- 3.012 Blog - Colloids of Life

8/14/2019 www.muliply.com - 3.012 Blog - Colloids of Life

1/99

Do youknow atp?

Become hercontact

Who is onMultiply?

Find your friends

Want tolearn more?

Take the Tour

Already aMember?

Sign In

"atpcorporation" Website: GODSENDProducts- Fulvic Acid ("Miracle Molecule")& Natural ZEOLITES , * * * " F R E E " inthe P H I L I P P I N E S ! ! ! . WithORGANIC GERMANIUM" -

SYNTHESIZED BY ATP WITH the DIVINEPROVIDENCE of our CREATOR * * * *

.

HomeNotesBlogPhotosVideoMusicCalendarReviewsLinks

Colloids of Life or Protits. By - ATP Global Foundation.Source: www.cellsalt.net

Oct 19, '08 1:16AMfor everyone

ATP Medical Literature: #05 Colloidof Life

atpcoop

ViewContacts(827)

ViewGroups(39)

Photos ofatp
http://multiply.com/user/join?connect=atpcoophttp://multiply.com/user/join?connect=atpcoophttp://multiply.com/findhttp://multiply.com/info/tour/1http://multiply.com/user/signinhttp://atpcoop.multiply.com/http://atpcoop.multiply.com/noteshttp://atpcoop.multiply.com/journalhttp://atpcoop.multiply.com/photoshttp://atpcoop.multiply.com/videohttp://atpcoop.multiply.com/musichttp://atpcoop.multiply.com/calendarhttp://atpcoop.multiply.com/reviewshttp://atpcoop.multiply.com/linkshttp://atpcoop.multiply.com/journal/item/23/Colloids_of_Life_or_Protits._By_-_ATP_Global_Foundation._Source_www.cellsalt.nethttp://atpcoop.multiply.com/journal/item/23/Colloids_of_Life_or_Protits._By_-_ATP_Global_Foundation._Source_www.cellsalt.nethttp://atpcorporation.wordpress.com/colloids-of-life-or-protits-atp-blog-series-006/http://atpcorporation.wordpress.com/colloids-of-life-or-protits-atp-blog-series-006/http://atpcoop.multiply.com/http://atpcoop.multiply.com/contactshttp://atpcoop.multiply.com/contactshttp://atpcoop.multiply.com/contactshttp://atpcoop.multiply.com/groupshttp://atpcoop.multiply.com/groupshttp://atpcoop.multiply.com/groupshttp://atpcoop.multiply.com/photos/of/mehttp://atpcoop.multiply.com/photos/of/mehttp://multiply.com/findhttp://multiply.com/info/tour/1http://multiply.com/user/signinhttp://atpcoop.multiply.com/http://atpcoop.multiply.com/noteshttp://atpcoop.multiply.com/journalhttp://atpcoop.multiply.com/photoshttp://atpcoop.multiply.com/videohttp://atpcoop.multiply.com/musichttp://atpcoop.multiply.com/calendarhttp://atpcoop.multiply.com/reviewshttp://atpcoop.multiply.com/linkshttp://atpcoop.multiply.com/journal/item/23/Colloids_of_Life_or_Protits._By_-_ATP_Global_Foundation._Source_www.cellsalt.nethttp://atpcoop.multiply.com/journal/item/23/Colloids_of_Life_or_Protits._By_-_ATP_Global_Foundation._Source_www.cellsalt.nethttp://atpcorporation.wordpress.com/colloids-of-life-or-protits-atp-blog-series-006/http://atpcorporation.wordpress.com/colloids-of-life-or-protits-atp-blog-series-006/http://atpcoop.multiply.com/http://atpcoop.multiply.com/contactshttp://atpcoop.multiply.com/contactshttp://atpcoop.multiply.com/contactshttp://atpcoop.multiply.com/groupshttp://atpcoop.multiply.com/groupshttp://atpcoop.multiply.com/groupshttp://atpcoop.multiply.com/photos/of/mehttp://atpcoop.multiply.com/photos/of/mehttp://multiply.com/user/join?connect=atpcoophttp://multiply.com/user/join?connect=atpcoop


2/99

Note : The informationcontained herein is for

informational purposes only.You may want to print ATP

MEDICAL LITERATURE andother educational documentsthat we have and give it them to

your doctor.Your doctor may very well be

grateful that you did.ATP Medical Literature #02 Dated : June 8, 2008

Subject : Colloids of Life or Protits.Discussion :Nourish the body and it will thrive for a time, Nourish the genes and itmay thrive for multiples of that time. . . .Dear GUEST / SPONSORS/ DONORSTERMINALLY ILL PERSON/GOVERNMENT / PRIVATE HOSPITALS/ MEDICAL DOCTORS

The undersigned would like to quote materials from :

Source: www.cellsalt.net

which highlights the . . .Ashes to ashes,as regards the inorganic parts, minerals

and salts of a corpse but thephysicallife part, not speaking of the Soul or

anything like that even, the

PersonalMessage

RSSFeed[?]

ReportAbuse
http://www.cellsalt.net/http://multiply.com/compose/pm?individual=atpcoophttp://multiply.com/compose/pm?individual=atpcoophttp://atpcoop.multiply.com/feed.rsshttp://atpcoop.multiply.com/feed.rsshttp://atpcoop.multiply.com/feedhttp://atpcoop.multiply.com/feedhttp://multiply.com/info/inquiry?report_user=atpcoophttp://multiply.com/info/inquiry?report_user=atpcoophttp://www.cellsalt.net/http://multiply.com/compose/pm?individual=atpcoophttp://multiply.com/compose/pm?individual=atpcoophttp://atpcoop.multiply.com/feed.rsshttp://atpcoop.multiply.com/feed.rsshttp://atpcoop.multiply.com/feedhttp://multiply.com/info/inquiry?report_user=atpcoophttp://multiply.com/info/inquiry?report_user=atpcoop


3/99

Protit, never dies.

Immortality is anature of Life andthe Protit too, asLife itself never

dies. The Protit is theelementary particleof life, not the cell,which can die.

The Video Testimonials of ATP patients regarding the use of ATPProducts Bio Minerals and Bio Energizers (whose formulation is composedof ZEOLITES & FULVIC ACID) also highlights the effects of Fulvic Acidin the bodys bio chemical reactions and its effects on the bodys electricalpotentialAt present Adenosine Triphosphate (ATP) Corporation is distributingATP Products (Zeolites & Fulvic Acid) for FREE to the followingrecipients:1. Daily patient/recipients at ATP Global Foundation- located at BoholMansion Office, 43 E.Lopez Ave., corner Sgt. Esguerra St., Quezon City,Philippines; and

2.Weekly patients of ATP/Salamat Dok TV program of ABS CBNnetwork, every Saturday 6-7 AM and Sunday 7-8 AM; venue ABS CBNcompound. (This weekly Medical Mission started last March 17, 2007 andcontinuing up to present)Please be guided accordingly.

/Print this document ! (For educational purposes)

>>


4/99

>>

[The link barfeature is not

available in this web]http://www.euroamericanhealth.com/gunth.html

Gnther Enderlein

>>

>>

Gnther Enderlein (1872-1968)sawthe healthy host as filled with primitive lifeforms which he called -

Colloids of Life orProtits.These reside in the red cells, white cells, inplasma and all other body fluids and tissues, are

0.01 micron in radius(about the size of a virus), and the larger formsof these can be seen under any microscopeshigh power, oil immersion lens, as tiny dots,

rolling, always moving. They are seen bestwith a dark-field microscope astiny shining, moving points. They

are visible because they

Links
http://www.euroamericanhealth.com/gunth.htmlhttp://www.euroamericanhealth.com/gunth.htmlhttp://www.euroamericanhealth.com/gunth.htmlhttp://members.iimetro.com.au/~hubbca/health-links.htmhttp://members.iimetro.com.au/~hubbca/health-links.htmhttp://www.euroamericanhealth.com/gunth.html


5/99

move. For Web Site reference regardingGnther Enderlein see the ExploreMaga zine at

explorepub.com.Gnther Enderlein was the last of the old

pleomorphists and has done the mostexhaustive and comprehensivecompilation and study of this informationto date. The basis for Enderleins work was the

book by the Frenchresearcher A.Bchamp, titledMycrozymas.Enderlein devoted the bulk of his scientific workwhich stretched for more that 40 years, to the

complex question ofpleomorphism,symbiosis andcyclogeny (the cycles organisms gothrough) of microorganisms.

From this he published his chief work,
http://www.explorepub.com/http://www.explorepub.com/


6/99

BAKTERIEN-CYCLOGENIE(publisher W.de Gruyter & Co.

Berlin, 1925). In it he presentedarguments and proofs forpleomorphism, which have to this dateremained undefeated.This book has justbecome available in English from EnderleinEnterprises, Inc., P.O. Box 704, Mt. Vernon, WA98273, phone 360-424-6029. That there hasbeen very little about any of this available inEnglish has been part of the problem for sure.

The following information and pictures, exceptwhere otherwise indicated, are from the book

Blood Examination in Darkfieldaccording to Prof. Dr. GntherEnderlein, available from Semmelweis-BVerlag, D-27316 Hoya, Germany, compiled byDr. med. Maria-M Bleker, 1993. This book isalso available, in English and German, at theabove address. In the following, unidentifiedquotes are placed for material taken from this

book. Maria Blekergivesseminars in Darkfield Microscopic examinationand has been one of the chief peopleresponsible for introducing Pleomorphism toAmerica. This has not been an easy job.

According to Enderlein, germs are


7/99

not representing unchanging organisms that are

independent of each other, but altogetherthey form a singular, common

cycle, which has its origin in thecolloidal, albuminoid

substances calledProtits that are contained

inside of each particular cell.

Enderlein called these Protits,

ENDOBIONTS (fromthe Greek endo internal and bios- life).We can never separate ourselves from them.

We coexist in amutually symbiotic(means we live

together, helping eachother) relationship. Wegive them a vehicle


8/99

for life, they give us

blood forms likeplatelets, without which we couldntexist (platelets areformed from the

Protits,not in thebone marrow astaught by modernscience).

The endobiont appearsin all mammalianspecies and has shown

evidence through some of

its developmental forms to be ofa plant nature.

Oursymbiotic union with


9/99

them evidently occurred

millions of years ago asour species grew into existence.Without some bloodclotting mechanism inplace, mammals couldnever have evolved.!

When the host is in health,Protits live in symbioticrelationship with the tissue cells,

and maintain the health of andregenerate all organs, we live togetherand help each other. They are the

smallest unit of life,not the cell.

They are physical lifeper se.

In the blood and tissue of humans and animals,


10/99

there live microbes

(Protits) which arenormally harmless andwhich maintain diverse regulatory mechanisms.According to Prof. Enderlein, these

Endobionts are

usually non-pathogenic phases ofthe mold fungusMucor racemosus

Fresen!,Aspergillus niger vanTieghem orPenicillium notatum.

One does not see these fungal forms in theblood of a living being, these are just what they

look like when

cultured in alaboratory or what theProtits devolve to in a


11/99

corpse.

The mummies inEgypt are composedtotally of Protits.

Put the dust from

these mummies inwater and there theyare, under themicroscope, turning,

moving, the Protits.* * *

THELAW OFCYCLOGENY

As with microbes the above Protits are subject

to the Law of Cyclogeny,which means, their


12/99

development cycles

through the followingstages: primitivephase (Protit) tobacterium to fungus,whereby the virulence and pathogenicity of the

parts of the cycle increases with the risingdevelopmental phase.

This means, they develop from the

apathogenic (cantmake you sick),non-

motile, tiniestalbuminoid, particle(Protit) which is to be classified insize with the viruses (0.01 m) viathe nonvirulentchondrit stageinto thefollowing parasitic, pathogenic (can make


13/99

you sick) stages.

As the patient becomes ill and therefore acid,

microorganisms form, inquantum-biological leaps,depending on the pH of thenutritive medium or the internalmilieu. The microorganisms get more

dangerous as one goes from

the strongly alkalinehigh of the pH-valuetowards the everdecreasing pH-valueof the acid side.This happens in the following manner. AS THEINTERNAL MILIEUBECOMES MORE ACID,

the Protits first begin to

join into threads (tailsor Filum) that sproutglobules, primitive


14/99

granules (heads). These,

Enderlein, calledSYMPROTITS.As from Dr. med. Maria-M Blekers, BloodExamination in Darkfield according to Prof. Dr.Gnther Enderlein;

In the new formation of filum and head, atomic-

physical and quantum-biological factors play adecisive role. This is visible from the suddenoccurrences by the leap of these new

formations. The formationalprocesses of a filum

with a head resultingin what is called theCHONDRIT, occurs within thesmallest fraction of a second, which is thereforenot observable by the eye looking through themicroscope; the new developmental forms aresuddenly there. The Protits come together and

join in the following manner:

Protits can


15/99

NATIONALIZE or

come together inthree ways. They can form:1. A one dimensional arrangement. This resultsin a shorter or longer thread, the FILUM; itsdiameter is that of the protit, namely 0.01 mm.However, it can constantly increase inthickness, after its formation.2. A two dimensional arrangement of the protits,into fine, skin-like surfaces that are found, forexample, in the spermit (bacteriophage) asswarmer-heads (see below). This is one filumwith one Protit head. The

SYMPROTIT is simply

a larger head than theProtit or the Spermithead.3. A three-dimensional arrangement, namelyinto more or less tiny granules, the physiologic,

often spherical SYMPROTITS which becomethe primary nuclei of the bacterial cell they areturning into.

* * *

FORMATION OF FILUM


16/99

The formation of these Fila

threads can beobserved only in thedark field, sometimes this occursvery rapidly, right before your eyes, in extremelyill patinets.

The fila in this pictureare the thread like

structures that fill the

background. These are whatcause blood to clot.Thecircles are red blood

cells.The circles that are stacked

together in the left hand pictureare red blood cells that havestuck together.

As from Maria Blekers


17/99

book;It is the first of the primitive phases that occurs

through the change in fila according to theformula x:2x. Because the x shows very greatdifferences in the lengths, the filit-phasecomprises very large numbers of individualphases. These threads begin to appear soonafter the blood is drawn. While watching underthe microscope the threads just pop intoview, increasing in length in quantum typejumps, 2X long then 4X, then 8X, 16X, etc..Actually, there appears to be constant quantumfluctuations between these formed products.Thereupon follow the primitive stage FILIT, theongoing change between the FILUM and afilum-piece of double its length.

If a person is totally healthy,none of these Fila will form. Ifthere is no appearance of Filaafter two days, that person istotally healthy. Personally, I have neverseen this, perhaps in a new born baby.

Base Powder reverses this process.

Actually, we had a patient one time in whom theFila started forming immediately. This is veryunusual as usually it takes some hours for thisprocess to start. This patient was very ill withextremely acid blood and cancer and we never


18/99

saw him again. How fast the

Fila form is a verygood indicator of howill you are as it is adirect reflection of

how acid you are.* * *

FORMATIONOF

SYMPROTITSNext, the Filit makes a quantum jump and uniteswith or produces, instantaneously sprouts, a

SYMPROTIT HEAD.The above tail simplydevelops a head, in a

quantum fashion andpoof.there is a filum


19/99

thread with a

symprotit head on it -out of nowhere?

This is called the CHONDRIT(see below), a filum

with a symprotit head.You have sperm, or do you? The similitudeamong sexual processes in Nature is pervasive

and awesome. The snake thatate itself. In fact

sometimes thesethreads or fila beginto move like a flagellaand you have what iscalled SPERMIT. This ispleomorphism and acid base is the key.

The spermits of the


20/99

microbes are tinyswarmers that consistof a tiny symprotitheads and filumflagellie, which

enables them tocopulate with allpathologicalsymprotits and all the

bacterial and fungalforms within the same cycle.The consequence of such copulation ofbacterial and fungal-nucleic apparatus is

naturally that the bacteria and

fungi immediatelybecome dissolved andthey degrade back into


21/99

more spermits andprotits/chondrits.The presence of spermits is a good thing asthese forms attack anything (higher pathogenic

forms). Spermits cannotbe photographed

because of theirminute size andintense mobility. Theyrepresent nothing but

a readiness to meetan alarming situation.Enderlein first discovered this process in 1916with his work on typhus. He re-discovered in the

blood of these patients, with darkfield, thetiniest moving beings, this having been seenbefore by Bchamp and others.

Enderlein saw too that


22/99

these tiny moving

beings entered intounion with higherorganized bacteria.When this happened the bacteria that had

joined with the tiny beings became instantlyinvisible. Enderlein surmised sexual processes,through which came about, not higher forms (asin embryonal development) but lower forms thatwere invisible to the eye in the light microscope.These vigorously moving elements had flagella.As indicated above he named these Spermits.

SYMPROTITS

This shows the variation in sizeof the Portits. The smalldots in this picture

are Protits, the largerdots are theSymprotits. The red


23/99

circles are red blood

cellsand the mass in the middle of the slide are

disintegrating blood cells.The heads can only be seen here,not the tails.

Symprotits are conglomerated Protit heads thatform varying sized globules or heads. As theProtits group together the heads get larger andlarger. As stated, the tails really cant be seen inthese pictures. The Symprotits then that we see

under the microscope are enlarged Protit typeforms occurring in various sizes. They arealways moving too, compared to other thingsseen under the microscope that look similar anddont move.

The small dots in this picture are larger and ofdifferent diameters than the ones in the above

picture. The Protits have stucktogether and formed the heads ofthe next larger nationalizationor grouping of the Protits. Eachadvancement to a higher stage orVALENCY as it is called represents an

increasing degree of pathogenicity. Theybecome more dangerous.

Then, these conglomerated


24/99

Protits (Symprotits)

use more proteincolloid, Protits, for their advancement,depositing it first in large numbers right on itssurface as nutritional reserves. This reservedliving, protein colloid grows even larger,surrounding the symprotit sphere with more andmore substance. These become

Macrosymprotits(macro - large,symprotits). The acid

base imbalance isbecomming worse.* * *

MACROSYMPROTITS

These represent exceptionally large

spheres of purelynucleic protein. They can befound free, or connected with the filum, or in theelements of tissues and cells of the host. In


25/99

connection with the filum, the fila are, then,usually very mobile.

One can tell by the diverse sizes of free

symprotits that are present, whether one isdealing with normal forms or abnormal ones.Namely, in that case, the formula is also x:2x,which means the presence of identical spheresplus other ones of twice their size. Whenseveral sphere-phases are found side-by-side,they will be indicated by a larger number ofvarieties in size, which is the more commoncondition. They just jump from one size to theother, no period in-betwe0en that is observable.

The resulting forms arethe large, heads or

primitive granulescalledMacrosymprotits.

MACROSYMPROTITS

The large dot the arrow is pointing to is a Macrosymprotit.Notice the difference in size of the tiny dots in this picture.

As the internal milieubecomes acid, as the pHdecreases, the primary tiny lumps and theirtails, the Protits begin to increase in size bysticking together in a three dimensionalarrangement; first one, then two, then eight,


26/99

then sixteen, then thirty-two according to theformula, x:2x, where x is the number of Protitscoming together. These increase in quantal

jumps too. You can watch it under themicroscope; first there is 1 Protit, then 2, then 4,8 and so on, all lumped together.

* * *

FREE CHONDRIT PHASE

The Chondrit Phase begins with the aboveenlargement of the Symprotits and of their Fila.

The Symprotits and their tails join end to endgiving the Chondrit forms a beaded appearance.This gives them a lively mobility as they have aneven denser arrangement of tiny symprotitsalong the length of the fila.

The primitive stage CHONDRIT can be seenmost frequently constantly changing betweenFILUM and PRIMITIVE GRANULE (Symprotit).Depending on the size of this tiny primitivegranule (between 0.02 m and 1m), verydiverse valences or degrees of pathogenicitymay occur at this stage.

FREE CHONDRIT PHASE

The large dots in this picture are Macrosymprotits. The

beaded threads like the one the lower arrow is pointing to arefree Chondrit heads on Fila threads. Some have coalesed

into, thick rid shaped forms, (see below). The large circles arered blood cells.

The Chondrit Stage


27/99

This is the Chondrit stage growing out from a red blood celledge. It has many Symprotit heads on a File thread. This

stage is very strong and mobile. This thread will close end toend and form a circle. This will become a bacterial cell as

below.The lower valenced Chondrits are notpathogenic and do not make you sick. In fact,these low valenced Chondrits plus the Protitdiscussed above and the Protitit(the forms thatare so small that they cant be seen with thelight microscope). The Protit and Protitit haveeven lower valency or pathogenicity than the

Chondrits and these three are what are used asIsopathic medicine. These Chondrits, beingquite mobile, seek out higher valencedmicroorganisms such as bacteria and fungalforms. The Chondrit forms copulate and fusegenetic material with these more pathogenicorganisms and they then break all apart into

Protits as described.The Chondrit Stage begins with that sphere ofthe developmental growth of the endobiont, inwhich only the low-valenced phases have fullapathogenicity and all higher phases reachpathogenicity to an ever rising degree. Thehigher valenced forms of these Chondrits havemore Symprotit heads, they are bigger andmore varied in size among other things. TheFree Chondrits are considered to be the viralphase and in their higher valenced forms theyare pathogenic as such.

THE ONLY EXCEPTIONS ARE THE VERY


28/99

FIRST PRIMITIVE STAGES which are thePROTIT and the CHONDRITS that are of lowestvalences. They are entirely nonvirulent and theplay a REGULATORY role toward the higherand more pathogenic stages by decomposingthese through copulatory processes. In thatsense, these stages are termedREGULATORS.

Isnt this all rather amazing?

Sperms, doing whatthey do and breakingdown higher andmore dangerous

forms of itsconglomerated self,back into itself. Thesnake eating its tail

for sure. This isIsopathic medicine.***

THE BIRTH OF A CELL


29/99

(BACTERIAL SPHERES)

Next, if the internal milieu, Pishingers Space,becomes worse, more acid, polluted, the

beaded, Free Chondrits, form circles (closedloops) by hooking end to end and looping

around to complete a circle. These circles arecomposed of symprotit heads, distributed

around the ring made of fila.

Symprotit heads distributed around a ring made of fila.

These symprotitheads will fuse

together and form thenucleus of the

developing bacterialcell.

Then, these small symprotit heads movetogether and fuse forming the nucleus (calledthe Mych),

and you have the newborn cell!

BACTERIAL SPHERES

The medium sized circles like the arrow is pointing, looking


30/99


31/99

protit, namely a protein-colloid, for itsadvancement, depositing it at first in largenumbers right on its surface as nutritionalreserves. This reserved living, protein colloidgrows ever larger, surrounding the symprotitsphere more and more. By this process, the firstcell has come to be, which is a sphericalprimary cell, the bacterial cell, the MYCHIT. Bythis process, the symprotit became the primarynucleus, the MYCH, and from the reservematerial collection of living colloids came the

CELL PLASMA of the primary cell, the Mychit.Reserve substances, which form a more or lessthick layer, may be deposited around theprimary nucleus. These primary nuclei with theircovering of reserve substances completelycorrespond physiologically to the fattysubstances in higher organisms. To the verylargest percentage of cases, these reserve

materials consist of LIPOIDS and alsoNUCLEIC ACID DERIVATIVES.

* * *

DEVELOPMENT OF BACTERIAL RODS

Through division, the above Bacterial

Sphere becomes thesource of amicrococcus with two


32/99

nuclei (DIPROTIT). Fromthem, bacteria with 4 - 8 nuclei develop, and

finally a bacillus with 16 and more nuclei. On theother hand, the nucleus divides and the ring canelongate and turn into rod forms. This is apicture drawn while looking though a

microscope in 1879. The bacterium,Leptotrichia buccalis,the usually harmlessbacteria found in ourmouths, is seen here to go from theround coccal form into a rod form. In the

process the nucleus divides and becomesmany.

To summarize, the small nuclei or tinysymprotits of the Chondrit around the edges ofthe ring in these pictures move together andmake one nucleus. The ring can enlarge andbecome a coccus or round, ball shaped germ orit can elongate and turn into a bacterial rod. TheSymprotit gathers Protits to it to feed it and toform the cellular plasma. The nucleus getslarger as the tiny symprotits coalesce and thering gets larger as the cell plasma fills the cell


33/99

up.

Coccus type germs

are the streptococcus,gonococcus,staphlococcus and the like.

Rod type germs are E.coli, pseudomonis,and so on. These forms actuallycome out of the cells themselves, red or white inthe blood. The blood, when it starts to breakdown first begins a fermentation process that

can lead to blood clots orrigor mortuus, twosides of the same process.

Red blood cell from a patient with stomach cancer. There aretwo bacterial rods exuding from it. The nuclei are stacked one

on top of the other.

The following pictures show rod forms budding

off of or extruding from red blood cells. You seeround buds pinching off of blood cells. You seelong hollow tubes that have come out of cellsand long, beaded strings of Chondrit forms thatcan be the pathogenic viral forms. There arealso some short stubby rods that are typical of


34/99

the ones we see in medical, micro biology labs.Acid base imbalance is severe.

The multitude ofvarious sizedots in the left hand

picture are

Symprotits andMacrosymprotits, Symplasts(heads and tails hooked end to end, not yet pulled togetherinto bacterial forms) and Free Chondrits (the beaded, longthread like forms). The right hand picture shows buds of

bacterial forms comming out of red blood cells.

***

What makes these life forms, Protits,advance so rapidly?(I prefer to use theword degenerate or

involve, devolve ratherthan advance or evolve.)

Our civilization causes or facilitates this throughartificial fertilizers, preservatives, coloring


35/99

substances, air pollution, etc., but in the veryfirst place stands our false nutrition, which

literally fattens theEndobiont by its high-content in protein andsugar.Animal protein fattens the Protit. As soon as the

balance in the blood serum between mineralsalts (bases, alkali) and acids has becomedisturbed toward the acidic side through long-continued, antibiological nutrition, the abovethings start sticking together. The

endobiont literally

feeds off animalprotein and getsbigger.The endobiont is the

ROBBER OFPROTEIN. The only non-plant protein that can


36/99

be taken in largeramounts, is theprotein of the milk, andthat in its acid form, such as cottage cheese and

other forms of cheese. FarmersCheese is the best

available in supermarkets. Theselactic proteins have developed a specialaccomplishment in the course of endless time,namely the capacity for producing a specificprotein synthesis, which does not give theendobiont an opportunity to feed on.

The normal healthyProtit is made up ofvegetable protein!The hydrogen-ion concentration (pH) of theblood gets shifted through the Endobiont,

whereby it must be especially emphasized thatthe Endobiont expressly devours protein. It isunderstandable that these facts create everenlarging conditions of the endlessly ongoingdevelopment of the Endobiont.


37/99

* * *

THE ANARTATIC LAW of Enderlein

The dependency of the development of

microorganisms upon the pH (acid base) of thenutritive medium or the internal melieu is aFUNDAMENTAL LAW called the AnartaticFundamental Law by Enderlein. As fromBlutuntersuchung Im Dunkelfeld nach Prof. Dr.Gnther Enderlein;

The Anartatic Fundamental Principle:

For the nationalization (coming together of) ofcomparative-morphologic units into higher andhighest developmental phases, the specificacids PRODUCED by each individualmicroorganism are the CAUSAL reason for thechanges of the internal milieuin the pH, andthat is tending to the ACIDIC side. In otherwords: the RISING steps of the total cyclogeny

are accompanied by and dependent on thePROPORTIONATELY DESCENDING pH. Thatis it demonstrates the summary of theASCENDING developmental tendency with theever more DESCENDING pH-value.

An interesting point here is that one can neverforce an advancement by increasing the acidity

of the culture medium. This wont, in and ofitself, cause the Protits to stick together andacquire tails and form spheres with nuclei ontheir edges that finally turn into bacterial andthen fungal forms.


38/99

On the other hand, if one alkalinizes a culturemedium already containing fully developedbacterial or fungal forms by adding a little

bacterial material or parts of fungal mycelia to ahanging drop of 5% sodium carbonate, which isa strongly alkaline medium with a high pH value,one can immediately observe the formation ofthe primitive stages, namely in the CHONDRITSTAGE.

So higher forms arereadily decomposedback into the ChondritStage, by making

them alkaline.So too, if one withdraws blood from a veinthrough a tube and then run the blood directlyinto a sugar water solution with 40% ethylalcohol in it, without exposing it to air, as perLouis Pasteur and Antoine Bchamp, it willbegin to ferment. This fermentation producesthe acids it needs to continue its evolution, de-evolution, involution, namely lactic and citricacids. The red blood cells begin to decompose.All the above things happen and what you endup with is nothing but Protits. It takes a month orso. Very interesting experiment.


39/99

* * *

http://www.euroamericanhealth.com/antoin.html

Antoine Bchamp

Antoine Bchamp(1816-1908) proved that (all thefollowing quotes are from The Third Element ofThe Blood, Antoine Bchamp, 1994, unlessindicated otherwise);

all natural organic matters (matters that oncelived), absolutely protected from atmosphericgerms, invariably and spontaneously alter andferment, because they necessarily andinherently contain within themselves the agentsof their spontaneous alteration, digestion,dissolution.

These agents are of course the self same

Protits of Enderlein. As noted, M.Bchamp called themMicrozymas.

Bchamp was able toprove that all animaland plant cells
http://www.euroamericanhealth.com/antoin.htmlhttp://www.euroamericanhealth.com/antoin.html


40/99

contain these tiny

particles which continueto live after the deathof the organism and outof which

microorganisms candevelop. In his book Mycrozymas,Bchamp laid the foundation for the concept ofpleomorphism.

Whenever there is

anything in naturethat is dying,beginning to decay,something comes andeats it up.

In this case the Protits do, as


41/99

they change into the

microbes that come out of the tissuecells to clean up any toxins or decaying stufffound in the body. That is what microbes,germs, are for. They are the result, not thecause of disease! Rene Dubious reflected thisconcept when he noted that Berioge in BernardShaws book The Doctors Dilemma, was notentirely wrong when he said

The characteristicmicrobe of a diseasemight be a symptom

instead of a cause.As a blood smear slide ages over one to twodays, organisms literally can be seen wigglingout of the red blood cells, organisms thatchange into more degenerate and pathologicalforms as the process proceeds. When therotting or putrefaction process is over, whenthere is nothing more for the newly formedviruses, bacteria and fungi to eat, they all breakapart again, disappear, and turn back into thelittle dots they came from, the

Protits/Microzymas/Somatids. They eat


42/99

themselves and are

reborn, the alchemicalsnake forever eatingits tail (the Uroboros)or the Phoenix, a

mythical bird of greatbeauty that wasreborn from the ashesof its own funeral

pyre.As the microzymas of the destroyed bacteriaare also living, it follows that these

microzymas are theliving end of allcellular organizationwhich in turn, turn into all living things, beings,

organs everything They are the


43/99

end and the beginningof all physical life. Allcells, organs, all livingforms are built fromthese little bodies.

When you break anelement down intosmaller and smallerpieces you end up

with an atom of thatelement.

When you break organicmatter, physical life,down into smaller andsmaller pieces you


44/99

end up with the

Protit!, no matterwhich form oforganic, live matteryou started with.Ashes to ashes, as regards the inorganic parts,minerals and salts of a corpse but thephysicallife part, not speaking of the Soul or anything

like that even, the Protit,never dies.

Immortality is a natureof Life and the Protittoo, as Life itselfnever dies. The Protit is

the elementaryparticle of life, not thecell, which can die.


45/99

The Protit is lifeper

se, it is in truth thesimple vital unit of oldand is immortal.

* * *

FERMENTATIONFermentation followed by putrefaction is a formof eating, nutrition. In the living and healthyorganism the Protits function as thephysiological and chemical agents of thetransformations which take place during theprocess of nutrition. It is only in illness that theybecome agents of fermentation. A great deal of

Bchamps work concerned the process offermentation and therefore nutrition.

Rather, living organization, Life, ischaracterized by the property of producing andsecreting enzymes, each according to thenature of its species; and the production of thechemical-physiological phenomena of

transformations called fermentation, acid base,which are facts of nutrition, that is to say, ofdigestion followed by absorption, assimilation,disassimilation, and so forth, and finally theability to reproduce itself if all conditions


46/99

dependent upon nutrition are fulfilled.

This is a nature of Life too, nutrition, andtherefore of the Protit. Things the Protits do are

turn into the bacteria and other organisms,yeast etc., that ferment the sugar in wine orcurdle milk or rot eggs (it isnt the germs fromthe air of Louis Pasteurs that do these things).The wastes or by products of these bacteria andother organisms are the alcohol, CO2, lacticacid, vinegar etc. that are produced in suchprocesses. Again, these waste products of

fermentation, which is followed by putrefaction,are what make us ill in disease, not the germs.

The above has been known since around 1830,because of the studies done concerning

fermentation and

putrefaction by manyscientists; the Tulasne brothers inFrance and the microbiologist Anton de Bary(1831-1888), Ernest Hallier (1831-1904),Robert Koch (1843-1910),Claude Bernard(physiologist -1813 to 1878) and Pasteur(microbiologist -1822 to 1895) and Bchamp

(1830). Enderlein came toward the end ofthis.

Pasteur achieved fame through work onfermentation. Challenged by local distillerscomplaints of setbacks in fermenting alcohol


47/99

from beets, Pasteur pinpointed accidentalcontamination by stray fungi. Before this it wasthought that the yeast arose by spontaneous

generation. This is the idea that life just comesout of nowhere, that matter organizes itself,takes on or is imbued with the property of lifeitself. Pasteur gave up this idea in the 1860sand took its opposite point of view, that of thegerms coming from the air, from outside onesself.

as I have demonstrated, it is only through theaction of germs of the air, whose existencewas denied, that this alteration (of organicmatters) occurred which had the appearance ofbeing spontaneous. [Monsieur] Pasteur havingrepeated my experiments, was so convincedthat germs really do exist in the air and that hehad been mistaken, thenceforward declared that

the sole origin of ferments, vibrios (germs) andthe organisms that come out of putrefyingorganic matters, was these germs he hadpreviously disregarded. The

excessive roleascribed to the germsof the air by [Pasteur]and his pretended demonstration of theimputrescibility (cant become rotten) of organicmatters in general when protected from the


48/99

germs of the air have diverted science down adeplorable road. (Antoine Bchamp, TheBlood, p. 286)

As from Maria Blekers book, BlutuntersuchungIm Dunkelfeld,

with this work of Bchamp pleomorphism hadbeen discovered and the foundation was laidfrom which additional research would havedeveloped, it Pasteur had not interrupted thisimportant work. Pasteur claimed that allmicrobes, regardless of their type and species,are unchangeable (Monomorphism); that eachtype would produce only one specific disease;

that bacteria andfungi would never

arise fromspontaneousgeneration; and thatblood and tissues are

sterile in healthyconditions.Diseases, he said,


49/99

have their origin frombacteria that attackthe body from theOUTSIDE, and stemfrom preexisting

bacteria. See the section on Historyon the Home Page for more on how and whypleomorphism is unknown to modern doctors,not controversial or anything like that, it is justunknown in this country. Isnt that strange?

* * *

In addition to and in spite of the fact that

Pasteur ignored and in fact plagiarized much ofBchamps work on fermentation, the followingfacts have been known for some time.

Chalk, limestone, is composed of the Protits ofthe bacteria which living beings of the geologicalepochs had become and these materials willstart sugar water fermenting. The

mummies in Egypt arecomposed only of leftover Protits which do


50/99

the same, start

fermentation.Putthese back in water,the mummies or thechalk, and their little

dots start rolling,moving once again.

They just start eatingagain, fermenting

their environmentdebending on acidbase, after thousandsor millions years. Itnever stops, Life.From Viennese Medical Week, No. 34;

After slow thawing, Protits


51/99

isolated from amammoth frozenmore than 50,000years ago were shownto spontaneously

show life again andbegin fermentation insugar solutions.The following is from SANUM-TherapieBetrachtungen und Erfahrungen Eine

Heilbehandlung an der Basis von Wilhelm Fries;the Russian researcher Ginsberg-Karagitschewa provided proof in 1926 thatProtits isolated from petroleum showedcomplete viability and started the fermentationof sugar. A German by the name of Shwartzconfirmed this also for German petroleum.

Both private instructor E. Santo and H. P. Ruschwere able to find the same results, namely the

isolation of livingProtits from German


52/99

hard coal. The researches of Santoand Rusch also showed that the Protit could not

be harmed by sulfuric acid or by temperaturesof 1300C in a ceramics oven.

In addition, Wilhelm Friez also states that theabove researchers and Enderlein, on suitable

nourishing media, were able togrow viable bacteriafrom the Protitsisolated from the coaland oil. Streptococci, coliform bacteriaand Proteus species were all isolated from

these substances.The form of the bacteria isolated by doing theabove,on suitable nourishing media, dependson the nourishing-growth media the Protits aregrown on. How acid that growth media is, whatit is made of, how much oxygen, the rH-oxidation/reduction factor, lots of things effect

this. It is the same in theliving body, theinternal milieu, the


53/99

environment the

Protits grow in,determines what formthe Protits take, i.e.whether they are good

guys or not so good.The good guys turninto the cells thatregenerate the body,organ spacific Protits or Somatides (Seechapter on Live Cell TherapyunderTreatmenton the Home Page. The not so good guys arethe Protits that go in the direction offermentation and putrifaction.

What happens after

the death of a cell?The above prove thatthe littlest form of the


54/99

Lebendssubstanz,Life substance, is notdestructible.Robert Mayer provedthe law of the

maintenance ofenergy so that noenergy can disappearwithout a trace.What happens to the power source that made

the cell as an expression of or only as thecarrier of the living substance? Because theliving substance is distinguished fundamentallyby the inanimate matter, one cannot let ittheoretically pass over also into inanimatematter without an essential characteristic loss..

This is the Law ofConservation ofEnergy. Life energy


55/99

too does not just

come from nothingwith birth and thendisappear intonothing with death. It

too is conserved. (Seesection on Life on the Home Page.)* * *

These Protits are what come form the air andget in sugar water, wine or whatever and dowhat they are supposed to do, eat. TheseProtits are everywhere, in the air, the ground, in

all living things, plants, animalsIn wine theyturn into the yeast cells that do what they haveto do, eat it, ferment it.

As perAntoine Bchamp,

All cells, organs, all living formsare built from these little

bodies.The way we were taught of course, was that itwas the cell that did that, that the cell was thesmallest living thing out of which all larger livingthings were made. Where did the cell come


56/99

from, the sperm, the egg?

The essential

biologicalcharacteristics of themicrozymas (Protit) isthat they are creatorsof cellules (cells) bysynthesis and ofvibrioniens (viruses,

bacteria, fungi) bypleomorphism andevolution.So the Protits turn into everything, every livingbeing and organ and every disease producingorganism which turn those very beings andorgans back into the Protits they came from inthe us up.

This type of medicine, Wholistic Medicine, isopposite in all ways from allopathic medicine,not opposite really but complimentary - as you


57/99

cant have one without the other. All

polarities are like that,good and bad, loveand hate, you canthave one without the

other. This is the yingand yang of it. Puttingwhat is known,together, does create

a New Biology.* * *

http://www.euroamericanhealth.com/eav.html

Vibrational Medicine

Electroacupuncture and the Rife Microscope

Electroacupuncture and the concept of the Rife

Microscope and Generator best objectify all thedifferent forms of what are now calledVibrational Medicine from Michael Gerbersbook by the same name.

These vibrational techniques include such,
http://www.euroamericanhealth.com/eav.htmlhttp://www.euroamericanhealth.com/eav.html


58/99

unfortunately specialized branches of medicineas; radionics, electroacupuncture, Biotensor,pendulums, Bioresonance testing, kinesic pulse

testing (RAC), Applied Kinesiology, ContactReflexology, Homeopathy, Pleomorphism,Herbal medicine, vitamin therapy and on toregular, modern allopathic medicine - in more orless descending order of vibrationalimportance.

* * *

EAV OR Electro Acupuncture According to Voll

EAV began in France in the 1940s with a doctornamed Roger de la Feu. Dr. de la Feu beganexperiments with skin conductivity and foundthere are points on the body more electricallyconductive than others. These points, for themost part, turned out to be acupuncture points.In 1953 a German medical doctor named

Reinhold Voll became intrigued with de la Feusresearch and explained it.

All the acupuncture points are connected bylines of force, like wires, that are calledmeridians. Voll and his colleagues mapped thecorrelation between conductive points on theskin and internal organs, organ systems and

bodily functions.Their starting point was their knowledge ofTraditional Chinese Medicine, specificallyacupuncture. Acupuncture has developed overthe last 5000 years. During this period of time,


59/99

specific points on the body were mapped asbeing responsive to disease and therapy.Groups of acupuncture points are connected

along fourteen major pathways calledmeridians. With the exception of the Governingand Conception Meridians, each of thesemeridians begins and ends on a finger or toe.Each meridian is connected to one major organfrom which it drives its name, such as the LiverMeridian and the Stomach Meridian.

The Heart Meridian, for example, ends on thetip of your middle finger, at an exact pointbeside the finger nail. If you inject a radioactivedye in this exact point it will trace a line to theheart. If you miss that point by a fraction of aninch, the dye will go no where. For every organthere is a point on the end of one of the fingersor toes. Is this any different than reflexology or

iridology? This is Wholistic Medicine, theWhole being more than the sum of its parts.

These points at the end of the meridians give offa current of a very particular frequency,impedance and amplitude, depending on theorgan involved. Everything vibrates at aparticular, very precise, frequency. Acid basebalance effects all of this.

If you hold an electrode, a metal contact point,not a needle, on the point at the end of theHeart Meridian or any meridian, it will give off asignal that is either low (a degenerativecondition or low energy condition of that organ)


60/99

or it will be normal or it will be high (aninflammatory condition). This can be done for allthe organs of the body and more, in a very short

time.Then, if you find an organ that has a low energy,for example, you can insert a medicinecontained in a vial into that circuit whichconsists of the patient, the medicine and themachine. If the medicine vibrates at the samefrequency as the weak signal being tested,synchronizes, harmonizes, literally,electronically, with the low signal from the weakorgan, the amplitude or strength of the signalwill get higher as the two frequencies willsuperimpose and add together. Then you knowthat what is in the vial is the right medicine forthat organ, for that patient.

All these Vibrational Testing Techniques are

similar and are based on the idea of the tester(person and machine - EAV machine, pendulumwhatever) coming into resonance with the testsubject. The tester must thus be highlysensitive, must be very good at maintaining aneutral state and must be able to register thevibrational changes of the test person.Radionics is the most sophisticated of thesetechniques.

E.A.V. and the rest have the additionaladvantage of being highly sensitive. E.A.V. forexample, can detect extremely small amounts ofany type of chemical in a patient; DDT, mercury


61/99

intoxication, any chemical. Also, extremelysensitive allergy testing can be done. Fine-materials testing as this is called cannot be

performed on many people, since they havemasking disorders such as amalgamintoxication, dental foci or toxic blockages. Forthe same reason, these patients cannot usuallybe treated homeopathically or isopathically, theirblockades have to be broken up and detoxifiedfirst, before pleomorphism and its medicines orany medicines. This is what Base Powder and

diet change are for.The Rife Microscope and Generator

Royal Raymond Rife with his microscope andgenerator provide another striking example ofvibrational medicineand pleomorphism. All thedifferent microorganisms and forms they comein also vibrate at a very precise, distinct

frequencies. Royal Raymond Rife invented amicroscope in the 1930s that could magnify upto 60,000 diameters, at a time when the bestexisting light microscopes could magnify only1000 - 2000 diameters. Light microscopes areno better today. The electron microscope canmagnify to 100,000 to 1,000,000 diameters andhad not been invented yet.

Rife Micrograph of Bacillus Typhosus (Typhoid)Magnification: 23,000X on 35 mm film

Most of Royal Rifes books were burned by thepowers that be so exactly how to build this


62/99

microscope is unclear. Yet, still to this day, ifany doctor is caught possessing one of thesemicroscopes he or she will go to jail and the

microscope will be confiscated. I include this insome detail as an example of the types ofsophisticated research that were done beforethe 1930s.

This microscope illuminated the specimen by anarrow, polarized light beam, composed of asingle frequency of monochromatic (one color)light which caused the specimen to vibrate, toglow. This microscope could project a beam ofpure color, a beam so finely tuned that it wascomposed of only a single frequency of light.These tunable frequencies went all the wayfrom the infrared to the ultraviolet.

A monochromatic beam of light, correspondingexactly to the frequency of the organism (for Dr.

Rife found that each disease organismresponds to and has a definite and distinct wavelength, a fact supported by British medicalresearch workers) is then sent up through thespecimen, thus enabling the observer to viewthe organism stained in its true chemical colorand revealing its own individual structure in afield which is brilliant with light.

Because these objects glowed with theircharacteristic chemical colors they could beseen at much lower magnification than if theydidnt. Therefore, Royal Rife was seeingviruses in the 1930s and that was just


63/99

considered impossible. Still, today, viruses canonly be seen with the electron microscope.

Royal R. Rifes discovery of the frequency

characteristics of organisms led him to believethat each individual type of microorganismshould have a resonant frequency that would bedetrimental to it.

His first attempts to electronically destroy themconsisted of unsuccessful tests with infraredand ulta-violet rays. These frequencies only

caused surface damage so next he tried audioand radio frequency waves which penetrateddeeper. He thought that somewhere in thespectrum a harmonic or resonant frequencywould resonate with the vibratroy rates ofdisease organisms. He believed that if such afrequency could be found and applied, the rayswould be fatal to the disease organisms but not

to the normal cells that didnt vibrate at thefrequency being sent into the patient. Thisproved to be exactly right.

When radio frequencies and audio frequencieswere transmitted through a large rare gas filledray tube, the destruction of the organisms byrays and frequencies is described as being

similar to the phenomenon of the combination oftransmitted potential electronic energy and thecoordinative resonance of critical frequencies ortheir harmonics. This is electromagneticelectrocution where a potential energy level isreached that is lethal to the microorganism. This


64/99

is likened to fragile glass which is shattered by asustained note of music tuned to a resonantpitch or where a potential energy charge is built

up to exceed that level of energy which themicroorganism can cope with and still live. Thiswas called the M.O.R or Mortal OscillatoryRate.

Using the glass as an example, it is thefrequency of the glass (organism) harmonizingand resonating with the frequency beingbeamed into it that shatters it.Electroacupuncture. Because both vibratetogether, the glass (organism) can pick up thatparticular frequency and literally shake itselfapart. Tuning forks will respond only to theirspecific frequency, one across the room excitinganother only if they are tuned to the samefrequency or some harmonic thereof.

Another way the precise frequency or mortaloscillatory rate for any particular organism canbe found is by isolating and seeing theoffending organism under the Rife (or any)microscope and then zapping it with frequencyafter frequency until the right one is found.

When the mortal oscillatory rate or potential

energy level is lethally reached, the organismappears to blow up and disintegrate in the fieldand form, at times, a group of agglutinophilicclumped masses or electrostatic lines.

The first radio type frequency instrument was


65/99

designed and built in 1920. Development of theRife Ray to the point where it could be used onhuman beings was a proven fact back in 1934.

Tubercular and cancer patients were treated inprivate practice and recovered. Most casesresponded within a period of one to two monthsin which time the diseases were renderednoninfectious.

Rifes first human clinical work on cancer wascompleted under the supervision of Dr. MilbankJohnson, M.D., Chairman of the Special MedicalResearch Committee of the University ofSouthern California which included Dr. GeorgeDock, Professor of the Theory and Practice ofMedicine, Medical Department, TulaneUniversity of Louisiana, New Orleans; Dr.Charles Fisher, M.D. of the Childrens Hospitalin New York; Dr. Wayland Morrison, M.D., Chief

Surgeon of the Santa Fe Railway; Dr. KarlMeyer, M.D., Director of the George WilliamsHooper Foundation; Dr. Arthur I. Kendall,Professor of Bacteriology at NorthwesternUniversity Medical School in Chicago. Theresearch was conducted at the Scripps Castlewhich was rented over the summer of 1934 forcancer and T.B. cases. Fourteen out of sixteen

were cured in seven days, Rife said.

There are Rife generators readily availabletoday that generate these frequencies. Yousimply hold an electrode in each hand and asthe signal passes through your body, you feel


66/99

nothing. However, without knowing what theexact frequency of the organism that you aretrying to destroy is, for which you need the

microscope, these Rife generators areworthless. Acid base balance is simple andavailable.

* * *

Pendulums, Contact Reflexology, AppliedKenesthesiology, Radionics,Electroacupuncture and may others techniques,

are all based on the idea of the tester or the testcoming into resonance with the test subject.

* * *

Electroacupuncture and the Rife Microscopewere chosen to represent these vibrationalqualities as these are two quite objective formsof Vibrational Medicine.

* * *http://www.euroamericanhealth.com/gaston.html

Gaston NaessensGaston Naessens (1924 to present). Here Iwould like to introduce the work of M. Naessensas the diagram of his below puts in schematic

form what we have been been talking about.Apparently M. Naessens rediscovered thiswhole pleomorphic idea and what were earliercalled Myrozymas or Protits

Naessens termed
http://www.euroamericanhealth.com/gaston.htmlhttp://www.euroamericanhealth.com/gaston.html


67/99

Somatids.Gaston was born in Roubaix France in 1924

and by early childhood had shown himself to bean inventive mind. He received his degree afterWW II and immediately began research intomicroscopy, as well as into the nature ofdisease including acid base..

Like Royal Rife, Naessens

developed a lightmicroscope of hisown design which hecalls the

Somatoscope whichpermits enlargementsto 30,000 diameterswith a high degree ofresolution (150angstroms).With this he followed Bchamp, Rife and


68/99

Enderlein in showing that bacteria and othermicroorganisms arise from degenerated sub-cellular components of higher organisms. What

were earlier called microzymas or Protitswere called by Naessens

Somatids immortal particles oflife which survive thedeath of theindividual. When the individual isunhealthy, the Somatid passes through amultistage cycle of degeneration andregeneration, each stage in turn being capable

of independent life and reproduction. Thedegenerated stages of Somatids give rise tobacteria and other microorganisms under acid,acid base conditions.

The following information and picture are takenfrom the Physicians Handbook for Power, 1995,by Charlie Pixley, President, WRITERS ANDRESEARCH, Inc., 4810 St. Paul Blvd.,

Rochester, NY 14617.

the Somatid isindestructible. It


69/99

cannot be killed eitherby heat or by anychemical product.Secondly, theSomatid has to be

present in any kind ofcellular division.The Somatid permits growth hormone and thatpermits the cell to divide correctly. It is not theSomatid that secrets the growth hormone. It isthe transformation of the Somatid that liberatesthe growth hormone, but it is not a secretion of

the Somatid. The Somatid originates in a liquidform inside the red blood cell. Eachtransformation of the Somatid generates a newsecretion of growth hormones. He also has

noted that Somatids are

elcetro-chargedparticles. Themembrane has a


70/99

negative charge, thenucleus has a positivecharge and this canbe verified by puttingthe positive pole of a

magnet near theslides, all theSomatids areattracted to the

positive pull of themagnet.Like the tiny organisms Rife discovered throughhis unique microscopes in the 1920s and 30s,Naessens Somatids are pleomorphic (changeform) in nature. Furthermore, Naessens has

discovered that Somatids, the process ofpleomorphism, living in healthy human bodiesgo through a normal, recurring 3-stagepleomorphic sub cellular developmental cycle,and that each stage of this recurring cycle is


71/99

directly related to healthy cellular development,acid base and growth.

These three stages are listed as 1, 2, 3, in the

diagram below and correspond exactly to whatwe have been talking about, the only differencebeings the names assigned to these forms.

* * *

The normal 3-stages he represents here are ofcourse the same as the PROTIT, FREE

CHONDRIT, and the LOWER VALENCEDCHONDRIT FORMS of Enderlein.

[#1] As can be seen here what Naessens calledcalls the SOMATID is the Protit we have beentalking about.[#2] in this diagram, called SPORES byNaessens are the primitive stage FREE

CHONDRITS which as stated, can be seenmost frequently constantly changing betweenFILUM and PRIMITIVE GRANULE (Symprotit).The sizes of these tiny primitive granules varybetween 0.02 m and 1m.[#3] Naessens calls these DOUBLE SPORESwhich represent the joining of the FreeChondrits. This CHONDRIT PHASE begins with

the above enlargement of the Symprotits and oftheir Fila. The symprotits and their tails join endto end giving the chondrit forms a beadedappearance. This gives them a lively mobility asthey have an even denser arrangement of tiny


72/99

symprotits along the length of the fila. The sizeof these particles is from 0.5 to 2.0 m.

While Enderlein andother investigatorspopularized theconcept of bacterial

growth cycles, mostbacteriologist werestill unwilling toaccept sexual forms

of reproduction.Another objection was that experimenters wererarely able to show the complete cycle fromstart to finish. Gaston Naessens was theresearcher that was finally able to do this.

It is often stated that although a sequence ofdevelopmental forms may be observedmicroscopically, they do not reveal a cyclicaltrend that brings them back to the startingpointsuch culture developments shouldinclude a reversion to the original culture stagerather that manifest merely indefinite transitions


73/99

leaving the new form hanging in the air, as itwere. (W. H. Park and A. Williams, 1939)

The above includes as its first three steps, the

3-stage pleomorphic sub cellular developmentalcycle that is normal in our bodies. These threeforms cause no disease and in fact are used asthe medicines of Isopathic Therapies. None-the-less, the pathogenicity of the microorganismalforms rises with the developmental stages andacid base conditions and as stated;

THE ONLY EXCEPTIONS ARE THE VERYFIRST PRIMITIVE STAGES which are thePROTIT and the CHONDRITS that are of lowestvalences. They are entirely non virulent and theplay a REGULATORY role toward the higherand more pathogenic stages by decomposingthese through copulatory processes. In thatsense, these stages are termed

REGULATORS. (Blutuntersuchung ImDunkelfeld nach Prof. Dr. Gunther Enderlein;Maria-M Bleaker, Compiler)

But, if the bodys immune system becomessubstantially weakened due to trauma such asshock, wrong nutrition, chemical pollution, oreven psychological depression, Naessens hasfound as Enderlein and Antoine Bchamp did,that the Somatids switch gears, so to speak,and rapidly go into a 16-stage pleomorphiccycle, producing bacterial forms similar to thebacterial microorganisms Rife had discovered.Rife too had documented a similar 16-stage sub


74/99

cellular growth cycle through his microscope.

Along these lines, the fourth stages and beyondin the above diagram can continue and develop

into the more dangerous and pathological formsthat are familiar to us;

[#4] Next the first bacterial forms appear. TheseChondrits form circles (closed loops) composedof symprotit heads distributed around the ringmade of fila. The small symprotit heads movetogether and fuse forming the nucleus. These

are of course the resultant quantum likeconglomeration of Protits which in theirmultiplication, the primary tiny lumps begin todifferentiate themselves and increase in sizeand get a small spherical form, with a nucleusresiding at the cell wall. These are pathogenic.[#5] From the above, bacteria with 4 - 8 nucleidevelop, and finally a bacillus or rod with 16 and

more nuclei. These are the DoubleBacterial Forms ofNaessens. These arethe progenitors of themasses of bacteriaand bacilli, the Rod


75/99

Forms which wedevelop in ourselves,according toEnderlein and nowaccording to modern

science.Cancers are known tobe full of rottingbacteria and now

heart disease is linkedwith the bacteriaChlamydiapneumoniae as discussed. Basepowder is necessary.These later stages get into what I call the

degenerative


76/99

(fermentative and

putrifactive) phases of thesemiroorganismal forms. As this degenerationstarts with fermentation type processes, by theformed microorganisms, these later stages arerefered to under the above topic,AntoineBechamp and Fermentation

***

http://www.euroamericanhealth.com/mono.html

MONOMORPHISMMonomorphism is the cornerstone of RobertKochs (1843-1910) and Louis Pasteurs (1822-

1895) Germ Theory of

disease. This theoryprofesses thatdisease has amicrobial cause that

is caught from theoutside;that there are differences among pathogenic
http://www.euroamericanhealth.com/mono.htmlhttp://www.euroamericanhealth.com/mono.html


77/99

bacteria (ones that can make you ill), and eachhas a constant natureeach distinct bacterialform corresponds to a specific disease and thatthe form of this microbe always stays thesamemonomorphism, and causes the samedisease however often the disease istransferred from one animal to another, the kindalways remains the same and never changesinto other kinds. How You Rot and RustbySteve Denk

In 1878 Robert Kochwrote Etiology ofWound Infectionswhich was the

beginning of the GermTheory of Disease.Where Pasteurs views were shaped by thestudy of fermentation, Koch was affected by hiscontact with wounded soldiers. He noted thatthe bodies of animals that die of artificially

infected wound diseases (pus from an infectedanimal injected into a healthy one) invariablycontained many bacteriaIn each case adefinite organism corresponded to a distinctdiseaseand that for every individual,
http://biomedx.com/microscopes/rrintro/rr2.htmlhttp://biomedx.com/microscopes/rrintro/rr2.htmlhttp://biomedx.com/microscopes/rrintro/rr2.htmlhttp://biomedx.com/microscopes/rrintro/rr2.htmlhttp://biomedx.com/microscopes/rrintro/rr2.htmlhttp://biomedx.com/microscopes/rrintro/rr2.html


78/99

traumatic, infective disease, a morphologicallydistinguishable microorganism could beidentified.

In 1880 Koch built on an essay of the relationsbetween microbial diseases and their causesfrom the work of Jacob Henle, his professor ofanatomy. These became known as

the>Koch-HenlePostulates.The following are these postulates whichrevolutionized medical epidemiology at the turnof the century, by laying out the standard proofof infectivity to the present day. The

postulates dictate that

a microbe must be:1. found in an animal(or person) with thedisease,

2. isolated and grownin culture and3. injected into a


79/99

healthy experimentalanimal, producing thedisease in question;and then recoveredfrom the

experimentallydiseased animal andshown to be the samepathogen as the

original.* * *

By the early twentieth century the wholelandscape of medicine had changed. Most of

the common killer

diseases, including smallpox,diphtheria, bubonic plague, flu, whoopingcough, yellow fever, and TB, were


80/99

understood to be

caused by pathogens.Vaccines were devised against some, and bythe 1950s antibiotics could easily cure manyothers.

By the 1960s and 1970s the prevailing moodwas one of optimism. At least in the developed

world, infectious diseasesno longer seemedvery threatening. Far morescary were the diseases that the medical worldsaid were not infectious: heart disease, cancer,diabetes, and so on. That these diseases are

now considered to be infectious (SeeAtlanticMonthly, A New Germ Theory, February 1999) ,is what this web page is about.

Also, no one foresaw the devastation of AIDS,or the serial outbreaks of deadly new infectionssuch as Legionnaires disease, Ebola andMarburg hemorrhagic fevers, antibiotic-resistanttuberculosis, flesh-eating staph infections, andRift Valley fever.

The infectious age is, we now know, far fromover. Furthermore, it appears that manydiseases we didnt think were infectious may because by infectious agents after all. These


81/99

include stomach ulcers, heart disease. The firstcancer virus discovered in 1910 called theRous sarcoma virus, certain leukemias,

lymphomas, nasopharyngeal cancercommon in south China, cervical cancer,stomach cancer, liver cancer, Kaposissarcoma with Herpes virus 8, mammary-gland tumors in mice, childhood obsessivecompulsive disorder, Sydenhamss choreawhich is a rare complication of streptococcalinfection.Streptococcal antibodies find their

way into the brain and attack a region called thebasal ganglia, causing characteristic clumsinessalong with obsessions. Schizophrenia has longbeen considered to be possibly infectious innature.The Atlantic Monthly, A New Germ TheorybyJudith Hooper, February 1999, pg. 44.

The catalogue of suspected chronic diseasescaused by infection/bacteria to David ARelman, an assistant professor of medicine,microbiology, and immunology at StanfordUniversity, now includes;

sarcoidosis, various forms of inflammatorybowel disease, rhumatoid arthritis, lupus,Wegeners granulomatosis, diabetes mellitus,primary biliary cirrhosis, tropical sprue, andKawasaki disease. Likely suspects includemany forms of heart disease, arteriosclerosis,Alzheimerss disease, most major psychiatricdiseases, Hashimotos thyroiditis, cerebral
http://www.euroamericanhealth.com/atln.htmlhttp://www.euroamericanhealth.com/atln.html


82/99

palsy, polycystic ovarian disease, and perhapsobesity and certain eating disorders. Multiplesclerosis has been linked to the human herpes

virus 6, the agent of Roseola infantum, a verymild disease of childhood (ibid.)

* * *

Where do these bacteria come from?

To modern science, this is still an unansweredquestion.

* * *

Regarding stomach ulcers;

In 1981 Barry J. Marshall became interested inincidences of spiral bacteria in the stomachlining. The bacteria were assumed to beirrelevant to ulcer pathology, but Marshall and J.R. Warren noticed, serendipitously, that whenone patient was treated with tetracycline for

unrelated reason, his pain vanished, and inendoscopy, revealed the ulcer was gone.

An article by Marshall and Warren on theirculturing of unidentified curved bacilliappeared in the British medical journal,TheLancetin 1984. No one listened until finallyMarshall personally ingested a batch of the

spiral bacteria and came down with painfulgastritis, thereby fulfilling all of Kochspostulates.

There is now little doubt that Helicobacter pylori,found in the stomachs of a third of adults in theUnited States, cause inflammation of the


83/99

stomach lining. In 20 percent of infected peopleit produces and ulcer, Nearly everyone with aduodenal ulcer is infected. H. pyloriinfections

can be readily diagnosed with endoscopicbiopsy tests, a blood test for antibodies, or abreath test. In 90 percent of cases the infectionscan be cured in less than a month withantibiotics.

* * *

Where do these bacteria come from?

You dont catch them, so infectious is not thecorrect word.

* * *

Regarding arteriosclerosis;

It has recently been discovered thatarteriosclerosis is also a bacterial process.Notice I did not say, caused by bacteria. The

plaques of 99% of patients with hardening of thearteries have the bacteria Chlamydia

pneumoniae in them.

According to The Atlantic Monthly, Feb. 1999,Chlamydia pneumoniae is a newly discoveredbacterium that causes pneumonia andbronchitis. The germ is a relative ofChlamydia

trachomatis, which cause trachoma, a leadingcause of blindness in parts of the Third World.C. trachomatisis perhaps more familiar to us asa sexually transmitted disease that, leftuntreated in women, can lead to scarring of thefallopian tubes.


84/99

Pekka Saikku and Maija Leinonen of Finlanddiscovered the new type of chlamydial infectionin 1985 though its existence was not officially

recognized until 1989. Saikku and Leinonenfound that 68 percent of Finnish patients whohad suffered heart attacks had high levels ofantibodies to C. pneumoniae, as did 50 percentof patients with coronary heart disease, incontrast to 17 percent of the healthy controls.

While examining coronary-artery tissues atautopsy in 1991, Allan Shor, a pathologist inJohannesburg, saw pear-shaped bodies thatlooked like nothing he had seen before. Cho-Chou Kuo, of the University of WashingtonSchool of Public Health, found that the cloggedarteries were full ofC. pneumoniae. Everywherethe bacterium lodges, it appears to precipitatethe same grim sequence of events: a chronic

inflammation, followed by a buildup of plaquethat occludes the opening of the artery (or, inthe case of venereal Chlamydia, a buildup ofscar tissue in the fallopian tube).

Recently a team of pathologists at MCP-Hahnemann School of Medicine, found thesame bacterium in the diseased section of theautopsied brains of seventeen out of nineteenAlzheimers patentsand in only one of nineteencontrols.

Whether antibiotics help any of these diseasesor not remains to be seen. The first majorclinical trial is under way in the United States,


85/99

sponsored by the National Institutes of Healthand the Pfizer Corporation: 4000 heart patientsat twenty-seven clinical centers will be given

either the antibiotic azithromycin or a placeboand followed for four years to gauge whetherthe antibiotic affects the incidence of furthercoronary events.

Whether the antibiotic helps coronary heartdisease or not does not explain where thesebacteria come from and thereby how to effect acausalor real cure. That this issue ofChlamydiain the tissues, is still being pursued by themodern pharmaceutical firms as infectious innature, amenable to the treatment withantibiotics and/or vaccines, is an anotherexample of how entrenched Pasteurs andKochs ideas are in the whole of medicine fromthe profit orientation of the petro-chemical

pharmaceutical companies on down.The above reference to the article from The

Atlantic Monthly, does add to its credit,

Even if heart patients can be shown to haveantibodies to C. pneumoniae, and even ifcolonies of the bacteria are found living andbreeding in diseased coronary arteries, is it

certain that the germ caused the damage?Perhaps it is there as an innocent bystander, assome critics have proposed.

As will be shown, the above bacteria,Chlamydia pneumoniae andHelicobacter pylori


86/99

come outthe red blood cells themselves Theblood is teaming with microorganisms,especially if it sits on the microscope slide for a

few hours. You can watch this process underany microscope, anywhere, anytime.

* * *

This is a funny situation really. Modern,allopathicly trained physicians


87/99

organs; depends on which way we want to go.One needs a source of Protits in the diet, organmeats provide these, organ specific

Protits/Somatides. (See Live Cell Therapy)Continue on to: The Hystory of theMonomorphism Pleomorphism Debate

http://www.euroamericanhealth.com/hysty.html

THE HISTORY OF THE PLEOMORPHISM/MONOMORPHISM DEBATE

WHY PLEOMORPHISM IS UNKNOWN TO

MODERN MEDICINEA dichotomy in medical speculation, anunresolved philosophical conflict, has existedfrom ancient times to the present. This conflict isbetween two theories known traditionally asEmpiricism and Rationalism.

While this conflict can be discerned in the

earliest writings of the Hippocratic Corpus, fromthe fifth century BC, the names Empirical andRationalist became current in Rome at thebeginning of the Christian era - designatinggroups of physicians competing with oneanother ideologically and economically.(Divided Legacy, Harris Counter, pg. xv.)

The main form of medicine practiced today is ofthe Rationalist orRationalist/Methodist pointof view. Rationalism involves a mechanistic orchemical understanding of the human organism.It maintains that life itself can be explained byphysics and chemistry, or, more generally
http://www.euroamericanhealth.com/hysty.htmlhttp://www.euroamericanhealth.com/hysty.htmlhttp://www.euroamericanhealth.com/hysty.htmlhttp://www.euroamericanhealth.com/hysty.htmlhttp://www.euroamericanhealth.com/hysty.htmlhttp://www.euroamericanhealth.com/hysty.html


88/99

speaking, by mechanics. Rationalism maintainsthat there is no essential difference between thestructural chemistry of life and that of inanimate

nature.This idea of the body viewed as a machinecomposed of many little machines is contrary tothe Empiricalview that the laws governing theliving organism differ from those of lifelessmatter. This concept is called Vitalism.

The person as a whole is something different

from a collection of viscera; the wholeness givessome extra, if undeniable, quality to theindividual organs. Today we pay for ourknowledge of the parts in ignorance of thewhole.

Vitalism maintains that;

the organism is reactive, at all times coping

with, and attempting to overcome, the stresseswhich impinge upon it from outside. It behavespurposively, the nature and form of its reactionbeing determined by the specific environmentalstress encountered. It responds to challenge,which no aggregate or assembly of non-livingsubstances can ever do. (Divided Legacy,Harris Counter, pg. xvii.)

In 1946, the quantum physicist ErwinSchroedinger pointed out

that biological material has a totally differentcharacter from all other states of matter densityof life - that is, the information stored per unit


89/99

volume - and that of any inorganic system thathas not been produced by living formsThesilicon chip must use many orders of magnitude

more atoms to store the same amount ofinformation as a gene.

This is vitalism, Quantum Vitalism.

According to Harris Coulter, no perfectRationalist therapeutic doctrine has ever beendevised. Even Galen, who of all physicians inhistory worked hardest at theoreticalconsistency, left a few loose ends. But theformulation which emerged in the latenineteenth century - the specificbacterialdisease treated by thecontrarymedicine -seemed to its devotees an almost unblemisheddepiction of the Rationalistic reality. The aboveis what is what modern, allopathic medicinehas become.

The microbe and the Germ Theory of Diseasebecame a new organizing principle in medicine,bringing much scattered clinical data togetherinto a series of new specificentities with somecures, specific cures. The germ theory wasbolstered by the doctrine of monomorphism -meaning again that microbial genera andspecies are fixed and eternal, that the form ofeach microorganism associated with a specificdisease always stays the same and alwayscauses that same disease.

Monomorphism was above all, a practicalresponse to an emergency situation in


90/99

bacteriology. This concept of disease, emergedin a context of intense anxiety over the socialdepredations inflicted in every country in Europe

and the United States by a series of diseaseswhose very names - tuberculosis, diphtheria,typhus, cholerawere chilling reminders ofhuman mortality, (Divided Legacy, HarrisCoulter, pg. 37)

More to the point;

involved in the concept of Pleomorphism was

the role and importance of thehost organism -THE PATIENT!Microbes altered their forms inresponse to the patient, in response to the diet,environmental stresses the patient encountered,what poisons the patient consumed etc.. (ibid.),Harris Coulter)

Such ideas have little to do with the doctor.

Pleomorphism meant that the host organismor patient was an active participant ininfection and disease - in contrast to Koch andPasteur and the monomorphists who held themicrobe to be all-powerful, the host organism apassive victim. Pleomorphism meantdowngrading the microbe, since the host, byresisting the latters onslaught, could alter its

characteristics and make it return to a normalform as again. The patient had control overthe bacteria, not the other way around. Themicrobes are the result, not the cause ofdisease.


91/99

Even the common communicable diseases,e.g. strep throat or chickenpox, can not takehold, grow, if the internal milieuis not conducive

to their reproduction. This is what base powderdoes. As stated before, one third of people inEurope did not get bubonic plague. In treatingcancer with isopathic medicine, for example,one does not attack the tumor at all, instead onechanges the environment, the internal milieuthat caused the cancer in the first place.

What this all means then, thispleomorphism/monomorphism controversy, isthat at its most fundamental level it hassocioeconomic dimensions that still effect usprofoundly today.

Accepting Pleomorphism meant acknowledgingthe host organisms, the patients capacity todefend itself (him or her) against, and

dominate, the microbe.Monomorphism, on the contrary, enhanced therole of the microbe in disease, andconsequently that of the physician who combatsthe microbe. This is the principal reason forthe instinctive hostility of the majority ofphysicians to Pleomorphism and

Whoistic/Alternative Medicine ingeneral.(Ibid. pg. 39)

***

This gives the responsibility for health backto the patient


92/99

if they want it!

***

Pleomorphism has been a great threat to this

control factor. This control factormeans;control of the disease with poisons that need monitoredand controlled, controlling therefore, the patient and theirpocket book.(Ibid, pg.39)

The phenomena are forced into categorieswhich can be manipulated to make a living fromthe practice of medicine. The monomorphistshave identified their doctrine with science itself,

as science itself, that Monomorphism is a law ofnature, which it is not. This viewpoint has,through the years, taken on such an aspect oftruth that to question it now seems a scientificsacrilege.

The followers of Koch proclaimedMonomorphism with religious fanaticism,

stated Max Gruber in 1885. F. Loehnis stated in1922 that the intransigence and verbal violencedisplayed by the various factions in this conflictresembled certain historic theological quarrels.

This battle has been going on for a long time!

For all these reasons, Monomorphism was atfirst excessively rigid, even dogmatic. Rene

Dubious states that Koch and Pasteur;overestablished the doctrine of the specificityof disease causes and that blind acceptance byseveral generations of bacteriologist of thedogma of constancy of cell forms andimmutability of cultural characteristics


93/99

- 3.012 Blog - Colloids of Life

Documents

Transcript of - 3.012 Blog - Colloids of Life