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Page 1 of 135 http://www.talkshoe.com/talkshoe/web/talkCast.jsp?masterId=31043&cmd=tc ndoor Toxic Mold Awareness - September 5 to October 5, 2008 The Mold Controversy There are two schools of thought in the medical community: One group believes that molds cause allergic responses only (i.e. asthma, fungal sinusitis) and the other group has “scientific” evidence showing that inhalation of mycotoxins causes adverse health effects and not just allergic responses. » National Indoor Mold Society What is the purpose of National Indoor Toxic Mold Awareness Month? The purpose of National Indoor Toxic Mold Awareness Month is to inform, educate, and raise awareness about the adverse health effects due to exposure of indoor molds and mycotoxins. What are molds? Molds are a common name for fungi. Molds are microscopic organisms that produce enzymes to digest organic matter and mold spores to reproduce. These organisms are part of the fungi kingdom, a realm shared with mushrooms, yeast, and mildews. In nature, molds play a key role in the decomposition of leaves, wood, and other plant debris. Molds need moisture to grow. What are mycotoxins? Mycotoxins are toxic vapors produced by mold spores when they sporulate, or grow, and have serious health effects on humans and animals. Mycotoxins are so poisonous that they have been used as a biological war weapon. Stachybotrys chartarum is the most studied and well-known toxic mold. It is known to produce trichothecene mycotoxins. Aspergillus produces aflatoxin mycotoxins. Aflatoxins are among the most carcinogenic substances known. How do you get sick from mycotoxins? Mycotoxins enter the body through inhalation, ingestion, or contact with the skin, and can result in a multitude of symptoms including but not limited to: dermatitis, cough, rhinitis, nose bleeds, cold and flu-like symptoms, headache, general malaise and fever. How can exposure to indoor mold and mycotoxins affect my health? Mycotoxin exposure can lead to toxic injury that may include multiple illnesses, affecting the skin and the nervous, vascular, respiratory, digestive, reproductive, urinary, and immune systems; including the formation of cancers and can be life-threatening. Can mold grow inside the human body? Yes. Certain species of molds referred to as “body temperature molds” can live and grow inside

Transcript of ndoor Toxic Mold Awareness - September 5 to October 5,€¦ · One group believes that molds cause...

Page 1: ndoor Toxic Mold Awareness - September 5 to October 5,€¦ · One group believes that molds cause allergic responses only (i.e. asthma, fungal sinusitis) and the other group has

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http://www.talkshoe.com/talkshoe/web/talkCast.jsp?masterId=31043&cmd=tc

ndoor Toxic Mold Awareness - September 5 to October 5,

2008

The Mold Controversy

There are two schools of thought in the medical community:

One group believes that molds cause allergic responses only (i.e. asthma, fungal sinusitis) and the other group has “scientific” evidence showing that inhalation of mycotoxins causes adverse health effects and not just allergic

responses.

» National Indoor Mold Society

What is the purpose of National Indoor Toxic Mold Awareness Month?

The purpose of National Indoor Toxic Mold Awareness Month is to inform, educate, and raise

awareness about the adverse health effects due to exposure of indoor molds and mycotoxins.

What are molds?

Molds are a common name for fungi. Molds are microscopic organisms that produce enzymes to

digest organic matter and mold spores to reproduce. These organisms are part of the fungi

kingdom, a realm shared with mushrooms, yeast, and mildews. In nature, molds play a key role

in the decomposition of leaves, wood, and other plant debris. Molds need

moisture to grow.

What are mycotoxins?

Mycotoxins are toxic vapors produced by mold spores when they sporulate, or grow, and have

serious health effects on humans and animals. Mycotoxins are so poisonous that they have been

used as a biological war weapon. Stachybotrys chartarum is the most studied and well-known

toxic mold. It is known to produce trichothecene mycotoxins. Aspergillus produces aflatoxin

mycotoxins. Aflatoxins are among the most carcinogenic substances known.

How do you get sick from mycotoxins?

Mycotoxins enter the body through inhalation, ingestion, or contact with the skin, and can result

in a multitude of symptoms including but not limited to: dermatitis, cough, rhinitis, nose bleeds,

cold and flu-like symptoms, headache, general malaise and fever.

How can exposure to indoor mold and mycotoxins affect my health?

Mycotoxin exposure can lead to toxic injury that may include multiple illnesses, affecting the

skin and the nervous, vascular, respiratory, digestive, reproductive, urinary, and immune

systems; including the formation of cancers and can be life-threatening.

Can mold grow inside the human body?

Yes. Certain species of molds referred to as “body temperature molds” can live and grow inside

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the human body, causing recurring infections and numerous other health problems as well as

death.

Should I use bleach to clean mold?

No. Bleach combined with certain mycotoxins and VOC’s (Volatile Organic Compounds), can

create neurotoxins and brain tumors. OSHA does not recommend using bleach in mold

remediation. Ammonia dissolves some molds and neutralizes the mycotoxins. It is important to

follow safety guidelines when using cleaners to remove molds. Consult the EPA website for

proper personal safety equipment when removing mold. If mold growth is over 10 square feet,

the recommendation is to contact a professional who is experienced in cleaning up mold; either a

reputable, certified industrial hygienist (CIH) or a qualified mold remediation company.

Toxic Mold Fact Sheet

The National Indoor Toxic Mold Awareness Month Planning Committee developed this Toxic

Mold Fact Sheet to provide information about molds and mycotoxins. Currently, there are no

Federal Government Standards for indoor air quality regarding molds and mycotoxins. This

information is provided to inform the public on the preventable health and development

problems that may be caused by exposure to toxic mold in their homes, schools, and

communities.

Important Mold Facts: People are routinely exposed to more than 200 species of fungi indoors and outdoors. There are

sixty species that produce the 180 trichothecene mycotoxins. Mycotoxins kill other things, like

bacteria and viruses, so mold can continue to grow. The American Cancer Society lists aflatoxin

mycotoxins as known human carcinogens. The FDA has enforced regulatory limits on aflatoxin

concentrations in foods and feeds since 1965.

Mold spores, whether dead or alive, can cause adverse health effects. Molds also produce a large

number of volatile organic compounds (VOCs). These chemicals are responsible for the musty

odors produced by growing molds.

According to the U.S. Environmental Protection Agency (EPA):

There is no practical way to eliminate all molds and mold spores in the indoor

environment; the way to control indoor mold growth is to control moisture.

Molds can be found almost anywhere; they can grow on virtually any substance,

providing moisture is present. There are molds that can grow on wood, paper, carpet, and

foods.

Clean and dry any damp or wet building materials and furnishings within 24-48 hours to

prevent mold growth.

Incidences: It is estimated that 500,000 deaths occur yearly in the United States due to exposure to indoor

toxic mold.

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According to an EPA study, an estimated 50% of our nation’s schools have problems linked to

poor indoor air quality.

Health Causes: Mycotoxin exposure can lead to toxic injury that may include multiple illnesses, affecting the

skin and the nervous, vascular, respiratory, digestive, reproductive, urinary, and immune

systems; including the formation of cancers and can be life-threatening.

Studies: In the mid-1990's, a study conducted from Cleveland, Ohio, involved infants who had died

suddenly from unexplained pulmonary hemorrhage (bleeding of the lungs). Upon investigation,

the researchers found that the infants resided in homes with high levels of Stachybotrys atra,

linking Stachybotrys atra exposure to serious health effects and even death. A government study

is now being conducted, with findings to be released in 2010.

A 1997 Mayo Clinic study found that 96% of recurring sinus infections are caused by fungus in

the sinuses. When participants were treated with anti-fungal sinus sprays, recurrence of infection

was considerably less, and in some cases, no recurring infections were noted.

Fifty percent of the 937 children tested in a large multicity asthma study sponsored by the

National Institutes of Health showed sensitivity to mold, indicating the importance of mold as an

asthma trigger among these children. Molds are thought to play a role in asthma in several ways.

Molds produce many potentially allergenic compounds, and molds may play a role in asthma via

release of irritants that increase potential for sensitization or release of toxins (mycotoxins) that

affect immune response.

Letitia Peters, Executive Director

[email protected]

DISCLAIMER: The purpose of this fact sheet is to inform, not treat or offer legal counsel to the

public about

mold/mycotoxin health related issues. It is not intended to diagnose, treat, cure or prevent any

disease or take the place of medical advice and treatment from your personal physician, nor is it

intended to serve as legal counsel. Please consult your own doctor or other qualified health

professional regarding the treatment of your medical problem and consult your attorney for legal

counsel.

September 2014 marks the 6th annual Mold Awareness Month started by the National Indoor

Mold Society. Executive director Letitia Peters states: “The purpose of National Indoor Toxic

Mold Awareness Month is to inform, educate, and raise awareness about the adverse health

effects due to exposure of indoor molds and mycotoxins.”

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When mold invades schools, illness ensues

And, while it appears that the good work of Ms. Peters and NIMS has been terminated (she could

not be reached by email and her NIMS Facebook account has had no updates since 2010),

September as Mold Awareness Month continues to be in the news.

What are mycotoxins?

Mycotoxins are the toxic vapors produced by mold spores when they sporulate, or grow. These

toxins can have serious health effects for both humans and animals.

How bad are they?

Mycotoxins are so poisonous that they have been used as a biological war weapon.

One mold, Stachybotrys chartarum, is the most studied and well-known toxic mold. It produces

trichothecene, a mycotoxin so deadly it killed 100,000 people in the Soviet Union when they

were exposed to it in their food.

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Mold in public schools is a growing problem!

Another mold, Aspergillus, produces a mycotoxin called aflatoxin. Aflatoxins are among the

most carcinogenic substances known. The FDA has enforced regulatory limits on aflatoxin

concentrations in foods and feeds since 1965. However, currently there are still no Federal

Government Standards for indoor air quality regarding molds and mycotoxins.

So why have a “mold awareness month”?

There are about 1,000 species of mold that can be found in the United States, with more than

100,000 known species worldwide.

Not all of them are poisonous; not all people are allergic to molds and mycotoxins.

When a roof leaks, ceiling mold forms in this public school in Southern New Jersey

The Great Mold Debate There are two schools of thought in the medical community concerning mold and toxicity.

One group believes that molds only cause “allergic responses” like asthma or fungal sinusitis.

The second group has research data that provides compelling evidence demonstrating that

inhalation of mycotoxins can cause serious adverse health effects in some people – and not just

“allergic responses.” This second group of physicians report that the research data suggests a

strong relationship between exposure to these toxins and

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mold growth on a classroom ceiling

exacerbation of asthma

respiratory infections

and chronic sinus problems

as well as a host of other diseases including:

cancer

attention deficit disorder

multiple sclerosis

and

Parkinson’s Disease

However, because the debate continues in the medical community, there remain no federal

government standards for indoor air quality regarding molds and mycotoxins.

But why pick September for Mold Awareness Month?

There may be several reasons why Ms. Peters picked the month of September to designate as

“mold awareness month.” Perhaps it’s because summer heat and humidity increases the growth

of mold indoors. But, more likely it’s because September is also the month children across the

nation return to school.

Mold in Schools

A report by CNN in 2012 “Are Schools Making Kids Sick?” stated that one-third of U.S. schools

have mold, dust and other indoor air problems.

A national survey of school nurses found that 40% knew children and staff who were adversely

affected by indoor pollutants. In the CNN interview, allergist Dr. John Santilli, reported that he

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has treated dozens of students sickened by school air. “Even when children don’t miss school,”

he said, “the medications they take for asthma and conditions like rhinitis, an allergic reaction to

mold or dust, can make it harder for them to do their best work. They’re on antihistamines,

they’re on nasal sprays, they’re on asthma medications, and this limits their ability to perform,”

Santilli said. “These kids can’t concentrate. They can’t focus on what’s going on.”

Headaches, fatigue, memory problems and slowed thinking are all present in the people who are

susceptible – and this includes the students as well as the teachers!

The mold problem in schools is so prevalent in the U.S. that the Environmental Protection

Agency has published a guideline: Mold Remediation in Schools and Commercial Buildings

And, while there are still no federal governmental standards for indoor air quality, some state

governments, like the State of New York have developed their own guidelines.

Most recently, in response to John Lee’s Office of Long-Term Planning and Sustainability

testimony “that the asthma hospitalization rate in some New York City neighborhoods is now

four times the national average,” which he attributed in part to the mold problem, New York

City’s Mayor de Blasio signed into effect the Green Codes to Promote Environmentally Friendly

Building Practices and Legislation to Modify Business Improvement on May 19 of this year.

The new codes require the use of mold-resistant gypsum board or cement board in areas where

there is continuous high humidity or direct exposure to water to reduce hazardous mold growth.

But I don’t live in New York.

What can be done to prevent mold growth in my child’s school?

According to the Environmental Protection Agency (EPA):

There is no practical way to eliminate all molds and mold spores in the indoor

environment; the way to control indoor mold growth is to control moisture.

Molds can be found almost anywhere; they can grow on virtually any substance,

providing moisture is present. There are molds that can grow on wood, paper, carpet, and

foods.

Therefore, the only way to prevent mold growth is to find and correct water damage and

leaks and to clean and dry any damp or wet building materials and furnishings within 24-

48 hours.

What can I do if I think there’s mold in my child’s school?

While the City of Philadelphia and the State of New Jersey don’t currently have legislation that

require a change in building codes to decrease the prevalence of mold in schools, they do have

recommendations for safe remediation and removal of mold from schools on their respective

Department of Health websites.

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For more information for New Jersey Residents: NJ Department of Health

For more information for Pennsylvania Residents: PA Department of Health

But, most importantly, if you believe your child’s health is being adversely

affected by exposure to mold in their school, give us a call at 877-750-7876.

Our trained professionals follow the EPA, State of New York, Pennsylvania, and New

Jersey guidelines for safe removal and remediation of mold – in schools, businesses and

homes. We’ve helped hundreds of people throughout the Delaware Valley with fast, safe,

mold removal

DISCLAIMER:

This blog post is for informational purposes only.

The information is provided to inform the public on the preventable health and developmental

problems that may be caused by exposure to mold and mycotoxins in their homes, schools, and

communities.

It is not intended to diagnose, treat, cure or prevent any disease or take the place of medical

advice and treatment from your personal physician, nor is it intended to serve as legal counsel.

Please consult your own doctor or the mold illness treatment professionals listed here: “How to

Survive the Heartbreak of Illness Caused by Mold Exposure regarding the treatment of medical

problems arising from mold exposure.

http://www.blubrry.com/indoormold/

Dear Disstinguished Family of the Toxic Mold Community,

For the past several weeks, the National Indoor Mold Society has

spearheaded putting together a coalition of organizationsand

individuals suffering from toxic mold exposure to expose the truth

about this environmental disease. They are Sharon Pawlak (TN Toxic

Mold State Rep) of www.moldmadness.com, Iris Brooks (GA. Toxic Mold

State Rep) of www.myspace.com/faceoftoxicmold and Lori Tondini (IL

Toxic Mold State Rep), a former school administrative assistant and we

formed the National Indoor Toxic Mold Planning Committee.

WORKING TOGETHER FOR THE COMMON GOAL:

The National Indoor Toxic Mold Toxic Planning Committee has prepared

for publication the first Toxic Mold Proclamation observing the

upcoming National Indoor Toxic Mold Awareness Month, September 5 to

October 5, 2008. We were aware that in 2004, a group of organizations,

doctors, and mold advocates assembled for 1 week in September for the

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1stNational Mold Awareness Week. We have prepared a draft National

Indoor Toxic Mold Month Proclamation. We want to make a significant

impact on increasing mold research and dispelling myths that exposure

to toxic mold can not make you ill. We want to give a voice to the

voiceless, which we can only do by partnering together in order to

create one voice. Let's Break the Mold together! We hope that you will

join us in supporting this massive endeavor. Together our voices

will

be heard as we work to bring toxic mold exposure as a health care

epidemic. We invite all organizations (related to toxic mold

exposure/indoor environment/indoor air quality/illnesses caused by

toxic mold exposure i.e. autism, toxic encephalopathy),

environmental/mold specialists doctors, physicians, (some have already

committed to this effort), businesses (real estate/mold remediation/law

firms), clubs, schools, churches, groups, and individuals suffering due

to toxic mold exposure to join us in this event.

WHAT CAN YOU DO TO HELP MAKE THIS EVENT BE A SUCCESS?

1. Become an Indoor ToxicMoldState Proclamation Representative:

We have commitments from several individuals in NJ, GA, IL, TN, CO as

well as, one International Representative. The Indoor Toxic Mold State

ProclamationRepresentative can be an individual, business, doctor or

organization.

As an Indoor Toxic Mold State Representatives, you will be responsible

for obtaining a signed proclamation from your Governor and working to

develop an event in your state. The governor probably will not sign the

proclamation unless an event is taking place in his/her state. In order

to help those who want to obtain a signed proclamation from their

Governor, we are putting together a complete, easy-to-follow guide,

which outline the steps to get the National Indoor Toxic Mold Month

Proclamation signed. We hope to have as many of the states participate

for the 1st National Indoor Toxic Mold

Month.

The Indoor Toxic Mold State Representatives will be sent the

Proclamation Package, which contains the Proclamation, Fact Sheet, and

other supporting documentation.

2. Write Letters to Be Part of the Proclamation Supporting

Documentation:

We need letters of support from organizations, environmental doctors,

businesses, and individuals affected from toxic mold exposure to be

sent to your legislatorsand to the Governor emphasizing how this

proclamation will have a positive impact on the overall community.

3. PROPOSED EVENTS/ SPEAKERS/SPONSORS:

You can host an Indoor Toxic Mold Symposiumbringing in mold expert(s),

i.e. Environment Doctors/Mold Remediators/Toxic Mold Attorneys to speak

at your event. You can have it at your church, club, library, or

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school. You can set-up a booth at a local community event or health

fair. Please take pictures/videotape your event so that we can post

them on the websites.

NIMS will be hosting the National Indoor Mold Society Internet Talk

Show on Saturdays evenings starting on Saturday, September 6, 2008

-October 4, 2008 (up to Nov. 1, 2008). We can do these shows live in

various locations across the country. This could be done for 4 states.

The shows will be held on Saturdays evenings starting September 6

through November 1, 2008 from 8:00 P.M - 10:00 P.M. EST. There are 2

speakers on the show, each doing a 1 hr. segment.

A

0

We would like to have national and local sponsors for the event.

Sponsorship may include making a contribution to pay for the location

of the symposium/event, printing materials, ads about the event in

local and national newspapers, speaker's travel expenses, mailings,

tee-shirts, wristbands, DVDs for the Faces of Mold project, paying for

a booth at a community event, etc. You can be an anonymous sponsor as

well.

4. FACES OF MOLD DVD: Indoor Toxic Mold State Rep Lori Tondini has

sent me the following letter of intent for the FACES OF MOLD DVD-

please get your before mold exposure and after mold exposure pictures

to Lori. This is an exciting project!

LETTER OF INTENT FOR "FACES OF MOLD" DVD

I would like to put a dvd together, showing "faces" of mold victims.

Hopefully, I can get it done in time for all the National Indoor Toxic

Mold Awareness Month events, and have it playing in the background,

before presentations or something...I think we talked about it

before...what I need is info on your websites, asking mold victims to

e-mail a photo, and condensed info, Such as: Susie, 42, lawyer,

exposed at work, lungs/brain affected - something to that

effect...photos should be Jpeg only, and sent to: [email protected]

Depending on amount of pics received, will try to include all who send

me a picture...and hopefully

, I will get enough to put it together!

Those who email pics to me will not be compensated in any way, and I

will receive no monetary gain for preparing the dvd. No information or

photo will be used for any other purpose other than what has been

stipulated. The dvd will not be "sold" or dispersed to anyone other

than those who wish to use it in conjunction with an educational and

informative "mold event", to be played only to show that we are real,

normal people from all walks of life, ...no different from anyone

else.

Lori Tending, LT Productions

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5. Upcoming Conference Calls

The conference calls will occur on the following days this week: All

callers will be asked to announce their names. The conference calls

will last for 1 to 1 ½ hour. )

Saturday, July 26, 2008 (3:00 p.m. EST/2:00 p.m. CST/1:00 p.m.

MST/12:00 p.m. PST)

Tuesday, July 29, 2008 (11:00 a.m. EST/10:00 a.m. CST/9:00 a.m.

MST/8:00 a.m PST The Conference Dial-in Number: (712) 432-1620,

Participant Access Code: 938857#

Enclosed is the National Indoor Toxic Mold Awareness Month form for you

to review and complete. Thank you in advance for your support. All

information about the National Indoor Toxic Mold Awareness Month event

will be posted on the following websites:

www.nationalindoormoldsociety.org, www.moldmadness.com, and

www.myspace.com/faceoftoxicmold.We are currently finalizing the

National Indoor Toxic Mold=2

0Awareness Month proclamation, fact sheet,

and flyer, therefore, these documents will not be on the websites until

Monday, July 28, 2008.

If you have any questions ideas, or concerns, please contact one of the

National Indoor Toxic Mold Committee Members listed below or send an

e-mail to [email protected].

We look forward to hearing from you.

I would like to say a BIG "thank you" to Iris, Lori, and Sharon who

supported this endeavor.

Sincerely,

Letitia Peters

Executive Director, National Indoor Mold Society

"Helping to provide a voice for the voiceless"

General E-mail for the National Indoor Toxic Mold Month:

[email protected]

National Indoor Toxic Mold Month Proclamation Planning Committee

Members:

Chairperson: Letitia Peters, National Indoor Mold Society,

www.nationalindoormoldsociety.org

[email protected] 609-403-2046 (New Jersey Mold

State Representative)

Members:

Iris Harden, www.myspace.com/faceoftoxicmold, 706-595-7620

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(Georgia Mold State Representative)

Lori Tondini, [email protected] (Illinois Mold State

Representative)

Sharon Pawlak, Mold Madness, www.moldmadness.com, 931-670-2398

(Tennessee Toxic Mold State

Representative)__________________________________________________________

______________________________

NATIONAL INDOOR TOXIC MOLD AWARENESS

MONTH - 2008 FORM

PLEASE COMPLETE THE FORM AND E-MAIL IT TO THE APPLICABLE E-MAIL

ADDRESS:

Date: _________

Name: _

______________________________________

Name of Organization/Business: ____________________________________

Title: ________________________________________________

Address: ______________________________________________________

City: ___________________________ State:________ Zip Code:

_____________

Phone: __________________ â?° Home â?° Work â?°Mobile Best time to contact

you: _________EST/CST/MST/PST

Phone: __________________ â?° Home â?° Work â?°Mobileâ?° Best time to contact

you: _________EST/CST/MST/PST

FAX: _________________

Email: ______________________________________________________

Website: ______________________________________________________

PLEASE CHECK THE APPLICABLE BOX(ES):

â?° I WANT TO BE AN INDOOR TOXIC MOLD PROCLAMATION REPRESENTATIVE

FOR THE

STATE OF ________________________. (Your responsibilities will conclude

on October 5, 2008 or sooner (at the conclusion of your event after

getting the proclamation signed). This can be an organization, doctor,

business, school, club, or an individual suffering from toxic mold

exposure. We have indoor toxic mold proclamation reps in NJ, TN, IL,

and GA. (Please e-mail your form to [email protected].)

â?° I WANT TO TOXICMOLDSTATE REPRESENTATIVE FOR THE STATE OF

_____________________. (You will be the Toxic Mold Representative for

your state. This position will include educating people in your state

about the toxic mold, speaking with other mold victors in your state,

as well as, par

ticipating in getting the proclamation signed and

hosting an event in your state.) We have toxic mold state reps in NJ,

TN, IL, and GA. (Please e-mail your form to

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[email protected].)

â?°I WOULD LIKE TO HELP THE INDOOR TOXIC MOLD PROCLAMATION REP IN

THE

STATE OF ___________ TO HOST THE EVENT. (Please e-mail your form to

[email protected].)

â?°I WILL HOST/CO-HOST AN EVENT IN THE STATE OF ___________________.

(Please e-mail your form to [email protected].)

â?° I WOULD LIKE TO BE A SPEAKER ON THE NIMS INTERNET TALK SHOW. THE

SHOWS MAY BE LIVE, AS WELL AS, ON-LINE IN VARIOUS STATES. The shows

will be held on Saturdays evenings starting September 6 through

November 1, 2008 from 8:00 P.M - 10:00 P.M. EST. There are 2 speakers

on the show, each doing a 1 hr. segment. (A Speaker's form will be

e-mailed to you.) (Please e-mail your form to

[email protected].)

â?°I WOULD LIKE BE A PROSPECTIVE SPONSOR FOR THE NATIONAL INDOOR

TOXIC

MOLD AWARENESS MONTH. Sponsorship may include paying for the location

of the symposium/event, printing materials, ads about the event in

local and national newspapers, speaker's travel expenses, mailings,

tee-shirts, wristbands, paying for a booth at a community event, etc.

You can be an anonymous sponsor as well.

â?°I WOULD LIKE TO BE A LOCAL SPONSOR IN THE=2

0STATE OF _______.

â?°I WOULD LIKE TO BE A NATIONAL SPONSOR FOR THE NATIONAL

INDOOR TOXIC MOLD MONTH.

(Please email your form to [email protected].)

â?° I WOULD LIKE TO MAKE PHONE CALLS. (Please e-mail your form to

[email protected].)

â?° I WOULD LIKE TO SEND INFORMATION VIA COMPUTER. (Please e-mail your

form to [email protected].)

â?°I WOULD LIKE TO HELP! My skills include: __________________. (Please

e-mail your form to [email protected].)

â?° I HAVE QUESTIONS, IDEAS, SUGGESTIONS, OR CONCERNS: My questions,

ideas, or concerns are

______________________________________________________. (Please e-mail

your form to [email protected] if this was the only box checked,

otherwise, please send it to the other e-mail address.)

You can contact the National Indoor Mold Society at 609-403-2046 or

send any general questions, suggestions, or ideas about the event to

[email protected].

Copyright ©2008. National Indoor Mold Society, Inc. All Rights Reserved.

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To inform, educate, and bring awareness about how exposure to indoor molds and mycotoxins

can affect your health.

September 2009 marks the 2nd anniversary of National Indoor Mold Society’s National Indoor

Toxic Mold Awareness Month (NITMAM). We developed NITMAM to inform, educate, and

bring awareness about how exposure to indoor molds and mycotoxins can affect your health.

Currently, there are no Federal Government

Standards for indoor air quality regarding molds and mycotoxins. We all know that molds are

everywhere, but when an abundance of molds are indoors, given the right conditions they can

cause serious health consequences. Molds and the mycotoxins they produce have affected people

from all walks of life and ages. They do not discriminate; even some well-known celebrities have

been affected. Even if you can’t see or smell them in your school, workplace, or residence these

mycotoxins are capable of affecting you, your family, your co-workers, classmates, or loved

ones’ health. This information is provided to inform the public on the

preventable health and development problems that may be caused by exposure to toxic mold in

your homes,

schools, places of worship, and communities.

National Indoor Mold Society is committed to working in partnership with stakeholders,

international, national,and regional organizations. We invite organizations, health care

professionals, businesses, schools, places of worship, and individuals suffering due to toxic mold

exposure to join us in this event. Your help, no matter how

great or small your contribution to this effort may be, is needed and appreciated in order to

“spread the word”.

We would like to say a great big “thank you” for everyone who supported NITMAM 2008 and

now is supporting

NITMAM 2009.

We hope that you will join us in supporting this massive endeavor, which can only be done by

partnering together in order to create ONE VOICE. Let's Break the Mold together!

1. Mycotoxins kill other things, like bacteria and viruses, so mold can continue to grow.

2. Mold spores, whether dead or alive, can cause adverse health effects.

3. There is no practical way to eliminate all molds and mold spores in the indoor environment;

the way to control indoor mold growth is to control moistu

September is National Indoor Toxic Mold Awareness Month (N.I.T.M.A.M.)

Do you have health problems? Have you heard of "Sick Building Syndrome"? I didn't

either. I have never heard of the term "sick building syndrome" or that a building could

make you sick, because it was "...sick". I went from being basically a healthy woman with

allergies, which I acquired from being in one "sick" building for 7 years. My immune

system was slowly being compromised due to my daily exposure of indoor toxic molds and

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mycotoxins in several water-damaged buildings where I worked. Toxic Mold Exposure has

been linked to cause many diseases including CANCER. Many women develop breast

cancer. As a result, I have been diagnosed with fibromyalgia, chronic fatigue syndrome,

neuralgia, severe edema, asthma (developed full-blown asthma which required me to be on

an inhaler, but it went away after being out of the building for 1 year), toxic

encephalopathy, and reversible airways disease. I am doing my part to inform, educate,

and bring awareness to this environmental disease. Did you know that there are 500,000

deaths yearly in the U.S.A. due to exposure of indoor toxic mold exposure? Based on an

EPA study, they estimate that 50% of the nation's schools have problems linked to poor

indoor air quality. In the video, I also refer to a poem written by a 13 years old girl named

Arielle Murray called Mold..The Destroyer. If a child can understand the implications that

mold can do to one's body and quality of life, then why can't adults get it? I don't what has

happen to me to happen to others, especially to me, children. Children, like Arielle should

be enjoying their childhood and not go through this horrific disease. I know that I did.

September 2008 was the first National Indoor Toxic Mold Awareness Month. The Nevada

Legislature declared September 2009 as N.I.T.M.A.M. Let's Break the Mold Together!!

Please share this video with everyone that you know it may save someone's life.

BRIEF SYNOPSIS OF LETITIA PETERS' STORY:

Let me introduce myself, my name is Letitia Peters. I am a former Federal Government

Electronics Engineer turned activist and I live in the United States & Jesus/Yeshua has

allowed me to live through the most horrific atrocity of my life since 2009. I am a woman of

God who was intentionally selected to be in a “secret” human subject research program,

like the NSA’s PRISM research. I was working in a unhealthy, work environment in

Washington, DC for years, which caused me to develop a compromised immune system.

My former employer, the Federal Aviation Administration (F.A.A.) allowed us to work in a

workplace, which they knew was manifested with toxic mold. My once very healthy body

became compromised after working in it for over 7 years. First, my face starting to break

out. The NASSIF building was declared a sick building. People were dying in the 10 story,

4 quadrant building, which the U.S. Government was paying David Nassif $50 million a

year. We moved to the F.A.A. Headquarters and my body became more sensitive. They had

water damage and toxic mold started developing in the building. Even though they denied

having any water damage or mold in the building, other employees told me differently. A

doctor confirmed that I was suffering from “sick building syndrone”. I never heard of the

term before. Have you? One day, I received a phone call telling me that black mold was

growing in the cafeteria. I took pictures of the black mold that was growing in the ceiling of

the cafeteria, before they tried to cover-up this evidence. Then I had 2 break-ins 6 months

apart, after living there for over 10 years. My car was stolen so I took public transportation

or called a taxi. One day, I saw a male peeping through my basement window while I was

laying down on my sofa. Was I being watched and by whom? I was meeting with my

supervisor when the second break-in occurred. What were they looking for? There was no

investigation by the police, which I thought was strange. I published the toxic mold pictures

in my video, which is posted at www.youtube.com/NIMSOCIETY.

I was allowed to work temporarily into a fairly “new” building, which did not have any

water damage or mold. At first, I was not having any problems, until the furniture and

computer arrived from the “old building”. There was no decontamination of the furniture

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and the computer from the “old building”. By bringing the furniture and the computer

from the “old buiding” into the new environment the once contaminated free area became

contaminated because the mold spores were on them and they became air-borne. No one

was aware of “cross-contamination”, but this is what happened. I developed full-blown

asthma, severe edema, and was retaining 15 to 20 pounds of water weight. The pathologist

diagnosed me with late stage 2, early stage 3 of mycotoxicosis. Mycotoxins have been used

in biological warfare to kill people & here it was growing throughout my entire body. Since

my body was highly toxic, I ate organic foods only and took plenty of vitamins and

supplements. I developed a weight problem, despite not ever having one before. I was

working out like I had always done, but I was between 20 to 30 lbs. over my normal

weight.

After I was fired after 16 years of U.S. Federal Government service as an engineer, I

turned my anger into activism. I was forced to become an activist because I wanted to right

the wrong that was done to me. I started an organization called National Indoor Mold

Society or N.I.M.S. for short to bring awareness to the public & lawmakers that toxic mold

exposure can cause adverse health effects and even death. I interviewed many of the top

mold specialists in the U.S., which is available for download at www.TalkShoe.com. I

developed and produced a 6 hour live radio show dedicated to toxic mold with the top 6

mold specialists in the country, which received rave reviews. They only agreed to come on

the show after they checked me out to make sure that I was not a mole or double agent.

Unfortunately, I was not able to get a copy of the show from the radio station or the host of

the show. In 2008, I spearheaded the National Indoor Toxic Mold Awareness Month

(N.I.T.M.A.M.) with other mold activists and survivors. Their names are Sharon Pawlak,

Lori Tondini author of Are You Moldy: A True Story of a Very Moldy Person (I am

mentioned in her book), and Iris Brooks and we formed the National Indoor Toxic Mold

Planning Committee. We were also the Toxic Mold State Representatives as well. We

developed the N.I.T.M.A.M. Proclamation, which was signed by many Governors and it

was proclaimed in their states during the month of September 2008. I attended a

Proclamation Ceremony with the Georgia Governor in September 2009. The Nevada

legislature passed legislation declaring September 2009 as N.I.T.M.A.M. God told me to

close down N.I.M.S. because I had another fight to do at the time, which was intertwined.

N.I.T.M.A.M. is still being celebrated by organizations, survivors, and businesses in the

United States today every year in September. One survivor, Brandy B. is still submitting

the N.I.T.M.A.M. Proclamation in honor of the hard work that we did for the state of

Georgia every year. I sought the treatment from the top mold specialists & pathologist in

the country, like Dr. Ritchie Shoemaker, Dr. Kaye Kilburn, and Dr. William Croft. A

fellow mold survivor told me about a Holistic Practitioner, Barbara Frank who specialize

in the lymphatic system; her detoxing methods and products saved my life. I am still her

client today and I have referred several people to her for treatment of their diseases. Ms.

Frank has been providing health information for the “Heal Our Nations” Event. Her

website is www.BarbaraFrank222.com.

UPDATE: The Federal Government has cost me 20 years of my life, which I can never get back.

I was railroaded by a group of people, which was lead by one bitter woman who

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obviously hated me to put me and my family in this lifetime, generational human

subject research project. Like Edward Snowden, I knew people and I knew how the

system worked and I worked the system. I knew that I could not miss a deadline and I

did not. When I could not get reasonable accommodation, I applied for other jobs, but

I was not selected. The reason why it was strange was because I was selected out of a

nationwide competition for the position in Washington, DC. It was a GS-801 12/13/14

and I received many accolades (humbly speaking). The people at the F.A.A.T.C.

thought that I was going to be the F.A.A. Administrator. I worked with some

awesome guys. It was a male who told me that I outgrew the F.A.A.T.C. and I should

go to F.A.A. Headquarters.

I was awarded worker's compensation and then three months later, someone reverse it.

I sent letters, made phone calls, and NO ONE CONTACTED ME. I applied for civil

rights case. I was told that I had a good discrimination case. I hired one of the top

firms in Washington, DC. I was told that they were "milking me". After putting out

close to $10,000, I did not receive anything. Another firm wanted $25,000 for a

retainer fee, which was too high for my pockets. I had a year to apply for my

disability retirement, which I did. An attorney wanted to charge me $5,000 to do my

paperwork. In the meantime, I was dealing with the United States Merit Systems

Protection Board (U.S.M.S.P.B.), because of the unscrupulous & illegal tactics and I

sent them letters indicating the rules and regulations that they violated. Some tactics

included: backdate paperwork, said that I could work from home & then do not pay

me, overpay me & say that they made an error in order to "dock" me later, put me in

Leave Without Pay Status even when I had leave available on the books, which they

would not let me use & they refused to provide me reasonable accommodation with

proper medical documentation. The F.A.A. failed to send me COBRA paperwork.The

U.S.M.S.P.B. was another nightmare. Since I was a project scheduler, someone

intentionally compressed the dates that was impossible to meet, but with the help of

Yeshua, I did not miss one deadline. It was the F.A.A. who did not do one thing. They

tried to say that they did not receive the judge's order. I file motions for the judge to

rule on and he NEVER ruled on any of my motions. I should have WON. They were

timely and on point. The judge went on vacation and arrogantly told me that this was

his courtroom. This is the problem that the judge believe that they would do anything

that they want to in their courtroom regardless of the rules, statutes, & laws. I sent

him a 50 page fax to recuse himself as judge, which he refused. I went to my mailbox

and there was letter stating that I was awarded my disability retirement. I called the

judge and he process my paperwork that day stating so that I could not pursue this

issue against the F.A.A. again. He was more than too happy to get rid of me. The

U.S.M.S.P.B. needs to be reformed. The F.A.A. failed to process my paperwork. I

sent my complaint to the late Senator Lautenberg's office and they helped me. I was to

tired to file a complaint against the judge. I filed a tort claim and that did not go

through either. Despite having all the evidence and going through ALL the normal

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channels, I lost everywhere I turned. When I received the letter from O.P.M about my

disability retirement. I was happy.

Since I was fired the F.A.A., many employees have died from cancer, heart attacks,

strokes, or debilitating diseases. Many of them would not contribute their premature

deaths due to working in the water-damaged buildings in Washington, DC. One of my

remedies/reliefs that I mentioned in my affidavits was to help those who are still

working in those contaminated buildings in Washington, DC. They should be tested,

their homes, and they should receive health care or disability retirement. One of the

first casualties of the NASSIF BUILDING was a young mother who died working out

in the gym there. They should be compensated. My concern is for their families

because of cross-contamination. They have been bringing contamination from toxic

mold to their vehicles, homes, spouses, children, and grandchildren for years. Even

their pets can be exposed to toxic mold.

The 10 story, 4 quadrant building was GUTTED OUT after the Department of

Transportation (D.O.T.) left & moved into their new building. The D.O.T.

employees were told not to take ANYTHING from the NASSIF BUILDING not

even a pen. All papers were scanned. How much did this cost the U.S. Federal

Government or should I say the taxpayers?

In 2010, it was confirmed by the prophet, Jeanne S. that it was a group of people who

put me and 3 generations of my family into this secret, lifetime generational human

subject research project. After careful analysis, the only place that I worked was the

F.A.A. When I started working with this woman who had a problem with my work,

the manager came back and told me that he never had any problem with my work. I

always remembered that one question that she asked me as she was looking me up and

down "Is that sik?" I was wearing a silk pantsuit that I brought from Neiman-Marcus.

Joanne K. had it in for me. The prophet told me that people were jealous of me and

that I did not have a jealous bone in my body. Yes To Justice

DID EXPOSING TOXIC MOLD IN U.S. FEDS BUILDINGS CAUSE LETITIA PETERS

& 3 GENERATIONS OF HER FAMILY TO BE INTENTIONALLY SELECTED TO BE

IN A NON-CONSENSUAL HUMAN SUBJECT RESEARCH/MEDICAL

EXPERIMENT?

This video was made in September 2009. It has taken me years to figure out what was

happening to me. People would say that you are just having a “string of bad luck”, but this

“bad luck” did not end, it actually got WORST.

Did exposing contamination of toxic mold to FAA Senior Management in several Federal

Government buildings in Washington, DC caused my family, friends, and loved ones to be

placed into non-consensual human experiments for the rest of our lives? Did they think

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that they could do this, not to only to me, but to my family, friends, and loved ones because

minorities have been categorized as one of the “UNDESIRABLES”?

I reviewed my life for the past 8 years and I have come to one conclusion. It was

inconceivable at first, but based on my knowledge and the preponderance of facts staring

me in my face: We, including my family, friends, & loved ones have been placed in a non-

consensual human subject research/medical experiment because on my complaints and

exposure about toxic mold exposure in several Federal Government buildings in

Washington, DC. Is it possible because I am a “whistle blower”? Was it also inconceivable

because there was jealous and even some bigotry and racism?

I have cried so many times thinking how could anyone do this to any human being. They

have no right to play “god” with my life or the lives of anyone that I love. The sad thing is

that they do not care about what happens to me or my loved ones. I was taught not to hate.

My paternal grandmother was bi-racial. I pray that the mercy of God rests on their souls

for what they did to my family, friends, and loved ones. The Creator/Yawheh will be our

vindicator, refuge, healer, deliverer, fortress, & redeemer.

Do you have health problems? Have you heard of “Sick Building Syndrome”? I didn’t either

until 6 years ago. I have never heard of the term “sick building syndrome” or that a building

could make you sick, because it was “…sick”. I went from being basically a healthy woman with

allergies, which I acquired from being in one “sick” building for 7 years. My immune system

was slowly being compromised due to my daily exposure of indoor toxic molds and mycotoxins

in several water-damaged buildings where I worked. Toxic Mold Exposure has been linked to

cause many diseases including CANCER. Many women develop breast cancer. As a result, I

have been diagnosed with fibromyalgia, chronic fatigue syndrome, neuralgia, severe edema,

asthma (developed full-blown asthma which required me to be on an inhaler, but it disappeared

after I was out of the building for 1 year), toxic encephalopathy, and reversible airways disease. I

am doing my part to inform, educate, and bring awareness to this environmental disease. Did you

know that there are 500,000 deaths yearly in the U.S.A. due to exposure of indoor toxic mold

exposure? Based on an EPA study, they estimate that 50% of the nation’s schools have problems

linked to poor indoor air quality. In the video, I also refer to a poem written by a 13 years old girl

named Arielle Murray called Mold..The Destroyer. If a child can understand the implications

that mold can do to one’s body and quality of life, then why can’t adults get it? I don’t what has

happen to me to happen to others, especially to children. Children, like Arielle should be

enjoying their childhood and they should not have to go through this horrific disease. It is

written, “lack of knowledge my people will perish”. Let’s Break the Mold Together!! Please

share this video with everyone that you know it may save someone’s life. This video is located

at www.youtube.com/nimsociety.

WHAT ARE MOLDS AND MYCOTOXINS?

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We all know that molds are everywhere, but when an abundance of molds are indoors,

given the right conditions they can cause serious health consequences.

Molds are defined as microscopic forms of fungi.

Mycotoxins are toxins produced by certain molds which are poisonous to animals and

man.

There are over 100,000 species of molds.

About three dozen cause health problems in humans.

EPA, FEMA and CDC government agencies agree that mold starts to grow and spread

24 to 48 hours after water damage.

We have known for a long time about the health effects of molds:

History of Molds

Molds are mentioned in Leviticus in the Bible (Chapter 14) • Molds were used by the Spartans in

their war against Athens in 430 B.C. • There were 65 mold epidemics worldwide between 1591

and 1889 • 1920’s: Fatal kidney disease caused by mold in Denmark and the Balkans • 1930’s:

Stachybotrycosis:30% of horses in Russia from eating moldy hay • 1944: Alimentary Toxic

Aleukia epidemic in Russia from eating moldy bread; 10% of the population was affected and it

was often fatal • 1952: Aflatoxicosis: killed poultry that ate moldy corn (Aspergillus)

Biological Warfare • Used in Southeast Asia from 1974-1981

Indoor molds and the mycotoxins they produce have affected people from all walks of life and

ages. They do not discriminate; even some well-known celebrities have been affected. Even if

you can’t see or smell them in your school, workplace, or residence these mycotoxins are

capable of affecting you, your family, your co-workers, classmates, or loved ones’ health.

WHAT’S THE CONTROVERSY?

First, there are two schools of thoughts in the medical community:

One group believes that molds cause allergic responses only (i.e. asthma, fungal sinusitis) and

the other group has “scientific” evidence showing that inhalation to mycotoxins causes adverse

health effects and not just allergic responses only, but the controversy continues.

Second, we do not have any federal laws governing indoor air quality for molds.

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Finally, we have two bills pending, which are stalled in the U.S. Congress.

What is the purpose of National Indoor Toxic Mold Awareness Month?

The purpose of National Indoor Toxic Mold Awareness Month is to inform, educate, and raise

awareness about the adverse health effects due to exposure of indoor molds and mycotoxins.

What are molds?

Molds are a common name for fungi. Molds are microscopic organisms that produce enzymes to

digest organic matter and mold spores to reproduce. These organisms are part of the fungi

kingdom, a realm shared with mushrooms, yeast, and mildews. In nature, molds play a key role

in the decomposition of leaves, wood, and other plant debris. Molds need moisture to grow.

What are mycotoxins?

Mycotoxins are toxic vapors produced by mold spores when they sporulate, or grow, and have

serious health effects on humans and animals. Mycotoxins are so poisonous that they have been

used as a biological war weapon. Stachybotrys chartarum is the most studied and well-known

toxic mold. It is known to produce trichothecene mycotoxins. Aspergillus produces aflatoxin

mycotoxins. Aflatoxins are among the most carcinogenic substances known.

How do you get sick from mycotoxins?

Mycotoxins enter the body through inhalation, ingestion, or contact with the skin, and can result

in a multitude of symptoms including but not limited to: dermatitis, cough, rhinitis, nose bleeds,

cold and flu-like symptoms, headache, general malaise and fever.

How can exposure to indoor mold and mycotoxins affect my health?

Mycotoxin exposure can lead to toxic injury that may include multiple illnesses, affecting the

skin and the nervous, vascular, respiratory, digestive, reproductive, urinary, and immune

systems; including the formation of cancers and can be life-threatening.

Can mold grow inside the human body?

Yes. Certain species of molds referred to as “body temperature molds” can live and grow inside

the human body, causing recurring infections and numerous other health problems as well as

death.

Should I use bleach to clean mold?

No. Bleach combined with certain mycotoxins and VOC’s (Volatile Organic Compounds), can

create neurotoxins and brain tumors. OSHA does not recommend using bleach in mold

remediation. Ammonia dissolves some molds and neutralizes the mycotoxins. It is important to

follow safety guidelines when using cleaners to remove molds. Consult the EPA website for

proper personal safety equipment when removing mold. If mold growth is over 10 square feet,

the recommendation is to contact a professional who is experienced in cleaning up mold; either a

reputable, certified industrial hygienist (CIH) or a qualified mold remediation company.

Toxic Mold Fact Sheet

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The National Indoor Toxic Mold Awareness Month Planning Committee developed this Toxic

Mold Fact Sheet to provide information about molds and mycotoxins. Currently, there are no

Federal Government Standards for indoor air quality regarding molds and mycotoxins. This

information is provided to inform the public on the preventable health and development

problems that may be caused by exposure to toxic mold in their homes, schools, and

communities.

Important Mold Facts: People are routinely exposed to more than 200 species of fungi indoors and outdoors. There are

sixty species that produce the 180 trichothecene mycotoxins. Mycotoxins kill other things, like

bacteria and viruses, so mold can continue to grow. The American Cancer Society lists aflatoxin

mycotoxins as known human carcinogens. The FDA has enforced regulatory limits on aflatoxin

concentrations in foods and feeds since 1965.

Mold spores, whether dead or alive, can cause adverse health effects. Molds also produce a large

number of volatile organic compounds (VOCs). These chemicals are responsible for the musty

odors produced by growing molds.

According to the U.S. Environmental Protection Agency (EPA):

There is no practical way to eliminate all molds and mold spores in the indoor

environment; the way to control indoor mold growth is to control moisture.

Molds can be found almost anywhere; they can grow on virtually any substance,

providing moisture is present. There are molds that can grow on wood, paper, carpet, and

foods.

Clean and dry any damp or wet building materials and furnishings within 24-48 hours to

prevent mold growth.

Incidences: It is estimated that 500,000 deaths occur yearly in the United States due to exposure to indoor

toxic mold.

According to an EPA study, an estimated 50% of our nation’s schools have problems linked to

poor indoor air quality.

Health Causes: Mycotoxin exposure can lead to toxic injury that may include multiple illnesses, affecting the

skin and the nervous, vascular, respiratory, digestive, reproductive, urinary, and immune

systems; including the formation of cancers and can be life-threatening.

Studies: In the mid-1990’s, a study conducted from Cleveland, Ohio, involved infants who had died

suddenly from unexplained pulmonary hemorrhage (bleeding of the lungs). Upon investigation,

the researchers found that the infants resided in homes with high levels of Stachybotrys atra,

linking Stachybotrys atra exposure to serious health effects and even death. A government study

is now being conducted, with findings to be released in 2010.

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A 1997 Mayo Clinic study found that 96% of recurring sinus infections are caused by fungus in

the sinuses. When participants were treated with anti-fungal sinus sprays, recurrence of infection

was considerably less, and in some cases, no recurring infections were noted.

Fifty percent of the 937 children tested in a large multicity asthma study sponsored by the

National Institutes of Health showed sensitivity to mold, indicating the importance of mold as an

asthma trigger among these children. Molds are thought to play a role in asthma in several ways.

Molds produce many potentially allergenic compounds, and molds may play a role in asthma via

release of irritants that increase potential for sensitization or release of toxins (mycotoxins) that

affect immune response.

DISCLAIMER: The purpose of this fact sheet is to inform, not treat or offer legal counsel to the

public about mold/mycotoxin health related issues. It is not intended to diagnose, treat, cure or

prevent any disease or take the place of medical advice and treatment from your personal

physician, nor is it intended to serve as legal counsel. Please consult your own doctor or other

qualified health professional regarding the treatment of your medical problem and consult your

attorney for legal counsel.

What is the purpose of National Indoor Toxic Mold Awareness Month? The purpose of National Indoor Toxic Mold Awareness Month is to inform, educate, and raise

awareness about the adverse health effects due to exposure of indoor molds and mycotoxins.

What are molds? Molds are a common name for fungi. Molds are microscopic organisms that produce enzymes to

digest organic matter and mold spores to reproduce. These organisms are part of the fungi

kingdom, a realm shared with mushrooms, yeast, and mildews. In nature, molds play a key role

in the decomposition of leaves, wood, and other plant debris. Molds need moisture to grow.

What are mycotoxins? Mycotoxins are toxic vapors produced by mold spores when they sporulate, or grow, and have

serious health effects on humans and animals. Mycotoxins are so poisonous that they have been

used as a biological war weapon. Stachybotrys chartarum is the most studied and well-known

toxic mold. It is known to produce trichothecene mycotoxins. Aspergillus produces aflatoxin

mycotoxins. Aflatoxins are among the most carcinogenic substances known.

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How do you get sick from mycotoxins? Mycotoxins enter the body through inhalation, ingestion, or contact with the skin, and can result

in a multitude of symptoms including but not limited to: dermatitis, cough, rhinitis, nose bleeds,

cold and flu-like symptoms, headache, general malaise and fever.

How can exposure to indoor mold and mycotoxins affect my health? Mycotoxin exposure can lead to toxic injury that may include multiple illnesses, affecting the

skin and the nervous, vascular, respiratory, digestive, reproductive, urinary, and immune

systems; including the formation of cancers and can be life-threatening.

Can mold grow inside the human body? Yes. Certain species of molds referred to as “body temperature molds” can live and grow inside

the human body, causing recurring infections and numerous other health problems as well as

death.

Should I use bleach to clean mold? No. Bleach combined with certain mycotoxins and VOC’s (Volatile Organic Compounds), can

create neurotoxins and brain tumors. OSHA does not recommend using bleach in mold

remediation. Ammonia dissolves some molds and neutralizes the mycotoxins. It is important to

follow safety guidelines when using cleaners to remove molds. Consult the EPA website for

proper personal safety equipment when removing mold. If mold growth is over 10 square feet,

the recommendation is to contact a professional who is experienced in cleaning up mold; either a

reputable, certified industrial hygienist (CIH) or a qualified mold remediation company.

Toxic Mold Fact Sheet

The National Indoor Toxic Mold Awareness Month Planning Committee developed this Toxic

Mold Fact Sheet to provide information about molds and mycotoxins. Currently, there are no

Federal Government Standards for indoor air quality regarding molds and mycotoxins. This

information is provided to inform the public on the preventable health and development

problems that may be caused by exposure to toxic mold in their homes, schools, and

communities.

Important Mold Facts: People are routinely exposed to more than 200 species of fungi indoors

and outdoors. There are sixty species that produce the 180 trichothecene mycotoxins.

Mycotoxins kill other things, like bacteria and viruses, so mold can continue to grow. The

American Cancer Society lists aflatoxin mycotoxins as known human carcinogens. The FDA has

enforced regulatory limits on aflatoxin concentrations in foods and feeds since 1965.

Mold spores, whether dead or alive, can cause adverse health effects. Molds also produce a large

number of volatile organic compounds (VOCs). These chemicals are responsible for the musty

odors produced by growing molds.

According to the U.S. Environmental Protection Agency (EPA):

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There is no practical way to eliminate all molds and mold spores in the indoor

environment; the way to control indoor mold growth is to control moisture.

Molds can be found almost anywhere; they can grow on virtually any substance,

providing moisture is present. There are molds that can grow on wood, paper, carpet, and

foods.

Clean and dry any damp or wet building materials and furnishings within 24-48 hours to

prevent mold growth.

Incidences: It is estimated that 500,000 deaths occur yearly in the United States due to exposure

to indoor toxic mold. According to an EPA study, an estimated 50% of our nation’s schools have

problems linked to poor indoor air quality.

Health Causes: Mycotoxin exposure can lead to toxic injury that may include multiple illnesses,

affecting the skin and the nervous, vascular, respiratory, digestive, reproductive, urinary, and

immune systems; including the formation of cancers and can be life-threatening.

Studies: In the mid-1990’s, a study conducted from Cleveland, Ohio, involved infants who had

died suddenly from unexplained pulmonary hemorrhage (bleeding of the lungs). Upon

investigation, the researchers found that the infants resided in homes with high levels of

Stachybotrys atra, linking Stachybotrys atra exposure to serious health effects and even death.

A 1997 Mayo Clinic study found that 96% of recurring sinus infections are caused by fungus in

the sinuses. When participants were treated with anti-fungal sinus sprays, recurrence of infection

was considerably less, and in some cases, no recurring infections were noted.

Fifty percent of the 937 children tested in a large multicity asthma study sponsored by the

National Institutes of Health showed sensitivity to mold, indicating the importance of mold as an

asthma trigger among these children. Molds are thought to play a role in asthma in several ways.

Molds produce many potentially allergenic compounds, and molds may play a role in asthma via

release of irritants that increase potential for sensitization or release of toxins (mycotoxins) that

affect immune response.

Letitia Peters, Executive Director [email protected]

DISCLAIMER: The purpose of this fact sheet is to inform, not treat or offer legal counsel to the

public about mold/mycotoxin health related issues. It is not intended to diagnose, treat, cure or

prevent any disease or take the place of medical advice and treatment from your personal

physician, nor is it intended to serve as legal counsel. Please consult your own doctor or other

qualified health professional regarding the treatment of your medical problem and consult your

attorney for legal counsel.

Jun 7

Smart? Are We Electromagnetic Radiation Guinea Pigs?

Someone agrees with me. We are electromagnetic radiation guinea pigs.

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Page 26 of 135

Posted 2 years ago

Jun 7

Int’l Call for Action for those who are Monitored, Targeted, Tortured, &

Tracked w/ Information & Communications Tech by Fellow Citizens Worldwide

INTERNATIONAL SPIRITUAL AWAKENING MINISTRIES

FOR IMMEDIATE RELEASE

CONTACT: Letitia Peters

Phone: 347-568-3537

Website: www.digitalgunsforhire.tumblr.com

Emails: [email protected] or [email protected]

INTERNATIONAL CALL FOR ACTION FOR THOSE WHO ARE MONITORED,

TARGETED, TORTURED, & TRACKED WITH INFORMATION &

COMMUNICATIONS TECHNOLOGY BY FELLOW CITIZENS WORLDWIDE

“Citizens Want Justice for Human Rights Violations Now in America and Other Nations”

June 7, 2012-Trenton, NJ- Human rights should be fundamental rights for all people, regardless

of race, creed, gender or religion, but it isn’t in 2012. Recently, President Obama launched a new

campaign against human rights violators and to stop genocide worldwide. A video clip of

President Obama’s speech is available for your review at

http://www.cbn.com/media/player/index.aspx?s=/CWN/CWN042712_WS.

On April 23, 2012, President Obama issued an Executive Order which states …”determine that

the commission of serious human rights abuses against the people of Iran and Syria by their

governments, facilitated by computer and network disruption, monitoring, and tracking by those

governments, and abetted by entities in Iran and Syria that are complicit in their governments’

malign use of technology for those purposes, threaten the national security and foreign policy of

the United States. The Governments of Iran and Syria are endeavoring to rapidly upgrade their

technological ability to conduct such activities. Cognizant of the vital importance of providing

technology that enables the Iranian and Syrian people to freely communicate with each other and

the outside world, as well as the preservation, to the extent possible, of global

telecommunications supply chains for essential products and services to enable the free flow of

information, the measures in this order are designed primarily to address the need to prevent

entities located in whole or in part in Iran and Syria from facilitating or committing serious

human rights abuses.” You can read the full text of President Obama’s Executive Order at

http://blog.alexanderhiggins.com/2012/04/23/obama-declares-syria-national-emergency-outlaws-

reporting-rebels-126061/.

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According to the Los Angeles Times article, “U.S. put sanctions on telecom firms in Syria, Iran”

states, “There are other countries, perhaps, China, Cuba, or Russia, where technology firms are

also state-controlled and may also be implicated in human rights abuses,” Howard said. “It could

open the door to other kinds of diplomatic actions. The Syrian General Intelligence Directorate

has been implicated in serious human rights abuses, such as arbitrary arrests and the deaths of

detainees. Datak Telecom, an Internet Service provider in Iran, collaborated with the government

there to monitor, track and target people who tried to get around the regime’s blocking of

Internet content. You can read the full text of this article at

http://articles.latimes.com/2012/apr/23/business/la-fi-obama-tech-sanctions-20120424.

Even though America has been the forerunner for human rights in other nations, a group of

Americans are speaking out against America’s silent secret. Letitia Peters, an advocate and

survivor states, “We applaud America for its efforts to saving countless of lives worldwide for

human rights violators, but now Americans need you the help of America to stop human rights

violators and genocide in America. Our rights are not being enforced and the victims feel

powerless. We have severe network and computer disruptions just like the people in Syria and

Iran. We are being monitored, tracked, and targeted with information technology, but it also

includes torture with information and communications technology. Many of us are experiencing

cyber-bullying, phishing, and masquerading as well. This is happening in America, Europe,

Canada, and many other nations. I recently watched this Lifetime Movie called “Shadow of

Fear”,which is a true story of a young waitress and her terrifying experiences with a

schizophrenic stalker. When she turns to the police to help, they actually try to arrest her.

She finally learns that the stalker is well connected and that is why his records are

SEALED and she cannot get any help from the police. She just wants him to leave her

alone. Distraught, Casey (waitress) begins to withdraw from life. But when Morgan

(schizophrenic stalker) crosses the line and hurts the people Casey loves, she must find the

strength inside herself to stop living in fear, and finally put a stop to this dangerous

attraction. This story sounds like the life that many of us are living daily, but on a much

larger scale. She only dealt with this for 1 year and many of us have been dealing us this for

10, 15, and 20 years. I recently got this letter from President Obama about his latest campaign

and I pray that Congress, International leaders and local leaders will support to stop genocide and

human rights violators in America and worldwide now. This is a well orchestrated organization

with informants, perps, or contractors who are preventing this information from getting to the

right people to investigate these atrocities in America and worldwide. Many of us have sent our

request to opt-out of this unethical human subject research to Health and Human Services

Secretary Kathleen Sebelius, but to date, we have not heard from her. This is not only a moral

issue, but this is also a religious issue for many of us. I decree in Jesus’ name that the TIs will no

longer allow “fear” to control them, but that they will find the strength inside to stop living in

fear and do everything possible to work towards getting your life back. We can only stop this

evil by coming together and it is time to come together now while the door of opportunity is

opened. In a recent Public Broadcasting Service (PBS) documentary, Swimming In Auschwitz

(www.swimminginauschwitz.com), which depicts the stories of 6 survivors of the Holocaust,

one of the survivors said, “We made a big mistake. We never spoke up.”As a result of them

not speaking up, over six million Jewish men, women, and children were tortured,

executed, and killed. Do we want history to repeat itself? ” Is there a remnant of people who

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Page 28 of 135

will stand up for justice like they did for Trayvon Martin? It is us today, but it could be you and

your loved ones tomorrow?

White House’s Response

Letitia’s letter from President Obama dated June 4, 2012

THE WHITE HOUSE

June 4, 2012

Dear Letitia:

Thank you for sharing your thoughts with me. Many Americans have written to me about

human rights around the world, and I appreciate your perspective.

The United States was founded on the principles of freedom and equality, and our history is

marked with triumphs and struggles in fulfilling these timeless ideals. Our task is not finished,

and

protecting these core values is a shared obligation and a priority for my Administration. No

nation

should be silent in the fight against human rights violations. When innocents in places like

Sudan,

Syria, and the Democratic Republic of Congo are raped, murdered, or tortured, it is a stain on our

collective conscience. I am committed to reinvigorating America’s leadership on a range of

international human rights issues.

As the struggle for human rights continues around the world, we have witnessed an

extraordinary change in the Middle East and NorthAfrica. Country by country, people have risen

up

across this region to demand their human rights; too often, these calls for change have been

answered

by violence. The United States opposes the use of violence and repression against these men and

women. Rather, we support a set of universal rights, including free speech, the freedom of

peaceful

assembly, freedom of religion, equality for men and women under the rule of law, and the right

of

people to choose their own leaders. We also support political and economic reform in the Middle

East and North Africa that can meet the legitimate aspirations of ordinary people throughout the

region. While change may not come easily, America will stand squarely on the side of those who

are

reaching for their rights, knowing their success will bring about a world that is more peaceful,

more

stable, and more just.

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Page 29 of 135

As you may know, the United States has joined the United Nations Human Rights Council and

is working to make this body as effective as possible. My Administration will also advocate for

human rights in other international settings. In our relations with other countries, the issue of

human

rights will continue to be raised as clearly, persistently, and effectively as possible. Among other

things,we will continue to promote accountability for mass atrocities; respect for the rights of

minorities and women; freedom of association, speech, and religion; and freedom for people to

live

as they choose and love whom they chose.

Our commitment to human rights is an essential element of American foreign policy and

serves our national security. Through it, we will help to shut down torture chambers, replace

tyranny

with good governance, and enlist free nations in the common cause of liberty. To learn more

about

my Administration’s human rights agenda, please visit www.HumanRights.gov or

www.WhiteHouse.gov/CPo. Thank you, again, for writing.

Sincerely,

Barack Obama

We are suffering severely, but let that stop you from seeking justice. We request the support of

all survivors to contact the following this week.

1. This is for International and National Survivors. Department of Homeland Security:

Immigration and Customs Enforcement:

Human Rights Law Division; Human Rights Violators and War Crimes Unit Contact: http://www.ice.gov/contact/inv/

URL: http://www.ice.gov/human-rights-violators/

Tip Line: 1-866-DHS-2-ICE (1-866-347-2423)

Victim Witness Assistance: 1-866-872-4973

Public Service Announcement: http://www.ice.gov/human-rights-violators/

Human rights violators, including those who have participated in war crimes and acts of

genocide, torture, extrajudicial killing, violations of religious freedom, and other acts of

persecution, frequently seek to evade justice by seeking shelter in the United States. These

individuals will frequently assume fraudulent identities to enter the country, seeking to blend into

American society and communities.

ICE places a high priority on targeting serious offenders through its Human Rights Violators and

War Crimes Unit. The unit mission is twofold. The first part is to prevent the admission of

foreign war crimes suspects, persecutors and human rights abusers into the United States. The

second part is to identify, prosecute and ultimately remove such offenders who are already

unlawfully in the United States and who have committed acts ranging from genocide, torture and

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Page 30 of 135

war crimes to serious violations of religious freedoms or other forms of persecution. In

performing both missions, we work closely with our counterpart the Human Rights Law Division

(HRLD).

2. Inter-America Commission on Human Rights at http://www.oas.org/en/iachr/ There are 2

reports to download to read. Inter-American Commission on Human Rights

1889 F Street, N. W.

Washington, D.C. 20006

USA and/or by fax to the following number 1-202-458-3992. Contact their office at: 1 (202)

458-3000

3. UN Working Group on Arbitrary Detention

http://www.ohchr.org/EN/Issues/Detention/Pages/WGADIndex.aspx

Select individual complaints; many may want to use the urgent appeal process.

4. Send this press release and your story to your Congressional and State Representatives and

request oversight and investigative hearings. You can find your representatives at

www.senate.gov and www.house.gov.

5. U.S. Attorneys are empowered to investigate suspected or alleged offenses against the United

States. You can locate your representative at http://www.justice.gov/usao/.

6. The Attorney General (AG) can create task forces. The Special Counsel Regulations of 1999

require the AG to appoint a Special Counsel from outside the Government when three conditions

are met: (1) he determines that a criminal investigation of a person or matter is warranted; (2) it

would present a conflict of interest for DOJ to conduct the investigation, or any subsequent

prosecution(s); and (3) the appointment of a Special Counsel would serve the public interest.

You can visithttp://www.justice.gov/ag/ to write to Attorney General Eric Holder and you can

contact your local U.S. Attorney for your state as well.

7. Contact Secretary of State Hillary Clinton at www.state.gov. Leave a comment at 202-647-

5291 or via fax at 202-647-8947. We need as many non-Americans to send her a letter.

We suggest that this note is included on every correspondence to let those who are obstructing

justice that there will be on held accountable for their actions. NOTE: “Whoever intentionally

obstruct the proceedings before depts., agencies, and committees, obstruct this criminal

investigation and/or retaliate against me because I am a

victim, you will be punished to the full extent of the applicable[law in 1505 of Title 18

Obstruction of proceedings before depts., agencies & committees, 1510 Obstruction of

Criminal investigations, 1513 of Title 18 Retaliating against a witness, victim or an

informant, or 1514 Civil Action to restrain harassment of a victim or witness. Whoever

intentionally alters, destroys, mutilates or conceals records, or documents with the intent to

impair the object’s integrity or availability for use in an official proceeding will be

punished to the full extent of law as defined in 1519 of Title 18 Destruction, Alteration or

Falsification of records in Federal investigations and bankruptcy.”

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In closing, Kofi Annan, Secretary-general of the United Nations said, “Human Rights are what

reason requires and conscience demands. They are us and we are them. Human rights are rights

that any person has as a human being. We are all human beings; we are all deserving of human

rights. One cannot be true without the other.” Amen

If you have any questions, please contact us via email or phone.

# # #

Posted 2 years ago

Jun 7

Int’l Call for Action for those who are Monitored, Targeted, Tortured, &

Tracked w/ Information & Communications Tech by Fellow Citizens Worldwide

INTERNATIONAL CALL FOR ACTION FOR THOSE WHO ARE MONITORED,

TARGETED, TORTURED, & TRACKED WITH INFORMATION &

COMMUNICATIONS TECHNOLOGY BY FELLOW CITIZENS WORLDWIDE

“Citizens Want Justice for Human Rights Violations Now in America and Other Nations”

June 7, 2012-Trenton, NJ- Human rights should be fundamental rights for all people, regardless

of race, creed, gender or religion, but it isn’t in 2012. Recently, President Obama launched a new

campaign against human rights violators and to stop genocide worldwide. A video clip of

President Obama’s speech is available for your review at

http://www.cbn.com/media/player/index.aspx?s=/CWN/CWN042712_WS.

On April 23, 2012, President Obama issued an Executive Order which states …”determine that

the commission of serious human rights abuses against the people of Iran and Syria by their

governments, facilitated by computer and network disruption, monitoring, and tracking by those

governments, and abetted by entities in Iran and Syria that are complicit in their governments’

malign use of technology for those purposes, threaten the national security and foreign policy of

the United States. The Governments of Iran and Syria are endeavoring to rapidly upgrade their

technological ability to conduct such activities. Cognizant of the vital importance of providing

technology that enables the Iranian and Syrian people to freely communicate with each other and

the outside world, as well as the preservation, to the extent possible, of global

telecommunications supply chains for essential products and services to enable the free flow of

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Page 32 of 135

information, the measures in this order are designed primarily to address the need to prevent

entities located in whole or in part in Iran and Syria from facilitating or committing serious

human rights abuses.” You can read the full text of President Obama’s Executive Order at

http://blog.alexanderhiggins.com/2012/04/23/obama-declares-syria-national-emergency-outlaws-

reporting-rebels-126061/.

According to the Los Angeles Times article, “U.S. put sanctions on telecom firms in Syria, Iran”

states, “There are other countries, perhaps, China, Cuba, or Russia, where technology firms are

also state-controlled and may also be implicated in human rights abuses,” Howard said. “It could

open the door to other kinds of diplomatic actions. The Syrian General Intelligence Directorate

has been implicated in serious human rights abuses, such as arbitrary arrests and the deaths of

detainees. Datak Telecom, an Internet Service provider in Iran, collaborated with the government

there to monitor, track and target people who tried to get around the regime’s blocking of

Internet content. You can read the full text of this article at

http://articles.latimes.com/2012/apr/23/business/la-fi-obama-tech-sanctions-20120424.

Even though America has been the forerunner for human rights in other nations, a group of

Americans are speaking out against America’s silent secret. Letitia Peters, an advocate and

survivor states, “We applaud America for its efforts to saving countless of lives worldwide for

human rights violators, but now Americans need you the help of America to stop human rights

violators and genocide in America. Our rights are not being enforced and the victims feel

powerless. We have severe network and computer disruptions just like the people in Syria and

Iran. We are being monitored, tracked, and targeted with information technology, but it also

includes torture with information and communications technology. Many of us are experiencing

cyber-bullying, phishing, and masquerading as well. This is happening in America, Europe,

Canada, and many other nations. I recently watched this Lifetime Movie called “Shadow of

Fear”,which is a true story of a young waitress and her terrifying experiences with a

schizophrenic stalker. When she turns to the police to help, they actually try to arrest her.

She finally learns that the stalker is well connected and that is why his records are

SEALED and she cannot get any help from the police. She just wants him to leave her

alone. Distraught, Casey (waitress) begins to withdraw from life. But when Morgan

(schizophrenic stalker) crosses the line and hurts the people Casey loves, she must find the

strength inside herself to stop living in fear, and finally put a stop to this dangerous

attraction. This story sounds like the life that many of us are living daily, but on a much

larger scale. She only dealt with this for 1 year and many of us have been dealing us this for

10, 15, and 20 years. I recently got this letter from President Obama about his latest campaign

and I pray that Congress, International leaders and local leaders will support to stop genocide and

human rights violators in America and worldwide now. This is a well orchestrated organization

with informants, perps, or contractors who are preventing this information from getting to the

right people to investigate these atrocities in America and worldwide. Many of us have sent our

request to opt-out of this unethical human subject research to Health and Human Services

Secretary Kathleen Sebelius, but to date, we have not heard from her. This is not only a moral

issue, but this is also a religious issue for many of us. I decree in Jesus’ name that the TIs will no

longer allow “fear” to control them, but that they will find the strength inside to stop living in

fear and do everything possible to work towards getting your life back. We can only stop this

evil by coming together and it is time to come together now while the door of opportunity is

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Page 33 of 135

opened. In a recent Public Broadcasting Service (PBS) documentary, Swimming In Auschwitz

(www.swimminginauschwitz.com), which depicts the stories of 6 survivors of the Holocaust,

one of the survivors said, “We made a big mistake. We never spoke up.”As a result of them

not speaking up, over six million Jewish men, women, and children were tortured,

executed, and killed. Do we want history to repeat itself? ” Is there a remnant of people who

will stand up for justice like they did for Trayvon Martin? It is us today, but it could be you and

your loved ones tomorrow?

White House’s Response

Letitia’s letter from President Obama dated June 4, 2012

THE WHITE HOUSE

June 4, 2012

Dear Letitia:

Thank you for sharing your thoughts with me. Many Americans have written to me about

human rights around the world, and I appreciate your perspective.

The United States was founded on the principles of freedom and equality, and our history is

marked with triumphs and struggles in fulfilling these timeless ideals. Our task is not finished,

and

protecting these core values is a shared obligation and a priority for my Administration. No

nation

should be silent in the fight against human rights violations. When innocents in places like

Sudan,

Syria, and the Democratic Republic of Congo are raped, murdered, or tortured, it is a stain on our

collective conscience. I am committed to reinvigorating America’s leadership on a range of

international human rights issues.

As the struggle for human rights continues around the world, we have witnessed an

extraordinary change in the Middle East and NorthAfrica. Country by country, people have risen

up

across this region to demand their human rights; too often, these calls for change have been

answered

by violence. The United States opposes the use of violence and repression against these men and

women. Rather, we support a set of universal rights, including free speech, the freedom of

peaceful

assembly, freedom of religion, equality for men and women under the rule of law, and the right

of

people to choose their own leaders. We also support political and economic reform in the Middle

East and North Africa that can meet the legitimate aspirations of ordinary people throughout the

region. While change may not come easily, America will stand squarely on the side of those who

are

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Page 34 of 135

reaching for their rights, knowing their success will bring about a world that is more peaceful,

more

stable, and more just.

As you may know, the United States has joined the United Nations Human Rights Council and

is working to make this body as effective as possible. My Administration will also advocate for

human rights in other international settings. In our relations with other countries, the issue of

human

rights will continue to be raised as clearly, persistently, and effectively as possible. Among other

things,we will continue to promote accountability for mass atrocities; respect for the rights of

minorities and women; freedom of association, speech, and religion; and freedom for people to

live

as they choose and love whom they chose.

Our commitment to human rights is an essential element of American foreign policy and

serves our national security. Through it, we will help to shut down torture chambers, replace

tyranny

with good governance, and enlist free nations in the common cause of liberty. To learn more

about

my Administration’s human rights agenda, please visit www.HumanRights.gov or

www.WhiteHouse.gov/CPo. Thank you, again, for writing.

Sincerely,

Barack Obama

We are suffering severely, but let that stop you from seeking justice. We request the support of

all survivors to contact the following this week.

1. This is for International and National Survivors. Department of Homeland Security:

Immigration and Customs Enforcement:

Human Rights Law Division; Human Rights Violators and War Crimes Unit Contact: http://www.ice.gov/contact/inv/

URL: http://www.ice.gov/human-rights-violators/

Tip Line: 1-866-DHS-2-ICE (1-866-347-2423)

Victim Witness Assistance: 1-866-872-4973

Public Service Announcement: http://www.ice.gov/human-rights-violators/

Human rights violators, including those who have participated in war crimes and acts of

genocide, torture, extrajudicial killing, violations of religious freedom, and other acts of

persecution, frequently seek to evade justice by seeking shelter in the United States. These

individuals will frequently assume fraudulent identities to enter the country, seeking to blend into

American society and communities.

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Page 35 of 135

ICE places a high priority on targeting serious offenders through its Human Rights Violators and

War Crimes Unit. The unit mission is twofold. The first part is to prevent the admission of

foreign war crimes suspects, persecutors and human rights abusers into the United States. The

second part is to identify, prosecute and ultimately remove such offenders who are already

unlawfully in the United States and who have committed acts ranging from genocide, torture and

war crimes to serious violations of religious freedoms or other forms of persecution. In

performing both missions, we work closely with our counterpart the Human Rights Law Division

(HRLD).

2. Inter-America Commission on Human Rights at http://www.oas.org/en/iachr/ There are 2

reports to download to read. Inter-American Commission on Human Rights

1889 F Street, N. W.

Washington, D.C. 20006

USA and/or by fax to the following number 1-202-458-3992. Contact their office at: 1 (202)

458-3000

3. UN Working Group on Arbitrary Detention

http://www.ohchr.org/EN/Issues/Detention/Pages/WGADIndex.aspx

Select individual complaints; many may want to use the urgent appeal process.

4. Send this press release and your story to your Congressional and State Representatives and

request oversight and investigative hearings. You can find your representatives at

www.senate.gov and www.house.gov.

5. U.S. Attorneys are empowered to investigate suspected or alleged offenses against the United

States. You can locate your representative at http://www.justice.gov/usao/.

6. The Attorney General (AG) can create task forces. The Special Counsel Regulations of 1999

require the AG to appoint a Special Counsel from outside the Government when three conditions

are met: (1) he determines that a criminal investigation of a person or matter is warranted; (2) it

would present a conflict of interest for DOJ to conduct the investigation, or any subsequent

prosecution(s); and (3) the appointment of a Special Counsel would serve the public interest.

You can visithttp://www.justice.gov/ag/ to write to Attorney General Eric Holder and you can

contact your local U.S. Attorney for your state as well.

7. Contact Secretary of State Hillary Clinton at www.state.gov. Leave a comment at 202-647-

5291 or via fax at 202-647-8947. We need as many non-Americans to send her a letter.

We suggest that this note is included on every correspondence to let those who are obstructing

justice that there will be on held accountable for their actions. NOTE: “Whoever intentionally

obstruct the proceedings before depts., agencies, and committees, obstruct this criminal

investigation and/or retaliate against me because I am a

victim, you will be punished to the full extent of the applicable[law in 1505 of Title 18

Obstruction of proceedings before depts., agencies & committees, 1510 Obstruction of

Criminal investigations, 1513 of Title 18 Retaliating against a witness, victim or an

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informant, or 1514 Civil Action to restrain harassment of a victim or witness. Whoever

intentionally alters, destroys, mutilates or conceals records, or documents with the intent to

impair the object’s integrity or availability for use in an official proceeding will be

punished to the full extent of law as defined in 1519 of Title 18 Destruction, Alteration or

Falsification of records in Federal investigations and bankruptcy.”

In closing, Kofi Annan, Secretary-general of the United Nations said, “Human Rights are what

reason requires and conscience demands. They are us and we are them. Human rights are rights

that any person has as a human being. We are all human beings; we are all deserving of human

rights. One cannot be true without the other.” Amen

If you have any questions, please contact us via email or phone.

# # #

Posted 2 years ago

May 26

(Part 2 of 3) “Informants” Utilizes Products, Services & Estabishments as their

“Own Personal Playground” to Commit Crimes against Fellow U.S. Citizens

“Taking A Stand Against Injustice” Series (Part 2 of Part 3)

In the first article, we discussed about the rights of the non-consensual human subjects/TIs and

how the Federal law allows them the right to “opt-out” or discontinue participation at any time

without penalty or loss of benefits to which the subject is otherwise entitled (45 CFR 46.116 (a)

(8). This request should be sent to the Department of Health & Human Services who is the

“authorized Federal agency” for human subject research. Many Americans have been placed in a

non-consensual human subject research, which violates Title 45 Public Welfare Part 46

Protection of Human Subjects, 45 CFR Subject A, “The Common Rule”, that has not been an

enforceable lawfully, promulgated regulation for the past 20 years. As a result, “the absence of

Federal jurisdiction over much privately funded research means that the U.S. Government cannot

know how many Americans currently are subjects in experiments, cannot influence how they

have been recruited, cannot ensure that research subjects know and understand the risks they are

undertaking and cannot ascertain whether they have been harmed.”

In this second article, we will discuss how these citizens are being monitored, tracked, and

targeted with technology for violence by fellow citizens, just like in Syria and Iran. The use of

technology is being used to perpetrate human rights abuses. This is an International epidemic and

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human rights atrocity. In his April 23, 2012 Executive Order, President Obama that Syria and

Iran has committed serious human rights abuses against their own people, facilitated by

computer and network disruption, monitoring, and tracking by those governments. He referred

to this as “digital guns for hire”. The Syrian General Intelligence Directorate has been implicated

in serious human rights abuses, such as arbitrary arrests and the deaths of detainees. Last year

U.S. officials ”encourage people all over the world to use digital media.. and denounced those

who harass, unfairly arrest, threaten or commit violent acts against the people who use these

technologies.” We will address the reasons why we believe that “digital guns for hire” or a more

suitable name “digital murder for hire” has infiltrated in the U.S. Kofi Annan, Secretary-general

of the United Nations said, “Human Rights are what reason requires and conscience demands.

They are us and we are them. Human rights are rights that any person has as a human being. We

are all human beings; we are all deserving of human rights. One cannot be true without the other.

The bar for justice has risen in this country so let’s expose the truth that fellow U.S. citizens are

monitoring, targeting, and tracking their own citizens with technology by Friday, May 25, 2012

so that they can enjoy a wonderful Memorial Day weekend. Reconciliation cannot occur until

truth is exposed.

“Informants” Utilizes Products, Services, and Establishments as their “Own Personal

Playground” to Commit Crimes against Fellow U.S. Citizens

“U.S. Citizens seek Justice for “Digital Guns for Hire”, which Exceeds “Monitoring and

Surveillance” under the Auspices of National Security & War Against Terror”

May 24, 2012

Dear Presidents/CEOs/Executive Heads,

I am writing this letter to inform you about crimes that are being committed against your

customers, members, other employees, or students in your corporations, businesses, schools,

religious institutions, City/State/Federal Government and Organizations, by people who are

“confidential informants” ,“informants” or even those part of the

neighborhood watch”, or Intelligence Agencies contractors without your knowledge and consent.

In some cases, you may be very aware of this issue, but you are either threatened, been lied to, or

you are a willing participant. This is not just prolonged covert monitoring and surveillance, but

this is monitoring, targeting, and tracking your customers, members, employees or students for

no rhyme or reason. There are many grave human rights abuses being committed and we request

your immediate action and support to bring justice expeditiously for countless men, women,

children and even babies in the U.S. and worldwide. If it is happening in Syria and Iran, is it

possible that it could happen in the U.S.?

I am writing this letter publicly because my ability to communicate freely with others and the

outside world is very, very limited. I have constant computer and network disruptions on a daily

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basis. I, like so many others are being monitored, tracked, and targeted, like animals with

electromagnetic radiation technology, advanced electronics technology, implants,

biochemical/chemical/radiological weapons and information technology with COINTELPRO

tactics. We are referred to as a non-consensual human subject or as a Targeted Individual or TI

for short. There are countless men, women, and children in America and worldwide who are

unaware that they are victims and they do not attribute their ongoing “bad luck”; mishaps;

animal killings; or mysterious, untreatable, disabling “environmental” diseases to covert

operatives using old COINTELPRO tactics plus new weapons of war to terrorize or neutralize

or kill them. These professional, well-orchestrated intrusions induce excruciating pain,

exhaustion, terror, alienation, and results in behavior changes, which are sometimes aggressive

or violent. In addition, we are illegally being tortured, covertly harassed, abused, stalked

(individually or by gangs), and spied upon 24/7. Many who have tried to expose the truth by

telling their family, friends, or even the police have been wrongfully committed to mental

institutions, prisons, maimed or killed. This is generational and it may involve 3 to 4 generations.

Can you imagine children being exposed to this type of “torture” since they were babies or even

elderly people being abused as well? President Obama has waged a war against genocide. Will

you?

In his April 23, 2012 Executive Order “BLOCKING THE PROPERTY AND SUSPENDING

ENTRY INTO THE UNITED STATES OF CERTAIN PERSONS WITH RESPECT TO

GRAVE HUMAN RIGHTS ABUSES BY THE GOVERNMENTS OF IRAN AND SYRIA

VIA INFORMATION TECHNOLOGY” states, “By the authority vested in me as President

by the Constitution and the laws of the United States of America, including the International

Emergency Economic Powers Act (50 U.S.C. 1701 et seq.) (IEEPA), the National Emergencies

Act (50 U.S.C. 1601 et seq.), section 212(f) of the Immigration and Nationality Act of 1952, as

amended (8 U.S.C. 1182(f)), and section 301 of title 3, United States Code, I, BARACK

OBAMA, President of the United States of America, hereby determine that the commission of

serious human rights abuses against the people of Iran and Syria by their governments, facilitated

by computer and network disruption, monitoring, and tracking by those governments, and

abetted by entities in Iran and Syria that are complicit in their governments’ malign use of

technology for those purposes, threaten the national security and foreign policy of the United

States. The Governments of Iran and Syria are endeavoring to rapidly upgrade their

technological ability to conduct such activities. Cognizant of the vital importance of providing

technology that enables the Iranian and Syrian people to freely communicate with each other and

the outside world, as well as the preservation, to the extent possible, of global

telecommunications supply chains for essential products and services to enable the free flow of

information, the measures in this order are designed primarily to address the need to prevent

entities located in whole or in part in Iran and Syria from facilitating or committing serious

human rights abuses.” You can read the full text of President Obama’s Executive Order at

http://blog.alexanderhiggins.com/2012/04/23/obama-declares-syria-national-emergency-outlaws-

reporting-rebels-126061/.

Letter from Representative Jim Guest

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On October 10, 2007, Representative Jim Guest wrote a letter to employee of the Legislature and

friends, here’s a brief excerpt:

“This letter is to ask your help for the many constituents in our country, who are being affected

unjustly by electronic weapons, torture and covert harassment groups. Serious privacy violations

and physical injuries have been caused by the activities of those groups and their use of so-called

non-lethal weapons on men, women, and even children.

I am asking you to play a role in helping these victims and also stopping the massive movement

in the use of Verichip and RFID technologies in tracking Americans”….

Sincerely,

Representative Jim Guest

Former PA Governor & 1 Yr. Contract that Targeted Peaceful Demonstrators

Do you recall the story about former Pennsylvania Governor Ed Rendell who was horrified that

there was a one year contract between the State Office of Homeland Security and the Institute of

Terrorism Research & Response because of wrongful and improper reports being disseminated

about environmental groups, tax protesters, people at gay and lesbian rallies and even supporters

of more funding for education. He stated that “I am appalled that this contract was entered

into without my knowledge,” he said. “I am appalled that information was disseminated

about groups that were exercising their constitutional right to free speech and to protest.

They shouldn’t be on any list [of possible security threats]. This is extraordinarily

embarrassing. Were these people terrorists? Of course not,” he said. I disagreed with them

about a moratorium, but they were just exercising their constitutional rights to free speech.

I was surrounded by a group of them for 35 minutes and I never felt threatened even for a

millisecond.” Read

more:http://old.postgazette.com/pg/10258/1087582454.stm#ixzz1pwfMBLP4

Yes, it may be hard to believe, actually incomprehensible, but it is happening in America and in

many other nations worldwide. In a recent Public Broadcasting Service (PBS) documentary,

Swimming In Auschwitz (www.swimminginauschwitz.com), which depicts the stories of 6

survivors of the Holocaust, one of the survivors said, “We made a big mistake. We never

spoke up.” As a result of them not speaking up, over six million Jewish men, women, and

children were tortured, executed, and killed. Do we want history to repeat itself? We have

been declared as “enemy of the corporate” or “undesirables”, even though, we are law-abiding

citizens. We are doing what is right by speaking out against those who are abusing their

authority and exposing their sin. We cannot do it, without your support. It is us today, but it

could be you and your loved ones tomorrow. We must stop this before it is too late. Will

you stand up with us starting right now? We want to have an enjoyable Memorial Day

weekend like you.

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Who are the Non-Consensual Human Subjects/TIs?

The Non-Consensual Human Subjects/TIs are whistleblowers, people of faith, people of color,

alternative media, journalists, human rights & peace workers, environmentalists, activists,

celebrities, dissidents and women, especially women who live alone. People with infirmities,

elderly people, and children are not exempt. Even the military is experimenting on its own;

without his or her informed consent. We are also referred to as Targeted Individuals or “TIs” for

short as well as, non-consensual human subjects. Even President Obama’s car is equipped with

electromagnetic pulses defenses.

Many heroes are risking their lives to stop the corruption that is happening around you every

day. Have you heard the story of Richard Taus, John Carman, Darlene Fitzgerald

(bordergate.net), or Rodney Stich? They are some of our heroes. Many have died, been

incarcerated, or even been committed to a mental institution. These heroes are listed on

www.defraudingamerica.com. They would whether do the right thing in order for justice to

prevail, than be silent, take a bribe, or look the other way. Many have suffered imaginable

pain, unless you lived through it. This is not being reported in your major newspapers or on the

nightly news, because they are being controlled. Many of you may not be aware of your rights if

a Federal Investigator contacts you. You may want to read, “IF AN AGENT KNOCKS”:

FEDERAL INVESTIGATORS AND YOUR RIGHTS, which can be found at

http://whatreallyhappened.com/RANCHO/POLITICS/COINTELPRO/agent.knocks.html.

What are Electromagnetic Radiation and Electromagnetic Energy?

Electromagnetic radiation (EM radiation or EMR) is a form of energy emitted and absorbed

by charged particles, which exhibits wave-like behavior as it travels through space. EMR has

both electric and magnetic field components, which stand in a fixed ratio of intensity to each

other, and which oscillate in phase perpendicular to each other and perpendicular to the direction

of energy and wave propagation. In vacuum, electromagnetic radiation propagates at a

characteristic speed, the speed of light.

Electromagnetic radiation is a particular form of the more general electromagnetic field (EM

field) that is defined as the field produced by moving charges. Electromagnetic radiation is

associated with only the type of EM field which is far enough away from the moving charges

that produced it, that absorption of the EM radiation no longer affects the behavior of these

moving charges.

In general, EM radiation (the designation ‘radiation’ excludes static electric and magnetic and

near fields) is classified by wavelength into radio, microwave, infrared, the visible spectrum we

perceive as visible light, ultraviolet, X-rays, and gamma rays. The behavior of EM radiation

depends on its frequency. Lower frequencies have longer wavelengths, and higher frequencies

have shorter wavelengths, and are associated with photons of higher energy.

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Electromagnetic radiation composed of photons that carry minimum-ionization energy, or more,

(which includes the entire spectrum with shorter wavelengths), is therefore termed ionizing

radiation. (There are also many other kinds of ionizing radiation made of non-EM particles).

Electromagnetic-type ionizing radiation extends from the extreme ultraviolet to all higher

frequencies and shorter wavelengths, which means that all X-rays and gamma rays are ionizing

radiation. These are capable of the most severe types of molecular damage, which can happen in

biology to any type of biomolecule, including mutation and cancer, and often at great depths

from the skin, since the higher end of the X-ray spectrum, and all of the gamma ray spectrum,

are penetrating to matter. It is this type of damage which causes these types of radiation to be

especially carefully monitored, due to their hazard, even at comparatively low-energies, to all

living organisms.

Electromagnetic energy can be used to influence, disable or kill humans at a distance. The

spoken word of the hypnotist may be conveyed by modulate electromagnetic energy directly into

the subconscious parts of the human brain. Almost anything could be inserted into the target

brain-mind systems.

Electromagnetic energy could be used to prevent voluntary muscular movements, control

emotions & thus actions, produce sleep, transmit suggestions, interfere with both short-term and

long-term memory, produce an experience or delete an experience. A microscopic brain chip

can also be implanted.

Ionization and extreme types of molecular damage from X-rays and gamma rays

At the higher end of the ultraviolet range, the energy of photons becomes large enough to impart

enough energy to electrons to cause them to be liberated from the atom, in a process called

photoionisation. The energy required for this is always larger than about 10 electron volts (eV)

corresponding with wavelengths smaller than 124 nm (some sources suggest a more realistic

cutoff of 33 eV, which is the energy required to ionize water). This high end of the ultraviolet

spectrum with energies in the approximate ionization range, is sometimes called “extreme UV.”

(Most of this is filtered by the Earth’s atmosphere).

Effects of Radiation on the Human Body

Here are the effects of radiation on the human body: This information was taken from the

website: http://www.atomicarchive.com/Effects/radeffects.shtml. In July 2005 the National

Academy of Sciences came to the conclusion that the preponderance of scientific evidence

shows that even very low doses of radiation pose a risk of cancer or other health problem and

there is no threshold below, which exposure can be viewed as harmless. Here are the effects of

radiation on the human body:

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1. Hair- The losing of hair quickly and in clumps occurs with radiation exposure at 200 rems or

higher.

2. Brain – Since brain cells do not reproduce, they won’t be damaged directly unless the

exposure is 5,000 rems or greater. Like the heart, kills nerve cells and small blood vessels and

can cause seizures and immediate death.

3. Thyroid – The certain body parts are more specifically affected by exposure to different types

of radiation sources. The thyroid gland is susceptible to radioactive iodine. In sufficient

amounts, radioactive iodine can destroy all or part of the thyroid. By taking potassium iodide,

one can reduce the effects of exposure.

4. Blood System- When a person is exposed to around 100 rems, the blood’s lymphocyte cell

count will be reduced, leave the victim more susceptible to infection. This is often referred to as

mild radiation sickness. Early symptoms of radiation sickness mimic those of flu and may go

unnoticed unless a blood count is done. According to data from Hiroshima and Nagasaki, show

that symptoms may persist for up to 10 years and may also have an increased long-term risk for

leukemia and lymphoma.

5. Heart- Intense exposure to radioactive material at 1,000 to 5,000 rems would do immediate

damage to small blood vessels and probably cause heart failure and death directly.

6. Gastrointestinal Tract – Radiation damage to the intestinal tract lining will cause nausea,

blood, vomiting and diarrhea. This occurs when the victim’s exposure is 200 rems or more. The

radiation will begin to destroy the cells in the body that divide rapidly. These including blood,

GI tract, reproductive and hair cells, and harms their DNA and RNA of surviving cells.

7. Reproductive Tract - Because reproductive tract cells divide rapidly, these areas of the body

can be damaged at rem levels as low as 200. Long-term, some radiation sickness victims will

become sterile.

COINTELPRO + Hi-Technology

This is a well-organized, well-funded, well-connected, well-orchestrated operation with vast

resources across state lines and Internationally. Since the U.S. Patriot Act, there is no oversight

of the Intelligence Agencies, Dept. of Defense, and Dept. of Homeland Security. COINTELPRO

is an acronym for Counter Intelligence Program. Wikipedia states, “it was a series of covert, and

often illegal, projects conducted by the United States Federal Bureaus of Investigation (FBI)

aimed at surveilling, infiltrating, discrediting, and disrupting domestic political organizations.

COINTELPRO tactics included discrediting through targets through psychological warfare,

planting false reports in the media, smearing through forged reports, harassment, wrongful

imprisonment, extralegal violence and assassination. COINTELPRO took place between 1956

and 1971. Officially, COINTELPRO was termination in April 1971, but was it? The last major

Congressional investigation of COINTELPRO operations was conducted in 1976-1978 by the

Church Committee. These horrifying reports did not provide any effective legislative remedies

for future victims. Nor did they produce any prosecutions of proven criminals within the Justice

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Department. All of them returned to their life of government crime. Not only did

COINTELPRO seek to defame, neutralize, discredit, and destroy the more militant

organizations of that day, the Black Panther Party, Republic of New Afrika, Nation of

Islam, American Indian Movement, anti-war, socialist and communist organizations; but it

also targeted anyone who stood up against racism and oppression, and who challenged

federal and state government to correct these ills and change its policies. There are hundreds

of political prisoners who have been incarcerated upwards of 40 years as a direct result of this

heinous program and should be exonerated and released from prison. How long must they and

their families continue to suffer? Many of them were young people and now they are elderly

people who are still being punished by the “illegal and unconstitutional system”.

Thus COINTELPRO covert operations have continued to the present, but now it has been

unleashed to neutralize the target by including high-technology. An outline of court cases related

to COINTELPRO or COINTELPRO-like programs (ongoing investigations of disfavored

organizations for political, rather than legitimate law-enforcement purposes, often using

harassment, break-ins, provocateurs, etc. to disrupt them) are available on The COINTELPRO

Casebook’s website at www.icdc.com/~paulwolf/cointelpro/law/cointelprocasebook.htm.

Who Could Be “Informants” or “Perps”?

Basically, any employee, customer, member, or students could be an informant. Even children

are involved in this. In his analysis, retired attorney and 57 year non-consensual human subject

and COINTELPRO survivor Robert S. writes that an example of typical COINTELPRO

operations is the

“Ability to arrange for numerous local people to participate in elaborate harassment operations.

The FBI maintains an army of people throughout the nation who work at full-time at regular

jobs, but who are available at any time to carry out whatever special work assignments the FBI

gives them to perform. The FBI calls these people “informants”. The victims of harassment by

these people call them “perps” (short for perpetrators).”

In the 13 page article by D.T. Stockton called United States Terrorism and Repression Against

Its Own People states,

“All doormen, maintenance workers, superintendents, management companies, which I have

investigated and observed in the past several years are government-controlled informants

involved in these unscrupulous and illegal activities. I have also found this to be true with airline

and airport employees.

Parking lot and garage companies and corporations have also fallen prey to these actions. Many

security guards and security companies, home security companies are also controlled under the

intelligence agencies.

Also, many secretaries and receptionists of politicians are controlled informants who are spying

on them, often blocking people and information such as deleting emails, voicemails and

intercepting letters from getting to the politicians.”

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“Informants” and FBI/DHS in the News and Proposed Informant Legislation

On February 7, 2012 Fox News broadcast a segment called, “Informants Gaming the System”.

During this broadcast, they undercover, that “informants cut deals and continue their life of

crime- murderers, con men and thieves are just some of the people our Government is

paying to help fight crime, trading information in exchange for money or lighter

sentences.” You can read the several stories pertaining to the FBI informants at

www.myfoxboston.com/subindex/news/undercover. You can also read “The ex-FBI Informant

with a Change of Heart: “There is no real hunt. It’s fixed” by Paul Harris at

http://www.guardian.co.uk/world/2012/mar/20/fbi-informant. The American Free Press has

interviewed many non-consensual human subjects. In their April 23 & 30, 2012 edition of the

American Free Press, www.AmericanFreePress.net, “Press Targeted by DHS” details how Laura

Poitras, an Oscar and Emmy- nominated filmmaker and intrepid journalist who has been targeted

and the DHS has been forced to admit that in six years they never found anything to justify their

continuing abuse and harassment other than they didn’t like her expressing non-official

viewpoints. You can read the April 17, 2012 Washington Post article, “DOJ review of flawed

FBI forensics processes lacked transparency” by Spencer S. Hsu. Alexandra Natapoff, a Loyola

Law School Professor, the author of the book, “Snitching, Criminal Informants, & the Erosion of

American Justice” and an expert on informants has briefed Congress about their used of

criminals as “informants”. Her website is www.snitching.org. Congressman Stephen Lynch (D-

MA) is author of the Confidential Informant Accountability Act of 2011, H.R. 3228, which

would require Federal law enforcement agencies to report to Congress serious crimes,

authorized, as well as, unauthorized, committed by their confidential informants, to amend title

28, United States Code, with respect to certain tort claims arising out of the criminal misconduct

of confidential informants and for other purposes.

How the Informants use COINTELPRO Tactics on the Non-consensual Human

Subjects/TIs?

Employees, members, customers, or students “informants” are corrupting, utilizing, and

exploiting your (1) other employees, members, or students (2) products, (3) services, or (4)

establishments for their own personal gain. Children are even involved. Children are being

“mobbed” in school. They are using our dwellings and our vehicles as well. Now, they are using

your businesses, organizations, churches, and schools as their “own personal playground” to do

whatever they want to, without any regards to the law. Up to now, they have been able to keep it

“under wraps”. Now, it is time to expose what has been in dark for so many decades. They have

the ability to obtain cooperation of your employee, as well as, your members or customers to

perform various forms of COINTELPRO tactics on a consistent basis. The rights, safety, and

welfare of the non-consensual human subjects/TIs have been affected. Listed below are the 21

examples of COINTELPRO tactics used by the informants, which are either authorized or

unauthorized:

1. Cyber stalking – The informant is stalking the non-consensual human subjects/TIs via the

internet

2. Electronic Harassment (via phone): The informant is sending direct energy through the

phone. The informant tries to keep the non-consensual human subjects/TIs on the phone

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as long as possible. When the non-consensual human subjects/TIs gets off the phone,

they have a headache, feel fatigue, face breaks out, heart rate increases,

3. Electronic Harassment (in person): The informant or (in many cases, customers or

visitors) are using the cell phone as a device or they have their hands in their pockets,

which contain the electromagnetic weapon. It can also be on their clothing or in a purse.

They are using a biological agent or toxin as a weapon or with a reckless disregard for the

safety of human life. In addition, they are using eye targeted lasers or lasers.

4. Vehicular stalking – using business vehicles to follow the non-consensual human

subjects/TIs by going pass his/her residence, workplace, or location whereever his/her is

at that particular time. They are shooting eye targeted lasers, lasers, or using their

computer or phone.

5. The informant is not concern who else may be affected when he/she is using these

chemicals, toxins, and electromagnetic radiation on food, product, clothing, vehicles and

on personal property. They are using these toxins on any item/document received/brought

by the non-consensual human subjects/TIs. There is a great chance for cross-

contamination to occur. The non-consensual human subjects/TIs are contaminating their

vehicles, dwellings, or workplace. In addition, the informants are affecting or damaging

the products or the employer’s property/establishment.

6. The informant refuses to elevate issue to someone else or gives the issue to someone who

is also an informant or perp. They want to keep it all within “the family.”

7. Altering or tampering with any information/records pertaining to the non-consensual

human subjects/TIs. Encrypted passwords are even changed.

8. The informant can be arrogant, rude, angry, accusatory, or disrespectful to the non-

consensual human subjects/TIs. In the Presidential Proclamation, it states, “These stalkers

inspire fear through intimidation, explicit or implied threats and nonconsensual

communication often by telephone, text message, or email that can cause physical and

emotional distress” to the non-consensual human subjects/TIs.

9. One of the maneuvers is to divert time and energy. The informant does not follow their

own rules, laws, or regulations when it comes to the non-consensual human subjects/TIs.

The informant gives the non-consensual human subjects/TIs the runaround. They are

always looking for a “loophole”.

10. The informant discontinues service or set them up with new service without the consent

or knowledge of the non-consensual human subjects/TIs.

11. The informant orders one product, but receives the wrong product (This can happen

several times, before it is corrected).

12. The informant ignore the non-consensual human subjects/TIs requests made by him or

her in writing or verbally.

13. The non-consensual human subjects/TIs buys a new product, but he/she receives a

defective, modified or tampered with (used) product. This new product maybe affected

by electromagnetic radiation. The unassuming non-consensual human subjects/TIs use

the product realizing later that some of the features are not working. In many cases the

non-consensual human subjects/TIs attempt to return the product, but they refuse to

accept it or they receive one with the same problem. The “informant” or “perp” insists

that it is a “new product”. No one could have tampered with this, because there is no sign

of break-in. This is called “covert entry”. The Federal Government intelligence agencies

and law enforcement officials are the only ones who are authorize to receive this

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specialized training. Have the Federal Government or law enforcement officials been

teaching “covert entry”, which is a trade secret to these “informants”, some who are

former criminals, murderers, or drug users to enter not only products, but also our

dwellings, vehicles, and workplaces bypassing any secured locks, windows, and alarm

system ?

14. The informant is participating in the libel and slander campaign against the non-

consensual human subjects/TIs.

15. The informants are creating “work assignments” without work orders, therefore

eliminating a paper trail. This has happened with cable or phone services. Sometimes,

the problem is caused by an outside source or the informant is acting like he/she is doing

“work” on behalf of the employer, but he/she is not. Many have stated that they feel

fatigue or had headaches after their service was “worked on”.

16. The “informant” will threaten, coerce, and get others to participate or to “look the other

way”.

17. If the non-consensual human subjects/TIs are entitled to money, there is usually a “long”

delay in receiving it or he/she never receives it. The excuse is that this was due to “human

error”.

18. The non-consensual human subjects/TIs are being financially destroyed. (a) They are

overcharged for services. Many non-consensual human subjects/TIs have complained of

high utilities bills, phone bills, or even credit card bills. Unbeknownst to the non-

consensual human subjects/TIs, the neighbor “informants” have broken into their homes,

while they are sleeping or away and hare using their services or changes were made

within their dwelling, which caused their extremely high utility bills. Many have reported

that they are paying 2 to 3 times than someone else and there is nothing that the non-

consensual human subject/TIs can do about it. (b) Documents are “generated” or

“created” with higher amounts or late fees. It looks like the “real McCoy”, but it is a

FRAUD to get as much money out of the non-consensual human subjects/TIs as possible.

The neighborhood “informants”, possibly part of the “neighborhood watch” have broken

into their homes, while they are sleeping or when he/she went out and there is no sign of

a break-in and have taken their original “documents”. Now, the “original” documents are

no longer in the possession of the non-consensual human subject/TIs and have been

replaced with these new “generated” or “created” documents. Many do not realize that

this is happening. (c) The “informant” are working together to ensure that the bills are

higher from the “field” informant to the “office” informant. (d) The non-consensual

human subjects/TIs have lost their job and are unable to get another one because of an

informant.

19. If the non-consensual human subjects/TIs request that an investigation is done. The final

report usually concludes that there is insufficient evident against the “informant’s”

employer. No one is ever persecuted or held accountable.

20. The informant is working with others “informants” in the private sector, City, State, and

Federal Government agencies in America (interstate and intrastate) and Internationally. It

is one big, cohesive, secret family. Private or personal information is given to countless

of interstate, intrastate, and International “informants” and those who do not need-to-

know about the non-consensual human subjects/TIs, as well as, about other members of

their families down to the three and fourth generations.

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21. The informant is responsible for exacerbating pre-existing diseases or sicknesses, or

creating new diseases or sicknesses of the non-consensual human subjects/TIs.

Informants have even intentionally dosed non-consensual human subjects/TIs with high

concentrations of chemicals, toxins, lethal weapons, and electromagnetic radiation.

Others have been implanted with implants, which will change a person’s DNA and cause

cancer. Some informants, like physicians have denied medical treatment or did not follow

the medical protocol prescribed for the symptoms of the non-consensual human

subjects/TIs. Many consensual human subjects/TIs have stated that even though they

have noticeable symptoms that the physicians have can be seen with the naked eye, the

medical tests ALWAYS return normal. Are the medical tests being altered as well?

Some of My Personal COINTELPRO Tactics Examples

Our taxpayer’s dollars are being used to prevent the non-consensual human subjects/TIs from

making a living, or even run a business. Currently, they are using a common maneuver known

as placing a “snitch jacket” or “bad jacket” on an activist, in order to damage the activist’s

effectiveness and generate “confusion, distrust, and paranoia”. This maneuver is used to divert

time and energy. I am being prevented from running and conducting a successful business, as

well as, living a normal life. Is anyone willing to pay my consultant’s fee for the harassment for

your “informant” employees’ participation? Time is money and I have wasted a lot of time. I

have good work ethics. This has caused me great emotional, financial, and physical distress. I am

a consumer and I expect the same level of quality in your products and services that you would

give to any of your valued customers without any added benefits. I should not be treated any

differently, because these people are doing unscrupulous activities, while working. I, like all of

the non-consensual human subjects/TIs are unable to bypass these “preps” or

“gatekeepers” because they have been assigned to address our issues. They are being told

what to say and do to me. Even prisoners and pets are treated better than this. I am bringing these

issues to your attention so that justice can prevail because they do not want me to go to the CEOs

or Presidents. There are so many that I would have to go to that I do not have the energy, time or

resource. According to many of the non-consensual human subjects/TIs, they have been

experiencing this type of harassment for years. Is anyone willing to pay my medical expenses for

the next 10 years due to being exposed to toxins, biological agents, or electromagnetic radiation

by your employees? These informants should be held accountable for their actions. They have

gone far beyond “routine monitoring”. We just want our lives back.

As a former Federal Government electronics engineer, I do understand this technology. I have

filed police reports in NJ and PA. In Md., the police filed “events” so that they would not have to

investigate my allegations. I have filed a complaint with the F.B.I. in Newark, NJ. Last year, I

sent Cease and Desist Letters to the Trenton Mayor and NJ Governor’s Office and this week, I

sent another letter about the retaliation and the lack of support from them. In addition, I

requested the immediate arrest of 1 family and 2 individuals in my neighborhood. I also faxed

letters to Senators Lautenberg & Menendez and Congressman Holt requesting assistance. I sent

several opt-out requests to Dept. of Health and Human Services and to the Congressional

representatives listed above, but there has been no word. I will hold everyone responsible for

their lack of actions, including the staffers, because many of them are “informants”. According

to Federal law, we can opt-out of a human subject research at any time, especially one which

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violates the Common Rule. They are using this technology against my family and they are trying

to intimidate me to be silent or be homeless. I have nothing to lose because I have the TRUTH

and the TRUTH ALWAYS PREVAIL.

Here are some of the major issues that are affecting me from running a successful business and

to live a normal life.

The Establishments: The moment I stop outside my parent’s house, the

vehicles racing up and down the street is heightened. This has been referred to as “street

drama”. I feel like I am the fox in a fox hunt. Since electromagnetic radiation is invisible to

the naked eye, no one will know that it is there unless you are looking for it. Many

establishments do not have an infrared security camera, which will capture all of this.

Sometimes, I cannot go into a store because the contaminants are so strong. Other times, I have

gotten so sick from the exposure that it took me days or weeks to recuperate. I filed police

reports against several establishments and the police did not have the food tested to see what was

causing me to be sick. I called the health dept. and even private companies, but to no avail. I

even went to the Governor’s office and they did not assist me. The police report to “an event” so

that it would not be investigated. I sent an overnight letter or fax request to several

establishments to do not destroy or overwrite their security tapes, because it should have

captured the “informants” on camera. The police depts. failed to investigate any of the crimes in

NJ, PA, and MD. Last week, I could not go out to enjoy my birthday because of the

possibility of being “intentional poisoned” and then for it to be covered up. I am getting

tired of carrying my bags of evidence around so that they will not steal it. This week, I

made a very hard decision to attend my oldest niece’s college graduation and leave the

house unoccupied all day or stay home while my entire family attended so that I can save

the residual evidence. Even though I had the most excruciating migraine due to the

targeting of my head, I would have made it. I sacrifice that one day so that she will not have

to endure this for the rest of her life. This weekend, I am planning to attend her graduation

party. In Jesus’ name, I pray that arrests need to be made by Friday, May 25, 2012 and

that Congress or the President will react expeditiously. Now I am being threatened to keep

silent or be homeless. Isn’t this violation of Tampering with a Witness, Victim or Informant

18 USC 1512 to obstruct justice by intimidation?

Internationally Being Targeted, Monitored, & Tracked (This should be brought to the

Secretary of State’s attention): Two weeks ago, I was locked out of my Hotmail account and I

was in this continuous loop. I searched the Internet and came across this company who provided

tech support for Hotmail. I contacted them and I was told by this “tech” named Nick Nelson that

227 emails were sent from my computer requesting people’s financial data. I entered a contract

with them for 3 years that they would provide all of the tech support for my computer. I later

found out that companies like DNF Global Solutions are ripping people off. The name of this

company is DNF Global Solutions who are located in India. The “tech” installed this Super

AntiSpyware virus, which made my computer slower and infected my computer with viruses; my

files were being deleted, uploaded and files were hidden. After I did my research, I learned that

was a rogue virus to annoy me and to infect my computer, which it did. The scary part is that

they were able to unblock my Hotmail account. I changed all of my passwords. While, I was

speaking to them, someone gained access to my online banking account. They became the

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Administrative of the computer and I have not been able to repair it. I was told to call 866-921-

5154 for tech support. They were calling me various phone numbers from 661-748-0244, 661-

748-0240, 661-748-0242, 661-380-3000, 661-748-0245, but when I called the numbers back, it

did not go through. I thought that was odd. After they failed to answer my questions, I decided to

terminate the relationship. I spoke to a manager named Sonya who was shooting the “energy”

over the phone. There is no DNF Global Solutions with Mike Hughes as the President. 866-921-

5154 is the Toll-free number to an all-inclusive exotic vacation; http://allinclusive-adult-

vacations.com/desinaion.htm, as well as, to an India phone number. The phone numbers that the

“technicians” were calling from apparently were fraudulent because many people were

complaining about how they were unethical telemarketers. My computer has not crashed so the

forensics can be obtained off it to get their IP Address so that their illegal activities can be

stopped. Even though I brought System Mechanic Premium $60.00, and the Administrator on the

computer is not allowing the Cd to run, but allowed the recovery console, which was on the c

drive to run. I never downloaded the SW so it could not repair the computer. I even told the Best

Buy representative that the computer is not allowing the SW to run to fix the computer. I was

told that I had to buy the same product, because of copy right infringements. I did not open the

new SW package because I know what would happen. I decided to buy another computer on

5/23/2012. I decided to check out if this was indeed a new computer. This is what I did to

determine. I went to Control Panel, selected Systems & Security, selected Administrative Tools

and selected Event Viewer. In Event Viewer, I selected Windows Logs and Applications and

Services Logs and searched them and I learned that there were some recent activities on May 6,

2012. There were no setup events, some features were blocked out, and I changed the feature

under properties to do not overwrite because I wanted to save the history. Then I went to the

installed programs and saw that Adobe Flash player and Bing bar was installed on May 6, 2012.

In order to install the Bing Bar and Adobe Flash player, you have to be connected to the Internet,

but there’s no activity for the Internet Explorer. My files are changing to hidden files or to

shortcuts so now there is a virus on this one as well even though Norton is running. Everything

was sealed perfectly. It did not look like it had been opened. This is where the ability to reseal

products, without any evidence of it being opened comes into play. By the way, I am not been

connected to the Internet. I have been on Microsoft Word all day. Are there any special operation

forces or law enforcement working in Wal-mart’s electronics department? How was this

possible?

Our Health: Since 2009, all of our health has declined due to the move in of our new

neighbors. I am very concerned about my elderly parents’ health. My once very healthy and

very active elderly parents now complain about aches and pains, headaches, bloodshot

eyes, diarrhea, certain part of the body hurting. My father has myeloma, which could be a

contributing factor to the environment. This was confirmed by his oncologist and it is even

mentioned on the Dept. of Veteran Affairs’ website. Many of their family members, friends,

and associated come to the house under the auspices of seeing them, but now they are coming to

contaminate the house with more toxins by getting me. It would be hard to believe that almost

everything that we buy is contaminated from stores in NJ or PA. I filed a complaint because

when I went to CVS and brought 2 products, Arizona Green Tea and CVS Cheese Doodles.

Minutes after eating or drinking the products, my throat, my mouth and down in my esophagus

broke out in blisters. I tried to contact both companies, but I was being blocked from contacting

them. We live in a semi-attached house and my neighbors have used a generator inside their

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house against the wall that we share. A generator produces electromagnetic radiation. This was

one irrefutable fact that I sent to the Mayor and to the Governor’s office about them, but I know

that my faxes are being intercepted. I have to go there in person like I did last May. We all have

implants or some medical devices, which the Stanley Stud Sensor 150 ($15.00 at Wal-mart)

picks up. I tried running a stud sensor on a complete stranger and it did not beep once, so I know

that we are implanted with something. Implants change your DNA according to L.A.

Marzulli. You can listen to him on Thursdays from 7 to 9 pm CST. You can listen live at

858-216-3403 ext. 123456# or you can speak to L.A. Marzulli at 1-800-787-5044.

Constant Computer and Network Disruptions: This has been consistent every day, even

with this “new” computer now. There has never been a time in the past 5 ½ years, which I

did not have some type of computer or network disruptions. As a result, I am not able to

communicate freely with others or send information to others. I feel like I am a slave.

Email Accounts: My email messages are delayed or never delivered, returned undelivered

several days later, or people are receiving the emails days later after my event. My email

messages are rearranged, edited, or deleted. I have been told that my emails are being

compromised; data changed or attachments are missing. I got a permanent failure message from

my own email account, which I had created a couple of days later. This is my biggest problem

because either (1) not all of the people who are on the email lists are receiving my emails in a

timely fashion, without any modification or (2) my emails are being re-routed to people who

were not on my email list. Then I received a message from someone who has an attitude, because

they received a message about God or prayer. I had to stop using one email account because I

kept getting an error message and I could not attach any documents. The only people that I

hear from are informants. All emails to the media are never delivered.

Websites/Blogs: In attempt to get the word out about my organization and events, I have

developed blogs and recently paid someone to develop a website. The content of the websites are

altered, deleted, or completely taken down. The passwords are changed on the blogs. People are

being redirected to an earlier version of my blogs or websites, which does not contain the

information about the current event. This is even true for my paid website. People have received

a message that my website/blog no longer exists or is under maintenance. I am blocked from

sending information on many websites.

Social Networks: I am not able to enjoy the full benefits of the services like all of the millions of

customers have been receiving email messages from my social network account indicating that

[such and such] has accepted your invitation. For example, when I went to the profile of one

person, I found out that she lived in the suburbs of Trenton, NJ and she was only in her 20’s. I

sent her an instant message and told her that I did not know her and how did she get on my

friends list. After I sent that message, someone removed her name off of my friends list

immediately. My latest acceptance was from my uncle who is in his 70’s. First, I did not send

him an invite and second, I did not know that he had a social network account. I thought that

social networks are an excellent tool to promoting my events, but I have been unsuccessful in

inviting people to my events because every single time, I get an error message and after 2 or 3

times of trying, I just give up. Even though, I reported that someone has been stalking me to

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them, now I got a message that I will lose my privileges, because someone has reported that I

sent them invitations, which I did not?

Hosting Conference Calls: I have been unsuccessful in hosting conference calls, unlike my

other 2 fellow organizations who use the same service. When I called conference call’s website

first it said that my pin was being utilized by another person. After the 3rd attempt, that message

was no longer there; now the number was being redirected somewhere. It never connected to the

conference call’s website to allow me to host my conference call. I verified the call id number

and pin number several times and it was correct. I called back and the same thing happened. I

reset my cell phone. I called back and the same thing happened. After 30 minutes, I decided to

get my parent’s landline phone. I called the conference call’s website number, enter my pin

number and call id number and the problem persisted and it never connected to conference call’s

website. The duration time on the phone was running, but I could not host my internet show. I

sent emails to them about the problems, which stopped when I said that I needed the

name/address of the attorney so that I could send a CEASE and DESIST letter to them.

Obviously, one can conclude that my phone calls are being redirected. Why did I go that far until

the harassment stopped?

Broadband Modem: This broadband Modem has never worked properly since July 2011.I had

one previously several years ago and I did not have any problems. I have spent hours on the

phone with customer representatives since July 2011. I overlooked the problems thinking that I

was not getting a good signal. I missed conference calls that I was suppose to host because my

broadband modem kept getting error messages. Even though there is a strong signal, the

problems persist. When I dialed in, I get the same repeated messages and when I called customer

service, I am told that this problem is on their end. I stopped calling the customer service and just

documented all the problems and the error messages. I have an airtight case that proves that all of

the problems are coming from there. I believe the vehicles that are speeding excessively beyond

the 25 m.p.h. are sending “energy” that affects the Broadband Modem.

Mobile Phone: I purchased this new phone during the Thanksgiving weekend. I was supposed to

have free delivery, but there was nowhere on the website for that option so I selected 3 days and

it cost me $4.95. Within the 30 days to return the phone, I called customer service because I

wanted a refund and a new phone. After being transferred 3 times, the call was disconnected or

the person hung up on me. When I activated the new phone immediately I received text

messages and phone calls from people that I did not know. I only gave this new number out to

less than 10 people. When I went to set-up my voicemail, it was already set-up. I am receiving

“network failure” when I call and I have 2 or 3 bars displayed, which indicates a strong signal.

The customer service representative is trying to keep me on the phone longer than I need to be

and every time I did not feel good after speaking to someone.

Internet Phone: People have informed me they have called my office number 347-568-3537

and that they have received a message saying that this number is out of order. This is a vanity

number so I am paying extra for a number, which says “out of order” all the time.

Customized Laptop: I brought this customized laptop, but there have been numerous problems.

Even though my laptop was under warranty, I was recently sent a “recertified hard drive”, which

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crashed after less than 3 hours of usage. I was not on the Internet. The factory installed software

has many software problems each and every time. Many of the features do not work. A product,

which I paid for, took 3 tries before, they got it right. I paid for it in order to expedite delivery

and they did not want to give me a refund because of their “human error”. The customer service

representative is trying to keep me on the phone longer than I need to be and every time I did not

feel good after speaking to someone.

Mailing Services: There has been interception of my most important letters, long delays in

delivery; and tampering with contents. There have been contaminants on almost all of my mail

that we receive in this house and at my post office box. I filed my complaint with the Post Office

and someone returned my call, without identifying himself or leaving any contact information

said that there could not be anything on the mail. He stated that since anthrax all of the mail is

screened for any contaminants. This would mean one thing that the contaminants are being

placed on all of our mail after the screening process. I had one package tested and it tested for

molds/mycotoxins. I had a certified Industrial Hygienist analyze the report and he determined

that due to the exposure, I may develop tumors in the next 10 years. He also determined that this

was HAZMAT. How many people are handling the mail after that process? Who should I send

the bill to be reimbursed for the testing, analysis by the Certified Industrial Hygienist and the

contamination of my Coach briefcase?

Alarm/ Security System: A security system should keep burglars out and protect your personal

belongings and property, but these “informants” are able to bypass the security system, secured

windows, secured doors and enter our dwellings, without any signs or evidence of a break-in.

They are also able to commit thefts without showing any signs of a break-in for vehicles as well.

This is called “covert entry”. Special Operations Forces and Law Enforcement Officers are

taught their tactical covert entry skills. Are they teaching informants, some who are thieves,

drug users and murderers this expertise? If they are doing this, it is a violation of Federal laws.

Who should pay the claims for the stolen, damaged, or contaminated contents in this house: the

security system company or the Federal Government? My car has been broken into and they

have placed my possessions that were in the house in the car. This is called “gas lighting”.

Information Changed on Copyrighted Materials: There has been illegal access to products

without leaving any evidence of opening the packages. I had brought brand new software

wrapped in the plastic and one day when I went to use it, the plastic was missing. When I

installed the software, some of the features were deactivated or missing. I have problems with

flash drives, memory cards, cameras, printers, software, and mobile phones. Some of the features

are deactivated. This is copyright infringement.

Theft/Tampering of Information/Records: My records have been changed, deleted, altered or

stolen. They were stealing complete folders of my bank accounts records, insurance, etc. They

want to make me as financially poor. My folder became empty or they left one piece of paper or

a couple. If someone came after me for a bill, I would not have any way to dispute that it was

wrong or right. I had to stop being so organized. This also included my email accounts.

Recently, I was in my parent’s house alone and I had just included the name of the person who I

was speaking to on the phone in my May 10th entry of my Franklin Covey planner. I took

meticulous notes about that company DNF Global Company. Someone bypassed the locks and

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took my banking information and my entire month of May in a matter of minutes. I knew where

I had it because I always keep it in my yellow pad, which I carry with me all the time.

Federal Government Has a Long History of Discrediting Non-Consensual Human Subjects

First, the U.S. has a 110 year history of experimenting on its own people without his or her

consent. It is safe to say that the U.S. has a lot of experience in this area. One famous African-

American writer, Gloria Naylor wrote a book, called “1996”, a fictionalized memoir about her

experience under Government surveillance. Eileen Welsome, Pulitzer Prize winning reporter and

author of The Plutonium Files: America’s Secret Medical Experiments in the Cold War said,

“Basically, they confirmed that thousands and thousands of experiments had been done on U.S.

Citizens. That the victims were the most vulnerable people in our society: the young, the

disenfranchised, the poor, people of color, people who did not know enough to ask questions. In

other words, the subjects were not doctor’s children or friends of their doctors; they were people

who were vulnerable. The biggest revelation for me was to see how cruel and inhuman these

very educated doctors were toward their patients.”

In the past, many of the non-consensual human subjects were clinically diagnosis with

“housewife syndrome”, “neurotic” and “paranoid schizophrenia”. They were also being given

disinformation. Many of them were experimented on for the rest of their lives. It appears that

history is repeating itself. Currently, many non-consensual human experiments participants are

still being clinically diagnosis with any type of mental illness, “neurotic”, “paranoid

schizophrenia” or “delusional” so that they would appear unbelievable to their family, friends,

and loved ones.

The ACHRE’S report depicts that Federal Government officials made them think that they were

“crazy”, but in essence, they were telling the truth. It’s the perfect plan: Discredit the “enemy”

so that no one would listen or believe him/her so that they can carry on with their evil

plans.

Here’s the excerpt from the ACHRE’s report:

Disinformation and Nuclear Fallout “In the nuclear arms race, government doctors and

scientists brainwashed the public into believing low dose radiation was not harmful. Some

officials even tried to convince people that “a little radiation is good for you.” Totally ignored

was the knowledge that the radiation from nuclear fallout could lead to an increased risk of

cancer, heart disease, neurological disorders, immune system disease, reproductive

abnormalities, sterility, birth defects, and genetic mutations which could be passed on from

generation to

generation. The full extent of this radiation damage to the American public during the Cold War

years will never be known.

A secret AEC document, dated 17 April 1947, reveals that physicians were aware of these

radiation hazards but simply ignored them. Under the title “Medical Experiments in Humans,”

the memorandum read: “It is desired that no document be released which refers to experiments

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with humans that might have an adverse effect on public opinion or result in legal suits.

Documents covering such field work should be classified ‘Secret’.”

According to Gallagher, many downwinders testified that the Public Health Service officials told

them that their ‘neurosis’ about the fallout was the only thing that would give them cancer,

particularly if they were female. Women with severe radiation illness, hair loss, and badly

burned skin, were clinically diagnosed in hospitals as “neurotic.” Other severely ill women were

diagnosed with “housewife syndrome.” When Gallagher’s investigation led her to ask a

Department of Energy spokesperson about the AEC/DOE’s practice of waiting until the wind

blew towards Utah before testing nuclear bombs or venting radiation in order to avoid

contaminating Las Vegas or Los Angeles, the unabashed and unconcerned official actually said

on tape, “Those people in Utah don’t give a s*** about radiation.” The sad part about Elmer

Allen’s story is that nobody believed him. He went to his doctor and told him, “I think I’ve been

injected with something.” His doctor diagnosed him as a paranoid schizophrenic at the same time

that he was conversing with the atomic energy scientists in Argon National Lab to provide them

with tissue samples.

Final Thoughts

Did you know that 25% of America’s budget, our taxpayers’ dollars is for national security?

Why are millions of innocent law-abiding American citizens’ rights being violated using our tax

payers dollars under the auspices of national security and War Against Terrorism? My family

and I have been exposed to high concentrations of biological/chemical/radiological weapons and

electromagnetic radiations due to these informants. It has been since last year that I have not

eaten food, without any type of toxins on it. This was because many of the Tis went to eat out

after the Bioethics Commission Meeting in New York. As Corporation/President, you are held

accountable for the actions of your employees. In the past 2 days, I have been to Wal-mart, Best

Buy, and Kinko’s and they were using their technology on me. In many cases, they came in

ahead of me and shot up the store with it on your products and in the air. They could have rode

by your establishment and shot the “toxins” in there. Last night, I blanked out in Best Buy for

one second. Should I go and file injury reports in these stores because I suffered bodily injuries?

I was in Shop-Rite and I was being shot in my lower back that it was affecting my walking. I had

to get out of that store quickly. I could barely walk and I was in pain for several days. I have

suffered in silence for the past years from going temporarily blind to my entire body swelling up

because of the technology being used on me. I am tired of being on the phone with customer

service representatives who want to keep me on the phone as long as possible so that I can get

sick. This is premeditated murder. If I suffer injuries because of “informants” either on the

phone or in your establishment should I file injury reports? Arrests should be made. Doctors

should lose their licenses. Restaurants should be fined. Police should lose their badges. We need

to stop this now, before it is too late.

Many non-consensual human subjects/TIs have suffered emotionally, financially, and physically

at the hands of your “informant” employees. Who should be held accountable? Sometimes, they

are parked or driving by your establishment shooting the contaminant into your store? Laws must

be ratified. Laws must be enforced. Many people cannot believe that they are part of something,

which is so sinister. People should be held accountable for their actions.

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Corporations/Businesses/Organizations/Religious Institutions participate in the proposed

Reconciliation Program. Your Congressional Representatives, Governors, and President Obama

should be contacted immediately. We need something done today like an Executive Order to be

issued here in America for citizens monitoring, tracking, and targeting using technology by

fellow citizens. In addition, you will assist us in bringing to justice those who have committed

these crimes. We cannot do it, without your support. It is us today, but it could be you and

your loved ones tomorrow. We must stop this before it is too late. Will you stand up with us

starting right now? We want to have an enjoyable Memorial Day weekend like you.

"These technologies should be in place to empower citizens, not to repress them," Obama said in

a somber speech at the United States Holocaust Memorial Museum in Washington. The Germans

were very good at deception. Letitia Peters states, “Once I lived in a rose-colored world. I

thought that if you lived a good life, got a good education and never bother anyone then

everything will be alright. No one would fathom to think that people could be so jealous or evil.

The people in the Federal Government are abusing their power and authority. They have played

god for too long with people’s lives; destroying families, people’s reputations, maiming them,

putting them in prison, mental institutions, driving them to suicide or worst killing them. They

are amaze that I am still alive, because of everything that they have done to me and tried to do to

my family, even to my little “babies” to get me to stop. They try to turn my family against me

who I love very much in spite of everything that has happened, because I know that it has been

external forces that are doing this to them. Many of the tactics were done by the Nazis. I have

been treated worse than an animal because I am a Prophetess. People seem to forget the rule,

“Do unto others like you would have done to them”. I give all the glory to the one and only true

God, Jesus Christ. The other day I saw an emblem that said “Black Ops” on this jeep. Is this

what my family and I have been placed in because I wanted to work in a healthy and safe

environment that was not making me so ill? Was it because I was an attractive (humbly

speaking) African-American woman? You can watch my movie at

www.youtube.com/nimsociety. One thing that they have focused on is my appearance. A

beautician put something in my hair to make it hard and when I went to a cousin’s house, they

were shooting my head. When I left, I had a headache and fine red bumps were in my scalp. A

couple of days later, my long hair was coming out in clumps. I looked like I was a cancer patient.

I started to wear a wig all the time, which I never had to do in my entire 40 years on this planet.

I know that they gave me a very high dosage of radiation because I did not have my menstrual

cycle for months and my body was never the same. I had to do very aggressive detoxification.

Many of them are found in this free e-book at www.radiationdetox.com. It is almost impossible

to get well, when even the things that are supposed to make you well like eating organic foods at

Trader’s Joe are also contaminated by these informants.

Last year, I was on my way to one of the Torture Treatment Centers so that I could be examined

and they used the “energy” on my parents; thanks to my neighbors next door. Has this what

America has come down to doing things to others because they think that they can? People have

allowed their personal opinions to interfere what they are supposed to be doing according to their

job description. If this is the future of America then we are in trouble? I recently watched a PBS

documentary called “Not In Our Town: Class Actions” (www.pbs.org/niot) and it illustrated

stories of people who were fighting against injustices and intolerances in towns across America.

We request the help & support of as many people as possible in America and in other nations.

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Will you be a bystander, perpetrator, victim, or victor? The choice is yours. Will you Cricket,

Straight Talk, Hewlett-Packard, Verizon, Comcast, Wal-mart, Staples, Best Buy, IHOP,

P.F. Chang’s, Acme, Wegman’s, Panera Bread, Amtrak, Fed Ex, Kinko’s, USPS,

Gatewood Marketing, Ning, Facebook, Twitter, Gmail, Hotmail, Marshall’s, PFC, Daystar,

Trader Joe’s, Whole Foods, Shop-Rite, CVS, Federal Government agencies (Social

Security, FDA, IRS & HHS to name a few), City of Trenton, NJ, State of New Jersey, State

of PA, State of MD, Congressional Reps and President Obama, the United States of

America etc. etc. take a “zero tolerance” approach against stalking, attempted murder,

fraud, stealing, tampering with your products, overcharging, use of a deadly weapons

(biological, chemical, & radiological), and crimes against humanity committed by

employees, customers, or members who are “informants”, “perps” or Intelligence

contractors? I had enough of this “craziness”. We can’t change the past, but we can change the

future right now. Everyone is entitled to life, liberty and security of person, freedom from slavery

and servitude, freedom from torture, or cruel, inhuman or degrading treatment or punishment,

equality before the law, not being subjected to arbitrary arrest, detention, or exile, freedom of

movement and residence, nationality, the right to marriage and to found a family, freedom of

thought, conscience and religion, peaceful assembly and association, work, health, and

education. Who’s the informant at your business, organization, school, church, workplace, in

your neighborhood, or among your family, friends, or associates? “

Thank you for your time and consideration. I thank you for your support in advance. If you have

any questions or concerns, please contact me at 347-568-3537 or at [email protected].

Sincerely,

Letitia Peters, Founder of International Spiritual Awakening Ministries

P.S. Please read the final article in the trilogy: The Proposed Solutions

Posted 2 years ago

3 notes

crimes, informants, perps contractors, President Obama, perps, digital guns for hire,

May 6

Non-Consensual Human Subjects Research Related Documents To Download

Coalition Against Non-Consensual Experiments to download. This link was updated as of May

6, 2012.

Posted 2 years ago

Apr 26

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Human Subjects/TIs to HHS Secretary & Congress: Request to “Opt-out” of

Unethical Research & Propose a Moratorium

In this first article, we will discuss justice for the non-consensual human subjects/TIs. Since the

non-consensual human subjects/TIs meet the definition of being a “human subject” in a

“research” or “medical experiment”, they can request to “opt-out” of the human subject research

at any time without prejudice. This is stated in Federal law. These “researchers” are operating

above the law and below the accepted standard of scientific, ethical, and humane research.

There is no way for the non-consensual human subjects/TIs to determine the name of the

research or medical experiment, because there are over 55,000 projects, which involves human

subject research and we were placed into this human subject research without our informed

consent or knowledge. Since January 15, 2009, all IRBs must use the Internet-based registration

maintained by HHS as stated in 45 CFR 46.501. Is the answer right on HHS’s website since all

IRBs have to register with HHS?

For the past 15-20 years, both HHS and Congress have failed to close the gaps or “loopholes” to

protect the human subjects. Year after year, they have continued to sponsor billions of dollars in

human subject research, without ratifying any laws to protect the human subjects. Currently,

NO ONE is IMMUNE from being used as a human “guinea pig” because the laws are not

there to protect you! First, we seek a moratorium on all U.S. human subject research. Second,

we want Congress to conduct hearings on COINTELPRO-like activities and pertaining to the

obstruction of justice being committed by “informants” or people part of the neighborhood

watch. Finally, how do HHS and Congress intend to ratify laws to protect human subjects in the

future? Recently, the world has seen in the killing of Trayvon Martin, which was an awful

tragedy in itself, where the police chose not to enforce the law, even with all of the evidence

presented. It took people from all ages and walks of life rallying, signing petitions in order for

justice to prevail. We thank God for answering our prayers. The case for Trayvon Martin

represents all of us who have been seeking justice, but were unable to get it before. Now the bar

has been raised to a higher level in America. The non-consensual human subjects/TIs are seeking

justice because the laws are in place, but the “people” are choosing not to enforce or adhere to

the laws. Our slogan is “We say NO to COINTELPRO and YES to JUSTICE. We say NO to

NON-CONSENSUAL HUMAN EXPERIMENTATION, and YES to JUSTICE. Will you

stand up with us to seek justice for the non-consensual human subjects/TIs as well?

HUMAN SUBJECTS/TIs TO HHS SECRETARY & CONGRESS: REQUEST TO “OPT-

OUT” OF UNETHICAL RESEARCH & PROPOSE A MORATORIUM ON ALL U.S.

HUMAN SUBJECT RESEARCH

“It is a moral issue, but for many it violates their religious beliefs and principles.”

April 24, 2012 -Trenton, NJ- In 1997, former Senator John Glenn said, “I want to put this in

personal terms once again. You just think about your own family, your own son, your own

daughter, or grandchildren who might be, the next time they go to a doctor, the subject of some

medical experiment that they are not even told about. I do not think there can be many things

more un-American than that. That is unconscionable, and we should not permit that.” Why are

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there still non-consensual human subject research occurring in 2012, which are maiming, killing

or driving people to suicide? Aren’t there laws in place to protect the human subjects?

In Dr. Harriett A. Washington’s book, Medical Apartheid documents many non-consensual

human subject research/experiment cases. In 1994, the Medical University of South Carolina in

Charleston was accused of enrolling poor African-American women into narcotic-treatment

research without their knowledge. In 1995, an experimental measles vaccine was tested on

mostly African-American and Hispanic children in Los Angeles, without receiving their parents’

informed consent. From 1994 to 1995, New York City law enforcement officials helped

researchers coerce African-American parents into enrolling their boys into a study that sought to

establish a genetic propensity for violence, without receiving their parents’ informed consent.

This scourge has spread beyond racial minorities, as detailed in her new book, Deadly

Monopolies. Since the 1980s, approximately 20 U.S. research projects have won legal waivers

allowing them to bypass any form of informed consent. In 2011, drug giant Pfizer paid $75

million to settle claims that children in Kano state, Nigeria, were injured or killed by non-

consensual administration of its experimental meningitis drug Trovan.

Letitia Peters, a former Federal Government electronics engineer and non-consensual human

subject states, “I would have never imagined that as a law-abiding U.S. citizen (except for a few

parking and speeding tickets) that I would be going through horrific ordeal in America and in

2012. All attempts to silence me with extreme persecution, torture or by any means possible have

failed. I have been treated worse than an animal. I speak on behalf of countless of men, women,

and children in the U.S. and around the world. We are Americans and are entitled to nothing

less than the full rights of every American. The acts of violence that have been taken

against us, should be condemned by all Americans and those worldwide who value freedom

and justice. We have become someone else’s property because our rights, welfare and safety

have been affected. Isn’t that slavery? Now, we are human subjects in a project involving human

subject research without our knowledge or informed consent. For many of us, it is a moral issue,

but for some this violates our religious beliefs and principles. The current Federal laws have not

protected us. I would never “volunteer” to be a human subject with my many health ailments

confirmed by several physicians. The three generations of my family has been placed in this

unethical, human subject research. I love my family, but to do this to the children and to my

elderly parents is totally unacceptable. Is this genocide? My family does not believe that they

have been placed in this unethical, human subject research. History is repeating itself. Logically,

it does not make sense and it is not the acceptable norm. No man has the right to do this to

another fellowman. Many of you would not like it if the tables were turned and this was being

done to your family. Why are you doing this? You are serving Satan who comes to kill, steal,

and destroy. In Jesus’ name, may the angel of the Lord persecute and chase them who are

adversaries to our souls and want to do us harm.

I WOULD NEVER DO THIS TO ANYONE: NOT TO MY FAMILY, FRIENDS,

NEIGHBORS, OR EVEN COMPLETE STRANGERS.

I have a strong spiritual faith and belief in God/Yahweh and this violates my faith as a follower

of Jesus Christ/Yeshua. I thank my enemies for helping me to develop a closer relationship with

Yahweh through Yeshua. He has been my provider, refuge, fortress, shield, vindicator, healer,

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fortress, restorer, and deliverer. He is the only reason why I am still alive because of His grace

and mercy. I stand on the Word of God in the Holy Bible because it is the only truth 24/7. I love

Yahweh with all of my heart, mind, soul, and strength and He is worthy of my praise. It is

finished! Hallelujah!

No Response from HHS about Opt-Out Requests

Letitia Peters, further states, “in my in-depth research, I discovered that America has a 100 year

history of using minorities, especially African-Americans and their children and women as

“guinea pigs” without the human subjects or parent’s knowledge or informed consent. In

addition, this human subject research does not comply with 45 CFR 46 Subpart A, “The

Common Rule” because the rights, welfare, and safety of the human subjects have been affected

and the research involves more than minimal risk. The research practices, which we are

experiencing can be reclassified as “cruel and unusual punishment” or “crimes against

humanity”, which goes way beyond the physical or psychological harm that is normally

encountered in the daily lives, or in the routine medical, dental, or psychological examination of

healthy person as defined by minimal risk. This is torture. Many are maimed, been diagnosed

with cancer or other illnesses, committed suicide or died a premature death. The basic ethical

principles of respect of persons, beneficence and justice as stated in the Belmont report have

been violated. Human subjects should be protected by the authorized agency, HHS and not by

the researchers.”

On March 2, 2012, I emailed an 8 page letter to HHS requesting to “opt-out” or discontinue

participation in this human subject research, but I have not received an official response from

them. On March 20, 2012 and April 12, 2012, I emailed a second request using this opt-out form.

Others have also written to HHS Secretary Kathleen Sebelius requesting that as a human subject,

we have a right to be “opt-out” or discontinue participation in a human subject research.

Case of Elmer Allen, a Non-Consensual Human Subject Diagnosed as Paranoid

Schizophrenic

It is documented in official Federal Government medical records/documents that the Federal

Government scientists diagnosed many non-consensual human subjects with “neurosis” or

“paranoid schizophrenic” who stated that he/she was being experimented on by the Federal

Government. For example, this was documented in the case of the late Elmer Allen. The sad part

about Elmer Allen’s story is that nobody believed him. He went to his doctor and told him, “I

think I’ve been injected with something.” His doctor diagnosed him as a paranoid schizophrenic

at the same time that he was conversing with the atomic energy scientists in Argon National Lab

to provide them with tissue samples. Elmer Allen was not only used in 1947 when he was

injected with this radioactive isotope, but he continued to be used as a guinea pig for the rest of

his life. When Elmer Allen’s daughter, Elmerine was interviewed, she told the story of when she

left for college, her father would tell her watch out, “Don’t let the U.S. government guinea-pig

you.” And they always thought that Elmer Allen had some kind of, well, Elmer was kind of

quirky, and he had this delusion that the government experimented on him.

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In the 1970’s, a second generation of atomic scientists rediscovered this experiment. So they

wanted to dig up all the people who were dead, who had been injected with plutonium, and they

also wanted to bring whoever survived them back into the lab for further studies. Elmer Allen

was one of those people who was still alive.

AMY GOODMAN: Under what pretext since he didn’t know, supposedly, that he was a U.S.

government guinea pig?

EILEEN WELSOME: They told Elmer, and this is all documented in the medical records, that

they knew he had a very serious cancer and they wanted to know how he had lived so long.

The entire transcript about Elmer Allen is at

http://www.democracynow.org/2004/5/5/plutonium_files_how_the_u_s.

Discredit the Non-Consensual Human Subjects/TIs by Committing them to a Mental

Institution by “Any Means Possible” so that the Evil, Unethical Research Continues

Elmer Allen was telling the truth about being a Government “human guinea pig”, but the sad part

of his story is that no one believed in until many years later. The researchers continued with

experimenting on him for the rest of his life. Today, the same thing is occurring, but the

experiment involves more advanced hi-technology. Technology is constantly changing and

people are unaware that some technology can be used on them without them even knowing it.

Electromagnetic radiation is one of them, because it is invisible to the naked eye. People are

unaware that electromagnetic radiation can change their pleasant, easy going personalities into

angry or hostile ones in a matter of seconds or even make someone irritated by bringing up a

particular subject. Many would not contribute their illness, like cancer, brain tumors, or even

aches and pain due to being exposed to electromagnetic radiation because it is invisible.

Like Elmer Allen, many non-consensual human subjects/Targeted Individuals (TIs) have tried to

bring this to the public’s, family’s, or friend’s attention, but they have been called “crazy”,

“delusional” or been diagnosed with a “mental illness”. The game is the same, but the “players”

have increased because the stakes are higher. Now, police officers, psychiatrists, judges,

physicians & the human subjects own family members, friends, and associates are being used to

“discredit” the non-consensual human subjects/TIs. Many of these individuals are “informants”

(perps or perpetrators, moles or double agents) or part of the “neighborhood watch”. The police

have been involved in many non-consensual human subjects/Targeted Individuals (TIs) being

committed “for observation” even though they were not harming themselves or others. Some

have said that the police lied to them and even put them in handcuffs to take them to a mental

institution. Who would believe a “crazy person”? Now the committed non-consensual human

subjects/Targeted Individuals (TIs) are afraid to speak about their ordeal because they fear that

they might be recommitted again and this time even longer. All of the non-consensual human

subjects have stated that it has never been suggested for them to see a psychiatrist, but the

human subjects/TIs are carried off to be committed to a mental institution. This tactic is

also a form of adult “bullying” in order to intimidate the non-consensual human subject to

keep silent. It can also be perceived as an “abuse of power” as well.

Many non-consensual human subjects have been wrongfully committed to mental institutions

and given a diagnosis of schizophrenia, neurosis, or other mental illnesses. Schizophrenia is a

disease that typically begins in early adulthood; between the ages of 15 and 25. Men tend to

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get develop schizophrenia slightly earlier than women; whereas most males become ill between

16 and 25 years old, most females develop symptoms several years later, and the incidence in

women is noticeably higher in women after age 30. The average age of onset is 18 in men and 25

in women. Schizophrenia onset is quite rare for people under 10 years of age, or over 40

years of age. Schizophrenia is a devastating disorder for most people who are afflicted, and very

costly for families and society. The overall U.S. 2002 cost of schizophrenia was estimated to be

$62.7 billion, with $22.7 billion excess direct health care cost ($7.0 billion outpatient, $5.0

billion drugs, $2.8 billion inpatient, $8.0 billion long-term care). (source: Analysis Group, Inc.)

This is being done so that no one will ever investigate these allegations and the scientists can

continue with their evil, unethical human subject research. There’s a saying “what’s done in the

dark will be brought to the light”. In Luke 8:17 states, “For nothing is secret, that shall not be

made manifest; neither any thing hid, that shall be known and come abroad.” This is what

happened in the case of Elmer Allen who lived to be told that he was in a human subject research

for over 20+ years, without his knowledge or informed consent. He was telling the truth and he

was not delusional. Truth did prevail. We will fight for all human subjects/TIs that were

wrongfully diagnosed with a mental illness to have this permanently expunged from their

medical records.

Non-Consensual Human Subjects/TIs Should Send their “Opt-Out” form to HHS and to

Congress

The “Common Rule” has not been updated in 20 years and has failed to protect the human

subject since 1991. Obviously, there are serious deficiencies with informed consent in the

“Common Rule”. There is no enforceable Federal regulation or International standard on the

books for informed consent to be required because Congress has failed to ratify any proposed

legislations pertaining to human subject protection in 1997, 2002, 2003, 2004, 2006, 2008, and

2011, thus allowing for unethical human subjects experiments to occur.

Non-consensual human subjects/Targeted Individuals (TIs) should revise this “opt-out” form by

inserting in their own story concentrating on their pain and the violation of their rights, safety,

and welfare as a human subject and send it to HHS Secretary Kathleen Sebelius at

[email protected]. The mailing address is:

The U.S. Department of Health & Human Services

H.H.S. Secretary Kathleen Sebelius

200 Independence Ave. SW, Room 120F

Washington, DC 20201

HHS Main Number: 877-696-6775

Comment Line: 202-205-5445 (Please leave a comment)

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Correspondence: 202-690-6392

Fax: 202-690-7203

HHS Secretary Sebelius conducted a special plenary presentation at the National Action Network

Conference in Washington, DC today.

Non-consensual human subjects/Targeted Individuals (TIs) should also send their form to their

Congressional representatives (www.congress.gov or contact the switchboard: H.R. 202-225-

3121 or Senate: 202-224-3121 to find out the name of your Congressional representatives.)

Non-consensual human subjects/TIs can also request a Microsoft word version of the form with

the highlighted areas which they should change by sending an email to [email protected].

This will also include an introductory letter to HHS Secretary Sebelius.

I echo the words of Dr. Harriett A. Washington, ”Just as U.S. physicians demanded justice at

Nuremberg, Nigerian parents stormed courts in Kano and Manhattan to demand that we live up

to our stated ideals. Sixty-five years on, it is high time we did.” Don’t you agree?

Here’s the “Opt-Out” form:

Introduction:

In the Bioethics Commission’s report released on December 15, 2011, the Bioethics Commission

suggested that to keep track of the more than 55,000 research projects using human subjects, the

Federal government should create a central online portal and database where basic information

about the projects are archived and made easily accessible and further concluded that it “cannot

say that all federally funded research provides optimal protections against avoidable harms

and unethical treatment”. The Bioethics Commission also said although human subjects in US

government-funded research are generally protected by existing rules and regulations, their

safety and well-being could be enhanced with stronger measures, including increased public

transparency and a system of compensating subjects who sustain research-related injuries.

Human subject research should adhere to the ethical principles and guidelines for the protection

of human research participants summarized in the uniform set of regulations, called the Federal

Policy for the Protection of Human Subjects, 45 CFR 46, Subpart A, formally known as the

“Common Rule.” The 45 CFR 46 regulations are based in large part on the Belmont Report and

were written to offer basic protections to human subjects involved in both biomedical and

behavioral research. Today, 45 CFR 46, Subjects A and E: Registration of Institutional Review

Boards (added 1/15/2009) is shared by 17 Departments and Agencies, representing most, but not

all, of the Federal Departments and Agencies sponsoring human subjects research. Many of them

have not adopted Subpart B: Additional Protections for Pregnant Women, Human Fetuses &

Neonates Involved in Research, Subpart C: Additional Protections Pertaining to Biomedical &

Behavior Research Involving Prisoners as Subjects, or Subject D: Additional Protections for

Children Involved as Subjects in Research. For the past 20 years, 45 CFR 46, have been

considered merely “guidelines” and is not a lawfully, promulgated regulation.

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Before a research project involving human subjects is initiated, it must be reviewed and

approved by an Institutional Review Board (IRB). The IRB has a central role in ensuring that all

human subject research is planned and conducted in an ethical manner, and in compliance with

federal, state and local regulations. The major responsibilities of the IRB are to assess the risks

and benefits of proposed research and to promote respect for its advice and counsel in

safeguarding the rights and welfare of human subjects.

Research is defined by the Common Rule regulations as “a systematic investigation, including

research development, testing, and evaluation, designed to develop or contribute to generalizable

knowledge. Activities which meet this definition constitute research for purposes of this policy,

whether or not they are conducted or supported under a program which is considered research for

other purposes. For example, some demonstration and service programs may include research

activities.” Medical experiment is defined by California Law, Health & Safety Code Section

24171 as “the severance or penetration or damaging of tissues of a human subject or the use of a

drug or device, electromagnetic radiation, heat or cold, or a biological substance or organism, in

or upon a human subject in the practice of research of medicine in a manner not reasonably

related to maintaining or improving the health of the subject or otherwise directly benefiting the

subject.

Human Subject is defined by the Common Rule regulations as “a living individual about whom

an investigator (whether professional or student) conducting research obtains either a) data

through intervention or interaction with the individual or b) identifiable private information.”

Human subject is defined by FDA regulations as “an individual who is or becomes a participant

in research, either as a recipient of the test article or as a control. A subject may be either a

healthy human or a patient. Subject [also] means a human who participates in an investigation,

either as an individual on whom or on whose specimen an investigational device is used or as a

control.”

Failure of OHRP to Investigate Allegations

In the March 14, 2006 letter to the then HHS Secretary Michael Leavitt from Senator Charles

Grassley states, “I am personally troubled that, for all intents and purposes, the FDA allowed a

clinical trial to proceed, which makes the inhabitants of 32 communities in 18 states, and anyone

living or traveling near these communities, potential “guinea pigs” without their consent and,

absent consent, without full awareness of the risks and benefits of the blood substitute… My

requests to the FDA did not seem unreasonable to me, especially given the serious nature of the

ethical and safety issues included with the PolyHeme Study.” According to the Alliance for

Human Research Protection (AHRP), OHRP does not appear to have the authority to put on hold

a commercially sponsored unethical human experiment that is under FDA jurisdiction. If OHRP

has such authority and failed to exercise it, then the public should know that there are, in effect,

no protections preventing unethical experiments to be conducted at the nation’s hospitals. The

public must be protected by an authorized agency not under the influence of biotech-

pharmaceutical companies.

On behalf of the Secretary, HHS, the Office on Human Research Protections (OHRP) approves

the terms of these written institutional assurances, which constitute binding commitments. In

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essence, OHRP holds accountable and depends on institutional officials, committees,

researchers, and other agents of the institution to comply with the institution’s assurance and the

regulations. In carrying out its oversight responsibility, OHRP’s Division of Compliance

Oversight monitors compliance through not-for-cause compliance oversight surveillance

activities and for-cause compliance oversight evaluations of allegations or indications of

noncompliance with the regulations. OHRP has the authority under Title IV of the Public

Health Service Act (42 USC 281 et seq.) to investigate complaints about human subject

protections in HHS-conducted or -funded research, as well as any other research covered

by the institution’s Assurance of Compliance. OHRP also promotes compliance through its

Division of Policy and Assurances, which provides policy and guidance documents pertaining to

the regulatory requirements in 45 CFR 46. If HHS receives an allegation or indication of

noncompliance related to human subject research that is conducted or supported solely by a

Common Rule department/agency other than HHS, HHS will refer the matter to that

department/agency for review and action as appropriate” as stated at

http://www.hhs.gov/ohrp/humansubjects/commonrule/.

On April 26, 2011, I met with Kristina C. Borror Ph.D., Division of Compliance Oversight

Director to file a formal complaint and to find out which Federal agency was responsible for

conducting non-consensual human experimentation on me and others. I was told by Ms. Borror

that there was nothing that her office could do for me and that I should contact each agency and

file a FOIA request with each one.” I knew there were a lot of research projects using human

subjects and it would be like looking for a needle in a haystack. It would be very difficult, if not

impossible to find, since there are more than 55,000 projects that involve human subjects. Since

January 15, 2009, all IRBs must use the Internet-based registration maintained by HHS as stated

in 45 CFR 46.501. Is the answer right on HHS’s website since all IRBs have to register with

HHS?

Non-Consensual Human Subjects Testimonies & Request for a Moratorium

Congress and HHS are sponsoring projects involving human subjects, without 45 CFR 46 being

an enforceable lawfully, promulgated regulation, informed consent being on the books or a

ratified Human Subjects Research Protection Law. As a result, “the absence of Federal

jurisdiction over much privately funded research means that the U.S. government cannot know

how many Americans currently are subjects in experiments, cannot influence how they

have been recruited, cannot ensure that research subjects know and understand the risks

they are undertaking, and cannot ascertain whether they have been harmed.” Many non-

consensual human subjects testified at the Bioethics Commission’s Meeting 4 Session 10 (March

1, 2011) and Meeting 5 Session 6 (May 18, 2011): Public Comments. There were others who

submitted their written testimonies. The archived transcripts and videos are available at

bioethics.gov/cms/meeting-four and bioethics.gov/cms/meeting-five. Several months later, the

Office of Human Research Protections (OHRP) requested public comments pertaining to the

update of 45 CFR 46 and has received 600+ pages of testimonies from human subjects and over

1100 responses, which did not include the public comments from the Bioethics Commission.

A moratorium is being requested so that the “Federal Government can get it right”. This is a

massive undertaken, which should require the support of HHS and Congress to ensure that any

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new regulations will benefit and protect the rights, safety, and welfare of future human subjects.

We are requesting Congress to conduct investigative hearings about illegal “COINTELPRO”

activities, ratify laws to protect the rights & welfare of the human subjects so that informed

consent is finally on the books and oversee the activities pertaining to the revision of 45 CFR 46

by HHS so that it will become a lawfully, promulgated regulation. Will the revised 45 CFR 46

address the issues of ACHRE, NBAC, Executive Orders/Memos by former President Clinton,

results of the EPA lawsuit, and former Senator John Glenn? How will 45 CFR 46 interact with

FDA regulations (21 CFR 50, 56), HIPAA Privacy Rule (45 CFR 164), Public Health Service

Act (42 USC 281) & other Federal & State regulations that impact the conduct of human subjects

research? The Common Rule offers more exceptions than FDA regulations do. Should that be

true? More importantly, will 45 CFR 46 become a strict, ethical, and enforceable, lawfully

promulgated Federal regulation, which researchers will be held accountable for their actions so

that unethical, human subject research/experiments will be eliminated in the future?

Request to “Opt-Out” or Discontinue Participation as a “Non-consensual” Human Subject

I, Letitia Petershave been randomly selected to be a participant or human subject in a

research/experiment without my voluntary, informed consent, either orally or written and

without my knowledge. In this research/ experiment, I am/have been exposed to

electronic/electromagnetic radiation technology (including gamma rays, microwave, & infrared)

and weapons (chemical, biological, direct energy, & radiological). In addition, my body has been

infiltrated with many “unidentified metal devices”. I meet the requirement of a “human subject”

in a “research/experiment” as defined above. I already had a compromised immune system

because of my exposure to toxic molds/mycotoxins while working in the Washington, DC

Federal buildings. I was far from being that “healthy person with no major health ailments”, but I

was working towards it everyday so that I would have a better quality of life and become a

productive U.S. citizen in the workplace and community once again. I am on disability

retirement & I would have never consented to be a “volunteer” in any human subject

research with all of my confirmed diagnoses; especially one which uses gamma rays,

microwave, infrared and weapons (biological, chemical, directed energy & radiological). I

believe that my selection was not equitable in my case as defined in 45 CFR 46.113. I have

endured unnecessary & unimaginable pain and suffering that presents a danger to my

well-being by continuing in this human research. I am in a life-threatening situation

everyday that I continue to be in this human subject research. Furthermore, this violates

my religious principles and beliefs. I want out now! In addition, the National Commission

for the Protection of Human Subjects believed that those who are already burdened (e.g.,

by disabilities or institutionalization) should not be asked to accept the burdens of research

unless other appropriate subjects cannot be found (i.e., if the research concerns their

particular disability or circumstance).

This human subject research/experiment involves noncompliance with 45 CFR 46. This part of

the “Common Rule” is intended to allow IRBs to waive informed consent in its entirety or any of

the required elements of informed consent In order for this human subject/experiment to waive

informed consent it had to meet the 4 criteria in 45 CFR 46.116 (d). An IRB may approve a

consent procedure which does not include, or which alters, some or all of the elements of

informed consent set forth in this section, or waive the requirements to obtain informed consent

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provided the IRB finds and documents that: (1) The research involves no more than minimal

risk to the subjects; (2) The waiver or alteration will not adversely affect the rights and

welfare of the subjects; (3) The research could not practicably be carried out without the

waiver or alteration; and (4) Whenever appropriate, the subjects will be provided with

additional pertinent information after participation.

Risk is defined in The IRB Guidebook as the probability of harm or injury (physical,

psychological, social, or economic) occurring as a result of participation in a research study.

Both the probability and magnitude of possible harm may vary from minimal to significant.

Federal regulations define only “minimal risk.” Minimal risk is defined in the Common Rule as

the probability and magnitude of physical or psychological harm that is normally encountered in

the daily lives, or in the routine medical, dental, or psychological examination of healthy

persons.

The daily exposures of electronic/electromagnetic radiation technology (including gamma rays,

microwave, & infrared) and weapons (chemical, biological, direct energy, & radiological)

presents a danger to my overall well-being and has violated my rights and welfare as a human

subject. The human research practices, which I am experiencing, should be reclassified as “cruel

and unusual punishment” or “crimes against humanity”, which goes way beyond the physical or

psychological harm that is “normally” encountered in our daily lives or in the routine medical,

dental, or psychological examination. I am experiencing intentional infliction of severe physical

pain or suffering, which violates my rights and falls under the purview of 18 USC § 2340

Torture. I am in pain everyday, but the degree of the pain varies from day to day and from hour

to hour; from minor discomfort pain to excruciating, agonizing pain, where I am in tears and

crying out for Jesus Christ to deliver me. It has been very unbearable. There have been times that

I could not even get out of bed to bathe or even cook for myself because of the extreme fatigue

and the severity of the pain in my body. I am in excruciating pain for hours and days while

suffering in silence because I did not want my parents to worry and also they do not believe that

we are in a human subject research. My feet would become so swollen due to edema that I could

barely walk. Each step that I would take the shooting pain would resonate throughout my legs.

My legs looked like they were going to “pop”. I would have to elevate them and stay completely

off my feet for a day or several days before they would return to normal & there was no pain. My

stomach, fingers, eyelids, face & head also swells. I would experience constant throbbing of pain

for hours. I went “temporary blind” after being intentionally dosed with chemical:

pesticides/insecticides and the emergency medical care failed to treat me. I could hear my rapid

heart rate when I am in the bed or resting; sometimes I would have heart palpitations. One

incident I developed “red fine bumps” in my head and a couple of days later, my hair fell out in

“clumps” as I was combing it. The National Academy of Sciences states this only occurs with

radiation exposures at 200 rems or higher. My vision has become blurry after these exposures.

My body is under tremendous stress, undue distress and inflicted pain, which affects my

performance to try to run my own business and to live a normal life. My body has been

infiltrated with “unidentifiable metal devices”, which is being picked up by a simple carpenter’s

tool: a stud sensor/finder. I could see two in my neck, because that particular area of my neck

pulsates, when my heart rate increases and another one came out of place in my wrist, which I

saw through my skin. I developed very painful red, blisters/mouth sores overnight, while I am

sleeping. According to the Mayo Clinic’s website in order for the blisters/mouth sores to

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develop, radiation was aimed at my head or neck. I have a very dry, metallic taste in my mouth.

My eyes are very dry. I also woke up to an excruciating pounding, headache, which has been

with me all day. My body is “aching” all over, as well as, my parents’ bodies. All of our

diseases have been exacerbated; my father has developed cancer, which could have been a

contributing factor from the environment and I recently spent the night in the hospital with my

mother due to her chest pains and very high blood pressure, which never occurred before. Even

people who visit us are being exposed, including children.

Personal privacy is important to ethical research as stated in 45 CFR 46.111. My confidentiality

and privacy rights have been violated. 45 CFR 46.116 (f) clearly states, “nothing in this policy is

intended to limit the authority of a physician to provide emergency medical care, to the extent

the physician is permitted to do so under applicable federal, state, or local law.” The

“researchers” have interfered with the physicians to provide me with the “appropriate”

emergency care. The physicians released private health information, did not adequately

addressed my complaints, failed to ensure patient care was provided in a safe and effective

manner, did not provide appropriate medical screening exams for me, and failed to treat a sick

and injured patient before releasing me, which violates the Emergency Medical Treatment and

Active Labor Act (EMTALA). Now there is a significant high health risk of me developing a

radiation-related disease that could have been greatly minimized through early detection and

appropriate medical treatment. The “researchers” have used disinformation to cause humiliation,

social stigmatization, and discrimination. Invasion of privacy concerns access to a person’s body

and the “researchers” has access to my body 24/7 and there are countless of men, women and

children, also called “informants” or “perps” who have access to my body 24/7 without my

informed consent or knowledge.

Human Subject Research Violates the Rights & Welfare of Vulnerable Population:

Children

Children have been included in this human subject research, without receiving the

parental/guardian permission consent documentation as defined in 45 CFR 46.408 and these

children/minors are not wards of the state or any other agency, institution, or entity as defined in

45 CFR 46.409. No adequate provisions were made for soliciting the assent of children and the

no permission was granted from their parents or guardians, as set forth in 45 CFR 46.408 as

stated in 45 CFR 46.407 (iii). These children/minor are involve in research, which involves

greater than minimal risk as defined in 45 CFR 46.404 and does not present the prospect of direct

benefit to them at defined in 45 CFR 46.406. Some of these children are not economically or

educationally disadvantaged, but they have been placed in because of their race. This research is

not being conducted in accordance with sound ethical principles as stated in 45 CFR 46.607 (ii).

Both the National Commission for the Protection of Human Subjects and the President’s

Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral

Research recommended that such waivers be granted only if subjects will not be denied benefits

or services to which they are otherwise legally entitled. The waiver of informed consent has

diminished the protection of my rights and welfare as a non-consensual human subject. I have

received no respect as a non-consensual human subject. There is a non-verbal element that

“whatever happens to the human subject is of no personal concern to the researcher. They can do

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whatever they want to the human subject and there is nothing that the human subject can do

about because no one will help the human subject.”

The waiver of informed consent has caused adverse consequences for my welfare and for my

general well-being, as well as, my loved ones. In addition, our rights, safety, dignity, welfare,

and privacy as non-consensual human subjects have been violated and do not comply with 45

CFR 46. This human subject research/experiment is incompliance with the policy, 45 CFR 46

therefore, as stated in 45 CFR 46.123, it should be terminated. If I continue in this “loosely

controlled” research/experiment, it will likely result in irreversible permanent injury, radiation-

induced diseases or even pre-mature death for myself (this request also includes my family

members who were systematically included in this because of me), because the “researchers”

are operating above the law and below the accepted standard of scientific, ethical, and

humane research. I am requesting to “opt-out” or discontinue my participation immediately

out of this non-consensual human subject research/experiment without prejudice. The

“Common Rule”, 45 CFR 46.116 (a) (8) states, “and the subject may discontinue participation

at any time without penalty or loss of benefits to which the subject is otherwise entitled.” I

am not waiving any legal claims, rights or remedies because of my participation as a non-

consensual human subject. The legal rights as a human subject may not be waived and the

human subject may not be asked to release or appear to release the investigator, the sponsor, the

institution or its agents from liability for negligence.

In the National Institutes of Health, Office for Protection from Research Risks (OPRR)

1993 Institutional Review Board Guidebook in the withdrawal from participation section,

it states, “attention should be paid to subjects’ rights when they decide to withdraw from

participation in the study. The federal regulations clearly require that subjects be free to

withdraw from participation without penalty or loss of benefits to which they are otherwise

entitled [Federal Policy §116(a) (8)].”

For research involving more than minimal risk, an explanation as to whether any compensation

and an explanation as to whether any medical treatments are availability of medical treatment

and compensation in the case of research-related injury, including who will pay for the treatment

and the availability of other financial compensation as stated in 45 CFR 46.116(a)(6). In July

2005 the National Academy of Sciences came to the conclusion that the preponderance of

scientific evidence shows that even very low doses of radiation pose a risk of cancer or other

health problem and there is no threshold below, which exposure can be viewed as harmless.

According to data from Hiroshima and Nagasaki, show that symptoms may persist for up to 10

years and may also have an increased long-term risk for leukemia and lymphoma. The

effects of radiation on the human body can be found at

www.atomicarchive.com/Effects/radeffects.shtml. Will the human subjects be compensated due

to research-related injury?

I, Letitia Peters certify that my decision to “opt-out” or discontinue participation in this human

experiment is without the intervention of any element of force, fraud, deceit, duress, coercion or

undue influence on my decision. I am requesting to “opt-out” or discontinue my participation

because of my rights as a human subject as stated in 45 CFR 46 116 (a) (8). This request includes

all of my immediate family members (my elderly parents, my sister’s family and my brother’s

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family) who were thrust in this unethical, human subject research/experiment without their

consent or without their knowledge.

In closing, I echo the words announced at the 1976 National Urban League National Conference

on Human Experimentation, “We don’t want to kill science, but we don’t want science to kill,

mangle, & abuse us”.

# # #

INTERNATIONAL SPIRITUAL AWAKENING MINISTRIES

FOR IMMEDIATE RELEASE

CONTACT: Letitia Peters

Phone: 347-568-3537

Website: www.thecanche.tumblr.com

Emails: [email protected] or [email protected]

“Taking A Stand Against Injustice” Series (Part 1 of 3)

In this first article, we will discuss justice for the non-consensual human subjects/TIs. Since the

non-consensual human subjects/TIs meet the definition of being a “human subject” in a

“research” or “medical experiment”, they can request to “opt-out” of the human subject research

at any time without prejudice. This is stated in Federal law. These “researchers” are operating

above the law and below the accepted standard of scientific, ethical, and humane research.

There is no way for us to determine the name of the research or medical experiment, because

there are over 55,000 projects, which involves human subject research and we were placed into

this human subject research without our informed consent or knowledge. For the past 15-20

years, both HHS and Congress have failed to close the gaps or “loopholes” to protect the human

subjects. Year after year, they have continued to sponsor billions of dollars in human subject

research, without ratifying any laws to protect the human subjects. Currently, NO ONE is

IMMUNE from being used as a human “guinea pig” because the laws are not there to

protect you! First, we seek a moratorium on all U.S. human subject research. Second, we want

Congress to conduct hearings on COINTELPRO activities and pertaining to the obstruction of

justice being committed by informants from the private sector, city, state, and even including the

Federal Government. Finally, how do HHS and Congress intend to ratify laws to protect human

subjects in the future? Recently, the world has seen in the case of the late Trayvon Martin, which

was an awful tragedy in itself, where the police chose not to enforce the law, even with all of the

evidence presented in the case. It took people from all ages and walks of life protesting, signing

petitions and receiving national and worldwide media publicity in order for justice to prevail. We

thank God for answering our prayers. The case for Trayvon Martin represents all of us who have

been seeking justice, but were unable to get it before. Now the bar has been raised to a higher

level in America. The non-consensual human subjects/TIs are seeking justice because the laws

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are in place, but the “people” are choosing not to enforce or adhere to the laws. Our slogan is

“We say NO to COINTELPRO and YES to JUSTICE. We say NO to NON-

CONSENSUAL HUMAN EXPERIMENTATION, and YES to JUSTICE. Will you stand up

with us to seek justice for the non-consensual human subjects/TIs as well?

HUMAN SUBJECTS/TIs TO HHS SECRETARY & CONGRESS: REQUEST TO “OPT-

OUT” OF UNETHICAL RESEARCH & PROPOSE A MORATORIUM ON ALL U.S.

HUMAN SUBJECT RESEARCH

“It is a moral issue, but for many it violates their religious beliefs and principles.”

April 24, 2012 -Trenton, NJ- In 1997, former Senator John Glenn said, “I want to put this in

personal terms once again. You just think about your own family, your own son, your own

daughter, or grandchildren who might be, the next time they go to a doctor, the subject of some

medical experiment that they are not even told about. I do not think there can be many things

more un-American than that. That is unconscionable, and we should not permit that.” Why are

there still non-consensual human subject research occurring in 2012, which are maiming, killing

or driving people to suicide? Aren’t there laws in place to protect the human subjects?

In Dr. Harriett A. Washington’s book, Medical Apartheid documents many non-consensual

human subject research/experiment cases. In 1994, the Medical University of South Carolina in

Charleston was accused of enrolling poor African-American women into narcotic-treatment

research without their knowledge. In 1995, an experimental measles vaccine was tested on

mostly African-American and Hispanic children in Los Angeles, without receiving their parents’

informed consent. From 1994 to 1995, New York City law enforcement officials helped

researchers coerce African-American parents into enrolling their boys into a study that sought to

establish a genetic propensity for violence, without receiving their parents’ informed consent.

This scourge has spread beyond racial minorities, as detailed in her new book, Deadly

Monopolies. Since the 1980s, approximately 20 U.S. research projects have won legal waivers

allowing them to bypass any form of informed consent. In 2011, drug giant Pfizer paid $75

million to settle claims that children in Kano state, Nigeria, were injured or killed by non-

consensual administration of its experimental meningitis drug Trovan.

Letitia Peters, a former Federal Government electronics engineer and non-consensual human

subject states, “I would have never imagined that as a law-abiding U.S. citizen (except for a few

parking and speeding tickets) that I would be going through horrific ordeal in America and in

2012. All attempts to silence me with extreme persecution, torture or by any means possible have

failed. I have been treated worse than an animal. I speak on behalf of countless of men, women,

and children in the U.S. and around the world. We are Americans and are entitled to nothing

less than the full rights of every American. The acts of violence that have been taken

against us, should be condemned by all Americans and those worldwide who value freedom

and justice. We have become someone else’s property because our rights, welfare and safety

have been affected. Isn’t that slavery? Now, we are human subjects in a project involving human

subject research without our knowledge or informed consent. For many of us, it is a moral issue,

but for some this violates our religious beliefs and principles. The current Federal laws have not

protected us. I would never “volunteer” to be a human subject with my many health ailments

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confirmed by several physicians. The three generations of my family has been placed in this

unethical, human subject research. I love my family, but to do this to the children and to my

elderly parents is totally unacceptable. Is this genocide? My family does not believe that they

have been placed in this unethical, human subject research. History is repeating itself. Logically,

it does not make sense and it is not the acceptable norm. No man has the right to do this to

another fellowman. Many of you would not like it if the tables were turned and this was being

done to your family. Why are you doing this? You are serving Satan who comes to kill, steal,

and destroy. In Jesus’ name, may the angel of the Lord persecute and chase them who are

adversaries to our souls and want to do us harm.

I WOULD NEVER DO THIS TO ANYONE: NOT TO MY FAMILY, FRIENDS,

NEIGHBORS, OR EVEN COMPLETE STRANGERS.

I have a strong spiritual faith and belief in God/Yahweh and this violates my faith as a follower

of Jesus Christ/Yeshua. I thank my enemies for helping me to develop a closer relationship with

Yahweh through Yeshua. He has been my provider, refuge, fortress, shield, vindicator, healer,

fortress, restorer, and deliverer. He is the only reason why I am still alive because of His grace

and mercy. I stand on the Word of God in the Holy Bible because it is the only truth 24/7. I love

Yahweh with all of my heart, mind, soul, and strength and He is worthy of my praise. It is

finished! Hallelujah!

No Response from HHS about Opt-Out Requests

Letitia Peters, further states, “in my in-depth research, I discovered that America has a 100 year

history of using minorities, especially African-Americans and their children and women as

“guinea pigs” without the human subjects or parent’s knowledge or informed consent. In

addition, this human subject research does not comply with 45 CFR 46 Subpart A, “The

Common Rule” because the rights, welfare, and safety of the human subjects have been affected

and the research involves more than minimal risk. The research practices, which we are

experiencing can be reclassified as “cruel and unusual punishment” or “crimes against

humanity”, which goes way beyond the physical or psychological harm that is normally

encountered in the daily lives, or in the routine medical, dental, or psychological examination of

healthy person as defined by minimal risk. This is torture. Many are maimed, been diagnosed

with cancer or other illnesses, committed suicide or died a premature death. The basic ethical

principles of respect of persons, beneficence and justice as stated in the Belmont report have

been violated. Human subjects should be protected by the authorized agency, HHS and not by

the researchers.”

On March 2, 2012, I emailed an 8 page letter to HHS requesting to “opt-out” or discontinue

participation in this human subject research, but I have not received an official response from

them. On March 20, 2012 and April 12, 2012, I emailed a second request using this opt-out form.

Others have also written to HHS Secretary Kathleen Sebelius requesting that as a human subject,

we have a right to be “opt-out” or discontinue participation in a human subject research.

Case of Elmer Allen, a Non-Consensual Human Subject Diagnosed as Paranoid

Schizophrenic

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It is documented in official Federal Government medical records/documents that the Federal

Government scientists diagnosed many non-consensual human subjects with “neurosis” or

“paranoid schizophrenic” who stated that he/she was being experimented on by the Federal

Government. For example, this was documented in the case of the late Elmer Allen. The sad part

about Elmer Allen’s story is that nobody believed him. He went to his doctor and told him, “I

think I’ve been injected with something.” His doctor diagnosed him as a paranoid schizophrenic

at the same time that he was conversing with the atomic energy scientists in Argon National Lab

to provide them with tissue samples. Elmer Allen was not only used in 1947 when he was

injected with this radioactive isotope, but he continued to be used as a guinea pig for the rest of

his life. When Elmer Allen’s daughter, Elmerine was interviewed, she told the story of when she

left for college, her father would tell her watch out, “Don’t let the U.S. government guinea-pig

you.” And they always thought that Elmer Allen had some kind of, well, Elmer was kind of

quirky, and he had this delusion that the government experimented on him.

In the 1970’s, a second generation of atomic scientists rediscovered this experiment. So they

wanted to dig up all the people who were dead, who had been injected with plutonium, and they

also wanted to bring whoever survived them back into the lab for further studies. Elmer Allen

was one of those people who was still alive.

AMY GOODMAN: Under what pretext since he didn’t know, supposedly, that he was a U.S.

government guinea pig?

EILEEN WELSOME: They told Elmer, and this is all documented in the medical records, that

they knew he had a very serious cancer and they wanted to know how he had lived so long.

The entire transcript about Elmer Allen is at

http://www.democracynow.org/2004/5/5/plutonium_files_how_the_u_s.

Discredit the Non-Consensual Human Subjects/TIs by Committing them to A Mental

Institution by “Any Means Possible”

Like Elmer Allen, many non-consensual human subjects/Targeted Individuals (TIs) have tried to

bring this to the public’s, family’s, or friend’s attention, but they have been called “crazy”,

“delusional” or been diagnosed with a “mental illness”. Police officers, psychiatrists, judges,

physicians, Federal intelligence agents & their family members, friends, and associates are being

used to discredit the non-consensual human subjects/TIs. Many of these individuals are

informants (perps or perpetrators, moles or double agents). The police were involved in non-

consensual human subjects/Targeted Individuals (TIs) being committed “for observation” even

though they were not harming themselves or others. Some have said that the police had lied to

them and even put them in handcuffs to take them to a mental institution. Who would believe a

“crazy person”? Now the committed non-consensual human subjects/Targeted Individuals (TIs)

are afraid to speak about their ordeal because they fear that they might be recommitted again and

this time even longer. All of the non-consensual human subjects have stated that it has never

been suggested for them to see a psychiatrist, but they always want the human subjects/TIs

to be committed to a mental institution. This tactic is also a form of adult “bullying” in

order to intimidate the non-consensual human subject to keep silent. It can also be

perceived as an “abuse of power” as well.

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Technology has changed and people are unaware that some technology can be used on them

without them even knowing it. Electromagnetic radiation is one of them, because it is invisible to

the naked eye. People are unaware that electromagnetic radiation can change their pleasant, easy

going personalities into angry or hostile ones in a matter of seconds or even make someone

irritated by bringing up a particular subject.

Many non-consensual human subjects have been wrongfully committed to mental institutions

and given a diagnosis of schizophrenia, neurosis, or other mental illnesses. Schizophrenia is a

disease that typically begins in early adulthood; between the ages of 15 and 25. Men tend to

get develop schizophrenia slightly earlier than women; whereas most males become ill between

16 and 25 years old, most females develop symptoms several years later, and the incidence in

women is noticably higher in women after age 30. The average age of onset is 18 in men and 25

in women. Schizophrenia onset is quite rare for people under 10 years of age, or over 40

years of age. Schizophrenia is a devastating disorder for most people who are afflicted, and very

costly for families and society. The overall U.S. 2002 cost of schizophrenia was estimated to be

$62.7 billion, with $22.7 billion excess direct health care cost ($7.0 billion outpatient, $5.0

billion drugs, $2.8 billion inpatient, $8.0 billion long-term care). (source: Analysis Group, Inc.)

This is being done so that no one will ever investigate these allegations and the scientists can

continue with their unethical human subject research. There’s a saying “what’s done in the dark

will be brought to the light”. In Luke 8:17 states, “For nothing is secret, that shall not be made

manifest; neither any thing hid, that shall be known and come abroad.” This is what happened in

the case of Elmer Allen who lived to be told that he was in a human subject research for over

20+ years, without his knowledge or informed consent. He was telling the truth and he was not

delusional. Truth did prevail. We will fight for all human subjects/TIs that were wrongfully

diagnosed with a mental illness to have this permanently expunged from their medical records.

Non-Consensual Human Subjects/TIs Should Send their “Opt-Out” form to HHS and to

Congress

The “Common Rule” has not been updated in 20 years and has failed to protect the human

subject since 1991. Obviously, there are serious deficiencies with informed consent in the

“Common Rule”. There is no enforceable Federal regulation or International standard on the

books for informed consent to be required because Congress has failed to ratify any proposed

legislations pertaining to human subject protection in 1997, 2002, 2003, 2004, 2006, 2008, and

2011, thus allowing for unethical human subjects experiments to occur.

Non-consensual human subjects/Targeted Individuals (TIs) should revise this “opt-out” form by

inserting in their own story concentrating on their pain and the violation of their rights, safety,

and welfare as a human subject and send it to HHS Secretary Kathleen Sebelius at

[email protected]. The mailing address is:

The U.S. Department of Health & Human Services

H.H.S. Secretary Kathleen Sebelius

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200 Independence Ave. SW, Room 120F

Washington, DC 20201

HHS Main Number: 877-696-6775

Comment Line: 202-205-5445 (Please leave a comment)

Correspondence: 202-690-6392

Fax: 202-690-7203

HHS Secretary Sebelius conducted a special plenary presentation at the National Action Network

Conference in Washington, DC today.

Non-consensual human subjects/Targeted Individuals (TIs) should also send their form to their

Congressional representatives (www.congress.gov or contact the switchboard: H.R. 202-225-

3121 or Senate: 202-224-3121 to find out the name of your Congressional representatives.)

Non-consensual human subjects/TIs can also request a Microsoft word version of the form with

the highlighted areas which they should change by sending an email to [email protected].

This will also include an introductory letter to HHS Secretary Sebelius.

I echo the words of Dr. Harriett A. Washington, ”Just as U.S. physicians demanded justice at

Nuremberg, Nigerian parents stormed courts in Kano and Manhattan to demand that we live up

to our stated ideals. Sixty-five years on, it is high time we did.” Don’t you agree?

Here’s the “Opt-Out” form:

Introduction:

In the Bioethics Commission’s report released on December 15, 2011, the Bioethics Commission

suggested that to keep track of the more than 55,000 research projects using human subjects, the

Federal government should create a central online portal and database where basic information

about the projects are archived and made easily accessible and further concluded that it “cannot

say that all federally funded research provides optimal protections against avoidable harms

and unethical treatment”. The Bioethics Commission also said although human subjects in US

government-funded research are generally protected by existing rules and regulations, their

safety and well-being could be enhanced with stronger measures, including increased public

transparency and a system of compensating subjects who sustain research-related injuries.

Human subject research should adhere to the ethical principles and guidelines for the protection

of human research participants summarized in the uniform set of regulations, called the Federal

Policy for the Protection of Human Subjects, 45 CFR 46, Subpart A, formally known as the

“Common Rule.” The 45 CFR 46 regulations are based in large part on the Belmont Report and

were written to offer basic protections to human subjects involved in both biomedical and

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behavioral research. Today, 45 CFR 46, Subjects A and E: Registration of Institutional Review

Boards (added 1/15/2009) is shared by 17 Departments and Agencies, representing most, but not

all, of the Federal Departments and Agencies sponsoring human subjects research. Many of them

have not adopted Subpart B: Additional Protections for Pregnant Women, Human Fetuses &

Neonates Involved in Research, Subpart C: Additional Protections Pertaining to Biomedical &

Behavior Research Involving Prisoners as Subjects, or Subject D: Additional Protections for

Children Involved as Subjects in Research. For the past 20 years, 45 CFR 46, have been

considered merely “guidelines” and is not a lawfully, promulgated regulation.

Before a research project involving human subjects is initiated, it must be reviewed and

approved by an Institutional Review Board (IRB). The IRB has a central role in ensuring that all

human subject research is planned and conducted in an ethical manner, and in compliance with

federal, state and local regulations. The major responsibilities of the IRB are to assess the risks

and benefits of proposed research and to promote respect for its advice and counsel in

safeguarding the rights and welfare of human subjects.

Research is defined by the Common Rule regulations as “a systematic investigation, including

research development, testing, and evaluation, designed to develop or contribute to generalizable

knowledge. Activities which meet this definition constitute research for purposes of this policy,

whether or not they are conducted or supported under a program which is considered research for

other purposes. For example, some demonstration and service programs may include research

activities.” Medical experiment is defined by California Law, Health & Safety Code Section

24171 as “the severance or penetration or damaging of tissues of a human subject or the use of a

drug or device, electromagnetic radiation, heat or cold, or a biological substance or organism, in

or upon a human subject in the practice of research of medicine in a manner not reasonably

related to maintaining or improving the health of the subject or otherwise directly benefiting the

subject.

Human Subject is defined by the Common Rule regulations as “a living individual about whom

an investigator (whether professional or student) conducting research obtains either a) data

through intervention or interaction with the individual or b) identifiable private information.”

Human subject is defined by FDA regulations as “an individual who is or becomes a participant

in research, either as a recipient of the test article or as a control. A subject may be either a

healthy human or a patient. Subject [also] means a human who participates in an investigation,

either as an individual on whom or on whose specimen an investigational device is used or as a

control.”

Failure of OHRP to Investigate Allegations

In the March 14, 2006 letter to the then HHS Secretary Michael Leavitt from Senator Charles

Grassley states, “I am personally troubled that, for all intents and purposes, the FDA allowed a

clinical trial to proceed, which makes the inhabitants of 32 communities in 18 states, and anyone

living or traveling near these communities, potential “guinea pigs” without their consent and,

absent consent, without full awareness of the risks and benefits of the blood substitute… My

requests to the FDA did not seem unreasonable to me, especially given the serious nature of the

ethical and safety issues included with the PolyHeme Study.”According to the Alliance for

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Human Research Protection (AHRP) is that OHRP does not appear to have the authority to put

on hold a commercially sponsored unethical human experiment that is under FDA jurisdiction.

If OHRP has such authority and failed to exercise it, then the public should know that there are,

in effect, no protections preventing unethical experiments to be conducted at the nation’s

hospitals. The public must be protected by an authorized agency not under the influence of

biotech-pharmaceutical companies.

On behalf of the Secretary, HHS, the Office on Human Research Protections (OHRP) approves

the terms of these written institutional assurances, which constitute binding commitments. In

essence, OHRP holds accountable and depends on institutional officials, committees,

researchers, and other agents of the institution to comply with the institution’s assurance and the

regulations. In carrying out its oversight responsibility, OHRP’s Division of Compliance

Oversight monitors compliance through not-for-cause compliance oversight surveillance

activities and for-cause compliance oversight evaluations of allegations or indications of

noncompliance with the regulations. OHRP has the authority under Title IV of the Public

Health Service Act (42 USC 281 et seq.) to investigate complaints about human subject

protections in HHS-conducted or -funded research, as well as any other research covered

by the institution’s Assurance of Compliance. OHRP also promotes compliance through its

Division of Policy and Assurances, which provides policy and guidance documents pertaining to

the regulatory requirements in 45 CFR 46. If HHS receives an allegation or indication of

noncompliance related to human subject research that is conducted or supported solely by a

Common Rule department/agency other than HHS, HHS will refer the matter to that

department/agency for review and action as appropriate” as stated at

http://www.hhs.gov/ohrp/humansubjects/commonrule/.

On April 26, 2011, I met with Kristina C. Borror Ph.D., Division of Compliance Oversight

Director to file a formal complaint and to find out which Federal agency was responsible for

conducting non-consensual human experimentation on me and others. I was told by Ms. Borror

that there was nothing that her office could do for me and that I should contact each agency and

file a FOIA request with each one.” I knew there were a lot of research projects using human

subjects and it would be like looking for a needle in a haystack. It would be very difficult, if not

impossible to find, since there are more than 55,000 projects that involve human subjects. Since

January 15, 2009, all IRBs must use the Internet-based registration maintained by HHS as stated

in 45 CFR 46.501. Is the answer right on HHS’s website since all IRBs have to register with

HHS?

Non-Consensual Human Subjects Testimonies & Request for a Moratorium

Congress and HHS are sponsoring projects involving human subjects, without 45 CFR 46 being

an enforceable lawfully, promulgated regulation, informed consent being on the books or a

ratified Human Subjects Research Protection Law. As a result, “the absence of Federal

jurisdiction over much privately funded research means that the U.S. government cannot know

how many Americans currently are subjects in experiments, cannot influence how they

have been recruited, cannot ensure that research subjects know and understand the risks

they are undertaking, and cannot ascertain whether they have been harmed.” Many non-

consensual human subjects testified at the Bioethics Commission’s Meeting 4 Session 10 (March

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1, 2011) and Meeting 5 Session 6 (May 18, 2011): Public Comments. There were others who

submitted their written testimonies. The archived transcripts and videos are available at

bioethics.gov/cms/meeting-four and bioethics.gov/cms/meeting-five. Several months later, the

Office of Human Research Protections (OHRP) requested public comments pertaining to the

update of 45 CFR 46 and has received 600+ pages of testimonies from human subjects and over

1100 responses, which did not include the public comments from the Bioethics Commission.

A moratorium is being requested so that the “Federal Government can get it right”. This is a

massive undertaken, which should require the support of HHS and Congress to ensure that any

new regulations will benefit and protect the rights, safety, and welfare of future human subjects.

We are requesting Congress to conduct investigative hearings about illegal “COINTELPRO”

activities, ratify laws to protect the rights & welfare of the human subjects so that informed

consent is finally on the books and oversee the activities pertaining to the revision of 45 CFR 46

by HHS so that it will become a lawfully, promulgated regulation. Will the revised 45 CFR 46

address the issues of ACHRE, NBAC, Executive Orders/Memos by former President Clinton,

results of the EPA lawsuit, and former Senator John Glenn? How will 45 CFR 46 interact with

FDA regulations (21 CFR 50, 56), HIPAA Privacy Rule (45 CFR 164), Public Health Service

Act (42 USC 281) & other Federal & State regulations that impact the conduct of human subjects

research? The Common Rule offers more exceptions than FDA regulations do. Should that be

true? More importantly, will 45 CFR 46 become a strict, ethical, and enforceable, lawfully

promulgated Federal regulation, which researchers will be held accountable for their actions so

that unethical, human subject research/experiments will be eliminated in the future?

Request to “Opt-Out” or Discontinue Participation as a “Non-consensual” Human Subject

I, Letitia Petershave been randomly selected to be a participant or human subject in a

research/experiment without my voluntary, informed consent, either orally or written and

without my knowledge. In this research/ experiment, I am/have been exposed to

electronic/electromagnetic radiation technology (including gamma rays, microwave, & infrared)

and weapons (chemical, biological, direct energy, & radiological). In addition, my body has been

infiltrated with many “unidentified metal devices”. I meet the requirement of a “human subject”

in a “research/experiment” as defined above. I already had a compromised immune system

because of my exposure to toxic molds/mycotoxins while working in the Washington, DC

Federal buildings. I was far from being that “healthy person with no major health ailments”, but I

was working towards it everyday so that I would have a better quality of life and become a

productive U.S. citizen in the workplace and community once again. I am on disability

retirement & I would have never consented to be a “volunteer” in any human subject

research with all of my confirmed diagnoses; especially one which uses gamma rays,

microwave, infrared and weapons (biological, chemical, directed energy & radiological). I

believe that my selection was not equitable in my case as defined in 45 CFR 46.113. I have

endured unnecessary & unimaginable pain and suffering that presents a danger to my

well-being by continuing in this human research. I am in a life-threatening situation

everyday that I continue to be in this human subject research. Furthermore, this violates

my religious principles and beliefs. I want out now! In addition, the National Commission

for the Protection of Human Subjects believed that those who are already burdened (e.g.,

by disabilities or institutionalization) should not be asked to accept the burdens of research

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unless other appropriate subjects cannot be found (i.e., if the research concerns their

particular disability or circumstance).

This human subject research/experiment involves noncompliance with 45 CFR 46. This part of

the “Common Rule” is intended to allow IRBs to waive informed consent in its entirety or any of

the required elements of informed consent In order for this human subject/experiment to waive

informed consent it had to meet the 4 criteria in 45 CFR 46.116 (d). An IRB may approve a

consent procedure which does not include, or which alters, some or all of the elements of

informed consent set forth in this section, or waive the requirements to obtain informed consent

provided the IRB finds and documents that: (1) The research involves no more than minimal

risk to the subjects; (2) The waiver or alteration will not adversely affect the rights and

welfare of the subjects; (3) The research could not practicably be carried out without the

waiver or alteration; and (4) Whenever appropriate, the subjects will be provided with

additional pertinent information after participation.

Risk is defined in The IRB Guidebook as the probability of harm or injury (physical,

psychological, social, or economic) occurring as a result of participation in a research study.

Both the probability and magnitude of possible harm may vary from minimal to significant.

Federal regulations define only “minimal risk.” Minimal risk is defined in the Common Rule as

the probability and magnitude of physical or psychological harm that is normally encountered in

the daily lives, or in the routine medical, dental, or psychological examination of healthy

persons.

The daily exposures of electronic/electromagnetic radiation technology (including gamma rays,

microwave, & infrared) and weapons (chemical, biological, direct energy, & radiological)

presents a danger to my overall well-being and has violated my rights and welfare as a human

subject. The human research practices, which I am experiencing, should be reclassified as “cruel

and unusual punishment” or “crimes against humanity”, which goes way beyond the physical or

psychological harm that is “normally” encountered in our daily lives or in the routine medical,

dental, or psychological examination. I am experiencing intentional infliction of severe physical

pain or suffering, which violates my rights and falls under the purview of 18 USC § 2340

Torture. I am in pain everyday, but the degree of the pain varies from day to day and from hour

to hour; from minor discomfort pain to excruciating, agonizing pain, where I am in tears and

crying out for Jesus Christ to deliver me. It has been very unbearable. There have been times that

I could not even get out of bed to bathe or even cook for myself because of the extreme fatigue

and the severity of the pain in my body. I am in excruciating pain for hours and days while

suffering in silence because I did not want my parents to worry and also they do not believe that

we are in a human subject research. My feet would become so swollen due to edema that I could

barely walk. Each step that I would take the shooting pain would resonate throughout my legs.

My legs looked like they were going to “pop”. I would have to elevate them and stay completely

off my feet for a day or several days before they would return to normal & there was no pain. My

stomach, fingers, eyelids, face & head also swells. I would experience constant throbbing of pain

for hours. I went “temporary blind” after being intentionally dosed with chemical:

pesticides/insecticides and the emergency medical care failed to treat me. I could hear my rapid

heart rate when I am in the bed or resting; sometimes I would have heart palpitations. One

incident I developed “red fine bumps” in my head and a couple of days later, my hair fell out in

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“clumps” as I was combing it. The National Academy of Sciences states this only occurs with

radiation exposures at 200 rems or higher. My vision has become blurry after these exposures.

My body is under tremendous stress, undue distress and inflicted pain, which affects my

performance to try to run my own business and to live a normal life. My body has been

infiltrated with “unidentifiable metal devices”, which is being picked up by a simple carpenter’s

tool: a stud sensor/finder. I could see two in my neck, because that particular area of my neck

pulsates, when my heart rate increases and another one came out of place in my wrist, which I

saw through my skin. I developed very painful red, blisters/mouth sores overnight, while I am

sleeping. According to the Mayo Clinic’s website in order for the blisters/mouth sores to

develop, radiation was aimed at my head or neck. I have a very dry, metallic taste in my mouth.

My eyes are very dry. I also woke up to an excruciating pounding, headache, which has been

with me all day. My body is “aching” all over, as well as, my parents’ bodies. All of our

diseases have been exacerbated; my father has developed cancer, which could have been a

contributing factor from the environment and I recently spent the night in the hospital with my

mother due to her chest pains and very high blood pressure, which never occurred before. Even

people who visit us are being exposed, including children.

Personal privacy is important to ethical research as stated in 45 CFR 46.111. My confidentiality

and privacy rights have been violated. 45 CFR 46.116 (f) clearly states, “nothing in this policy is

intended to limit the authority of a physician to provide emergency medical care, to the extent

the physician is permitted to do so under applicable federal, state, or local law.” The

“researchers” have interfered with the physicians to provide me with the “appropriate”

emergency care. The physicians released private health information, did not adequately

addressed my complaints, failed to ensure patient care was provided in a safe and effective

manner, did not provide appropriate medical screening exams for me, and failed to treat a sick

and injured patient before releasing me, which violates the Emergency Medical Treatment and

Active Labor Act (EMTALA). Now there is a significant high health risk of me developing a

radiation-related disease that could have been greatly minimized through early detection and

appropriate medical treatment. The “researchers” have used disinformation to cause humiliation,

social stigmatization, and discrimination. Invasion of privacy concerns access to a person’s body

and the “researchers” has access to my body 24/7 and there are countless of men, women and

children, also called “informants” or “perps” who have access to my body 24/7 without my

informed consent or knowledge.

Human Subject Research Violates the Rights & Welfare of Vulnerable Population:

Children

Children have been included in this human subject research, without receiving the

parental/guardian permission consent documentation as defined in 45 CFR 46.408 and these

children/minors are not wards of the state or any other agency, institution, or entity as defined in

45 CFR 46.409. No adequate provisions were made for soliciting the assent of children and the

no permission was granted from their parents or guardians, as set forth in 45 CFR 46.408 as

stated in 45 CFR 46.407 (iii). These children/minor are involve in research, which involves

greater than minimal risk as defined in 45 CFR 46.404 and does not present the prospect of direct

benefit to them at defined in 45 CFR 46.406. Some of these children are not economically or

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educationally disadvantaged, but they have been placed in because of their race. This research is

not being conducted in accordance with sound ethical principles as stated in 45 CFR 46.607 (ii).

Both the National Commission for the Protection of Human Subjects and the President’s

Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral

Research recommended that such waivers be granted only if subjects will not be denied benefits

or services to which they are otherwise legally entitled. The waiver of informed consent has

diminished the protection of my rights and welfare as a non-consensual human subject. I have

received no respect as a non-consensual human subject. There is a non-verbal element that

“whatever happens to the human subject is of no personal concern to the researcher. They can do

whatever they want to the human subject and there is nothing that the human subject can do

about because no one will help the human subject.”

The waiver of informed consent has caused adverse consequences for my welfare and for my

general well-being, as well as, my loved ones. In addition, our rights, safety, dignity, welfare,

and privacy as non-consensual human subjects have been violated and do not comply with 45

CFR 46. This human subject research/experiment is incompliance with the policy, 45 CFR 46

therefore, as stated in 45 CFR 46.123, it should be terminated. If I continue in this “loosely

controlled” research/experiment, it will likely result in irreversible permanent injury, radiation-

induced diseases or even pre-mature death for myself (this request also includes my family

members who were systematically included in this because of me), because the “researchers”

are operating above the law and below the accepted standard of scientific, ethical, and

humane research. I am requesting to “opt-out” or discontinue my participation immediately

out of this non-consensual human subject research/experiment without prejudice. The

“Common Rule”, 45 CFR 46.116 (a) (8) states, “and the subject may discontinue participation

at any time without penalty or loss of benefits to which the subject is otherwise entitled.” I

am not waiving any legal claims, rights or remedies because of my participation as a non-

consensual human subject. The legal rights as a human subject may not be waived and the

human subject may not be asked to release or appear to release the investigator, the sponsor, the

institution or its agents from liability for negligence.

In the National Institutes of Health, Office for Protection from Research Risks (OPRR)

1993 Institutional Review Board Guidebook in the withdrawal from participation section,

it states, “attention should be paid to subjects’ rights when they decide to withdraw from

participation in the study. The federal regulations clearly require that subjects be free to

withdraw from participation without penalty or loss of benefits to which they are otherwise

entitled [Federal Policy §116(a) (8)].”

For research involving more than minimal risk, an explanation as to whether any compensation

and an explanation as to whether any medical treatments are availability of medical treatment

and compensation in the case of research-related injury, including who will pay for the treatment

and the availability of other financial compensation as stated in 45 CFR 46.116(a)(6). In July

2005 the National Academy of Sciences came to the conclusion that the preponderance of

scientific evidence shows that even very low doses of radiation pose a risk of cancer or other

health problem and there is no threshold below, which exposure can be viewed as harmless.

According to data from Hiroshima and Nagasaki, show that symptoms may persist for up to 10

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years and may also have an increased long-term risk for leukemia and lymphoma. The

effects of radiation on the human body can be found at

www.atomicarchive.com/Effects/radeffects.shtml. Will the human subjects be compensated due

to research-related injury?

I, Letitia Peters certify that my decision to “opt-out” or discontinue participation in this human

experiment is without the intervention of any element of force, fraud, deceit, duress, coercion or

undue influence on my decision. I am requesting to “opt-out” or discontinue my participation

because of my rights as a human subject as stated in 45 CFR 46 116 (a) (8). This request includes

all of my immediate family members (my elderly parents, my sister’s family and my brother’s

family) who were thrust in this unethical, human subject research/experiment without their

consent or without their knowledge.

In closing, I echo the words announced at the 1976 National Urban League National Conference

on Human Experimentation, “We don’t want to kill science, but we don’t want science to kill,

mangle, & abuse us”.

# # #

Posted 2 years ago

Apr 12

1st Request to HHS to “Opt-Out” & Propose Moratorium on all U.S. Human

Subject Experiments

March 1, 2012

The U.S. Department of Health & Human Services

H.H.S. Secretary Kathleen Sebelius

200 Independence Ave. SW

Washington, DC 20201

Re: Request to Discontinue Participation in Non-consensual Human Subject Experiment & to

Propose A 90 day Moratorium on All U.S. Human Subjects Experiments/Experiments that

Receive Federal Funding Internationally

Madam Secretary:

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I am writing this letter to request your intervention because many of our avenues to bring this

issue to light have been “obstructed” by informants. While in other cases, the government term

“on a need- to-know basis” comes into practice. The issue is: non-consensual human subjects in

the U.S. I am not only speaking for myself and for my family, but also on behalf of the countless

of my fellow Americans and those worldwide who have been placed in a human subject

experiment, without our voluntary, informed oral or written consent or knowledge. The current

deficiencies in the U.S. human subject research system have made this possible. The Belmont

Report and the Nuremberg Code both addressed voluntary, informed consent as a requirement

for the ethical conduct of human subject research. In 1991, 16 federal agencies adopted 45 CFR

46, Subpart A, which then became known as the “Common Rule”, governs the research on

human subjects. Even though the “Common Rule” has the requirement for informed consent, it

has many “loop holes”, which has not been closed in 20 years, and as a result this has caused

unethical human subjects experimentation on men, women, and children in the U.S. and

Internationally.

Let me introduce myself. My name is Letitia Peters and I was a former Electrical/Electronics

Engineer (GS-14/J) with the Federal Government in NJ and Washington, DC. During my 16

years career, I worked as a project manager managing 3 acquisition programs worth close to

$100 million, test engineer, and a program scheduler. I received accolades for my achievements

at my workplace and in the community. I volunteered as a math tutor in the public school

systems in Washington, DC and I was active in numerous organizations. I loved tutoring

children, which I would like to do again real soon. I also started my own event management

business in 2001 after earning a Master’s Certificate in Event Management from George

Washington University. I started to get very ill in 2003 and I was diagnosed with sick building

syndrome. Toxic mold was prevalent in several Federal buildings in Washington, DC and it was

making several of us sick. Unfortunately, I was terminated in 2006. I developed a 3 minute

video, which you can watch at www.youtube.com/nimsociety. I turned my anger to activism and

I started an organization called National Indoor Mold Society (NIMS). Humbly speaking, in 3 ½

years, we brought awareness to the public, medical field, and lawmakers that exposure to indoor

toxic molds and mycotoxins can cause adverse health effects to humans and pets. The 75th

Nevada legislature passed legislation declared September 2009 as National Indoor Toxic Mold

Awareness Month (NITMAM) in their state. Even though I was forced to close NIMS, the

people, businesses and organizations are still today celebrating September as NITMAM, which

was spearheaded by NIMS. Many of the archived radio shows are still available at

www.talkshoe.com. I was feeling better and I was working towards being active in the

community once again. My life changed drastically in September 2009, after I attempted to file a

cyber stalking report and to request that computer forensics be done. One NJ police officer told

me that no one will look at your computer. He was right. Since then, my life has been a

rollercoaster to say the least. I have not done anything to anyone to warrant such unusual and

cruel punishment. I realize that these people will never stop until I am dead so I will stop at

nothing for justice. I have done extensive research on the human subjects experiments in the U.S.

and Internationally. It has taken me years to figure out what was happening to me. At first, I

thought it was because of my activism work so I stopped doing the radio shows and eventually

closed NIMS. My health did not improve it got worse because I was receiving the most

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aggressive form of torture that a human person could ever endure. I suffered many nights in

silence, thinking how a human being could do this to another human being. My nightmare began

while I was still employed as a Federal Government employee. As unbelievable, and as

unthinkable this may sound, but I reasonably believe that my family and I (includes children and

elderly), have been placed in this non-consensual human subject experiment as a form of

retaliation because I was a Federal whistleblower. I only wanted to work in a healthy work

environment because the exposure to toxic mold was causing adverse health effects for me

Madam Secretary, I, like so many other non-consensual human subjects are enduring inhumane

treatment everyday 24/7. We would like to eat food that is not contaminated with chemicals,

radiation, or heaven knows what. We would like to have one solid night of sleep, without being

wakened out of sleep, because our neighbors are beaming us with electromagnetic weapons. We

want our lives back now. I will do everything possible with the help of Jesus Christ to ensure that

the next generation is not a “guinea pig” for the rest of his/her lives. Many non-consensual

human subjects testified at the Bioethics Commission 4thand 5th meetings. You can watch

Meeting 4 session 10 (March 1, 2011) and Meeting 5 Session 6 (May 18, 2011): Public

Comments at bioethics.gov/cms/meeting-four and bioethics.gov/cms/meeting-five. In addition,

you can download the transcript in pdf file or watch the live archived sessions. I echo the words

that were announced at the 1976 National Urban League National Conference on Human

Experimentation, “we don’t want to kill science, but we don’t want science to kill, mangle, &

abuse us”.

How do I know that I am/we are in an experiment/research?

We meet the definition of being a human subject in an experiment/research as defined in 45 CFR

46.102, as well as, according to California Law, Health & Safety Code Section 24171, a medical

experiment is defined as “the severance or penetration or damaging of tissues of a human subject

or the use of a drug or device, electromagnetic radiation, heat or cold, or a biological substance

or organism, in or upon a human subject in the practice of research of medicine in a manner not

reasonably related to maintaining or improving the health of the subject or otherwise directly

benefiting the subject.” The informants are utilizing COINTELPRO tactics. COINTELPRO is a

well-organized, well-funded, well-connected, well-orchestrated operation with vast resources

across state lines and Internationally. COINTELPRO is an acronym for Counter Intelligence

Program. Wikipedia states, “it was a series of covert, and often illegal, projects conducted by the

United States Federal Bureaus of Investigation (FBI) aimed at surveilling, infiltrating,

discrediting, and disrupting domestic political organizations. COINTELPRO tactics included

discrediting through targets through psychological warfare, planting false reports in the media,

smearing through forged reports, harassment, wrongful imprisonment, extralegal violence and

assassination. COINTELPRO took place between 1956 and 1971. Officially, COINTELPRO

was termination in April 1971, but was it? The last major Congressional investigation of

COINTELPRO operations was conducted in 1976-1978 by the Church Committee. These

horrifying reports did not provide any effective legislative remedies for future victims. Nor did

they produce any prosecutions of proven criminals within the Justice Department.

COINTELPRO covert operations have been unleashed to neutralize the non-consensual human

subjects, which includes advanced electronic/electromagnetic radiation technology (including

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gamma rays, microwave, & infrared), weapons (chemical, biological, direct energy, &

radiological), implants, and satellites/drones. You can read more information about the current

COINTELPRO tactics at www.COINTELPROContinuesToday.org.

Recently, Congressman Stephen Lynch (D-MA) has authored the Confidential Informant

Accountability Act of 2011, H.R. 3228, which would require Federal law enforcement agencies

to report to Congress serious crimes, authorized, as well as, unauthorized, committed by their

confidential informants, to amend title 28, United States Code, with respect to certain tort claims

arising out of the criminal misconduct of confidential informants and for other purposes.

Deficiencies with the Current Regulations in the Human Research System

Since 1991, the Common Rule has not been a strict, ethical, enforceable and lawfully,

promulgated regulation. The Common Rule “was originally written by the National Institutes of

Health and do not always appropriately address the ethical issues in research outside of the

biomedical context.” It is now being updated after 20 years. Year and year, Congress, HHS &

other Federal agencies continued to sponsor federally funded human subjects experiments,

without ratifying any Federal regulations & International standards, which would protect the

human subjects. Congress and HHS have failed to ratified legislation which would have closed

the loopholes for the protection of the human research subjects. These deficiencies have

benefited the researchers and have not protected the human subjects. There are:

1. Former President Clinton & the Advisory Committee on Human Radiation

Experiments (ACHRE): He directed the ACHRE to uncover the truth, recommend steps to

right past wrongs and propose ways to prevent unethical human subjects research from occurring

in the future. The Federal Government and Government officials failed ignored to implement

many of the 18 recommendations outlined in the ACHRE’s final report as well as, the March 27,

1997 former President William Clinton’s Memorandum: Directive to Strengthened Protections

for Human Subjects of Classified Research; thus allowing continuous waivers for informed

consent of classified and secret human subjects experiments; no sanctions for conducting

research unethically; allowing for research conducted by Federal agencies that do not follow the

Common Rule, privately funded research that is not regulated by the Food and Drug

Administration or private individuals or institutions that do not receive any Federal funding to

conduct human subjects research without requiring that informed consent must be obtained for

the past 15 to 20 years. DHHS failed to implement the memorandum, but NASA has included it

in their policy. As a result, many human subjects’ experiments are being conducted without

being required to obtain informed consent.

2. Former Senator John Glenn: There is no law on the books requiring that

informed consent must be obtained. Informed consent must be obtained prior to conducting

research on human subjects. Former Senator John Glenn cited this issue in 1997 in his remarks

for his proposed legislation S. 193, Human Research Subject Protection Act to the 105th

Congress. The intent therefore of this legislation is twofold: First, to fill in the gaps of coverage

of the common rule by requiring all research involving human subjects to abide by the rule; and

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second, to elevate the importance of conducting research ethically, the bill provides criminal

fines and penalties for failure to comply with the requirements of this law, and by extension 45

CFR 46. The full text is available for your review at

http://home.swipnet.se/allez/Eng/HumExpEn.htm. Former Senator John Glenn said, “I want to

put this in personal terms once again. You just think about your own family, your own son, your

own daughter, or grandchildren who might be, the next time they go to a doctor, the subject of

some medical experiment that they are not even told about. I do not think there can be many

things more un-American than that. That is unconscionable, and we should not permit that.”

3. Proposed Congressional Legislation to Protect the Human Subjects: Congress

passed the Defense Authorization Act of 2012 in less than a year, but Congress has failed to

ratify any proposed legislation for the protection of human subjects in 1997, 2002, 2003, 2006,

2008 and 2011 for the past 15 years. In the April 29, 2002 press release, Congress Examines

Research Protection Oversight System: Legislation Needed”, Congress examines research

protection oversight system and states that legislation is needed, but it is never ratified. The full

press release can be found at http://www.cossa.org/hsbackground.htm.Year after year, Congress

and HHS has funded human subjects’ experiments, without having proper legislation to protect

the human subjects. This has allowed for unethical, non-consensual human subject experiments

to continue. A list of the proposed laws is at www.circare.org.

4. President Clinton & National Bioethics Advisory Commission: The issue of

informed consent were addressed in 4 reports (1998, 1999a, 1999b, and 2001) because the topic

is central to the protections offered to research. As a first priority, NBAC shall direct its attention

to the consideration of the protection of the rights and welfare of humans research subjects. On

May 17, 1997, the National Bioethics Advisory Commission (NBAC) unanimously adopted a

resolution that “No person in the United States should be enrolled in research without the twin

protection of informed consent by an authorized persons and independent review of the risks and

benefits of the research. Later that month, Former President Clinton stated that “Science must

respect the dignity of every American. We must never allow our citizens to be unwitting guinea

pigs in scientific experiments that put them at risk without their consent and full knowledge.”

Almost 15 years later, the former Senator John Glenn’s, NBAC’s and former President

Clintons’goals remains unmet. In the May 4, 1999 letter, NBAC Chair, Harold T. Shapiro’s

memo to former President Clinton stated in his memo “Consistent with your October 3, 1995,

Executive Order 12975, the NBAV has focused a good deal of its efforts over the last three years

on issues surrounding the protection of human research subjects…I know of your interest, as

well as that of the Congress, which has rightfully inquired about the adequacy of existing

protections… our key concerns are

the following:

· Federal protections for persons serving as human research subjects do not yet

extend to all Americans.

· Despite widespread implementation of federal regulations by those departments

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and agencies sponsoring substantial amounts of biomedical research, a number of

departments and agencies who sponsor primarily non-biomedical research or little research

overall have failed to implement these federal protections.

· Federal protections do not always include specific provisions for especially

vulnerable populations of research subjects.

· Many federal agencies find the interpretation and implementation of the Common Rule

confusing and/or unnecessarily burdensome.

· Federal protections are difficult to enforce and improve effectively throughout the Federal

Government, in part because no single authority or office oversees research protections across all

government agencies and departments.

· New techniques are needed to ensure implementation at the local level.

5. EPA sued by the Pesticide Industry: March 2002 — the pesticide industry sued EPA

over this approach, and the U.S. Court of Appeals for the District of Columbia Circuit ruled that

EPA’s interim approach was not established through required notice and comment rulemaking

and should be vacated. In a June 2003 decision, the court stated that, as a consequence, "the

agency’s previous practice of considering third-party human studies on a case-by-case

basis, applying statutory requirements, the Common Rule, and high ethical standards as a

guide, is reinstated and remains in effect unless and until it is replaced by a lawfully

promulgated regulation."

In conclusion, there have been many attempts to ensure that the safety and welfare of the human

subjects are protected, but many Federal agencies have failed to implement these federal

protections, including DHHS and Congress. In the 2001 NBAC’s final report states, “Despite the

fact that many research institutions voluntarily apply the Common Rule-even to their privately

financed research-there are other significant sectors of privately funded research that remain

ungoverned either by State or Federal law. NBAC finds that the absence of Federal jurisdiction

over much privately funded research means that the U.S. government cannot know how many

Americans currently are subjects in experiments, cannot influence how they have been

recruited, cannot ensure that research subjects know and understand the risks they are

undertaking, and cannot ascertain whether they have been harmed. Not only does this

prevent the Federal Government from protecting Americans enrolling in research, but it affects

the Federal Government’s ability to craft policies governing emerging technologies. While

preparing its 1997 report Cloning Human Beings, for example, NBAC noted that the Common

Rule’s lack of jurisdiction over privately funded research made it impossible to rely on

IRBs as the primary mechanism for protecting human subjects against inappropriate uses

of those technologies.” I have completed a 41 page analysis, which discuss these issues in depth

is available for review.

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Failure of OHRP to Investigate Allegations

"If HHS receives an allegation or indication of noncompliance related to human subject research

that is conducted or supported solely by a Common Rule department/agency other than HHS,

HHS will refer the matter to that department/agency for review and action as appropriate" as

stated at http://www.hhs.gov/ohrp/humansubjects/commonrule/ . In May 2011, I went to

OHRP’s office to file a formal complaint to find out which Federal agency was responsible for

conducting non-consensual human experimentation on my family and on those Americans in the

U.S.A. I was told by OHRP’s management that “there was nothing that this office could do for

you and that you should contact each agency and request a FOIA request.” In addition, she was

not aware of any agency, which was using electromagnetic radiation. I walked out with a copy of

the Belmont report and the 45 CFR 46 in my hands, which I received. Others who contacted

OHRP have received a similar response by letter, which states: "OHRP has determined that it

does not have jurisdiction over the matters referenced in your letter. Therefore, OHRP

will not be able to pursue this matter on your behalf.” If it is not OHRP’s jurisdiction, to

ensure compliance oversight over human subject research, then who is responsible? Since

January 15, 2009, all IRBs must use the Internet-based registration maintained by DHHS as

stated in 45 CFR 46.501. Is the answer right on DHHS’s website?

Madam Secretary, this is why 11 years later from the issue of the final NBAC report, we are

coming to you, as non-consensual human research subjects to ask for your intervention to honor

our 3 requests as per the “Common Rule.” Many of us are in life-threatening situations.

1. “Non-consensual” Human Research Subjects Request to Discontinue Participation

I am speaking for myself and for my family, as well as, on behalf of the countless of my fellow

Americans and those worldwide who have been placed in a human experiment, without our

voluntary, informed written or oral consent or knowledge. I am writing you today to request that

we would like to discontinue or “opt-out” our participation in these human subject experiments

without prejudice. As stated in 45 CFR 46.116 (a)(8)) states , ” and the subject may discontinue

participation at any time without penalty or loss of benefits to which the subject is otherwise

entitled.” I am not waiving any legal claims, rights or remedies because of my participation as a

non-consensual human subject. The legal rights of subjects may not be waived and human

subjects may not be asked to release or appear to release the investigator, the sponsor, the

institution or its agents from liability for negligence.

2. Human Subject Research Fails to Meet the 4 Criteria to Waive Informed Consent

According to 45 CFR 46.116 (d), ALL of the 4 criteria listed must be met to waive informed

consent. An IRB may approve a consent procedure which does not include, or which alters,

some or all of the elements of informed consent set forth in this section, or waive the

requirements to obtain informed consent provided the IRB finds and documents that:

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(1) The research involves no more than minimal risk to the subjects; Minimal risk is the

probability and magnitude of physical or psychological harm that is normally encountered in the

daily lives, or in the routine medical, dental, or psychological examination of healthy persons.

(2) The waiver or alteration will not adversely affect the rights and welfare of the subjects;

(3) The research could not practicably be carried out without the waiver or alteration; and

(4) Whenever appropriate, the subjects will be provided with additional pertinent information

after participation.

Each one of the 4 criteria to waive informed consent has been violated:

In response to (1) The research practices, which myself and many other non-consensual human

subjects can be reclassified as “cruel and unusual punishment” or “crimes against humanity”,

which goes way beyond the physical or psychological harm that is “normally” encountered or in

the routine of a medical, dental, or psychological examination. This is torture. As a result, many

non-consensual human subjects are/were diagnosed with cancer and other illnesses; many are

maimed or died as a result of the daily torture with lasers, electromagnetic radiation- gamma

rays, infrared, microwave. Some even committed suicide. Many have lost their hair and teeth.

In response to (2): The rights and welfare of the subjects have been affected. The basic ethical

principles of respect of persons, beneficence and justice as stated in the Belmont report have

been violated. According to 45 CFR 46.123, the department or agency head may require that

department or agency support for any project be terminated or suspended in the manner

prescribed in applicable program requirements, when the department or agency head finds an

institution has materially failed to comply with the terms of this policy. In addition, whether the

applicant or the person or persons who would direct or has/have directed the scientific and

technical aspects of an activity has/have, in the judgment of the department or agency head,

materially failed to discharge responsibility for the protection of the rights and welfare of human

subjects (whether or not the research was subject to federal regulation).

In response to (3) If the research could not be carried out without the waiver or alteration, then

maybe it should not be doing it in the first place.

In response to (4): This is an ambiguous and open-ending statement with no timeframe attached

to it. My family and I have never received any additional pertinent information after

participation. When appropriate could mean anytime including after I am dead.

3. Human Subject Research Violates the Rights & Welfare of Vulnerable Population:

Children

Many children/minors have been included in this human subject research, without receiving

parental/guardian permission consent documentation as defined in 45 CFR 46.408 and these

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children/minors are not wards of the state or any other agency, institution, or entity as defined in

45 CFR 46.409. No adequate provisions were made for soliciting the assent of children and the

permission of their parents or guardians, as set forth in 45 CFR 46.408 as stated in 45 CFR

46.407 (iii). These children/minor are involve in research, which involves greater than minimal

risk as defined in 45 CFR 46.404 and does not present the prospect of direct benefit to them at

defined in 45 CFR 46.406. In July 2005 the National Academy of Sciences came to the

conclusion that the preponderance of scientific evidence shows that even very low doses of

radiation pose a risk of cancer or other health problem and there is no threshold below, which

exposure can be viewed as harmless. According to data from Hiroshima and Nagasaki, show that

symptoms may persist for up to 10 years and may also have an increased long-term risk for

leukemia and lymphoma.The effects of radiation on the human body can be found at

www.atomicarchive.com/Effects/radeffects.shtml. As a result, the children’s DNA has been

altered and now these ” DNA mutations” will become part of their permanent DNA. Now, when

they will have children and this new modified DNA will become part of their hereditary and

passed on for future generations to their children and their children’s children. Some of these

children are not economically or educationally disadvantaged, but they have been placed in

because of their race. This research is not being conducted in accordance with sound ethical

principles as stated in 45 CFR 46.607 (ii).

Request a 90 day Moratorium on all U.S. Human Research Subjects/ Federally Funded

Human Subjects Experiments Internationally: Serious Concerns about the Current Update

of the “Common Rule” and the Future of Human Subjects Research/Experiments

I am requesting a 90 day moratorium on all U.S. Human Research Subjects/Federally Funded

Human Subjects Experiments Internationally until laws are ratified because the current Federal

laws and International standards do not protect the human research subjects. This is a massive

undertaking. It has been 20 years since this document has been updated. Even thought we have

been treated like “animals”, we are human beings. We should have the same rights as everyone

else. This will allow Congress and the DHHS to develop a comprehensive plan to resolve this

important issue that affects the lives of human beings. It appears that this is no big thing, but it is

a MASSIVE thing for us, because you have no clue how it feels to lose your eyesight

(temporarily and then regain it) or not being able to barely walk because of the excruciating pain

. There has been poor oversight by HHS and Congress in the past 15 to 20 years for the

protection of human subjects. Will the new revised “Common Rule” include the issues of

ACHRE, NBAC, Executive Orders and Memorandums by former President Clinton, results of

the EPA lawsuit, and former Senator John Glenn? If these issues are not even in the new revised

Common Rule we will have the same problem today of “non-consensual” human subjects in the

future.

Is there a conflict of interest with DHHS sponsoring experiments & those who are on the

Advisory Board? How can DHHS “police” itself? In FY 1999, DHHS was the largest sponsor of

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federally funded programs. There was a proposal to have an independent organization to provide

oversight for human subject research.

Has HHS reviewed the Europeans laws on the protection of human subjects’ experiments? The

European has stricter laws and many of them have come to conduct their clinical trials in the

U.S. because it is “easier”. Everyone is aware of the “easy pass”, which is available. What steps

will be taken to mitigate that the new laws are advantageous to the human subjects? The

Common Rule should include regulations for biomedical and non-biomedical.I propose that

Congress and DHHS should work closely together during while ratifying the Common Rule.

DHHS has received over 1153 responses and not including the comments from the Bioethics

Commission. Based on the past history of the DHHS, can they be objective to develop a Federal

regulation, which is beneficial to the protection of human subjects and not advantageous to the

researchers? Does DHHS have the resources, knowledge, skills, and ability to revise “The

Common Rule” to become a strict, ethical, enforceable and lawfully, promulgated regulation that

will protect the human subjects? If the Federal regulation, “The Common Rule” is revised

correctly, then (1) Many human subjects’ experiments will decrease dramatically (2) Researchers

will face criminal charges, therefore eliminating the “free pass” for researchers to persecute,

maim, mutilate, and even kill their human subjects and (3) informed consent will be required,

therefore eliminating the researchers ability to “select anyone that they want of their chosen,

without informing them” to participate in their experiments. More importantly, will it be an

enforceable Federal regulation, which researchers will be held accountable for their actions

and it will eliminate many future unethical, human experiments? In addition, there will no

longer be people in lifelong non-consensual human subjects. All human subjects’ experiments

will be transparent. Will HHS bring in outside experts? How long will they take? The ACHRE

used hundreds of people to go through all of those documents. Is Congress going to ratify its

Human Subjects Protection Act? Will the revised “Common Rule” go out for review to the

public again? Will the resolution of those public comments be posted? I am proposing a monthly

update by HHS to Congress in this process and then to the public. Can the public be involved?

Approximately 600 pages of U.S. victims’ testimonies were submitted to the Department of

Health & Human Services, Office of Human Research Protections (OHRP) in Oct. /Nov. 2011.

On Nov. 23, 2011, I sent a letter via email to the Bioethics Commission & to OHRP to respond

to OHRP’s Federal Register that OHRP will accept the public comments from the Bioethics

Commission. In addition, one other victim also forwarded a letter to them as well. Was this

action completed? I also sent my comments, which I provided to the Bioethics Commission.

HHS should have received the 25 pages of legal analyses: 12 pages of analysis by G. Mason cites

legal cases (many attorneys would like this one) proves the inadequacy of 45 CFR 46 in

enforcing the right to informed consent and retired attorney Robert S., provides more proof that

the Federal Government agencies are involved and he discusses modern-day COINTELPRO

tactics. This document is also available for review at www.COINTELPROContinuesToday.org.

In Dec. 20111, Bioethics Commission received 41 pages of analysis by Former Federal Govt.

engineer, Letitia Peters provides proof that the Federal Government agencies and Congress have

not ratified laws to protect human subjects in almost 20 years. From pages 36 to the end, she

presents information relevant to HHS, Congress, & to the Federal Government agencies. My

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concerns about DHHS capabilities to handle a massive undertaking of updating 45 CFR 46 after

20 years are a serious concern. What will be Congress’ role? This document will be available for

review at www.thecanche.tumblr.com.

In closing, I support the efforts that America has done to condone crimes against humanity and

torture in other nations, but now we need America to be here for us: the American people. My

religious beliefs have been violated by being in a non-consensual human subject research as

well. There are countless of men, women, and children in America and worldwide who are

unaware that they are victims of COINTELPRO abuse and/or have been placed in a non-

consensual human subject research. They do not attribute their ongoing “bad luck”; mishaps;

animal killings; or mysterious, untreatable, disabling “environmental” diseases to covert

operatives using old COINTELPRO tactics plus new weapons of war to terrorize, neutralize, and

prevent resisting the treatment. These professional, well-orchestrated intrusions induce

excruciating pain, exhaustion, terror, alienation, and sometimes result in violent behavior against

themselves or others - eventually, one way or another, “neutralizing” and killing the non-

consensual human subject. We want our lives back now. Princeton Theologian, Paul Ramsey

whose 1970 work, The Patient as a Person states, “No man is good enough to experiment upon

another without his consent.”

Thank you for your time and consideration. If you have any questions or concerns, I can be

reached at [email protected] or you can call me at 347-568-3537. You can visit my

website www.thecanche.tumblr.com, which will contain many of the supporting documentation

like my analysis report.

Sincerely,

Letitia M. Peters

International Spiritual Awakening Ministries

Posted 2 years ago

Mar 20

(Part 1 of (Paer 1 of 3) Non-Consensual Human Subjects/TIs Request to “Opt-

Out” & Propose a Moratorium on all U.S. Human Subject Research

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INTERNATIONAL SPIRITUAL AWAKENING MINISTRIES

FOR IMMEDIATE RELEASE

CONTACT: Letitia Peters

Phone: 347-568-3537

Website: www.thecanche.tumblr.com

Emails: [email protected] or [email protected]

“Taking A Stand Against Injustice” Series (Part 1 of 3)

In this first article, we will discuss justice for the non-consensual human subjects/TIs. Since the

non-consensual human subjects/TIs meet the definition of being a “human subject” in a

“research” or “medical experiment”, they can request to “opt-out” of the human subject research

at any time without prejudice. This is stated in Federal law. These “researchers” are operating

above the law and below the accepted standard of scientific, ethical, and humane research.

There is no way for us to determine the name of the research or medical experiment, because

there are over 55,000 projects, which involves human subject research and we were placed into

this human subject research without our informed consent or knowledge. For the past 15-20

years, both HHS and Congress have failed to close the gaps or “loopholes” to protect the human

subjects. Year after year, they have continued to sponsor billions of dollars in human subject

research, without ratifying any laws to protect the human subjects. Currently, NO ONE is

IMMUNE from being used as a human “guinea pig” because the laws are not there to

protect you! First, we seek a moratorium on all U.S. human subject research. Second, we want

Congress to conduct hearings on COINTELPRO activities and pertaining to the obstruction of

justice being committed by informants from the private sector, city, state, and even including the

Federal Government. Finally, how do HHS and Congress intend to ratify laws to protect human

subjects in the future? Recently, the world has seen in the case of the late Trayvon Martin, which

was an awful tragedy in itself, where the police chose not to enforce the law, even with all of the

evidence presented in the case. It took people from all ages and walks of life protesting, signing

petitions and receiving national and worldwide media publicity in order for justice to prevail. We

thank God for answering our prayers. The case for Trayvon Martin represents all of us who have

been seeking justice, but were unable to get it before. Now the bar has been raised to a higher

level in America. The non-consensual human subjects/TIs are seeking justice because the laws

are in place, but the “people” are choosing not to enforce or adhere to the laws. Our slogan is

“We say NO to COINTELPRO and YES to JUSTICE. We say NO to NON-

CONSENSUAL HUMAN EXPERIMENTATION, and YES to JUSTICE. Will you stand up

with us to seek justice for the non-consensual human subjects/TIs as well?

HUMAN SUBJECTS/TIs TO HHS SECRETARY & CONGRESS: REQUEST TO “OPT-

OUT” OF UNETHICAL RESEARCH & PROPOSE A MORATORIUM ON ALL U.S.

HUMAN SUBJECT RESEARCH

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“It is a moral issue, but for many it violates their religious beliefs and principles.”

April 24, 2012 -Trenton, NJ- In 1997, former Senator John Glenn said, “I want to put this in

personal terms once again. You just think about your own family, your own son, your own

daughter, or grandchildren who might be, the next time they go to a doctor, the subject of some

medical experiment that they are not even told about. I do not think there can be many things

more un-American than that. That is unconscionable, and we should not permit that.” Why are

there still non-consensual human subject research occurring in 2012, which are maiming, killing

or driving people to suicide? Aren’t there laws in place to protect the human subjects?

In Dr. Harriett A. Washington’s book, Medical Apartheid documents many non-consensual

human subject research/experiment cases. In 1994, the Medical University of South Carolina in

Charleston was accused of enrolling poor African-American women into narcotic-treatment

research without their knowledge. In 1995, an experimental measles vaccine was tested on

mostly African-American and Hispanic children in Los Angeles, without receiving their parents’

informed consent. From 1994 to 1995, New York City law enforcement officials helped

researchers coerce African-American parents into enrolling their boys into a study that sought to

establish a genetic propensity for violence, without receiving their parents’ informed consent.

This scourge has spread beyond racial minorities, as detailed in her new book, Deadly

Monopolies. Since the 1980s, approximately 20 U.S. research projects have won legal waivers

allowing them to bypass any form of informed consent. In 2011, drug giant Pfizer paid $75

million to settle claims that children in Kano state, Nigeria, were injured or killed by non-

consensual administration of its experimental meningitis drug Trovan.

Letitia Peters, a former Federal Government electronics engineer and non-consensual human

subject states, “I would have never imagined that as a law-abiding U.S. citizen (except for a few

parking and speeding tickets) that I would be going through horrific ordeal in America and in

2012. All attempts to silence me with extreme persecution, torture or by any means possible have

failed. I have been treated worse than an animal. I speak on behalf of countless of men, women,

and children in the U.S. and around the world. We are Americans and are entitled to nothing

less than the full rights of every American. The acts of violence that have been taken

against us, should be condemned by all Americans and those worldwide who value freedom

and justice. We have become someone else’s property because our rights, welfare and safety

have been affected. Isn’t that slavery? Now, we are human subjects in a project involving human

subject research without our knowledge or informed consent. For many of us, it is a moral issue,

but for some this violates our religious beliefs and principles. The current Federal laws have not

protected us. I would never “volunteer” to be a human subject with my many health ailments

confirmed by several physicians. The three generations of my family has been placed in this

unethical, human subject research. I love my family, but to do this to the children and to my

elderly parents is totally unacceptable. Is this genocide? My family does not believe that they

have been placed in this unethical, human subject research. History is repeating itself. Logically,

it does not make sense and it is not the acceptable norm. No man has the right to do this to

another fellowman. Many of you would not like it if the tables were turned and this was being

done to your family. Why are you doing this? You are serving Satan who comes to kill, steal,

and destroy. In Jesus’ name, may the angel of the Lord persecute and chase them who are

adversaries to our souls and want to do us harm.

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I WOULD NEVER DO THIS TO ANYONE: NOT TO MY FAMILY, FRIENDS,

NEIGHBORS, OR EVEN COMPLETE STRANGERS.

I have a strong spiritual faith and belief in God/Yahweh and this violates my faith as a follower

of Jesus Christ/Yeshua. I thank my enemies for helping me to develop a closer relationship with

Yahweh through Yeshua. He has been my provider, refuge, fortress, shield, vindicator, healer,

fortress, restorer, and deliverer. He is the only reason why I am still alive because of His grace

and mercy. I stand on the Word of God in the Holy Bible because it is the only truth 24/7. I love

Yahweh with all of my heart, mind, soul, and strength and He is worthy of my praise. It is

finished! Hallelujah!

No Response from HHS about Opt-Out Requests

Letitia Peters, further states, “in my in-depth research, I discovered that America has a 100 year

history of using minorities, especially African-Americans and their children and women as

“guinea pigs” without the human subjects or parent’s knowledge or informed consent. In

addition, this human subject research does not comply with 45 CFR 46 Subpart A, “The

Common Rule” because the rights, welfare, and safety of the human subjects have been affected

and the research involves more than minimal risk. The research practices, which we are

experiencing can be reclassified as “cruel and unusual punishment” or “crimes against

humanity”, which goes way beyond the physical or psychological harm that is normally

encountered in the daily lives, or in the routine medical, dental, or psychological examination of

healthy person as defined by minimal risk. This is torture. Many are maimed, been diagnosed

with cancer or other illnesses, committed suicide or died a premature death. The basic ethical

principles of respect of persons, beneficence and justice as stated in the Belmont report have

been violated. Human subjects should be protected by the authorized agency, HHS and not by

the researchers.”

On March 2, 2012, I emailed an 8 page letter to HHS requesting to “opt-out” or discontinue

participation in this human subject research, but I have not received an official response from

them. On March 20, 2012 and April 12, 2012, I emailed a second request using this opt-out form.

Others have also written to HHS Secretary Kathleen Sebelius requesting that as a human subject,

we have a right to be “opt-out” or discontinue participation in a human subject research.

Case of Elmer Allen, a Non-Consensual Human Subject Diagnosed as Paranoid

Schizophrenic

It is documented in official Federal Government medical records/documents that the Federal

Government scientists diagnosed many non-consensual human subjects with “neurosis” or

“paranoid schizophrenic” who stated that he/she was being experimented on by the Federal

Government. For example, this was documented in the case of the late Elmer Allen. The sad part

about Elmer Allen’s story is that nobody believed him. He went to his doctor and told him, “I

think I’ve been injected with something.” His doctor diagnosed him as a paranoid schizophrenic

at the same time that he was conversing with the atomic energy scientists in Argon National Lab

to provide them with tissue samples. Elmer Allen was not only used in 1947 when he was

injected with this radioactive isotope, but he continued to be used as a guinea pig for the rest of

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his life. When Elmer Allen’s daughter, Elmerine was interviewed, she told the story of when she

left for college, her father would tell her watch out, “Don’t let the U.S. government guinea-pig

you.” And they always thought that Elmer Allen had some kind of, well, Elmer was kind of

quirky, and he had this delusion that the government experimented on him.

In the 1970’s, a second generation of atomic scientists rediscovered this experiment. So they

wanted to dig up all the people who were dead, who had been injected with plutonium, and they

also wanted to bring whoever survived them back into the lab for further studies. Elmer Allen

was one of those people who was still alive.

AMY GOODMAN: Under what pretext since he didn’t know, supposedly, that he was a U.S.

government guinea pig?

EILEEN WELSOME: They told Elmer, and this is all documented in the medical records, that

they knew he had a very serious cancer and they wanted to know how he had lived so long.

The entire transcript about Elmer Allen is at

http://www.democracynow.org/2004/5/5/plutonium_files_how_the_u_s.

Discredit the Non-Consensual Human Subjects/TIs by Committing them to A Mental

Institution by “Any Means Possible”

Like Elmer Allen, many non-consensual human subjects/Targeted Individuals (TIs) have tried to

bring this to the public’s, family’s, or friend’s attention, but they have been called “crazy”,

“delusional” or been diagnosed with a “mental illness”. Police officers, psychiatrists, judges,

physicians, Federal intelligence agents & their family members, friends, and associates are being

used to discredit the non-consensual human subjects/TIs. Many of these individuals are

informants (perps or perpetrators, moles or double agents). The police were involved in non-

consensual human subjects/Targeted Individuals (TIs) being committed “for observation” even

though they were not harming themselves or others. Some have said that the police had lied to

them and even put them in handcuffs to take them to a mental institution. Who would believe a

“crazy person”? Now the committed non-consensual human subjects/Targeted Individuals (TIs)

are afraid to speak about their ordeal because they fear that they might be recommitted again and

this time even longer. All of the non-consensual human subjects have stated that it has never

been suggested for them to see a psychiatrist, but they always want the human subjects/TIs

to be committed to a mental institution. This tactic is also a form of adult “bullying” in

order to intimidate the non-consensual human subject to keep silent. It can also be

perceived as an “abuse of power” as well.

Technology has changed and people are unaware that some technology can be used on them

without them even knowing it. Electromagnetic radiation is one of them, because it is invisible to

the naked eye. People are unaware that electromagnetic radiation can change their pleasant, easy

going personalities into angry or hostile ones in a matter of seconds or even make someone

irritated by bringing up a particular subject.

Many non-consensual human subjects have been wrongfully committed to mental institutions

and given a diagnosis of schizophrenia, neurosis, or other mental illnesses. Schizophrenia is a

disease that typically begins in early adulthood; between the ages of 15 and 25. Men tend to

get develop schizophrenia slightly earlier than women; whereas most males become ill between

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16 and 25 years old, most females develop symptoms several years later, and the incidence in

women is noticably higher in women after age 30. The average age of onset is 18 in men and 25

in women. Schizophrenia onset is quite rare for people under 10 years of age, or over 40

years of age. Schizophrenia is a devastating disorder for most people who are afflicted, and very

costly for families and society. The overall U.S. 2002 cost of schizophrenia was estimated to be

$62.7 billion, with $22.7 billion excess direct health care cost ($7.0 billion outpatient, $5.0

billion drugs, $2.8 billion inpatient, $8.0 billion long-term care). (source: Analysis Group, Inc.)

This is being done so that no one will ever investigate these allegations and the scientists can

continue with their unethical human subject research. There’s a saying “what’s done in the dark

will be brought to the light”. In Luke 8:17 states, “For nothing is secret, that shall not be made

manifest; neither anything hid, that shall be known and come abroad.” This is what happened in

the case of Elmer Allen who lived to be told that he was in a human subject research for over

20+ years, without his knowledge or informed consent. He was telling the truth and he was not

delusional. Truth did prevail. We will fight for all human subjects/TIs that were wrongfully

diagnosed with a mental illness to have this permanently expunged from their medical records.

Non-Consensual Human Subjects/TIs Should Send their “Opt-Out” form to HHS and to

Congress

The “Common Rule” has not been updated in 20 years and has failed to protect the human

subject since 1991. Obviously, there are serious deficiencies with informed consent in the

“Common Rule”. There is no enforceable Federal regulation or International standard on the

books for informed consent to be required because Congress has failed to ratify any proposed

legislations pertaining to human subject protection in 1997, 2002, 2003, 2004, 2006, 2008, and

2011, thus allowing for unethical human subjects experiments to occur.

Non-consensual human subjects/Targeted Individuals (TIs) should revise this “opt-out” form by

inserting in their own story concentrating on their pain and the violation of their rights, safety,

and welfare as a human subject and send it to HHS Secretary Kathleen Sebelius at

[email protected]. The mailing address is:

The U.S. Department of Health & Human Services

H.H.S. Secretary Kathleen Sebelius

200 Independence Ave. SW, Room 120F

Washington, DC 20201

HHS Main Number: 877-696-6775

Comment Line: 202-205-5445 (Please leave a comment)

Correspondence: 202-690-6392

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Fax: 202-690-7203

HHS Secretary Sebelius conducted a special plenary presentation at the National Action Network

Conference in Washington, DC today.

Failure of OHRP to Investigate Allegations

On behalf of the Secretary, HHS, the Office on Human Research Protections (OHRP) approves

the terms of these written institutional assurances, which constitute binding commitments. In

essence, OHRP holds accountable and depends on institutional officials, committees,

researchers, and other agents of the institution to comply with the institution’s assurance and the

regulations. In carrying out its oversight responsibility, OHRP’s Division of Compliance

Oversight monitors compliance through not-for-cause compliance oversight surveillance

activities and for-cause compliance oversight evaluations of allegations or indications of

noncompliance with the regulations. OHRP has the authority under Title IV of the Public

Health Service Act (42 USC 281 et seq.) to investigate complaints about human subject

protections in HHS-conducted or -funded research, as well as any other research covered

by the institution’s Assurance of Compliance. OHRP also promotes compliance through its

Division of Policy and Assurances, which provides policy and guidance documents pertaining to

the regulatory requirements in 45 CFR 46. If HHS receives an allegation or indication of

noncompliance related to human subject research that is conducted or supported solely by a

Common Rule department/agency other than HHS, HHS will refer the matter to that

department/agency for review and action as appropriate” as stated at

http://www.hhs.gov/ohrp/humansubjects/commonrule/.

On April 26, 2011, I met with Kristina C. Borror Ph.D., Division of Compliance Oversight

Director to file a formal complaint and to find out which Federal agency was responsible for

conducting non-consensual human experimentation on me and others. I was told by Ms. Borror

that there was nothing that her office could do for me and that I should contact each agency and

file a FOIA request with each one. I knew there were a lot of research projects using human

subjects and it would be like looking for a needle in a haystack. It would be very difficult, if not

impossible to find, since there are more than 55,000 projects that involve human subjects. Others

who contacted OHRP have received this response by letter, which states: “OHRP has determined

that it does not have jurisdiction over the matters referenced in your letter. Therefore, OHRP

will not be able to pursue this matter on your behalf.” Since January 15, 2009, all IRBs must use

the Internet-based registration maintained by HHS as stated in 45 CFR 46.501. Is the answer

right on HHS’s website?

Non-Consensual Human Subjects Testimonies & Request for a Moratorium

Congress and HHS are sponsoring projects involving human subjects, without 45 CFR 46 being

an enforceable lawfully, promulgated regulation, informed consent being on the books or a

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ratified Human Subjects Research Protection Law. As a result, “the absence of Federal

jurisdiction over much privately funded research means that the U.S. government cannot know

how many Americans currently are subjects in experiments, cannot influence how they

have been recruited, cannot ensure that research subjects know and understand the risks

they are undertaking, and cannot ascertain whether they have been harmed.” Many non-

consensual human subjects testified at the Bioethics Commission’s Meeting 4 Session 10 (March

1, 2011) and Meeting 5 Session 6 (May 18, 2011): Public Comments. There were others who

submitted their written testimonies. The archived transcripts and videos are available at

bioethics.gov/cms/meeting-four and bioethics.gov/cms/meeting-five. Several months later, the

Office of Human Research Protections (OHRP) requested public comments pertaining to the

update of 45 CFR 46 and has received 600+ pages of testimonies from human subjects and over

1100 responses, which did not include the public comments from the Bioethics Commission.

A moratorium is being requested so that the “Federal Government can get it right”. This is a

massive undertaken, which should require the support of HHS and Congress to ensure that any

new regulations will benefit and protect the rights, safety, and welfare of future human subjects.

We are requesting Congress to conduct investigative hearings about illegal “COINTELPRO”

activities, ratify laws to protect the rights & welfare of the human subjects so that informed

consent is finally on the books and oversee the activities pertaining to the revision of 45 CFR 46

by HHS so that it will become a lawfully, promulgated regulation. Will the revised 45 CFR 46

address the issues of ACHRE, NBAC, Executive Orders/Memos by former President Clinton,

results of the EPA lawsuit, and former Senator John Glenn? How will 45 CFR 46 interact with

FDA regulations (21 CFR 50, 56), HIPAA Privacy Rule (45 CFR 164), Public Health Service

Act (42 USC 281) & other Federal & State regulations that impact the conduct of human subjects

research? The Common Rule offers more exceptions than FDA regulations do. Should that be

true? More importantly, will 45 CFR 46 become a strict, ethical, and enforceable, lawfully

promulgated Federal regulation, which researchers will be held accountable for their actions so

that unethical, human subject research/experiments will be eliminated in the future?

Request to “Opt-Out” or Discontinue Participation as a “Non-consensual” Human Subject

I, Letitia Petershave been randomly selected to be a participant or human subject in a

research/experiment without my voluntary, informed consent, either orally or written and

without my knowledge. In this research/ experiment, I am/have been exposed to

electronic/electromagnetic radiation technology (including gamma rays, microwave, & infrared)

and weapons (chemical, biological, direct energy, & radiological). In addition, my body has been

infiltrated with many “unidentified metal devices”. I meet the requirement of a “human subject”

in a “research/experiment” as defined above. I already had a compromised immune system due

to the exposure of toxic molds/mycotoxins in the Federal buildings in Washington, DC. I was far

from being that “healthy person with no major health ailments”, but I was working towards it

everyday so that I would have a better quality of life and become a productive U.S. citizen in the

workplace and community once again. I am on disability retirement & I would have never

consented to be a “volunteer” in any human subject research with all of my confirmed

diagnoses; especially one which uses gamma rays, microwave, infrared and weapons

(biological, chemical, directed energy & radiological). I believe that my selection was not

equitable in my case as defined in 45 CFR 46.113. I have endured unnecessary &

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unimaginable pain and suffering that presents a danger to my well-being by continuing in

this human research. I am in a life-threatening situation everyday that I continue to be in

this human subject research. Furthermore, this violates my religious principles and beliefs.

I want out now! In addition, the National Commission for the Protection of Human Subjects

believed that those who are already burdened (e.g., by disabilities or institutionalization) should

not be asked to accept the burdens of research unless other appropriate subjects cannot be found

(i.e., if the research concerns their particular disability or circumstance).

This human subject research/experiment has failed to comply with the terms in Title 45 Public

Welfare Part 46 Protection of Human Subjects (45 CFR 46). This part of the “Common Rule” is

intended to allow IRBs to waive informed consent in its entirety or any of the required elements

of informed consent. In order for this human subject/experiment to waive informed consent it

had to meet the 4 criteria in 45 CFR 46.116 (d). An IRB may approve a consent procedure which

does not include, or which alters, some or all of the elements of informed consent set forth in this

section, or waive the requirements to obtain informed consent provided the IRB finds and

documents that: (1) The research involves no more than minimal risk to the subjects; (2) The

waiver or alteration will not adversely affect the rights and welfare of the subjects; (3) The

research could not practicably be carried out without the waiver or alteration; and (4)

Whenever appropriate, the subjects will be provided with additional pertinent information

after participation.

Risk is defined in The IRB Guidebook as the probability of harm or injury (physical,

psychological, social, or economic) occurring as a result of participation in a research study.

Both the probability and magnitude of possible harm may vary from minimal to significant.

Federal regulations define only “minimal risk.” Minimal risk is defined in the Common Rule as

the probability and magnitude of physical or psychological harm that is normally encountered in

the daily lives, or in the routine medical, dental, or psychological examination of healthy

persons.

The daily exposures of electronic/electromagnetic radiation technology (including gamma rays,

microwave, & infrared) and weapons (chemical, biological, direct energy, & radiological)

presents a danger to my overall well-being and has violated my rights and welfare as a human

subject. The human research practices, which I am experiencing, should be reclassified as “cruel

and unusual punishment” or “crimes against humanity”, which goes way beyond the physical or

psychological harm that is “normally” encountered in our daily lives or in the routine medical,

dental, or psychological examination. I am experiencing intentional infliction of severe physical

pain or suffering, which violates my rights and falls under the purview of 18 USC § 2340

Torture. I am in pain everyday, but the degree of the pain varies from day to day and from hour

to hour; from minor, discomfort pain to excruciating, agonizing pain, where I am in tears and

crying out for Jesus Christ to deliver me. It has been very unbearable. There have been times that

I could not even get out of bed to bathe or even cook for myself because of the extreme fatigue

and the severity of the pain in my body. I am in excruciating pain for hours and days while

suffering in silence because I did not want my parents to worry and also they do not believe that

we are in a human subject research. My feet would become so swollen due to edema that I could

barely walk. Each step that I would take the shooting pain would resonate throughout my legs.

My legs looked like they were going to “pop”. I would have to elevate them and stay completely

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off my feet for a day or several days before they would return to normal & there was no pain. My

stomach, fingers, eyelids, face & head also swells. I would experience constant throbbing of pain

for hours. I went “temporary blind” after being intentionally dosed with chemical:

pesticides/insecticides and the emergency medical care failed to treat me. I could hear my rapid

heart rate when I am in the bed or resting; sometimes I would have heart palpitations. One

incident I developed “red fine bumps” in my head and a couple of days later, my hair fell out in

“clumps” as I was combing it. The National Academy of Sciences states this only occurs with

radiation exposures at 200 rems or higher. My vision has become blurry after these exposures.

My body is under tremendous stress, undue distress and inflicted pain, which affects my

performance to try to run my own business and to live a normal life. My body has been

infiltrated with “unidentifiable metal devices”, which is being picked up by a simple carpenter’s

tool: a stud sensor/finder. I could see the two in my neck, because my neck pulsates, when my

heart rate increases. Several times, I developed very painful red, blisters/mouth sores overnight,

while I am sleeping. According to the Mayo Clinic’s website in order for the blisters/mouth sores

to develop, radiation was aimed at my head or neck. I have a very dry, metallic taste in my

mouth. I also woke up to an excruciating pounding, headache, which has been with me all day.

My body is “aching” all over, as well as, my parents’ bodies. All of our diseases have been

exacerbated; my father has developed cancer, which could have been a contributing factor from

the environment and I recently spent the night in the hospital with my mother due to her chest

pains and very high blood pressure, which never occurred before. Even people who visit us are

being exposed, including children.

Personal privacy is important to ethical research as stated in 45 CFR 46.111. My confidentiality

and privacy rights have been violated. 45 CFR 46.116 (f) clearly states, “nothing in this policy is

intended to limit the authority of a physician to provide emergency medical care, to the extent

the physician is permitted to do so under applicable federal, state, or local law.” The

“researchers” have interfered with the physicians to provide me with the “appropriate”

emergency care. The physicians released private health information, did not adequately

addressed my complaints, failed to ensure patient care was provided in a safe and effective

manner, did not provide appropriate medical screening exams for me, and failed to treat a sick

and injured patient before releasing me, which violates the Emergency Medical Treatment and

Active Labor Act (EMTALA). Now there is a significant high health risk of me developing a

radiation-related disease that could have been greatly minimized through early detection and

appropriate medical treatment. The “researchers” have used disinformation to cause humiliation,

social stigmatization, and discrimination. Invasion of privacy concerns access to a person’s body

and the “researchers” has access to my body 24/7 and there are countless of men, women and

children, also called “informants” or “perps” who have access to my body 24/7 without my

informed consent or knowledge.

Human Subject Research Violates the Rights & Welfare of Vulnerable Population:

Children

Children have been included in this human subject research, without receiving the

parental/guardian permission consent documentation as defined in 45 CFR 46.408 and these

children/minors are not wards of the state or any other agency, institution, or entity as defined in

45 CFR 46.409. No adequate provisions were made for soliciting the assent of children and the

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no permission was granted from their parents or guardians, as set forth in 45 CFR 46.408 as

stated in 45 CFR 46.407 (iii). These children/minor are involve in research, which involves

greater than minimal risk as defined in 45 CFR 46.404 and does not present the prospect of direct

benefit to them at defined in 45 CFR 46.406. Some of these children are not economically or

educationally disadvantaged, but they have been placed in because of their race. This research is

not being conducted in accordance with sound ethical principles as stated in 45 CFR 46.607 (ii).

Both the National Commission for the Protection of Human Subjects and the President’s

Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral

Research recommended that such waivers be granted only if subjects will not be denied benefits

or services to which they are otherwise legally entitled. The waiver of informed consent has

diminished the protection of my rights and welfare as a non-consensual human subject. I have

received no respect as a non-consensual human subject. There is a non-verbal element that

“whatever happens to the human subject is of no personal concern to the researcher. They can do

whatever they want to the human subject and there is nothing that the human subject can do

about because no one will help the human subject.”

The waiver of informed consent has caused adverse consequences for my welfare and for my

general well-being, as well as, my loved ones. In addition, our rights, safety, dignity, welfare,

and privacy as non-consensual human subjects have been violated. This human subject

research/experiment has also failed to comply with the terms of the policy, 45 CFR 46 therefore,

as stated in 45 CFR 46.123 it should be subject to termination or suspension. If I continue in this

“loosely controlled” research/experiment, it will likely result in irreversible permanent injury,

radiation-induced diseases or even pre-mature death for myself (this request also includes my

family members who were systematically included in this because of me), because the

“researchers” are operating above the law and below the accepted standard of scientific,

ethical, and humane research. I am requesting to “opt-out” or discontinue my participation

immediately out of this non-consensual human subject research/experiment without prejudice.

The “Common Rule”, 45 CFR 46.116 (a) (8) states, “and the subject may discontinue

participation at any time without penalty or loss of benefits to which the subject is

otherwise entitled.” I am not waiving any legal claims, rights or remedies because of my

participation as a non-consensual human subject. The legal rights as a human subject may not be

waived and the human subject may not be asked to release or appear to release the investigator,

the sponsor, the institution or its agents from liability for negligence.

In the National Institutes of Health, Office for Protection from Research Risks (OPRR)

1993 Institutional Review Board Guidebook states, “attention should be paid to subjects’

rights when they decide to withdraw from participation in the study. The federal regulations

clearly require that subjects be free to withdraw from participation without penalty or loss of

benefits to which they are otherwise entitled [Federal Policy §116(a) (8)].”

For research involving more than minimal risk, an explanation as to whether any compensation

and an explanation as to whether any medical treatments are availability of medical treatment

and compensation in the case of research-related injury, including who will pay for the treatment

and the availability of other financial compensation as stated in 45 CFR 46.116(a)(6). In July

2005 the National Academy of Sciences came to the conclusion that the preponderance of

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scientific evidence shows that even very low doses of radiation pose a risk of cancer or other

health problem and there is no threshold below, which exposure can be viewed as harmless.

According to data from Hiroshima and Nagasaki, show that symptoms may persist for up to 10

years and may also have an increased long-term risk for leukemia and lymphoma. The

effects of radiation on the human body can be found at

www.atomicarchive.com/Effects/radeffects.shtml. Will the human subjects be compensated due

to research-related injury?

I, Letitia Peters certify that my decision to “opt-out” or discontinue participation in this human

experiment is without the intervention of any element of force, fraud, deceit, duress, coercion or

undue influence on my decision. I am requesting to “opt-out” or discontinue my participation

because of my rights as a human subject as stated in 45 CFR 46 116 (a) (8). This request includes

all of my immediate family members (my elderly parents, my sister’s family and my brother’s

family) who were thrust in this unethical, human subject research/experiment without their

consent or without their knowledge.

I echo the words of Dr. Harriett A. Washington, ”Just as U.S. physicians demanded justice at

Nuremberg, Nigerian parents stormed courts in Kano and Manhattan to demand that we live up

to our stated ideals. Sixty-five years on, it is high time we did.” Don’t you agree?

In closing, I echo the words announced at the 1976 National Urban League National Conference

on Human Experimentation, “We don’t want to kill science, but we don’t want science to kill,

mangle, & abuse us”.

Posted 2 years ago

Mar 20

Action Requested by all Non-consensual Human Subjects/TIs

Hello Fellow Non-consensual Human Subject/TIs:

It is time for the TI community to get organize. Spring is here and I refuse to carry all of my

“evidence” around any longer or to spend another year in this experiment. Is there anyone out

there in agreement with me? Don’t be shy now?

Let’s come together and get organize.

We need your time and support.

I have seen plenty of websites, which talk about our problem, but I did not find any information

about a SOLUTION until recently and it was right under our noses.

I am writing to inform you that based on irrefutable facts, you can request to withdraw

participation from the human subject research. IT IS YOUR RIGHT AS A HUMAN

SUBJECT. We have a leg up on many other people because we know that we are in an

unethical, human subject research/experiment. I have done the research and developed a form to

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be submitted to HHS and to your Congressional representatives. I have done the research and I

have found a SOLUTION to our situation. I invite you to join me by revising the attached opt-

out form.

Do you have 30 minutes? You only have to discuss your pain, and the violation of your rights,

safety, and welfare as a human subject. I put everything in ***red where you would need to

discuss your pain, safety, and welfare** on the following pages to make it easier. You can even

use my words, if you can’t come up with any of your own. Many of us are suffering from “brain

fog”, which is affecting our mind. You can do something about it. If you follow the steps outline

below to do spring cleaning from the inside out. The other areas do not require any changes,

unless you want to do it. Don’t forget to sign the form or use a script font.

Please also send it to your Congressional representatives as well. Please send the attached press

release (70.5 kb) to media (newspapersand tv stations) along with your story or alone.

Attached is the opt-out form to be revised (52.5 k file). You can use the words, which I provided

and make them your own or use your own words. I know that many of us have “brain fog.” I am

tired of hearing EXCUSES! Well, it is EXCUSES , NO MORE! If you can’t do this, then you

don’t want this to end this. Only the perps, informants, double agents, and spies want this to

continue so that they can get their “comps” and the devil have their souls. Many of them should

be going to jail for obstructing justice.

The “researchers” waived informed consent by telling HHS that the research involves no more

than minimal risk, like going to the dentist. We know that our pain has been more than a

toothache. In many cases, it has been crimes against humanity or torture. This is why we need to

talk about the pain and the violation of our rights, welfare & safety as human subjects. We need

as many testimonies as possible going to HHS Secretary Sebelius and to your Congressional

representatives.

Why should we be contacting HHS? ( A perp wanted to know the answer to this question so

here’s the answer.)

The OHRP has the authority under Title IV of the Public Health Service Act (42 USC 281 et

seq.) to investigate complaints about human subject protections in HHS-conducted or -funded

research, as well as any other research covered by the institution’s Assurance of Compliance.

Here are 8 ways: Just do what you can every day.

1. Contact HHS: We need to write and call the comment line.

Her e-mail address is [email protected]. The mailing address is:

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The U.S. Department of Health & Human Services

H.H.S. Secretary Kathleen Sebelius

200 Independence Ave. SW, Room 120F

Washington, DC 20201

877-696-6775

Comment Line: 202-205-5445 (Everyone can leave a comment)

Correspondence: 202-690-6392

Fax: 202-690-7203

I did receive a response that my email was received.

Propose introduction for the letter and cc: Senator

The U.S. Department of Health & Human Services

H.H.S. Secretary Kathleen Sebelius

200 Independence Ave. SW, Room 120F

Washington, DC 20201

VIA E-MAIL, FAX AND REGULAR MAIL

Re: Request to “Opt-Out” or Discontinue Participation in Non-consensual Human Subject

Experiment & to Propose A 90 day Moratorium on All U.S. Human Subjects

Experiments/Experiments that Receive Federal Funding Internationally

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Madam Secretary:

I am writing to request your intervention on a very important issue: non-consensual human

subjects in the U.S. I am not only speaking for myself and for my family, but also on behalf of

the countless of my fellow Americans and those worldwide who have been placed in a human

subject experiment, without our voluntary, informed consent, whether orally or written. I have

the right as a human subject to request to “opt-out” or discontinue participation in the human

subject research. In addition, this human subject research has failed to comply with the terms in

Title 45 Public Welfare Part 46 Protection of Human Subjects, 45 CFR 46 Subpart A, “The

Common Rule” to waive informed consent for this human subject research.” Attached is

Statement of XXX XXX, a Non-consensual Human Subject to “Opt-Out” or Discontinue

Participation in the Human Subjects Research/Experiment for your review.

A moratorium is being requested so that the “Federal Government can get it right”. This is a

massive undertaken, which should require the support of HHS and Congress to ensure that any

new regulations will benefit and protect the rights, safety, and welfare of future human subjects.

We are requesting Congress to conduct investigative hearings about illegal “COINTELPRO”

activities, ratify laws to protect the rights & welfare of the human subjects so that informed

consent is finally on the books and oversee the activities pertaining to the revision of 45 CFR 46

by HHS so that it will become a lawfully, promulgated regulation. Will the revised 45 CFR 46

address the issues of ACHRE, NBAC, Executive Orders/Memos by former President Clinton,

results of the EPA lawsuit, and former Senator John Glenn? How will 45 CFR 46 interact with

FDA regulations (21 CFR 50, 56), HIPAA Privacy Rule (45 CFR 164), Public Health Service

Act (42 USC 281) & other Federal & State regulations that impact the conduct of human subjects

research? The Common Rule offers more exceptions than FDA regulations do. Should that be

true? More importantly, will 45 CFR 46 become a strict, ethical, and enforceable, lawfully

promulgated Federal regulation, which researchers will be held accountable for their actions so

that unethical, human subject research/experiments will be eliminated in the future?

Thank you for your time and consideration. If you have any questions or concerns, please contact

me at xxx-xxx-xxxx or via e-mail at [email protected]. I look forward to hearing from you

expeditiously.

Sincerely,

Cc:

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Senator

Congressman

Attachment: Statement of Letitia Peters, a Non-consensual Human Subject to “Opt-Out” or

Discontinue Participation in the Human Subjects Research/Experiment

2. Contact your Congressional Representatives:

Please also send the form to your Congressional representatives (www.congress.gov or contact

the HR switchboard: 202-225-3121 or Senate: 202-224-3121 to find out the name of your

Congressional representatives. ) You can send him or her copy of your completed form.

3. Contact Media (secular and alternative) in America and Internationally

Send the press release to the editor or to the reporter who did a story pertaining to human

subject, bioethics, or research. This can be sent in America and Internationally. Just cut

and paste. Keep doing it. You can add your story to the press release and request a story is

done.

Google: “worldwide news media directory”, local news media or national newspaper etc.

A couple of weeks ago, CNN did a story about vets who were secretly experimented on by the

U.S. Government. Please send your testimonies to Dr. Sanjay Gupta who did the story as well as,

to the attorneys in CA. Gordon Erspamer of Morrison & Foerster at [email protected]

reporter who did follow-up: Hope Hodge at [email protected] or call at 910-219-8453.

In the U.S., we want EVERYONE TO SEND THEIR STORIES TO THE Washington Post, New

York Times, USA Today, American Free Press, Democracy NOW!, NPR, for starters. There is

no reason why they should receive less than 1,000 stories, unless like I believe that most of the

people who I am interacting with are double agents, spies, or informants.

4. Join us on the conference call: If anyone wants to be interviewed, please call in or send

an email to “[email protected]" or call and leave a message at 347-568-3537. We

welcome those who have written books on the subject, as well as, those who are victors;

those who are human subjects and are not perps, double agents, or informants and does

not want to sabotage the efforts of exposing the truth.

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Conference Call starting March 19, 2012 to March 23, 2012 at 9:00 p.m. EST

Phone/Calling:

The call-in number is (724) 444-7444, Enter: 118668# (Call ID), Enter: 1# or your Pin.

Computer via 2 ways:

1. You can become a TalkShoe Member at www.talkshoe.com to be able to listen, text, or talk

live.

2. You can click on this link to join the call or just listen

along:http://www.talkshoe.com/talkshoe/web/talkCast.jsp?masterId=118668&cmd=tc

5. INCLUDE THIS WORDING ON ALL CORRESPONDENCES:

They are among you and you have to stop dealing at the lower levels of these Federal

agencies/Companies/organizations. The infiltrators have been blocking all of the

correspondences. You should add this language to your emails, faxes, and mailings so when

the perps, double agents, and informants receive our request forms, they will think again:

“Whoever intentionally obstruct the proceedings before depts., agencies, and committees,

obstruct this criminal investigation and/or retaliate against me because I am a victim, you

will be punished to the full extent of the applicable law in 1505 of Title 18 Obstruction of

proceedings before depts., agencies & committees, 1510 Obstruction of Criminal

investigations, 1513 of Title 18 Retaliating against a witness, victim or an informant, or

1514 Civil Action to restrain harassment of a victim or witness. Whoever intentionally

alters, destroys, mutilates or conceals records, or documents with the intent to impair the

object’s integrity or availability for use in an official proceeding will be punished to the full

extent of law as defined in 1519 of Title 18 Destruction, Alteration or Falsification of

records in Federal investigations and bankruptcy.”)

6. Follow-up with everyone. Get people’s names and contact information.

7. Change Your Mind, Body, and Spirit. IT IS TIME TO DO SPRING CLEANING FROM

THE INSIDE OUT.

NO SUGAR. NO JUNK FOOD. NO SODAS.

Download the book at www.radiationdetox.com to start detoxing your body of the radiation.

DMG is one supplement, which will increase your body by 300%.I use baking soda and

hydrogen peroxide as a paste and scrub it on my body with a loofah brush. You should always

brush towards your heart. The baking soda will exfoliate your skin and then put oil (emu,

coconut, extra virgin olive oil or essential oils) as a barrier on your skin. In my hair, I combine

the baking soda with the shampoo and then for the 3rd wash, I use the baking soda and hydrogen

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peroxide paste so that it will not cause a chemical reaction in my hair. My hair has turned blonde

on its own because of the chemical reaction. Eat green foods to alkaline your body in a powder

form (with no fillers if you can afford): wheatgrass, spirulina, and chlorophyll. Drink plenty of

water with lemons to hydrate your body. Coconut water and coconut oil are excellent sources,

Drinking bentonite clay.

Your body has its own electrical frequency. You can change it by what you do, think, and eat.

They know your body frequency so that is why you feel the pain. In addition, these lethal

weapons hurt anyway. When your body frequency is low, that is when cancer and other diseases

develop. Complaining lowers your body frequency. Think of thoughts of love and happiness

increases your body’s frequency. Think positive. Praying increases your frequency. Drinking

green tea, roobios tea and other teas will help. Eating vegetables will increase your frequency.

Buy oxygen to oxygenate your body. Eat bananas. Exercise will change your frequency.

Remember this: You have to get as much oxygen in your body as possible. Google: Increase

your body’s frequency, alkaline your body, kill parasites

8. PRAY, PRAY & PRAY.

Diseases are curses. If you want to start changing your situation, please say this:” I curse,

break, and destroy the spirit of Fear and I curse, break, and destroy the roots of the spirit

of insecurity and the roots of the spirit of inferiority in the name of Jesus Christ and

command you to leave my mind, body, and soul and never return. In the name of Jesus

Christ, I command all spirits associated with spirits of fear, insecurity, and inferiority to

come out of my body now. Hold your tongues and leave me now! In Jesus name, I

command you to go to the abyss and never return again.”

Say the Lord’s Prayer.

Visit www.demonbuster.com for more deliverance prayers. Break the generational and

individual curses over your life.

I had not heard that what I provided was INCORRECT. It is based on sound, irrefutable facts.

Can you believe that there was someone who actually wrote that they were happy to see that the

Bioethics Commission said that the laws are adequate. Instead of doing something that sounds

feasible and does not cost any money, but your time. The enemy wants to tell you about what

will NOT WORK before you even try it! Does that make sense? They don’t want you to DO

ANYTHING! THINK POSITIVE! How would anyone know what will work unless you try it? I

know what will work. NO ACTION. COMPLAINING. NO ACTION. TALKING ABOUT

YOUR SITUATION ALL THE TIME AND NEVER MOVING FORWARD BECAUSE

OF FEAR. FEAR IS FALSE EVIDENCE APPEARING REAL. THE THINGS THAT

HAVE BEEN GOING ON FOR THE PAST 8-9 YEARS. Divide and conquer in the TI

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community has ended in the name of Jesus Christ! We are united in the non-consensual human

subjects/TI community in the name of Jesus Christ.

THEY WANT TO KNOW YOUR EVERY MOVE SO THAT THEY CAN SABOTAGE

IT. This is a quote that I keep in mind. “Sabotage is used to defeat people.”

WHY HASN’T THE TI COMMUNITY GONE TO DC? Obviously, they do not want you to

go to DC as a group! We want a remnant of people to go to DC. It is time to get organized.

Wake up people! In the name of Jesus Christ, Satan and his demons are defeated! Spring is here!

Don’t you want to have a new beginning?

I pray for the people who have been sent to sabotage us. May the mercy of Jesus Christ be on

your souls; perps; double agents, and informants. You are not fooling me. The gig is up. They

went too far with my mother and now it is on. If I have to expose everyone and every

organization, then I will do it.

If anyone has a website or want to expose the truth, then enter the information at

www.yestojustice.tumblr.com.

Beware of NAYSAYERS or THOSE WHO HAVE EXCUSES or THOSE WHO WILL NOT

SEND THIS PACKAGE TO THE OTHER MEMBERS IN THEIR

GROUPS/ORGANIZATIONS.

I want you to think for a moment what has been going on with this community. It is a HOT

MESS! CHILDISH BEHAVIOR! I HAVE NEVER SEEN ANYTHING LIKE THIS IN MY

LIFE AND I HAD ENOUGH!

The vehicles are flying in this residential area. The aircrafts have gotten off of their flight plans.

Will you trust and believe with me? That is all that I ask of you. I hope to see more on the

conference call tonight.

I am only doing what God has told me to do.

Blessings,

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Letitia Peters

www.thecanche.tumblr.com

347-568-3537

Posted 2 years ago

action, human subjects, non-consensual, guinea pig, spring cleaning,

Mar 19

Form to Request “Opt-Out” or Discontinue From Human Subject Research

Please change the information with the ***and the letters in italics. This note could be included

on your fax page or in your emails. The perps, informants, and double agents have been

blocking the TIs/Human Subjects’ correspondences from reaching the appropriate destination.

You can right-click and select copy to paste this form in Word.

Her e-mail address is [email protected]. The mailing address is:

The U.S. Department of Health & Human Services

H.H.S. Secretary Kathleen Sebelius

200 Independence Ave. SW, Room 120F

Washington, DC 20201

877-696-6775

Comment Line: 202-205-5445 (leave a comment)

Correspondence: 202-690-6392

Fax: 202-690-7203

I did receive a response that my email was received.

NOTE: “Whoever intentionally obstruct the proceedings before depts., agencies, and

committees, obstruct this criminal investigation and/or retaliate against me because I am a

victim, you will be punished to the full extent of the applicable law in 1505 of Title 18

Obstruction of proceedings before depts., agencies & committees, 1510 Obstruction of

Criminal investigations, 1513 of Title 18 Retaliating against a witness, victim or an

informant, or 1514 Civil Action to restrain harassment of a victim or witness. Whoever

intentionally alters, destroys, mutilates or conceals records, or documents with the intent to

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impair the object’s integrity or availability for use in an official proceeding will be

punished to the full extent of law as defined in 1519 of Title 18 Destruction, Alteration or

Falsification of records in Federal investigations and bankruptcy.”

Date: March 19, 2012

From: ____________________________________________

To: Health & Human Services Secretary Kathleen Sebelius

Re: Request to “Opt-Out” or Discontinue Participation from Non-consensual Human

Subject Research/Experiment;

I am pleased to submit my request to “opt-out” or discontinue participation from this non-

consensual human subject research/experiment. I have a right to “opt-out” or discontinue

participation from this research/experiment. This research involves more than minimal risk. My

family and I are being torture. The “researchers” are violating my rights to obtain medical care. I

am in a life-threatening situation. This research should be terminated because it does not comply

with 45 CFR 46. We are requesting a moratorium for all human subject research.

******* FORM BEGINS **************************************

Statement of your name, a Non-consensual Human Subject to “Opt-Out” or Discontinue

Participation in the Human Subject Research/Experiment

Introduction:

In the Bioethics Commission’s report released on December 15, 2011, the Bioethics Commission

suggested that to keep track of the more than 55,000 research projects using human subjects, the

Federal government should create a central online portal and database where basic information

about the projects are archived and made easily accessible and further concluded that it “cannot

say that all federally funded research provides optimal protections against avoidable harms and

unethical treatment”. The Bioethics Commission also said although human subjects in US

government-funded research are generally protected by existing rules and regulations, their

safety and well-being could be enhanced with stronger measures, including increased public

transparency and a system of compensating subjects who sustain research-related injuries.

Research is defined by the Common Rule regulations as “a systematic investigation, including

research development, testing, and evaluation, designed to develop or contribute to generalizable

knowledge. Activities which meet this definition constitute research for purposes of this policy,

whether or not they are conducted or supported under a program which is considered research for

other purposes. For example, some demonstration and service programs may include research

activities.” Medical experiment is defined by California Law, Health & Safety Code Section

24171 as “the severance or penetration or damaging of tissues of a human subject or the use of a

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drug or device, electromagnetic radiation, heat or cold, or a biological substance or organism, in

or upon a human subject in the practice of research of medicine in a manner not reasonably

related to maintaining or improving the health of the subject or otherwise directly benefiting the

subject.

Human Subject is defined by the Common Rule regulations as “a living individual about whom

an investigator (whether professional or student) conducting research obtains either a) data

through intervention or interaction with the individual or b) identifiable private information.”

Human subject is defined by FDA regulations as “an individual who is or becomes a participant

in research, either as a recipient of the test article or as a control. A subject may be either a

healthy human or a patient. Subject [also] means a human who participates in an investigation,

either as an individual on whom or on whose specimen an investigational device is used or as a

control.”

Human subject research should adhere to the ethical principles and guidelines for the protection

of human research participants summarized in the uniform set of regulations, called the Federal

Policy for the Protection of Human Subjects, 45 CFR 46, Subpart A, formally known as the

“Common Rule.” The 45 CFR 46 regulations are based in large part on the Belmont Report and

were written to offer basic protections to human subjects involved in both biomedical and

behavioral research. Today, 45 CFR 46, Subjects A and E: Registration of Institutional Review

Boards (added 1/15/2009) is shared by 17 Departments and Agencies, representing most, but not

all, of the Federal Departments and Agencies sponsoring human subjects research. Many of them

have not adopted Subpart B: Additional Protections for Pregnant Women, Human Fetuses &

Neonates Involved in Research, Subpart C: Additional Protections Pertaining to Biomedical &

Behavior Research Involving Prisoners as Subjects, or Subject D: Additional Protections for

Children Involved as Subjects in Research. For the past 20 years, 45 CFR 46, have been

considered merely “guidelines” and is not a lawfully, promulgated regulation.

Before a research project involving human subjects is initiated, it must be reviewed and

approved by an Institutional Review Board (IRB). The IRB has a central role in ensuring that all

human subject research is planned and conducted in an ethical manner, and in compliance with

federal, state and local regulations. The major responsibilities of the IRB are to assess the risks

and benefits of proposed research and to promote respect for its advice and counsel in

safeguarding the rights and welfare of human subjects.

Failure of OHRP to Investigate Allegations

On behalf of the Secretary, HHS, the Office on Human Research Protections (OHRP) approves

the terms ofthese written institutional assurances, which constitute binding commitments. In

essence, OHRP holds accountable and depends on institutional officials, committees,

researchers, and other agents of the institution to comply with the institution’s assurance and the

regulations. In carrying out its oversight responsibility, OHRP’s Division of Compliance

Oversight monitors compliance through not-for-cause compliance oversight surveillance

activities and for-cause compliance oversight evaluations of allegations or indications of

noncompliance with the regulations. OHRP has the authority under Title IV of the Public

Health Service Act (42 USC 281 et seq.) to investigate complaints about human subject

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protections in HHS-conducted or -funded research, as well as any other research covered

by the institution’s Assurance of Compliance. OHRP also promotes compliance through its

Division of Policy and Assurances, which provides policy and guidance documents pertaining to

the regulatory requirements in 45 CFR 46. If HHS receives an allegation or indication of

noncompliance related to human subject research that is conducted or supported solely by a

Common Rule department/agency other than HHS, HHS will refer the matter to that

department/agency for review and action as appropriate” as stated at

http://www.hhs.gov/ohrp/humansubjects/commonrule/.On April 26, 2011, I met with Kristina C.

Borror Ph.D., Division of Compliance Oversight Director to file a formal complaint and to find

out which Federal agency was responsible for conducting non-consensual human

experimentation on me and others. I was told by Ms. Borror that there was nothing that her

office could do for me and that I should contact each agency and file a FOIA request with each

one.” I knew there were a lot of research projects using human subjects and it would be like

looking for a needle in a haystack. It would be very difficult, if not impossible to find, since there

are more than 55,000 projects that involve human subjects. Others who contacted OHRP have

received this response by letter, which states: “OHRP has determined that it does not have

jurisdiction over the matters referenced in your letter. Therefore, OHRP will not be able

to pursue this matter on your behalf.” Since January 15, 2009, all IRBs must use the Internet-

based registration maintained by HHS as stated in 45 CFR 46.501. Is the answer right on HHS’s

website?

Non-Consensual Human Subjects Testimonies & Request for a Moratorium

Congress and HHS are sponsoring projects involving human subjects, without 45 CFR 46 being

an enforceable lawfully, promulgated regulation, informed consent being on the books or a

ratified Human Subjects Research Protection Law. As a result, “the absence of Federal

jurisdiction over much privately funded research means that the U.S. government cannot know

how many Americans currently are subjects in experiments, cannot influence how they

have been recruited, cannot ensure that research subjects know and understand the risks

they are undertaking, and cannot ascertain whether they have been harmed.” Many non-

consensual human subjects testified at the Bioethics Commission’s Meeting 4 Session 10 (March

1, 2011) and Meeting 5 Session 6 (May 18, 2011): Public Comments. There were others who

submitted their written testimonies. The archived transcripts and videos are available at

bioethics.gov/cms/meeting-four and bioethics.gov/cms/meeting-five. Several months later, the

Office of Human Research Protections (OHRP) requested public comments pertaining to the

update of 45 CFR 46 and has received 600+ pages of testimonies from human subjects and over

1100 responses, which did not include the public comments from the Bioethics Commission..

A moratorium is being requested so that the “Federal Government can get it right”. This is a

massive undertaken, which should require the support of HHS and Congress to ensure that any

new regulations will benefit and protect the rights, safety, and welfare of future human subjects.

We are requesting Congress to conduct investigative hearings about illegal “COINTELPRO”

activities, ratify laws to protect the rights & welfare of the human subjects so that informed

consent is finally on the books and oversee the activities pertaining to the revision of 45 CFR 46

by HHS so that it will become a lawfully, promulgated regulation.. Will the revised 45 CFR 46

address the issues of ACHRE, NBAC, Executive Orders/Memos by former President Clinton,

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results of the EPA lawsuit, and former Senator John Glenn? How will 45 CFR 46 interact with

FDA regulations (21 CFR 50, 56), HIPAA Privacy Rule (45 CFR 164), Public Health Service

Act (42 USC 281) & other Federal & State regulations that impact the conduct of human subjects

research? The Common Rule offers more exceptions than FDA regulations do. Should that be

true? More importantly, will 45 CFR 46 become a strict, ethical, and enforceable, lawfully

promulgated Federal regulation, which researchers will be held accountable for their actions so

that unethical, human subject research/experiments will be eliminated in the future?

Statement of your name, a Non-consensual Human Subject to “Opt-Out” or Discontinue

Participation in the Human Subject Research/Experiment

Request to “Opt-Out” or Discontinue Participation as a “Non-consensual” Human Subject

***Revise, keep high level here*** I, your name________have been randomly selected to be a

participant or human subject in a research/experiment without my voluntary, informed

consent, either orally or written and without my knowledge. In this research/ experiment, I

am/have been exposed to electronic/electromagnetic radiation technology (including gamma

rays, microwave, & infrared) and weapons (chemical, biological, direct energy, &

radiological). In addition, my body has been infiltrated with many “unidentified metal

devices”. I meet the requirement of a “human subject” in a “research/experiment” as defined

above. I already had a compromised immune system. I was far from being that “healthy

person with no major health ailments”, but I was working towards it everyday so that I would

have a better quality of life and become a productive U.S. citizen in the workplace and

community once again. I am on disability retirement & I would have never consented to be a

“volunteer” in any human subject research with all of my confirmed diagnoses; especially one

which uses gamma rays, microwave, infrared and weapons (biological, chemical, directed

energy & radiological). I believe that my selection was not equitable in my case as defined in

45 CFR 46.113. I have endured unnecessary & unimaginable pain and suffering that it

presents a danger to my well-being by continuing in this human research. I am in a life-

threatening situation everyday that I continue to be in this human subject research.

Furthermore, this violates my religious principles and beliefs. I want out now! In addition, the

National Commission for the Protection of Human Subjects believed that those who are already

burdened (e.g., by disabilities or institutionalization) should not be asked to accept the burdens of

research unless other appropriate subjects cannot be found (i.e., if the research concerns their

particular disability or circumstance).

This human subject research/experiment involves noncompliance with 45 CFR 46. This part of

the “Common Rule” is intended to allow IRBs to waive informed consent in its entirety or any of

the required elements of informed consent In order for this human subject/experiment to waive

informed consent it had to meet the 4 criteria in 45 CFR 46.116 (d). An IRB may approve a

consent procedure which does not include, or which alters, some or all of the elements of

informed consent set forth in this section, or waive the requirements to obtain informed consent

provided the IRB finds and documents that: (1) The research involves no more than minimal

risk to the subjects; (2) The waiver or alteration will not adversely affect the rights and

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welfare of the subjects; (3) The research could not practicably be carried out without the

waiver or alteration; and (4) Whenever appropriate, the subjects will be provided with

additional pertinent information after participation.

Risk is defined in The IRB Guidebook as the probability of harm or injury (physical,

psychological, social, or economic) occurring as a result of participation in a research study.

Both the probability and magnitude of possible harm may vary from minimal to significant.

Federal regulations define only “minimal risk.” Minimal risk is defined in the Common Rule as

the probability and magnitude of physical or psychological harm that is normally encountered in

the daily lives, or in the routine medical, dental, or psychological examination of healthy

persons.

***ReviseGo in detail about your pain, violation of your rights, welfare, privacy, and

safety*** The daily exposures of electronic/electromagnetic radiation technology (including

gamma rays, microwave, & infrared) and weapons (chemical, biological, direct energy, &

radiological) presents a danger to my well-being and has violated my rights and welfare as a

human subject. The human research practices, which I am experiencing, should be

reclassified as “cruel and unusual punishment” or “crimes against humanity”, which goes

way beyond the physical or psychological harm that is “normally” encountered in our daily

lives or in the routine medical, dental, or psychological examination. I am experiencing

intentional infliction of severe physical pain or suffering, which violates my rights and falls

under the purview of 18 USC § 2340 Torture. I am in pain everyday, but the degree of the pain

varies from day to day and from hour to hour; from minor discomfort pain to excruciating,

agonizing pain, where I am in tears and crying out for God to deliver me. It has been very

unbearable. There have been times that I could not even get out of bed to bathe or even cook

for myself because of the extreme fatigue and the severity of the pain in my body. I am in

excruciating pain for hours and days while suffering in silence because I did not want my

parents to worry and also they do not believe that we are in a human subject research. My feet

would become so swollen due to edema that I could barely walk. Each step that I would take

the shooting pain would resonate throughout my legs. My legs looked like they were going to

“pop” any minute. I would have to elevate them and stay completely off my feet for a day or

several days before they would return to normal & there was no pain. My stomach, fingers,

eyelids, face & head also swells. I would experience constant throbbing of pain for hours. I

went “temporary blind” after being intentionally dosed with chemical: pesticides/insecticides

and the emergency medical care failed to treat me. I could hear my rapid heart rate when I am

in the bed or resting; sometimes I would have heart palpitations. One incident I developed

“red fine bumps” in my head and a couple of days later, my hair fell out in “clumps” as I was

combing it. The National Academy of Sciences states this only occurs with radiation exposures

at 200 rems or higher. My vision has become blurry after these exposures. My body is under

tremendous stress, undue distress and inflicted pain, which affects my performance to try to

run my own business and to live a normal life. My body has been infiltrated with

“unidentifiable metal devices”, which is being picked up by a simple carpenter’s tool: a stud

sensor/finder. I developed very painful red, blisters/mouth sores overnight, while I am

sleeping. According to the Mayo Clinic’s website in order for the blisters/mouth sores to

develop, radiation was aimed at my head or neck. I have a very dry, metallic taste in my

mouth. My eyes are very dry. I also woke up to an excruciating pounding, headache, which

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has been with me all day. My body is “aching” all over, as well as, my parents’ bodies. All of

our diseases have been exacerbated; my father has developed cancer, which could have been a

contributing factor from the environment and I recently spent the night in the hospital with

my mother due to her chest pains and very high blood pressure, which never occurred before.

Even people who visit us are being exposed, including children.

Personal privacy is important to ethical research as stated in 45 CFR 46.111. My

confidentiality and privacy rights have been violated. 45 CFR 46.116 (f) clearly states,

“nothing in this policy is intended to limit the authority of a physician to provide emergency

medical care, to the extent the physician is permitted to do so under applicable federal, state,

or local law.” The “researchers” have interfered with the physicians to provide me with the

“appropriate” emergency care. The physicians released private health information, did not

adequately addressed my complaints, failed to ensure patient care was provided in a safe and

effective manner, did not provide appropriate medical screening exams for me, and failed to

treat a sick and injured patient before releasing me, which violates the Emergency Medical

Treatment and Active Labor Act (EMTALA). Now there is a significant high health risk of me

developing a radiation-related disease that could have been greatly minimized through early

detection and appropriate medical treatment. The “researchers” have used disinformation to

cause humiliation, social stigmatization, and discrimination. Invasion of privacy concerns

access to a person’s body and the “researchers” has access to my body 24/7 and there are

countless of men, women and children, also called “informants” or “perps” who have access

to my body 24/7 without my informed consent or knowledge.

***Include this section or delete it if it does not impact you or your loved ones***Human

Subject Research Violates the Rights & Welfare of Vulnerable Population: Children

Children have been included in this human subject research, without receiving the

parental/guardian permission consent documentation as defined in 45 CFR 46.408 and these

children/minors are not wards of the state or any other agency, institution, or entity as defined

in 45 CFR 46.409. No adequate provisions were made for soliciting the assent of children and

the no permission was granted from their parents or guardians, as set forth in 45 CFR 46.408

as stated in 45 CFR 46.407 (iii). These children/minor are involve in research, which involves

greater than minimal risk as defined in 45 CFR 46.404 and does not present the prospect of

direct benefit to them at defined in 45 CFR 46.406. Some of these children are not

economically or educationally disadvantaged, but they have been placed in because of their

race. This research is not being conducted in accordance with sound ethical principles as

stated in 45 CFR 46.607 (ii).

Both the National Commission for the Protection of Human Subjects and the President’s

Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral

Research recommended that such waivers be granted only if subjects will not be denied benefits

or services to which they are otherwise legally entitled. The waiver of informed consent has

diminished the protection of my rights and welfare as a non-consensual human subject. I have

received no respect as a non-consensual human subject. There is a non-

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verbal element that “whatever happens to the human subject is of no personal concern to the

researcher. They can do whatever they want to the human subject and there is nothing that the

human subject can do about because no one will help the human subject.”

The waiver of informed consent has caused adverse consequences for my welfare and for my

general well-being, as well as, my loved ones. In addition, our rights, safety, dignity, welfare,

and privacy as non-consensual human subjects have been violated and do not comply with 45

CFR 46. This human subject research/experiment is incompliance with the policy, 45 CFR 46

therefore, as stated in 45 CFR 46.123, it should be terminated. If I continue in this “loosely

controlled” research/experiment, it will likely result in irreversible permanent injury, radiation-

induced diseases or even pre-mature death for myself (this request also includes my family

members who were systematically included in this because of me), because the “researchers”

are operating above the law and below the accepted standard of scientific, ethical, and

humane research. I am requesting to “opt-out” or discontinue my participation immediately

out of this non-consensual human subject research/experiment without prejudice. The

“Common Rule”, 45 CFR 46.116 (a) (8) states, “and the subject may discontinue participation

at any time without penalty or loss of benefits to which the subject is otherwise entitled.” I

am not waiving any legal claims, rights or remedies because of my participation as a non-

consensual human subject. The legal rights as a human subject may not be waived and the

human subject may not be asked to release or appear to release the investigator, the sponsor, the

institution or its agents from liability for negligence.

In the National Institutes of Health, Office for Protection from Research Risks (OPRR)

1993 Institutional Review Board Guidebook in the withdrawal from participation section,

it states, “attention should be paid to subjects’ rights when they decide to withdraw from

participation in the study. The federal regulations clearly require that subjects be free to

withdraw from participation without penalty or loss of benefits to which they are otherwise

entitled [Federal Policy §116(a) (8)].”

For research involving more than minimal risk, an explanation as to whether any compensation

and an explanation as to whether any medical treatments are availability of medical treatment

and compensation in the case of research-related injury, including who will pay for the treatment

and the availability of other financial compensation as stated in 45 CFR 46.116(a)(6). In July

2005 the National Academy of Sciences came to the conclusion that the preponderance of

scientific evidence shows that even very low doses of radiation pose a risk of cancer or other

health problem and there is no threshold below, which exposure can be viewed as harmless.

According to data from Hiroshima and Nagasaki, show that symptoms may persist for up to 10

years and may also have an increased long-term risk for leukemia and lymphoma. The

effects of radiation on the human body can be found at

www.atomicarchive.com/Effects/radeffects.shtml. Will the human subjects be compensated due

to research-related injury?

I, ____________certify that my decision to “opt-out” or discontinue participation in this

human experiment is without the intervention of any element of force, fraud, deceit, duress,

coercion or undue influence on my decision. I am requesting to “opt-out” or discontinue my

participation because of my rights as a human subject as stated in 45 CFR 46 116 (a) (8). This

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request includes all of my immediate family members (my elderly parents, my sister’s family

and my brother’s family) who were thrust in this unethical, human subject

research/experiment without their consent or without their knowledge.

Print Name: ______________________________________

Signature:________________________________________

Date: _________________________

Address:______________________________________________

Phone No.:____________

Posted 2 years ago

Mar 4

Conference Calls March 19-22, 2012 at 9:00 PM EST (Click Here)

Conference Call starting March 19, 2012 to March 22, 2012 at 9:00 p.m. EST

Phone/Calling:

The call-in number is (724) 444-7444, Enter: 118668# (Call ID), Enter: 1# or your Pin.

Computer via 2 ways:

1. You can become a TalkShoe Member at www.talkshoe.com to be able to listen, text, or talk

live.

2. You can click on this link to join the call or just listen

along:http://www.talkshoe.com/talkshoe/web/talkCast.jsp?masterId=118668&cmd=tc

Posted 2 years ago

Mar 3

Letter to HHS Secretary to Request “Discontinuation” in Non-consensual

Human Subject Experiment & Propose a 90 Day Moratorium

Fellow Non-Consensual Human Subjects/TIs,

Please join us as we have found the loopholes to benefit ALL human subjects.

This is part 1 of 3 parts so be on the look out for the other 2 parts in the next few days.

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Please read the following letter. I have been looking for a solution to our situation about how to

get out of it and guess what? I found the loopholes for us, which was in the “Common Rule” all

the time. One is that we can ask to discontinue our participation as a human subject. It is our

right to do so as a human subject. Does that make sense? We do have rights. The other is that

they violated the requirements to waive the informed consent. They also violated the rights and

welfare of the children: vulnerable population. This does not cost anything, but your time.

Knowledge is power!

Here’s the letter, which I sent to HHS Secretary Kathleen Sebelius. Please feel free to revise the

letter by replacing your information with mine and then send your letter to her. Her phone

number is 202-619-0257 (I got a message saying that this is disconnected.) or call 1-877-696-

6775 to see if you get the same number. Her email address is [email protected]. If

anyone gets a fax number, please send it to me so that I can post it. The mailing address is:

The U.S. Department of Health & Human Services

H.H.S. Secretary Kathleen Sebelius

200 Independence Ave. SW, Room 120F

Washington, DC 20201

It may take a few days. I did receive a response that my email was received.

I will do a conference call on Sunday night at 9:00 p.m. If you follow me at

www.thecanche.tumblr.com, then you will get a message every time that I post something.

More laws to check out: http://uscode.house.gov/download/pls/18c73.txt.

18 USC 1505 Obstruction of proceedings before depts., agencies and committees

18 USC 1512 Tampering with a Witness, Victim or Informant

Obstruction may consist of any attempt to hinder the discovery, apprehension, conviction or

punishment of anyone who has committed a crime. The acts by which justice is obstructed may

include bribery, murder, intimidation or the use of physical force. The purpose is to influence,

delay or prevent communication of information to law enforcement, to alter or destroy evidence.

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The informants are obstructing justice. 95% to 99% (I will give them the 1%) of the people you

are interfacing with are perps or informants. They were blocking your correspondences.

The doors of opportunity are opened for us until Friday, March 23, 2012. Spring is around the

corner and it is time for new beginnings. We have to expose these informants, perps, or double

agents. It is time for you to get out of your residence and start talking to people. Bob S. and G.

Mason also have done an outstanding job. With all 3; it is an airtight case. I will send out my

analysis, once I have updated it so look for it tomorrow and you can post it, just reference my

website www.thecanche.tumblr.com. The analysis which I did shows that the Federal

Government has a history of discrediting non-consensual human subjects. It is documented in

official U.S. Federal Government papers. They have referred to them as neurotic, paranoid

schizophrenia, or delusional so that they will appear “not all the way there”. Now, we have the

proof that this is a pattern of the Federal Government have done in the past and is continuing

doing. It is a perfect plan: Discredit the victim so that no one would believe him/her so that they

can continue with their evil plans.

Proposed Schedule:

Sunday, March 4, 2012 start fasting 3 hours before daybreak and end Wednesday, March 7, 2012

at sundown. Drinking water with lemons during a fast will helps our immune system. You can

download the free e-book at www.radiationdetox.com to learn how to repair your body from

radiation exposure.

Evening conference calls begins on Sunday, March 4, 2012 at 9:00 p.m. EST to Friday, March

23, 2012. Mark your calendars!

1 day fast from March 7, 2012 from 3 hours before daybreak to sundown - We would like as

many people as possible to do this.

Join us in Washington, DC on Wednesday, March 7, 2012. Send an email to

[email protected] and put in the subject: Ready to Join You in DC. Anyone is welcome to

join us. They do not want you to come to DC. Only the perps and informants want you to stay

out of DC. We need a group of people. We will keep going until we get action!!!

Prayers-We need as many people as possible to pray.

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Perps/Informants- We will pray that you will confess and repent of your sins.

Former Federal Employee/ Whistleblowers- 115 (a) (2) of Title 18 and for your families 115 (b)

Visit www.justicegov/usao/eousa/foia_reading_room/usam/title9/crm01601.htm

If the lawsuit was so feasible, then how come an attorney will not file a class action suit on our

behalf?

No one knows that we exist; our stories are not on the nightly news or in a major newspaper.

Even the journalists who came to the Bioethics Commission, they all left before they heard our

testimonies. Your website can be redirected. The petitions have been tampered with so that you

will not get the numbers. We need to get out in the public and tell our stories.

I know that I will. Will you?

PLEASE WRITE YOUR STORY THIS WEEKEND. We will need your story in the next week.

www.COINTELPROContinuesToday.org has an excellent format to follow to help you with

your story. They will even help you. We need as many stories as possible to be done. (I just

found them a couple of days ago.)

Let’s think about our freedom now!!!

We will have flyers for you to pass out. Get involved! The enemy is already defeated and he

knows it. We have the truth. It is now up to you to do your part. Please share this with others

Blessings,

Letitia

347-568-3537

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March 1, 2012

P.O. Box 77181

Ewing, NJ 08628

The U.S. Department of Health & Human Services

H.H.S. Secretary Kathleen Sebelius

200 Independence Ave. SW, Room 120F

Washington, DC 20201

Re: Request to Discontinue Participation in Non-consensual Human Subject Experiment & to

Propose A 90 day Moratorium on All U.S. Human Subjects Experiments/Experiments that

Receive Federal Funding Internationally

Madam Secretary:

I am writing this letter to request your intervention because many of our avenues to bring this

issue to light have been “obstructed” by informants. While in other cases, the government term

“on a need- to-know basis” comes into practice. The issue is: non-consensual human subjects in

the U.S. I am not only speaking for myself and for my family, but also on behalf of the countless

of my fellow Americans and those worldwide who have been placed in a human subject

experiment, without our voluntary, informed consent, whether orally or written. The current

deficiencies in the U.S. human subject research system have made this possible. The Belmont

Report and the Nuremberg Code both addressed voluntary, informed consent as a requirement

for the ethical conduct of human subject research. In 1991, 16 federal agencies adopted 45 CFR

46, Subpart A, which then became known as the “Common Rule”, governs the research on

human subjects. Even though the “Common Rule” has the requirement for informed consent, it

has many “loop holes”, which has not been closed in 20 years, and as a result this has caused

unethical human subjects experimentation on men, women, and children in the U.S. and

Internationally.

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Let me introduce myself. My name is Letitia Peters and I was a former Electrical/Electronics

Engineer (GS-14/J) with the Federal Government in NJ and Washington, DC. During my 16

years career, I worked as a project manager managing 3 acquisition programs worth close to

$100 million, test engineer, and a program scheduler. I received accolades for my achievements

at my workplace and in the community. I volunteered as a math tutor in the public school

systems in Washington, DC and I was active in numerous organizations. I loved tutoring

children, which I would like to do again real soon. I also started my own event management

business in 2001 after earning a Master’s Certificate in Event Management from George

Washington University. I started to get very ill in 2003 and I was diagnosed with sick building

syndrome. Toxic mold was prevalent in several Federal buildings in Washington, DC and it was

making several of us sick. Unfortunately, I was terminated in 2006. I developed a 3 minute

video, which you can watch at www.youtube.com/nimsociety. I turned my anger to activism and

I started an organization called National Indoor Mold Society (NIMS). Humbly speaking, in 3 ½

years, we brought awareness to the public, medical field, and lawmakers that exposure to indoor

toxic molds and mycotoxins can cause adverse health effects to humans and pets. The 75th

Nevada legislature passed legislation declared September 2009 as National Indoor Toxic Mold

Awareness Month (NITMAM) in their state. Even though I was forced to close NIMS, the

people, businesses and organizations are still today celebrating September as NITMAM, which

was spearheaded by NIMS. Many of the archived radio shows are still available at

www.talkshoe.com. I was feeling better and I was working towards being active in the

community once again. My life changed drastically in September 2009, after I attempted to file a

cyber stalking report and to request that computer forensics be done. One NJ police officer told

me that no one will look at your computer. He was right. Since then, my life has been a

rollercoaster to say the least. I have not done anything to anyone to warrant such unusual and

cruel punishment. I realize that these people will never stop until I am dead so I will stop at

nothing for justice. I have done extensive research on the human subjects experiments in the U.S.

and Internationally. It has taken me years to figure out what was happening to me. At first, I

thought it was because of my activism work so I stopped doing the radio shows and eventually

closed NIMS. My health did not improve it got worse because I was receiving the most

aggressive form of torture that a human person could ever endure. I suffered many nights in

silence, thinking how a human being could do this to another human being. My nightmare began

while I was still employed as a Federal Government employee. As unbelievable, and as

unthinkable this may sound, but I reasonably believe that my family and I (includes children and

elderly), have been placed in this non-consensual human subject experiment as a form of

retaliation because I was a Federal whistleblower. I only wanted to work in a healthy work

environment because the exposure to toxic mold was causing adverse health effects for me.

Madam Secretary, I, like so many other non-consensual human subjects are enduring inhumane

treatment everyday 24/7. We would like to eat food that is not contaminated with chemicals,

radiation, or heaven knows what. We would like to have one solid night of sleep, without being

wakened out of sleep, because our neighbors are beaming us with electromagnetic weapons. We

want our lives back now. I will do everything possible with the help of Jesus Christ to ensure that

the next generation is not a “guinea pig” for the rest of his/her lives. Many non-consensual

human subjects testified at the Bioethics Commission 4thand 5th meetings. You can watch

Meeting 4 session 10 (March 1, 2011) and Meeting 5 Session 6 (May 18, 2011): Public

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Comments at bioethics.gov/cms/meeting-four and bioethics.gov/cms/meeting-five. In addition,

you can download the transcript in pdf file or watch the live archived sessions. I echo the words

that were announced at the 1976 National Urban League National Conference on Human

Experimentation, “we don’t want to kill science, but we don’t want science to kill, mangle, &

abuse us”.

How do I know that I am/we are in an experiment/research?

We meet the definition of being a human subject in an experiment/research as defined in 45 CFR

46.102, as well as, according to California Law, Health & Safety Code Section 24171, a medical

experiment is defined as “the severance or penetration or damaging of tissues of a human subject

or the use of a drug or device, electromagnetic radiation, heat or cold, or a biological substance

or organism, in or upon a human subject in the practice of research of medicine in a manner not

reasonably related to maintaining or improving the health of the subject or otherwise directly

benefiting the subject.” The informants are utilizing COINTELPRO tactics. COINTELPRO is a

well-organized, well-funded, well-connected, well-orchestrated operation with vast resources

across state lines and Internationally. COINTELPRO is an acronym for Counter Intelligence

Program. Wikipedia states, “it was a series of covert, and often illegal, projects conducted by the

United States Federal Bureaus of Investigation (FBI) aimed at surveilling, infiltrating,

discrediting, and disrupting domestic political organizations. COINTELPRO tactics included

discrediting through targets through psychological warfare, planting false reports in the media,

smearing through forged reports, harassment, wrongful imprisonment, extralegal violence and

assassination. COINTELPRO took place between 1956 and 1971. Officially, COINTELPRO

was termination in April 1971, but was it? The last major Congressional investigation of

COINTELPRO operations was conducted in 1976-1978 by the Church Committee. These

horrifying reports did not provide any effective legislative remedies for future victims. Nor did

they produce any prosecutions of proven criminals within the Justice Department.

COINTELPRO covert operations have been unleashed to neutralize the non-consensual human

subjects, which includes advanced electronic/electromagnetic radiation technology (including

gamma rays, microwave, & infrared), weapons (chemical, biological, direct energy, &

radiological), implants, and satellites/drones. You can read more information about the current

COINTELPRO tactics at www.COINTELPROContinuesToday.org.

Recently, Congressman Stephen Lynch (D-MA) authored the Confidential Informant

Accountability Act of 2011, H.R. 3228, which would require Federal law enforcement agencies

to report to Congress serious crimes, authorized, as well as, unauthorized, committed by their

confidential informants, to amend title 28, United States Code, with respect to certain tort claims

arising out of the criminal misconduct of confidential informants and for other purposes.

Deficiencies with the Current Regulations in the Human Research System

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Since 1991, the Common Rule has not been a strict, ethical, enforceable and lawfully,

promulgated regulation. The Common Rule “was originally written by the National Institutes of

Health and do not always appropriately address the ethical issues in research outside of the

biomedical context.” It is now being updated after 20 years. Year and year, Congress, HHS &

other Federal agencies continued to sponsor federally funded human subjects experiments,

without ratifying any Federal regulations & International standards, which would protect the

human subjects. Congress and HHS have failed to ratified legislation which would have closed

the loopholes for the protection of the human research subjects. These deficiencies have

benefited the researchers and have not protected the human subjects. There are:

1. Former President Clinton & the Advisory Committee on Human Radiation

Experiments (ACHRE): He directed the ACHRE to uncover the truth, recommend steps to

right past wrongs and propose ways to prevent unethical human subjects’ research from

occurring in the future. The Federal Government and Government officials failed ignored to

implement many of the 18 recommendations outlined in the ACHRE’s final report as well as, the

March 27, 1997 former President William Clinton’s Memorandum: Directive to Strengthened

Protections for Human Subjects of Classified Research; thus allowing continuous waivers for

informed consent of classified and secret human subjects experiments; no sanctions for

conducting research unethically; allowing for research conducted by Federal agencies that do not

follow the Common Rule, privately funded research that is not regulated by the Food and Drug

Administration or private individuals or institutions that do not receive any Federal funding to

conduct human subjects research without requiring that informed consent must be obtained for

the past 15 to 20 years. HHS failed to implement the memorandum, but NASA has included it in

their policy. As a result, many human subjects’ experiments are being conducted without being

required to obtain informed consent, whether orally or written.

2. Former Senator John Glenn: There is no law on the books requiring that informed

consent must be obtained. Informed consent must be obtained prior to conducting research on

human subjects. Former Senator John Glenn cited this issue in 1997 in his remarks for his

proposed legislation S. 193, Human Research Subject Protection Act to the 105th Congress. The

intent therefore of this legislation is twofold: First, to fill in the gaps of coverage of the common

rule by requiring all research involving human subjects to abide by the rule; and second, to

elevate the importance of conducting research ethically, the bill provides criminal fines and

penalties for failure to comply with the requirements of this law, and by extension 45 CFR 46.

The full text is available for your review at http://home.swipnet.se/allez/Eng/HumExpEn.htm.

Former Senator John Glenn said, “I want to put this in personal terms once again. You just think

about your own family, your own son, your own daughter, or grandchildren who might be, the

next time they go to a doctor, the subject of some medical experiment that they are not even told

about. I do not think there can be many things more un-American than that. That is

unconscionable, and we should not permit that.”

3. Proposed Congressional Legislation to Protect the Human Subjects: Congress passed

the Defense Authorization Act of 2012 in less than a year, but Congress has failed to ratify any

proposed legislation for the protection of human subjects in 1997, 2002, 2003, 2006, 2008 and

2011 for the past 15 years. In the April 29, 2002 press release, Congress Examines Research

Protection Oversight System: Legislation Needed”, Congress examines research protection

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oversight system and states that legislation is needed, but it is never ratified. The full press

release can be found at http://www.cossa.org/hsbackground.htm.Year after year, Congress and

HHS has funded human subjects’ experiments, without having proper legislation to protect the

human subjects. This has allowed for unethical, non-consensual human subject experiments to

continue. A list of the proposed laws is at www.circare.org.

4. President Clinton & National Bioethics Advisory Commission: The issue of informed

consent were addressed in 4 reports (1998, 1999a, 1999b, and 2001) because the topic is central

to the protections offered to research. As a first priority, NBAC directed its attention to the

consideration of the protection of the rights and welfare of humans’ research subjects. On May

17, 1997, the National Bioethics Advisory Commission (NBAC) unanimously adopted a

resolution that “No person in the United States should be enrolled in research without the twin

protection of informed consent by an authorized persons and independent review of the risks and

benefits of the research.” Later that month, Former President Clinton stated that “Science must

respect the dignity of every American. We must never allow our citizens to be unwitting guinea

pigs in scientific experiments that put them at risk without their consent and full knowledge.”

Almost 15 years later, the former Senator John Glenn’s, NBAC’s and former President

Clintons’goals remains unmet. In the May 4, 1999 letter, NBAC Chair, Harold T. Shapiro’s

memo to former President Clinton stated in his memo “Consistent with your October 3, 1995,

Executive Order 12975, the NBAV has focused a good deal of its efforts over the last three years

on issues surrounding the protection of human research subjects…I know of your interest, as

well as that of the Congress, which has rightfully inquired about the adequacy of existing

protections… our key concerns are

the following:

· Federal protections for persons serving as human research subjects do not yet

extend to all Americans.

· Despite widespread implementation of federal regulations by those departments

and agencies sponsoring substantial amounts of biomedical research, a number of

departments and agencies who sponsor primarily non-biomedical research or little research

overall have failed to implement these federal protections.

· Federal protections do not always include specific provisions for especially

vulnerable populations of research subjects.

· Many federal agencies find the interpretation and implementation of the Common Rule

confusing and/or unnecessarily burdensome.

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· Federal protections are difficult to enforce and improve effectively throughout the Federal

Government, in part because no single authority or office oversees research protections across all

government agencies and departments.

· New techniques are needed to ensure implementation at the local level.

5. EPA sued by the Pesticide Industry: March 2002 — the pesticide industry sued EPA

over this approach, and the U.S. Court of Appeals for the District of Columbia Circuit ruled that

EPA’s interim approach was not established through required notice and comment rulemaking

and should be vacated. In a June 2003 decision, the court stated that, as a consequence, "the

agency’s previous practice of considering third-party human studies on a case-by-case

basis, applying statutory requirements, the Common Rule, and high ethical standards as a

guide, is reinstated and remains in effect unless and until it is replaced by a lawfully

promulgated regulation."

In conclusion, there have been many attempts to ensure that the safety and welfare of the human

subjects are protected, but many Federal agencies have failed to implement these federal

protections, including HHS and Congress. In the 2001 NBAC’s final report states, “Despite the

fact that many research institutions voluntarily apply the Common Rule—even to their privately

financed research—there are other significant sectors of privately funded research that remain

ungoverned either by State or Federal law. NBAC finds that the absence of Federal jurisdiction

over much privately funded research means that the U.S. government cannot know how many

Americans currently are subjects in experiments, cannot influence how they have been

recruited, cannot ensure that research subjects know and understand the risks they are

undertaking, and cannot ascertain whether they have been harmed. Not only does this

prevent the Federal Government from protecting Americans enrolling in research, but it affects

the Federal Government’s ability to craft policies governing emerging technologies. While

preparing its 1997 report Cloning Human Beings, for example, NBAC noted that the Common

Rule’s lack of jurisdiction over privately funded research made it impossible to rely on

IRBs as the primary mechanism for protecting human subjects against inappropriate uses

of those technologies.” I have completed a 41 page analysis, which discuss these issues in depth

is available for review.

Failure of OHRP to Investigate Allegations

“If HHS receives an allegation or indication of noncompliance related to human subject research

that is conducted or supported solely by a Common Rule department/agency other than HHS,

HHS will refer the matter to that department/agency for review and action as appropriate” as

stated at http://www.hhs.gov/ohrp/humansubjects/commonrule/ . In May 2011, I went to

OHRP’s office to file a formal complaint to find out which Federal agency was responsible for

conducting non-consensual human experimentation on my family and on those Americans in the

U.S.A. I was told by OHRP’s management that “there was nothing that this office could do for

you and that you should contact each agency and request a FOIA request.” In addition, she was

not aware of any agency, which was using electromagnetic radiation. I walked out with a copy of

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the Belmont report and the 45 CFR 46 in my hands, which I received. Others who contacted

OHRP have received a similar response by letter, which states: “OHRP has determined that it

does not have jurisdiction over the matters referenced in your letter. Therefore, OHRP

will not be able to pursue this matter on your behalf.” If it is not OHRP’s jurisdiction, to

ensure compliance oversight over human subject research, then who is responsible? Since

January 15, 2009, all IRBs must use the Internet-based registration maintained by HHS as stated

in 45 CFR 46.501. Is the answer right on HHS’s website?

Madam Secretary, this is why 11 years later from the issue of the final NBAC report, we are

coming to you, as non-consensual human research subjects to ask for your intervention to honor

our 3 requests as per the “Common Rule.” Many of us are in life-threatening situations.

1. “Non-consensual” Human Research Subjects Request to Discontinue Participation

I am speaking for myself and for my family, as well as, on behalf of the countless of my fellow

Americans and those worldwide who have been placed in a human experiment, without our

voluntary, informed written or oral consent or knowledge. I am writing you today to request that

we would like to discontinue or “opt-out” our participation in these human subject experiments

without prejudice. As stated in 45 CFR 46.116 (a)(8)) states , “ and the subject may discontinue

participation at any time without penalty or loss of benefits to which the subject is otherwise

entitled.” I am not waiving any legal claims, rights or remedies because of my participation as a

non-consensual human subject. The legal rights of subjects may not be waived and human

subjects may not be asked to release or appear to release the investigator, the sponsor, the

institution or its agents from liability for negligence.

2. Human Subject Research Fails to Meet the 4 Criteria to Waive Informed Consent

According to 45 CFR 46.116 (d), ALL of the 4 criteria listed must be met to waive informed

consent. An IRB may approve a consent procedure which does not include, or which alters,

some or all of the elements of informed consent set forth in this section, or waive the

requirements to obtain informed consent provided the IRB finds and documents that:

(1) The research involves no more than minimal risk to the subjects; Minimal risk is the

probability and magnitude of physical or psychological harm that is normally encountered in the

daily lives, or in the routine medical, dental, or psychological examination of healthy persons.

(2) The waiver or alteration will not adversely affect the rights and welfare of the subjects;

(3) The research could not practicably be carried out without the waiver or alteration; and

(4) Whenever appropriate, the subjects will be provided with additional pertinent information

after participation.

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Each one of the 4 criteria to waive informed consent has been violated:

In response to (1) The research practices, which myself and many other non-consensual human

subjects can be reclassified as “cruel and unusual punishment” or “crimes against humanity”,

which goes way beyond the physical or psychological harm that is “normally” encountered or in

the routine of a medical, dental, or psychological examination. This is torture. As a result, many

non-consensual human subjects are/were diagnosed with cancer and other illnesses; many are

maimed or died as a result of the daily torture with lasers, electromagnetic radiation- gamma

rays, infrared, microwave. Some even committed suicide. Many have lost their hair and teeth.

In response to (2): The rights and welfare of the subjects have been affected. The basic ethical

principles of respect of persons, beneficence and justice as stated in the Belmont report have

been violated. According to 45 CFR 46.123, the department or agency head may require that

department or agency support for any project be terminated or suspended in the manner

prescribed in applicable program requirements, when the department or agency head finds an

institution has materially failed to comply with the terms of this policy. In addition, whether the

applicant or the person or persons who would direct or has/have directed the scientific and

technical aspects of an activity has/have, in the judgment of the department or agency head,

materially failed to discharge responsibility for the protection of the rights and welfare of human

subjects (whether or not the research was subject to federal regulation).

In response to (3) If the research could not be carried out without the waiver or alteration, then

maybe it should not be doing it in the first place.

In response to (4): This is an ambiguous and open-ending statement with no timeframe attached

to it. My family and I have never received any additional pertinent information after

participation. When appropriate could mean anytime including after I am dead.

3. Human Subject Research Violates the Rights & Welfare of Vulnerable Population:

Children

Many children/minors have been included in this human subject research, without receiving

parental/guardian permission consent documentation as defined in 45 CFR 46.408 and these

children/minors are not wards of the state or any other agency, institution, or entity as defined in

45 CFR 46.409. No adequate provisions were made for soliciting the assent of children and the

permission of their parents or guardians, as set forth in 45 CFR 46.408 as stated in 45 CFR

46.407 (iii). These children/minor are involve in research, which involves greater than minimal

risk as defined in 45 CFR 46.404 and does not present the prospect of direct benefit to them at

defined in 45 CFR 46.406. In July 2005 the National Academy of Sciences came to the

conclusion that the preponderance of scientific evidence shows that even very low doses of

radiation pose a risk of cancer or other health problem and there is no threshold below, which

exposure can be viewed as harmless. According to data from Hiroshima and Nagasaki, show that

symptoms may persist for up to 10 years and may also have an increased long-term risk for

leukemia and lymphoma.The effects of radiation on the human body can be found at

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www.atomicarchive.com/Effects/radeffects.shtml. As a result, the children’s DNA has been

altered and now these “ DNA mutations” will become part of their permanent DNA. Now, when

they will have children and this new modified DNA will become part of their hereditary and

passed on for future generations to their children and their children’s children. Some of these

children are not economically or educationally disadvantaged, but they have been placed in

because of their race. This research is not being conducted in accordance with sound ethical

principles as stated in 45 CFR 46.607 (ii).

Request a 90 day Moratorium on all U.S. Human Research Subjects/ Federally Funded

Human Subjects Experiments Internationally: Serious Concerns about the Current Update

of the “Common Rule” and the Future of Human Subjects Research/Experiments

I am requesting a 90 day moratorium on all U.S. Human Research Subjects/Federally Funded

Human Subjects Experiments Internationally until laws are ratified because the current Federal

laws and International standards do not protect the human subjects. This is a massive

undertaking. It has been 20 years since this document has been updated. Even though we have

been treated like “animals”, we are human beings. We should have the same rights as everyone

else. This will allow Congress and the HHS to develop a comprehensive plan to resolve this

important issue that affects the lives of human beings. It appears that this is no big thing, but it is

a MASSIVE thing for us, because you have no clue how it feels to lose your eyesight

(temporarily and then regain it) or not being able to barely walk because of the excruciating pain.

There has been poor oversight by HHS and Congress in the past 15 to 20 years for the protection

of human subjects. Will the new revised “Common Rule” include the issues of ACHRE, NBAC,

Executive Orders and Memorandums by former President Clinton, results of the EPA lawsuit,

and former Senator John Glenn? If these issues are not even in the new revised Common Rule

we will have the same problem today of “non-consensual” human subjects in the future.

Is there a conflict of interest with HHS sponsoring experiments & those who are on the Advisory

Board? How can HHS “police” itself? In FY 1999, HHS was the largest sponsor of federally

funded programs. There was a proposal to have an independent organization to provide

oversight for human subject research.

Has HHS reviewed the Europeans laws on the protection of human subjects’ experiments? The

European has stricter laws and many of them have come to conduct their clinical trials in the

U.S. because it is “easier”. Everyone is aware of the “easy pass”, which is available. What steps

will be taken to mitigate that the new laws are advantageous to the human subjects? The

Common Rule should include regulations for biomedical and non-biomedical. I propose that

Congress and HHS should work closely together while ratifying the Common Rule. HHS has

received over 1153 responses and not including the comments from the Bioethics Commission.

Based on the past history of the HHS, can they be objective to develop a Federal regulation,

which is beneficial to the protection of human subjects and not advantageous to the researchers?

Does HHS have the resources, knowledge, skills, and ability to revise “The Common Rule” to

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become a strict, ethical, enforceable and lawfully, promulgated regulation that will protect the

human subjects? If the Federal regulation, “The Common Rule” is revised correctly, then (1)

Many human subjects’ experiments will decrease dramatically (2) Researchers will face criminal

charges, therefore eliminating the “free pass” for researchers to persecute, maim, mutilate, and

even kill their human subjects and (3) informed consent will be required, therefore eliminating

the researchers ability to “select anyone that they want of their chosen, without informing them”

to participate in their experiments. More importantly, will it be an enforceable, lawfully

promulgated Federal regulation, which researchers will be held accountable for their

actions and it will eliminate many future unethical, human experiments? In addition, there

will no longer be people in lifelong non-consensual human subjects. All human subjects’

experiments will be transparent. Will HHS bring in outside experts? How long will they take?

The ACHRE used hundreds of people to go through all of those documents. Is Congress going to

ratify its Human Subjects Protection Act? Will the revised “Common Rule” go out for review to

the public again? Will the resolution of those public comments be posted? I am proposing a

monthly update by HHS to Congress in this process and then to the public. Can the public be

involved?

Approximately 600 pages of U.S. victims’ testimonies were submitted to the Department of

Health & Human Services, Office of Human Research Protections (OHRP) in Oct. /Nov. 2011.

On Nov. 23, 2011, I sent a letter via email to the Bioethics Commission & to OHRP to respond

to OHRP’s Federal Register that OHRP will accept the public comments from the Bioethics

Commission. In addition, one other victim also forwarded a letter to them as well. Was this

action completed? I also sent my comments, which I provided to the Bioethics Commission.

HHS should have received the 25 pages of legal analyses: 12 pages of analysis by G. Mason cites

legal cases (many attorneys would like this one) proves the inadequacy of 45 CFR 46 in

enforcing the right to informed consent and retired attorney Robert S., provides more proof that

the Federal Government agencies are involved and he discusses modern-day COINTELPRO

tactics. This document is also available for review at www.COINTELPROContinuesToday.org.

In Dec. 20111, Bioethics Commission received 41 pages of analysis by Former Federal Govt.

engineer, Letitia Peters provides proof that the Federal Government agencies and Congress have

not ratified laws to protect human subjects in almost 20 years. From pages 36 to the end, she

presents information relevant to HHS, Congress, & to the Federal Government agencies. My

concerns about HHS capabilities to handle a massive undertaking of updating 45 CFR 46 after

20 years are a serious concern. What will be Congress’ role? This document will be available for

review at www.thecanche.tumblr.com.

In closing, I support the efforts that America has done to condone crimes against humanity and

torture in other nations, but now we need America to be here for us: the American people. My

religious beliefs have been violated by being in a non-consensual human subject research as

well. There are countless of men, women, and children in America and worldwide who are

unaware that they are victims of COINTELPRO abuse and/or have been placed in a non-

consensual human subject research. They do not attribute their ongoing “bad luck”; mishaps;

animal killings; or mysterious, untreatable, disabling “environmental” diseases to covert

operatives using old COINTELPRO tactics plus new weapons of war to terrorize, neutralize, and

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prevent resisting the treatment. These professional, well-orchestrated intrusions induce

excruciating pain, exhaustion, terror, alienation, and sometimes result in violent behavior against

themselves or others – eventually, one way or another, “neutralizing” and killing the non-

consensual human subject. We want our lives back now. Princeton Theologian, Paul Ramsey

whose 1970 work, The Patient as a Person states, “No man is good enough to experiment upon

another without his consent.”

Thank you for your time and consideration. If you have any questions or concerns, I can be

reached at [email protected] or you can call me at 347-568-3537. For additional

information, you can visit www.thecanche.tumblr.com, which will contain many of the

supporting documentation including my analysis report.

Sincerely,

Letitia M. Peters

Letitia M. Peters

International Spiritual Awakening Ministries/Coalition Against Non-Consensual Human

Experiments

Welcome to the International Council Against Non-consensual Human Subject Research (I.C.A.N.H.S.R.) Blog! My name is Letitia Peters. You are also welcome to visit the other blog for videos, recommended list of documents, reports to download at www.YesToJustice.tumblr.com. Our Cause: Bring awareness about the violation of the serious human, civil & constitutional rights of countless men, women, and children who are being monitored, tracked, tortured and targeted with technology by fellow citizens like those in Syria and Iran. President Obama has said that technology should not be used to repress people. Those who are involve includes minorities, celebrities, activists, journalists,people of faith, minorities, people with disabilities, people with mental health, prisoners, children in the state/government care, and the poor. Many have been classified as “undesirables". Others include members of the Armed Forces; the military, human rights activists, peace activists, dissidents, and Liberals. COINTELPRO has been deemed unconstitutional in the courts. The informants or perps using highly advanced electronics/electromagnetic technology (includes gamma rays, infrared and microwave), weapons( biological,chemical, direct energy and radiological), implants, and satellites/drones. It may take people years before they realized that they have been placed in a "digital guns for hire" program. We are victims now, but you and your loved ones, may be next, if you aren't already? WE NEED YOU in order for our VOICES TO BE HEARD! You are Invited to join us in our campaign: "We say

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NO to Non-consensual Human Subject Research and YES to Justice! We say NO to COINTELPRO and YES to Justice!" Will you join us to stop tjhis genocide?

U.S. puts sanctions on telecom firms in Syria,

Iran

The Obama administration announces sanctions for

recording cellphone calls, monitoring Internet traffic and

employing other technological tools to 'facilitate grave

human rights abuses.'

April 23, 2012|By Jim Puzzanghera, Los Angeles Times

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WASHINGTON — The Internet and social media helped fuel last year's "Arab Spring" pro-

democracy uprisings. Now, the Obama administration wants to prevent companies from using

the same technology to help repressive regimes in Syria and Iran target dissidents.

Taking aim at what it called "digital guns for hire," the administration unveiled new sanctions

against major telecom firms in those countries as well as the governments themselves for

recording cellphone calls, monitoring Internet traffic and employing other technological tools to

"facilitate grave human rights abuses."

"These technologies should be in place to empower citizens, not to repress them," President

Obama said in announcing the sanctions Monday in a speech at the U.S. Holocaust Memorial

Museum.

The sanctions freeze any assets or property in the United States controlled by the companies or

the Syrian and Iranian governments. The sanctions also ban government officials or company

executives implicated in using technology to "track and target citizens for violence" from

obtaining visas to enter the U.S.

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The U.S. has used sanctions against companies in the past. In fact, the Treasury Department in

August announced sanctions against one of the telecom firms named Monday, Syriatel.

U.S. officials said the private company, Syria's largest mobile phone carrier, was controlled by

an insider in the regime of the country's president, Bashar Assad.

But focusing on specific technologies used in repression is a novel approach, said Philip N.

Howard, director of the Project on Information Technology and Political Islam at the University

of Washington.

"There are other countries, perhaps China, Cuba or Russia, where technology firms are also

state-controlled and may also be implicated in human rights abuses," Howard said. "It could

open the door to other kinds of diplomatic actions."

Still, there are complexities to targeting technology in repressive countries such as Iran, he said.

"The tough policy choice would be to figure out how to have effective information technology

sanctions on Iran that would cripple the infrastructure of the regime while still allowing civil

society groups to use Facebook, Google or Twitter to get news or information about the world

and get news and information to their family and friends," he said.

The administration's international cyberspace strategy released last year said U.S. officials

"encourage people all over the world to use digital media ... and denounce those who harass,

unfairly arrest, threaten or commit violent acts against the people who use these technologies."

The Internet and social media tools such as Facebook and Twitter played a pivotal role in the

pro-democracy uprisings of last year's Arab Spring, which led to the toppling of repressive

regimes in Egypt, Tunisia and other countries.

U.S. officials and activists say the governments of Syria and Iran have used technology to

prevent their regimes from falling.

In Syria, the Assad government has killed about 9,000 people as part of a yearlong crackdown on

armed rebels, according to the United Nations. The Obama administration said the Syrian

government had directed Syriatel, which controls 55% of that nation's cellphone market, to cut

off network access in areas where the government planned attacks on rebels. The company also

recorded mobile phone calls on the government's behalf, the administration said.

Datak Telecom, an Internet service provider in Iran, collaborated with the government there to

monitor, track and target people who tried to get around the regime's blocking of Internet

content, the administration said.

Datak also assisted in surveillance of Iranians who used a popular commercial email service, and

it planned to expand the operation to potentially include millions of Iranian Internet users,

according to the White House.

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The administration also aimed the new sanctions at Syrian and Iranian government agencies and

officials who directed the surveillance operations.

One person specifically named was Ali Mamluk, who the administration said oversaw a

communications program by the Syrian General Intelligence Directorate that was directed at

opposition groups.

Mamluk worked with Iran's Ministry of Intelligence and Security to provide the Syrian

government with training in the use of Internet monitoring technology, the administration said.

He also requested Iran's help with monitoring social networks, it said.

The Syrian General Intelligence Directorate has been implicated in serious human rights abuses,

such as arbitrary arrests and the deaths of detainees, the administration said.

[email protected]