Do you Who is on Want to Already a

know atp? Multiply? learn more? Member?

Become her
Find your friends Take the Tour Sign In
contact

"atpcorporation" Website: GODSEND

Products- Fulvic Acid ("Miracle Molecule")
& Natural ZEOLITES , * * * " F R E E " in
the P H I L I P P I N E S ! ! ! . With
ORGANIC GERMANIUM" -
SYNTHESIZED BY ATP WITH the DIVINE
PROVIDENCE of our CREATOR * * * *

HomeNotesBlogPhotosVideoMusicCalendarReviewsLinks

Oct 19, '08 1:16

Colloids of Life or Protits. By - ATP Global Foundation.
AM atpcoop
Source: www.cellsalt.net
for everyone • View
Contacts
(827)

ATP Medical Literature: #05 Colloid • View

Groups
of Life (39)
• Photos of
atp
 • Personal
Note : The information Message
•
contained herein is for RSS
Feed [?]
•
informational purposes only. Report
Abuse
•
You may want to print ATP
MEDICAL LITERATURE and
other educational documents
that 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 it
may thrive for multiples of that time”. . . .
Dear GUEST / SPONSORS/ DONORS…TERMINALLY 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 the physical
life part, not speaking of the Soul or

anything like that even, the

 Protit, never dies.
Immortality is a
nature of Life and
the Protit too, as
Life itself never
dies. The Protit is the
elementary particle
of life, not the cell,
which can die. “
The Video Testimonials of ATP patients regarding the use of ATP
Products Bio Minerals and Bio Energizers (whose formulation is composed
of ZEOLITES & FULVIC ACID) also highlights the effects of Fulvic Acid
in the body’s bio chemical reactions and its effects on the body’s electrical
potential
At present Adenosine Triphosphate (ATP) Corporation is distributing
ATP Products (Zeolites & Fulvic Acid) for FREE to the following
recipients:
1. Daily patient/recipients at ATP Global Foundation- located at Bohol
Mansion Office, 43 E.Lopez Ave., corner Sgt. Esguerra St., Quezon City,
Philippines; and
2. Weekly patients of ATP/Salamat Dok –TV program of ABS CBN
network, every Saturday 6-7 AM and Sunday 7-8 AM; venue –ABS CBN
compound. (This weekly Medical Mission started last March 17, 2007 and
continuing up to present)
Please be guided accordingly.

/Print this document ! (For educational purposes)

>>
>>
[The link bar Links
feature is not
available in this web]
http://www.euroamericanhealth.com/gunth.html
Günther Enderlein
>>

>>

Günther Enderlein (1872-1968) saw

the healthy host as filled with primitive life
forms which he called -
Colloids of Life or
Protits.
These reside in the red cells, white cells, in
plasma and all other body fluids and tissues, are

0.01 micron in radius

(about the size of a virus), and the larger forms
of these can be seen under any microscope’s
high power, oil immersion lens, as tiny dots,
rolling, always moving. They are seen best
with a dark-field microscope as
tiny shining, moving points. They
are visible because they
move. For Web Site reference regarding
Günther Enderlein see the ExploreMagazine at
explorepub.com.
Günther Enderlein was the last of the old
pleomorphists and has done the most
exhaustive and comprehensive
compilation and study of this information
to date. The basis for Enderlein’s work was the

French
book by the

researcher A.
Béchamp, titled
Mycrozymas.
Enderlein devoted the bulk of his scientific work
which stretched for more that 40 years, to the

complex question of
pleomorphism,
symbiosis and
cyclogeny (the cycles organisms go
through) of microorganisms.
From this he published his chief work,
BAKTERIEN-CYCLOGENIE
(publisher W.de Gruyter & Co.
Berlin, 1925). In it he presented
arguments and proofs for
pleomorphism, which have to this date
remained undefeated.This book has just
become available in English from Enderlein
Enterprises, Inc., P.O. Box 704, Mt. Vernon, WA
98273, phone 360-424-6029. That there has
been very little about any of this available in
English has been part of the problem for sure.
The following information and pictures, except
where otherwise indicated, are from the book
Blood Examination in Darkfield
according to Prof. Dr. Günther
Enderlein, available from Semmelweis-
BVerlag, D-27316 Hoya, Germany, compiled by
Dr. med. Maria-M Bleker, 1993. This book is
also available, in English and German, at the
above address. In the following, unidentified
quotes are placed for material taken from this

book. Maria Bleker gives

seminars in Darkfield Microscopic examination
and has been one of the chief people
responsible for introducing Pleomorphism to
America. This has not been an easy job.

“According to Enderlein, ‘germs’ are

not representing unchanging organisms that are
independent of each other, but altogether
they form a singular, common
cycle, which has its origin in the
colloidal, albuminoid
substances called
Protits that are contained
inside of each particular cell.”
Enderlein called these Protits,

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

Wecoexist in a
mutually symbiotic
(means we live
together, helping each
other) relationship. We
give them a vehicle
for life, they give us
blood forms like
platelets, without which we couldn’t
exist (platelets are

formed from the

Protits, not in the
bone marrow as
taught by modern
science).
The endobiont appears

in all mammalian
species and has shown
evidence through some of
its developmental forms to be of
a plant nature.
Our symbiotic union with
 evidently occurred
them

millions of years ago as

our species grew into existence.

Without some blood

clotting mechanism in
place, mammals could
never have evolved.!
When the host is in health,
Protits live in symbiotic
relationship with the tissue cells,
and maintain the health of and
regenerate all organs, we live together
and help each other. They are the

smallest unit of life,

not the cell.
They are physical life
per se.
In the blood and tissue of humans and animals,
 microbes
there live

(Protits) which are

normally harmless and
which maintain diverse regulatory mechanisms.
According to Prof. Enderlein, these

‘Endobionts’ are
usually non-
pathogenic phases of
the mold fungus
Mucor racemosus
Fresen!, Aspergillus niger van
Tieghem or Penicillium notatum.
One does not see these fungal forms in the
blood of a living being, these are just what they

look like when

cultured in a
laboratory or what the
Protits devolve to in a
corpse.
The mummies in
Egypt are composed
totally of Protits.
Put the dust from
these mummies in
water and there they
are, under the
microscope, turning,
moving, the Protits.
***

THE LAW OF
CYCLOGENY
As with microbes the above Protits are subject

Law of Cyclogeny,
to the

which means, their

development cycles
through the following
stages: primitive
phase (Protit) to
bacterium to fungus,
whereby the virulence and pathogenicity of the
parts of the cycle increases with the rising
developmental phase.
This means, they develop from the

apathogenic (can’t
make you sick), non-
motile, tiniest
albuminoid, particle
(Protit) — which is to be classified in
size with the viruses (0.01 µm) — via

the nonvirulent
chondrit stage into the
following parasitic, pathogenic (can make
you sick) stages.
As the patient becomes ill and therefore acid,
microorganisms form, in
quantum-biological leaps,
depending on the pH of the
nutritive medium or the internal
milieu. The microorganisms get more
one goes from
dangerous as

the strongly alkaline

high of the pH-value
towards the ever
decreasing pH-value
of the acid side.
This happens in the following manner. AS THE
INTERNAL MILIEU BECOMES MORE ACID,

Protits first begin to

the

join into threads (tails

or Filum) that sprout
globules, primitive
granules (heads). These,
Enderlein, called
SYMPROTITS.
As from Dr. med. Maria-M Bleker’s, Blood
Examination in Darkfield according to Prof. Dr.
Günther Enderlein;
“In the new formation of filum and head, atomic-
physical and quantum-biological factors play a
decisive role. This is visible from the sudden
occurrences by the leap of these new

formational
formations. The

processes of a filum
with a head resulting
in what is called the
CHONDRIT, occurs within the
smallest fraction of a second, which is therefore
not observable by the eye looking through the
microscope; the new developmental forms are
suddenly there. The Protits come together and
join in the following manner:

Protits can
NATIONALIZE or
come together in
three ways. They can form:
1. A one dimensional arrangement. This results
in a shorter or longer thread, the FILUM; its
diameter is that of the protit, namely 0.01 mm.
However, it can constantly increase in
thickness, after its formation.
2. A two dimensional arrangement of the protits,
into fine, skin-like surfaces that are found, for
example, in the spermit (bacteriophage) as
swarmer-heads (see below). This is one filum
with one Protit head. The

SYMPROTIT is simply
a larger head than the
Protit or the Spermit
head.
3. A three-dimensional arrangement, namely
into more or less tiny granules, the physiologic,
often spherical SYMPROTITS which become
the primary nuclei of the bacterial cell they are
turning into.”
***
FORMATION OF FILUM
 Fila
The formation of these

threads can be
observed only in the
dark field, sometimes this occurs
very rapidly, right before your eyes, in extremely
ill patinets.

The fila in this picture

are the thread like
structures that fill the
background. These are what

cause blood to clot. The

circles are red blood

cells circles that are stacked
.The

together in the left hand picture

are red blood cells that have
stuck together.
As from Maria Bleker’s
book;
“It is the first of the primitive phases that occurs
through the change in fila according to the
formula x:2x. Because the x shows very great
differences in the lengths, the filit-phase
comprises very large numbers of individual
phases. These threads begin to appear soon
after the blood is drawn. While watching under
the microscope the threads just pop into
view, increasing in length in quantum type
jumps, 2X long then 4X, then 8X, 16X, etc..
Actually, there appears to be constant quantum
fluctuations between these formed products.
Thereupon follow the primitive stage FILIT, the
ongoing change between the FILUM and a
filum-piece of double its length.”
If a person is totally healthy,
none of these Fila will form. If
there is no appearance of Fila
after two days, that person is
totally healthy. Personally, I have never
seen this, perhaps in a new born baby.
Base Powder reverses this process.
Actually, we had a patient one time in whom the
Fila started forming immediately. This is very
unusual as usually it takes some hours for this
process to start. This patient was very ill with
extremely acid blood and cancer and we never
 How fast the
saw him again.

Fila form is a very

good indicator of how
ill you are as it is a
direct reflection of
how acid you are.
***

FORMATION OF
SYMPROTITS
Next, the Filit makes a quantum jump and unites
with or produces, instantaneously sprouts, a

SYMPROTIT HEAD.
The above tail simply
develops a head, in a
quantum fashion and
poof….there is a filum
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 similitude
among sexual processes in Nature is pervasive

The snake that

and awesome.

ate itself. In fact

sometimes these
threads or fila begin
to move like a flagella
and you have what is
called SPERMIT. This is
pleomorphism and acid base is the key.

“The spermits of the

microbes are tiny
swarmers that consist
of a tiny symprotit
heads and filum
flagellie, which
enables them to
copulate with all
pathological
symprotits and all the
bacterial and fungal
forms within the same cycle.
The consequence of such copulation of
bacterial and fungal-nucleic apparatus is

bacteria and
naturally that the

fungi immediately
become dissolved and
they degrade back into
more spermits and
protits/chondrits.
The presence of spermits is a good thing as
these forms attack anything (higher pathogenic

Spermits cannot
forms).

be photographed
because of their
minute size and
intense mobility. They
represent nothing but
a readiness to meet
an alarming situation.
”
Enderlein first discovered this process in 1916
with his work on typhus. He re-discovered in the
blood of these patients, with darkfield, “the
tiniest moving beings”, this having been seen
before by Béchamp and others.

Enderlein saw too that

these tiny moving
beings “entered into
union with higher
organized bacteria”.
When this happened the bacteria that had
joined with the tiny beings “became instantly
invisible. Enderlein surmised sexual processes,
through which came about, not higher forms (as
in embryonal development) but lower forms that
were invisible to the eye in the light microscope.
These vigorously moving elements had flagella.”
As indicated above he named these Spermits.
SYMPROTITS

variation in size
This shows the

of the Portits. small The

dots in this picture

are Protits, the larger
dots are the
Symprotits. red The
 circles are red blood
cells and 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 that
form varying sized globules or heads. As the
Protits group together the heads get larger and
larger. As stated, the tails really can’t be seen in
these pictures. The Symprotits then that we see
under the microscope are enlarged Protit type
forms occurring in various sizes. They are
always moving too, compared to other things
seen under the microscope that look similar and
don’t move.
The small dots in this picture are larger and of
different diameters than the ones in the above
picture. The Protits have stuck
together and formed the heads of
the next larger “nationalization”
or grouping of the Protits. Each
advancement to a higher stage or
VALENCY as it is called represents an
increasing degree of pathogenicity. They
become more dangerous.

Then, these conglomerated

Protits (Symprotits)
use more protein
colloid, Protits, for their advancement,
depositing it first in large numbers right on its
surface as nutritional reserves. This reserved
living, protein colloid grows even larger,
surrounding the symprotit sphere with more and
more substance. These become

Macrosymprotits
(macro - large,
symprotits). The acid
base imbalance is
becomming worse.
***
MACROSYMPROTITS

large
These represent exceptionally

spheres of purely
nucleic protein. They can be
found free, or connected with the filum, or in the
elements of tissues and cells of the host. In
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 is
dealing with normal forms or abnormal ones.
Namely, in that case, the formula is also x:2x,
which means the presence of identical spheres
plus other ones of twice their size. When
several sphere-phases are found side-by-side,
they will be indicated by a larger number of
varieties in size, which is the more common
condition. They just jump from one size to the
other, no period in-betwe0en that is observable.

resulting forms are

The

the large, heads or

primitive granules
called
Macrosymprotits.”
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 milieu becomes acid, as the pH
decreases, the primary tiny lumps and their
tails, the Protits begin to increase in size by
sticking together in a three dimensional
arrangement; first one, then two, then eight,
then sixteen, then thirty-two according to the
formula, x:2x, where x is the number of Protits
coming together. These increase in quantal
jumps too. You can watch it under the
microscope; 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 above
enlargement of the Symprotits and of their Fila.
The Symprotits and their tails join end to end
giving the Chondrit forms a beaded appearance.
This gives them a lively mobility as they have an
even denser arrangement of tiny symprotits
along the length of the fila.
“The primitive stage CHONDRIT can be seen
most frequently constantly changing between
FILUM and PRIMITIVE GRANULE (Symprotit).
Depending on the size of this tiny primitive
granule (between 0.02 µm and 1µm), very
diverse valences or degrees of pathogenicity
may 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 are
free Chondrit heads on Fila threads. Some have coalesed
into, thick rid shaped forms, (see below). The large circles are
red blood cells.
The Chondrit Stage
 This is the Chondrit stage growing out from a red blood cell
edge. It has many Symprotit heads on a File thread. This
stage is very strong and mobile. This thread will close end to
end and form a circle. This will become a bacterial cell as
below.
The lower valenced Chondrits are not
pathogenic and do not make you sick. In fact,
these low valenced Chondrits plus the Protit
discussed above and the Protitit (the forms that
are so small that they can’t be seen with the
light microscope). The Protit and Protitit have
even lower valency or pathogenicity than the
Chondrits and these three are what are used as
Isopathic medicine. These Chondrits, being
quite mobile, seek out higher valenced
microorganisms such as bacteria and fungal
forms. The Chondrit forms copulate and fuse
genetic material with these more pathogenic
organisms and they then break all apart into
Protits as described.
The Chondrit Stage begins with that sphere of
the developmental growth of the endobiont, in
which only the low-valenced phases have full
apathogenicity and all higher phases reach
pathogenicity to an ever rising degree. The
higher valenced forms of these Chondrits have
more Symprotit heads, they are bigger and
more varied in size among other things. The
Free Chondrits are considered to be the viral
phase and in their higher valenced forms they
are pathogenic as such.
“THE ONLY EXCEPTIONS ARE THE VERY
FIRST PRIMITIVE STAGES which are the
PROTIT and the CHONDRITS that are of lowest
valences. They are entirely nonvirulent and the
play a REGULATORY role toward the higher
and more pathogenic stages by decomposing
these through copulatory processes. In that
sense, these stages are termed
REGULATORS.”
Isn’t this all rather amazing?

“Sperms”, doing what

they do and breaking
down higher and
more dangerous
forms of its
conglomerated self,
back into itself. The
snake eating its tail
for sure. This is
Isopathic medicine.
***
THE BIRTH OF A CELL
 (BACTERIAL SPHERES)
Next, if the internal milieu, Pishinger’s Space,
becomes worse, more acid, polluted, the
beaded, Free Chondrits, form circles (closed
loops) by hooking end to end and looping
around to complete a circle. These circles are
composed of symprotit heads, distributed
around the ring made of fila.

Symprotit heads distributed around a ring made of fila.

These symprotit
heads will fuse
together and form the
nucleus of the
developing bacterial
cell .

Then, these small symprotit heads move

together and fuse forming the nucleus (called
the Mych),

and you have the newborn cell!

BACTERIAL SPHERES

The medium sized circles like the arrow is pointing, looking

 Bacterial
like bubbles, are

Spheres (Mychits) or
spherical, primary
bacterial cells. The larege circles
are red blood cells and the mass in the middle is a
disintegrating white blood cell with the many ring forms being
extruded from it.

growth forms
The above are the

of the primitive
phases (the Protit,
Symprotit,
Macrosymprotit and
lower valenced
Chondrits). These come
together and form the
cell.
“Each higher developmental step represents the
nationalization or coming together of these
growth forms. In this way, the symprotit uses the
protit, namely a protein-colloid, for its
advancement, depositing it at first in large
numbers right on its surface as nutritional
reserves. This reserved living, protein colloid
grows ever larger, surrounding the symprotit
sphere more and more. By this process, the first
cell has come to be, which is a spherical
primary cell, the bacterial cell, the MYCHIT. By
this process, the symprotit became the primary
nucleus, the MYCH, and from the reserve
material collection of living colloids came the
CELL PLASMA of the primary cell, the Mychit.”
“Reserve substances, which form a more or less
thick layer, may be deposited around the
primary nucleus. These primary nuclei with their
covering of reserve substances completely
correspond physiologically to the fatty
substances in higher organisms. To the very
largest percentage of cases, these reserve
materials consist of LIPOIDS and also
NUCLEIC ACID DERIVATIVES.”
***
DEVELOPMENT OF BACTERIAL RODS

Bacterial
Through division, the above

Sphere becomes the

source of a
micrococcus with two
nuclei (DIPROTIT). From
them, bacteria with 4 - 8 nuclei develop, and
finally a bacillus with 16 and more nuclei. On the
other hand, the nucleus divides and the ring can
elongate and turn into rod forms. This is a
picture drawn while looking though a

bacterium,
microscope in 1879. The

Leptotrichia buccalis,
the usually harmless
bacteria found in our
mouths, is seen here to go from the
round coccal form into a rod form. In the
process the nucleus divides and becomes
many.

To summarize, the small nuclei or tiny

symprotits of the Chondrit around the edges of
the ring in these pictures move together and
make one nucleus. The ring can enlarge and
become a coccus or round, ball shaped germ or
it can elongate and turn into a bacterial rod. The
Symprotit gathers Protits to it to feed it and to
form the cellular plasma. The nucleus gets
larger as the tiny symprotits coalesce and the
ring gets larger as the cell plasma fills the cell
up.

Coccus type germs

are the streptococcus,
gonococcus,
staphlococcus and the like.
Rod type germs are E.
coli, pseudomonis,
and so on. These forms actually
come out of the cells themselves, red or white in
the blood. The blood, when it starts to break
down first begins a fermentation process that
can lead to blood clots or rigor mortuus, two
sides of the same process.

Red blood cell from a patient with stomach cancer. There are
two 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 see
round buds pinching off of blood cells. You see
long hollow tubes that have come out of cells
and long, beaded strings of Chondrit forms that
can be the pathogenic viral forms. There are
also some short stubby rods that are typical of
the ones we see in medical, micro biology labs.
Acid base imbalance is severe.

various size
The multitude of

dots in the left hand

picture are
Symprotits and
Macrosymprotits , Symplasts
(heads and tails hooked end to end, not yet pulled together
into bacterial forms) and Free Chondrits (the beaded, long
thread like forms). The right hand picture shows buds of
bacterial forms comming out of red blood cells.
***

Protits,
What makes these life forms,

‘advance’ so rapidly?
(I prefer to use the
word degenerate or
involve, devolve – rather
than advance or evolve.)
“Our civilization causes or facilitates this through
artificial fertilizers, preservatives, coloring
substances, air pollution, etc., but in the very
first place stands our false nutrition, which

literally “fattens” the

Endobiont by its high-
content in protein and
sugar.
Animal protein fattens the Protit. As soon as the
balance in the blood serum between mineral
salts (bases, alkali) and acids has become
disturbed toward the acidic side through long-
continued, antibiological nutrition, the above
things start sticking together. The

endobiont literally
feeds off animal
protein and gets
bigger.”
“The endobiont is the
ROBBER OF
PROTEIN. The only non-
plant protein that can
be taken in larger
amounts, is the
protein of the milk, and
that in its acid form, such as cottage cheese and

Farmers
other forms of cheese.

Cheese is the best

available in supermarkets. These
lactic proteins have developed a special
accomplishment in the course of endless time,
namely the capacity for producing a specific
protein synthesis, which does not give the
endobiont an opportunity to feed on.”

The normal healthy

Protit is made up of
vegetable protein!
“The hydrogen-ion concentration (pH) of the
blood gets shifted through the Endobiont,
whereby it must be especially emphasized that
the Endobiont expressly devours protein. It is
understandable that these facts create ever
enlarging conditions of the endlessly ongoing
development of the Endobiont.”
 ***
THE ANARTATIC LAW of Enderlein
The dependency of the development of
microorganisms upon the pH (acid base) of the
nutritive medium or the internal melieu is a
FUNDAMENTAL LAW called the Anartatic
Fundamental Law by Enderlein. As from
Blutuntersuchung Im Dunkelfeld nach Prof. Dr.
Günther Enderlein;
The Anartatic Fundamental Principle:
“For the nationalization (coming together of) of
comparative-morphologic units into higher and
highest developmental phases, the specific
acids PRODUCED by each individual
microorganism are the CAUSAL reason for the
changes of the internal milieu in the pH, and
that is tending to the ACIDIC side. In other
words: the RISING steps of the total cyclogeny
are accompanied by and dependent on the
PROPORTIONATELY DESCENDING pH. That
is it demonstrates the summary of the
ASCENDING developmental tendency with the
ever more DESCENDING pH-value.”
An interesting point here is that one can never
force an advancement by increasing the acidity
of the culture medium. This won’t, in and of
itself, cause the Protits to stick together and
acquire tails and form spheres with nuclei on
their edges that finally turn into bacterial and
then fungal forms.
“On the other hand, if one alkalinizes a culture
medium already containing fully developed
bacterial or fungal forms by adding a little
bacterial material or parts of fungal mycelia to a
hanging drop of 5% sodium carbonate, which is
a strongly alkaline medium with a high pH value,
one can immediately observe the formation of
the primitive stages, namely in the CHONDRIT
STAGE.”

Sohigher forms are

readily ‘decomposed’
back into the Chondrit
Stage, by making
them alkaline.
So too, if one withdraws blood from a vein
through a tube and then run the blood directly
into a sugar water solution with 40% ethyl
alcohol in it, without exposing it to air, as per
Louis Pasteur and Antoine Béchamp, it will
begin to ferment. This fermentation produces
the acids it needs to continue its evolution, de-
evolution, involution, namely lactic and citric
acids. The red blood cells begin to decompose.
All the above things happen and what you end
up with is nothing but Protits. It takes a month or
so. Very interesting experiment.
 ***
http://www.euroamericanhealth.com/antoin.html
Antoine Béchamp

Antoine Béchamp
(1816-1908) proved that (all the
following quotes are from The Third Element of
The Blood, Antoine Béchamp, 1994, unless
indicated otherwise);
“all natural organic matters (matters that once
lived), absolutely protected from atmospheric
germs, invariably and spontaneously alter and
ferment, because they necessarily and
inherently contain within themselves the agents
of their spontaneous alteration, digestion,
dissolution”.
These agents are of course the self same

M.
Protits of Enderlein. As noted,

Béchamp called them

Microzymas.
Béchamp was able to
prove that all animal
and plant cells
contain these tiny
particles which continue
to live after the death
of the organism and out
of which
microorganisms can
develop. In his book Mycrozymas,
Béchamp laid the foundation for the concept of
pleomorphism.

Whenever there is
anything in nature
that is dying,
beginning to decay,
something comes and
eats it up.
In this case the Protits do, as
they change into the
microbes that come out of the tissue
cells to clean up any toxins or decaying stuff
found in the body. That is what microbes,
germs, are for. They are the result, not the
cause of disease! Rene Dubious reflected this
concept when he noted that Berioge in Bernard
Shaw’s book The Doctor’s Dilemma, was not
entirely wrong when he said…

“The characteristic
microbe of a disease
might be a symptom
instead of a cause.”
As a blood smear slide ages over one to two
days, organisms literally can be seen wiggling
out of the red blood cells, organisms that
change into more degenerate and pathological
forms as the process proceeds. When the
rotting or putrefaction process is over, when
there is nothing more for the newly formed
viruses, bacteria and fungi to eat, they all break
apart again, disappear, and turn back into the
“little dots” they came from, the

Protits/Microzymas/Somatids. T hey eat

themselves and are
reborn, the alchemical
snake forever eating
its tail (the Uroboros)
or the Phoenix, a
mythical bird of great
beauty that was
reborn from the ashes
of its own funeral
pyre.
“As the microzymas of the destroyed bacteria
are also living, it follows that these

microzymas are the

living end of all
cellular organization
which in turn, turn into all living things, beings,

organs everything They are the

end and the beginning
of all physical life. All
cells, organs, all living
forms are built from
these ‘little bodies’.”
When you break an
element down into
smaller and smaller
pieces you end up
with an atom of that
element.
When you break organic

matter, physical life,

down into smaller and
smaller pieces you
end up with the
Protit!, no matter
which form of
organic, live matter
you started with.
Ashes to ashes, as regards the inorganic parts,
minerals and salts of a corpse but the physical
life part, not speaking of the Soul or anything

the Protit,
like that even,

never dies.
Immortality is a nature
of Life and the Protit
too, as Life itself
never dies. The Protit is
the elementary
particle of life, not the
cell, which can die.
The Protit is life per
se, it is in truth the
simple vital unit of old
and is immortal.
***

FERMENTATION
Fermentation followed by putrefaction is a form
of eating, nutrition. In the living and healthy
organism the Protits function as the
physiological and chemical agents of the
transformations which take place during the
process of nutrition. It is only in illness that they
become agents of fermentation. A great deal of
Béchamp’s work concerned the process of
fermentation and therefore nutrition.
“Rather, living organization, Life, is
characterized by the property of producing and
secreting enzymes, each according to the
nature of its species; and the production of the
chemical-physiological phenomena of
transformations called fermentation, acid base,
which are facts of nutrition, that is to say, of
digestion followed by absorption, assimilation,
disassimilation, and so forth, and finally the
ability to reproduce itself if all conditions
dependent upon nutrition are fulfilled.”
This is a nature of Life too, nutrition, and
therefore of the Protit. Things the Protits do are
turn into the bacteria and other organisms,
yeast etc., that ferment the sugar in wine or
curdle milk or rot eggs (it isn’t the “germs from
the air” of Louis Pasteur’s that do these things).
The wastes or by products of these bacteria and
other organisms are the alcohol, CO2, lactic
acid, vinegar etc. that are produced in such
processes. 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 many
scientists; the Tulasne brothers in
France 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 Béchamp
(1830). Enderlein came toward the end of
this.
Pasteur achieved fame through work on
fermentation. Challenged by local distillers’
complaints of setbacks in fermenting alcohol
from beets, Pasteur pinpointed accidental
contamination by stray fungi. Before this it was
thought that the yeast arose by spontaneous
generation. This is the idea that life just comes
out of nowhere, that matter organizes itself,
takes on or is imbued with the property of life
itself. Pasteur gave up this idea in the 1860s
and took its opposite point of view, that of the
germs coming from the air, from outside one’s
self.
“…as I have demonstrated, it is only through the
action of germs of the air, whose existence…
was denied, that this alteration (of organic
matters) occurred which had the appearance of
being spontaneous. [Monsieur] Pasteur having
repeated my experiments, was so convinced
that germs really do exist in the air and that he
had been mistaken, thenceforward declared that
the sole origin of ferments, vibrios (germs) and
the organisms that come out of putrefying
organic matters, was these germs he had
previously disregarded. The

excessive role
ascribed to the germs
of the air by [Pasteur]
and his pretended demonstration of the
imputrescibility (can’t become rotten) of organic
matters in general when protected from the
germs of the air have diverted science down a
deplorable road.” (Antoine Béchamp, “The
Blood,” p. 286)
As from Maria Bleker’s book, Blutuntersuchung
Im Dunkelfeld,
“with this work of Béchamp pleomorphism had
been discovered and the foundation was laid
from which additional research would have
developed, it Pasteur had not interrupted this
important work. Pasteur claimed that all
microbes, regardless of their type and species,
are unchangeable (Monomorphism); that each
type would produce only one specific disease;

that bacteria and

fungi would never
arise from
spontaneous
generation; and that
blood and tissues are
sterile in healthy
conditions.
Diseases, he said,
have their origin from
bacteria that attack
the body from the
OUTSIDE, and stem
from preexisting
bacteria.” See the section on History
on the Home Page for more on how and why
pleomorphism is unknown to modern doctors,
not controversial or anything like that, it is just
unknown in this country. Isn’t that strange?
***
In addition to and in spite of the fact that
Pasteur ignored and in fact plagiarized much of
Béchamp’s work on fermentation, the following
facts have been known for some time.
Chalk, limestone, is composed of the Protits of
the bacteria which living beings of the geological
epochs had become and these materials will
start sugar water fermenting. The

mummies in Egypt are

composed only of left
over Protits which do
the same, start
fermentation. Put
these back in water,
the mummies or the
chalk, and their “little
dots” start rolling,
moving once again.
They just start eating
again, fermenting
their environment
debending on acid
base, after thousands
or millions years. It
never stops, Life.
From Viennese Medical Week, No. 34;

“After slow thawing, Protits

isolated from a
mammoth frozen
more than 50,000
years ago were shown
to spontaneously
show life again and
begin fermentation in
sugar 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 that
Protits isolated from petroleum showed
complete viability and started the fermentation
of sugar. A German by the name of Shwartz
confirmed this also for German petroleum.”
Both private instructor E. Santo and H. P. Rusch
were able to find the same results, namely the

isolation of living
Protits from German
hard coal. The researches of Santo
and Rusch also showed that the Protit could not
be harmed by sulfuric acid or by temperatures
of 1300°C in a ceramics oven.
In addition, Wilhelm Friez also states that the
above researchers and Enderlein, on suitable

able to
nourishing media, were

grow viable bacteria

from the Protits
isolated from the coal
and oil. Streptococci, coliform bacteria
and Proteus species were all isolated from
these substances.
The form of the bacteria isolated by doing the
above,”on suitable nourishing media”, depends
on the nourishing-growth media the Protits are
grown on. How acid that growth media is, what
it is made of, how much oxygen, the rH-
oxidation/reduction factor, lots of things effect

It is the same in the

this.

living body, the

internal milieu, the
environment the
Protits grow in,
determines what form
the Protits take, i.e.
whether they are good
guys or not so good.
The ‘good guys’ turn
into the cells that
regenerate the body,
organ spacific Protits or Somatides (See
chapter on Live Cell Therapy under Treatment
on the Home Page. The not so good guys are
the Protits that go in the direction of
fermentation and putrifaction.

“What happens after

the death of a cell?
The above prove that
the littlest form of the
Lebendssubstanz,
Life substance, is not
destructible.
Robert Mayer proved
the law of the
maintenance of
energy so that no
energy can disappear
without a trace.
What happens to the power source that made
the cell as an expression of or only as the
carrier of the living substance? Because the
living substance is distinguished fundamentally
by the inanimate matter, one cannot let it
theoretically pass over also into inanimate
matter without an essential characteristic loss..”

Law of
This is the

Conservation of
Energy. Life energy
too does not just
come from nothing
with birth and then
disappear into
nothing with death. It
too is conserved. (See
section on Life on the Home Page.)
***
These Protits are what come form the air and
get in sugar water, wine or whatever and do
what they are supposed to do, eat. These
Protits are everywhere, in the air, the ground, in
all living things, plants, animals…In wine they
turn into the yeast cells that do what they have
to do, eat it, ferment it.
As per Antoine Béchamp,
“All cells, organs, all living forms
are built from these ‘little
bodies’.”
The way we were taught of course, was that it
was the cell that did that, that the cell was the
smallest living thing out of which all larger living
things were made. Where did the cell come
from, the sperm, the egg?

“The essential
biological
characteristics of the
microzymas (Protit) is
that they are creators
of cellules (cells) by
synthesis and of
vibrioniens (viruses,
bacteria, fungi) by
pleomorphism and
evolution.”
So the Protits turn into everything, every living
being and organ and every disease producing
organism which turn those very beings and
organs back into the Protits they came from in
the us up.
This type of medicine, Wholistic Medicine, is
opposite in all ways from allopathic medicine,
not opposite really but complimentary - as you
 All
can’t have one without the other.

polarities are like that,

good and bad, love
and hate, you can’t
have one without the
other. This is the ying
and yang of it. Putting
what 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 the
different forms of what are now called
Vibrational Medicine from Michael Gerber’s
book by the same name.
These vibrational techniques include such,
unfortunately ‘specialized’ branches of medicine
as; radionics, electroacupuncture, Biotensor,
pendulums, Bioresonance testing, kinesic pulse
testing (RAC), Applied Kinesiology, Contact
Reflexology, Homeopathy, Pleomorphism,
Herbal medicine, vitamin therapy and on to
regular, modern allopathic medicine - in more or
less descending order of ‘vibrational’
importance.
***
EAV OR Electro Acupuncture According to Voll
EAV began in France in the 1940s with a doctor
named Roger de la Feu. Dr. de la Feu began
experiments with skin conductivity and found
there are points on the body more electrically
conductive than others. These points, for the
most part, turned out to be acupuncture points.
In 1953 a German medical doctor named
Reinhold Voll became intrigued with de la Feu’s
research and explained it.
All the acupuncture points are connected by
lines of force, like wires, that are called
meridians. Voll and his colleagues mapped the
correlation between conductive points on the
skin and internal organs, organ systems and
bodily functions.
Their starting point was their knowledge of
Traditional Chinese Medicine, specifically
acupuncture. Acupuncture has developed over
the last 5000 years. During this period of time,
specific points on the body were mapped as
being responsive to disease and therapy.
Groups of acupuncture points are connected
along fourteen major pathways called
meridians. With the exception of the Governing
and Conception Meridians, each of these
meridians begins and ends on a finger or toe.
Each meridian is connected to one major organ
from which it drives its name, such as the Liver
Meridian and the Stomach Meridian.
The Heart Meridian, for example, ends on the
tip of your middle finger, at an exact point
beside the finger nail. If you inject a radioactive
dye in this exact point it will trace a line to the
heart. If you miss that point by a fraction of an
inch, the dye will go no where. For every organ
there is a point on the end of one of the fingers
or toes. Is this any different than reflexology or
iridology? This is Wholistic Medicine, the
“Whole” being more than the sum of its parts.
These points at the end of the meridians give off
a current of a very particular frequency,
impedance and amplitude, depending on the
organ involved. Everything vibrates at a
particular, very precise, frequency. Acid base
balance effects all of this.
If you hold an electrode, a metal contact point,
not a needle, on the point at the end of the
Heart Meridian or any meridian, it will give off a
signal that is either low (a degenerative
condition or low energy condition of that organ)
or it will be normal or it will be high (an
inflammatory condition). This can be done for all
the 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 medicine
contained in a vial into that circuit which
consists of the patient, the medicine and the
machine. If the medicine vibrates at the same
frequency as the weak signal being tested,
synchronizes, harmonizes, literally,
electronically, with the low signal from the weak
organ, the amplitude or strength of the signal
will get higher as the two frequencies will
superimpose and add together. Then you know
that what is in the vial is the right medicine for
that 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, pendulum
whatever) coming into resonance with the test
subject. The tester must thus be highly
sensitive, must be very good at maintaining a
neutral state and must be able to register the
vibrational changes of the test person.
Radionics is the most sophisticated of these
techniques.
E.A.V. and the rest have the additional
advantage of being highly sensitive. E.A.V. for
example, can detect extremely small amounts of
any type of chemical in a patient; DDT, mercury
intoxication, any chemical. Also, extremely
sensitive allergy testing can be done. Fine-
materials testing as this is called cannot be
performed on many people, since they have
masking disorders such as amalgam
intoxication, dental foci or toxic blockages. For
the same reason, these patients cannot usually
be treated homeopathically or isopathically, their
blockades have to be broken up and detoxified
first, before pleomorphism and its medicines or
any medicines. This is what Base Powder and
diet change are for.
The Rife Microscope and Generator
Royal Raymond Rife with his microscope and
generator provide another striking example of
‘vibrational medicine’and ‘pleomorphism’. All the
different microorganisms and forms they come
in also vibrate at a very precise, distinct
frequencies. Royal Raymond Rife invented a
microscope in the 1930s that could magnify up
to 60,000 diameters, at a time when the best
existing light microscopes could magnify only
1000 - 2000 diameters. Light microscopes are
no better today. The electron microscope can
magnify to 100,000 to 1,000,000 diameters and
had not been invented yet.

Rife Micrograph of Bacillus Typhosus (Typhoid)

Magnification: 23,000X on 35 mm film
Most of Royal Rife’s books were burned by the
powers that be so exactly how to build this
microscope is unclear. Yet, still to this day, if
any doctor is caught possessing one of these
microscopes he or she will go to jail and the
microscope will be confiscated. I include this in
some detail as an example of the types of
sophisticated research that were done before
the 1930s.
This microscope illuminated the specimen by a
narrow, polarized light beam, composed of a
single frequency of monochromatic (one color)
light which caused the specimen to vibrate, to
glow. This microscope could project a beam of
pure color, a beam so finely tuned that it was
composed of only a single frequency of light.
These tunable frequencies went all the way
from the infrared to the ultraviolet.
A monochromatic beam of light, corresponding
exactly to the frequency of the organism (for Dr.
Rife found that each disease organism
responds to and has a definite and distinct wave
length, a fact supported by British medical
research workers) is then sent up through the
specimen, thus enabling the observer to view
the organism stained in its true chemical color
and revealing its own individual structure in a
field which is brilliant with light.
Because these objects glowed with their
characteristic chemical colors they could be
seen at much lower magnification than if they
didn’t. Therefore, Royal Rife was ‘seeing’
viruses in the 1930s and that was just
considered impossible. Still, today, viruses can
only be seen with the electron microscope.
Royal R. Rife’s discovery of the frequency
characteristics of organisms led him to believe
that each individual type of microorganism
should have a resonant frequency that would be
detrimental to it.
His first attempts to electronically destroy them
consisted of unsuccessful tests with infrared
and ulta-violet rays. These frequencies only
caused surface damage so next he tried audio
and radio frequency waves which penetrated
deeper. He thought that somewhere in the
spectrum a harmonic or resonant frequency
would resonate with the vibratroy rates of
disease organisms. He believed that if such a
frequency could be found and applied, the rays
would be fatal to the disease organisms but not
to the normal cells that didn’t vibrate at the
frequency being sent into the patient. This
proved to be exactly right.
“When radio frequencies and audio frequencies
were transmitted through a large rare gas filled
ray tube, the destruction of the organisms by
rays and frequencies is described as being
similar to the phenomenon of the combination of
transmitted potential electronic energy and the
coordinative resonance of critical frequencies or
their harmonics. This is electromagnetic
electrocution where a potential energy level is
reached that is lethal to the microorganism. This
is likened to fragile glass which is shattered by a
sustained note of music tuned to a resonant
pitch or where a potential energy charge is built
up to exceed that level of energy which the
microorganism can cope with and still live. This
was called the M.O.R or Mortal Oscillatory
Rate.”
Using the glass as an example, it is the
frequency of the glass (organism) harmonizing
and resonating with the frequency being
beamed into it that shatters it.
Electroacupuncture. Because both vibrate
together, the glass (organism) can pick up that
particular frequency and literally shake itself
apart. Tuning forks will respond only to their
specific frequency, one across the room exciting
another only if they are tuned to the same
frequency or some harmonic thereof.
Another way the precise frequency or mortal
oscillatory rate for any particular organism can
be found is by isolating and seeing the
offending organism under the Rife (or any)
microscope and then zapping it with frequency
after frequency until the right one is found.
“When the mortal oscillatory rate or potential
energy level is lethally reached, the organism
appears to blow up and disintegrate in the field
and form, at times, a group of agglutinophilic
clumped masses or electrostatic lines”.
The first radio type frequency instrument was
designed and built in 1920. Development of the
Rife Ray to the point where it could be used on
human beings was a proven fact back in 1934.
Tubercular and cancer patients were treated in
private practice and recovered. Most cases
responded within a period of one to two months
in which time the diseases were rendered
‘noninfectious’.
“Rife’s first human clinical work on cancer was
completed under the supervision of Dr. Milbank
Johnson, M.D., Chairman of the Special Medical
Research Committee of the University of
Southern California which included Dr. George
Dock, Professor of the Theory and Practice of
Medicine, Medical Department, Tulane
University of Louisiana, New Orleans; Dr.
Charles Fisher, M.D. of the Children’s Hospital
in New York; Dr. Wayland Morrison, M.D., Chief
Surgeon of the Santa Fe Railway; Dr. Karl
Meyer, M.D., Director of the George Williams
Hooper Foundation; Dr. Arthur I. Kendall,
Professor of Bacteriology at Northwestern
University Medical School in Chicago. The
research was conducted at the Scripps Castle
which was rented over the summer of 1934 for
cancer and T.B. cases. Fourteen out of sixteen
were cured in seven days, Rife said.”
There are Rife generators readily available
today that generate these frequencies. You
simply hold an electrode in each hand and as
the signal passes through your body, you feel
nothing. However, without knowing what the
exact frequency of the organism that you are
trying to destroy is, for which you need the
microscope, these Rife generators are
worthless. Acid base balance is simple and
available.
***
Pendulums, Contact Reflexology, Applied
Kenesthesiology, Radionics,
Electroacupuncture and may others techniques,
are all based on the idea of the tester or the test
coming into resonance with the test subject.
***
Electroacupuncture and the Rife Microscope
were chosen to represent these vibrational
qualities as these are two quite objective forms
of Vibrational Medicine.
***
http://www.euroamericanhealth.com/gaston.html

Gaston Naessens
Gaston Naessens (1924 to present). Here I
would like to introduce the work of M. Naessens
as the diagram of his below puts in schematic
form what we have been been talking about.
Apparently M. Naessens rediscovered this
whole pleomorphic idea and what were earlier
called “Myrozymas” or “Protits”

Naessens termed
“Somatids”.
Gaston was born in Roubaix France in 1924
and by early childhood had shown himself to be
an inventive mind. He received his degree after
WW II and immediately began research into
microscopy, as well as into the nature of
disease including acid base..

Naessens
Like Royal Rife,

developed a light
microscope of his
own design which he
calls the
Somatoscope which
permits enlargements
to 30,000 diameters
with a high degree of
resolution (150
angstroms).
With this he followed Béchamp, Rife and
Enderlein in showing that bacteria and other
microorganisms arise from degenerated sub-
cellular components of higher organisms. What
were earlier called “microzymas” or “Protits”
were called by Naessens —

“Somatids” —
immortal particles of
life which survive the
death of the
individual. When the individual is
unhealthy, the Somatid passes through a
multistage cycle of degeneration and
regeneration, each stage in turn being capable
of independent life and reproduction. The
degenerated stages of Somatids give rise to
bacteria and other microorganisms under acid,
acid base conditions.
The following information and picture are taken
from the Physician’s Handbook for Power, 1995,
by Charlie Pixley, President, WRITER’S AND
RESEARCH, Inc., 4810 St. Paul Blvd.,
Rochester, NY 14617.

“…the Somatid is
indestructible. It
cannot be killed either
by heat or by any
chemical product.
Secondly, the
Somatid has to be
present in any kind of
cellular division.
The Somatid permits growth hormone and that
permits the cell to divide correctly. It is not the
Somatid that secrets the growth hormone. It is
the transformation of the Somatid that liberates
the growth hormone, but it is not a secretion of
the Somatid. The Somatid originates in a liquid
form inside the red blood cell. Each
transformation of the Somatid generates a new
secretion of growth hormones. He also has

Somatids are
noted that

elcetro-charged
particles. The
membrane has a
negative charge, the
nucleus has a positive
charge and this can
be verified by putting
the positive pole of a
magnet near the
slides, all the
Somatids are
attracted to the
positive pull of the
magnet.”
Like the tiny organisms Rife discovered through
his unique microscopes in the 1920s and 30s,
Naessens’ Somatids are pleomorphic (change
form) in nature. Furthermore, Naessens has
discovered that Somatids, the process of
pleomorphism, living in healthy human bodies
go through a normal, recurring 3-stage
pleomorphic sub cellular developmental cycle,
and that each stage of this recurring cycle is
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 what
we have been talking about, the only difference
beings the names assigned to these forms.

***
The normal 3-stages he represents here are of
course the same as the PROTIT, FREE
CHONDRIT, and the LOWER VALENCED
CHONDRIT FORMS of Enderlein.
[#1] As can be seen here what Naessens called
calls the SOMATID is the Protit we have been
talking about.
[#2] in this diagram, called SPORES by
Naessens are the primitive stage FREE
CHONDRITS which as stated, can be seen
most frequently constantly changing between
FILUM and PRIMITIVE GRANULE (Symprotit).
The sizes of these tiny primitive granules vary
between 0.02 µm and 1µm.
[#3] Naessens calls these DOUBLE SPORES
which represent the joining of the Free
Chondrits. This CHONDRIT PHASE begins with
the above enlargement of the Symprotits and of
their Fila. The symprotits and their tails join end
to end giving the chondrit forms a beaded
appearance. This gives them a lively mobility as
they have an even denser arrangement of tiny
symprotits along the length of the fila. The size
of these particles is from 0.5 to 2.0 µm.

Enderlein and
While

other investigators
popularized the
concept of bacterial
growth cycles, most
bacteriologist were
still unwilling to
accept sexual forms
of reproduction.
Another objection was that experimenters were
rarely able to show the complete cycle from
start to finish. Gaston Naessens was the
researcher that was finally able to do this.
“It is often stated that although a sequence of
developmental forms may be observed
microscopically, they do not reveal a cyclical
trend that brings them back to the starting
point…such culture developments should
include a reversion to the original culture stage
rather that manifest merely indefinite transitions
–leaving the new form hanging in the air, as it
were.” (W. H. Park and A. Williams, 1939)
The above includes as it’s first three steps, the
3-stage pleomorphic sub cellular developmental
cycle that is normal in our bodies. These three
forms cause no disease and in fact are used as
the medicines of Isopathic Therapies. None-the-
less, the pathogenicity of the microorganismal
forms rises with the developmental stages and
acid base conditions and as stated;
“THE ONLY EXCEPTIONS ARE THE VERY
FIRST PRIMITIVE STAGES which are the
PROTIT and the CHONDRITS that are of lowest
valences. They are entirely non virulent and the
play a REGULATORY role toward the higher
and more pathogenic stages by decomposing
these through copulatory processes. In that
sense, these stages are termed
REGULATORS.” (Blutuntersuchung Im
Dunkelfeld nach Prof. Dr. Gunther Enderlein;
Maria-M Bleaker, Compiler)
But, if the body’s immune system becomes
substantially weakened due to trauma such as
shock, wrong nutrition, chemical pollution, or
even psychological depression, Naessens has
found as Enderlein and Antoine Béchamp did,
that the Somatids switch gears, so to speak,
and rapidly go into a 16-stage pleomorphic
cycle, producing bacterial forms similar to the
bacterial microorganisms Rife had discovered.
Rife too had documented a similar 16-stage sub
cellular growth cycle through his microscope.
Along these lines, the fourth stages and beyond
in the above diagram can continue and develop
into the more dangerous and pathological forms
that are familiar to us;
[#4] Next the first bacterial forms appear. These
Chondrits form circles (closed loops) composed
of symprotit heads distributed around the ring
made of fila. The small symprotit heads move
together and fuse forming the nucleus. These
are of course the resultant quantum like
conglomeration of Protits which in their
multiplication, the primary tiny lumps begin to
differentiate themselves and increase in size
and get a small spherical form, with a nucleus
residing at the cell wall. These are pathogenic.
[#5] From the above, bacteria with 4 - 8 nuclei
develop, and finally a bacillus or rod with 16 and

Double
more nuclei. These are the

Bacterial Forms of
Naessens. These are
the progenitors of the
masses of bacteria
and bacilli, the Rod
Forms which we
develop in ourselves,
according to
Enderlein and now
according to modern
science.
Cancers are known to
be full of rotting
bacteria and now
heart disease is linked
with the bacteria
Chlamydia
pneumoniae as discussed. Base
powder is necessary.
These later stages get into what I call the

degenerative
(fermentative and
putrifactive) phases of these
miroorganismal forms. As this degeneration
starts with fermentation type processes, by the
formed microorganisms, these later stages are
refered to under the above topic,Antoine
Bechamp and Fermentation
***
http://www.euroamericanhealth.com/mono.html

MONOMORPHISM
Monomorphism is the cornerstone of Robert
Koch’s (1843-1910) and Louis Pasteur’s (1822-

Germ Theory of
1895)

disease. This theory

professes that
disease has a
microbial cause that
is “caught” from the
outside;
“that there are differences among pathogenic
bacteria (ones that can make you ill), and each
has a constant nature…each distinct bacterial
form corresponds to a specific disease and that
the form of this microbe always stays the
samemonomorphism, and causes the same
disease however often the disease is
transferred from one animal to another, the kind
always remains the same and never changes
into other kinds”. How You Rot and Rust by
Steve Denk

1878 Robert Koch

In

wrote Etiology of
Wound Infections
which was the
beginning of the Germ
Theory of Disease.
Where Pasteur’s views were shaped by the
study of fermentation, Koch was affected by his
contact with wounded soldiers. He noted that
the bodies of animals that die of artificially
infected wound diseases (pus from an infected
animal injected into a healthy one) invariably
contained many bacteria…In each case a
definite organism corresponded to a distinct
disease…and that for every individual,
traumatic, infective disease, a morphologically
distinguishable microorganism could be
identified.
In 1880 Koch built on an essay of the relations
between microbial diseases and their causes
from the work of Jacob Henle, his professor of
anatomy. These became known as

Koch-Henle
the>

Postulates.
The following are these postulates which
revolutionized medical epidemiology at the turn
of the century, by laying out the standard proof
of infectivity to the present day. The

postulates dictate that

a microbe must be:
1. found in an animal
(or person) with the
disease,
2. isolated and grown
in culture and
3. injected into a
healthy experimental
animal, producing the
disease in question;
and then recovered
from the
experimentally
diseased animal and
shown to be the same
pathogen as the
original.
***
By the early twentieth century the whole
landscape of medicine had changed. Most of

common killer
the

diseases, including smallpox,

diphtheria, bubonic plague, flu, whooping

cough, yellow fever, and TB, were

understood to be
caused by pathogens.
Vaccines were devised against some, and by
the 1950s antibiotics could easily cure many
others.
By the 1960s and 1970s the prevailing mood
was one of optimism. At least in the developed

infectious diseases
world,

no longer seemed
very threatening. Far more
scary were the diseases that the medical world
said were not infectious: heart disease, cancer,
diabetes, and so on. That these diseases are
now considered to be “infectious” (See Atlantic
Monthly, 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 infections
such as Legionnaire’s disease, Ebola and
Marburg hemorrhagic fevers, antibiotic-resistant
tuberculosis, “flesh-eating” staph infections, and
Rift Valley fever.
“The infectious age is, we now know, far from
over. Furthermore, it appears that many
diseases we didn’t think were infectious may be
cause by infectious agents after all. These
include stomach ulcers, heart disease. The first
cancer virus discovered in 1910 called the
Rous sarcoma virus, certain leukemias,
lymphomas, nasopharyngeal cancer
common in south China, cervical cancer,
stomach cancer, liver cancer, Kaposi’s
sarcoma with Herpes virus 8, mammary-
gland tumors in mice, childhood obsessive
compulsive disorder, Sydenhams’s chorea
which is a rare complication of streptococcal
infection. Streptococcal antibodies find their
way into the brain and attack a region called the
basal ganglia, causing characteristic clumsiness
along with obsessions. Schizophrenia has long
been considered to be possibly “infectious” in
nature.”
The Atlantic Monthly, A New Germ Theory by
Judith Hooper, February 1999, pg. 44.
The catalogue of suspected chronic diseases
caused by “infection”/bacteria to David A
Relman, an assistant professor of medicine,
microbiology, and immunology at Stanford
University, now includes;
“sarcoidosis, various forms of inflammatory
bowel disease, rhumatoid arthritis, lupus,
Wegener’s granulomatosis, diabetes mellitus,
primary biliary cirrhosis, tropical sprue, and
Kawasaki disease. Likely suspects include
many forms of heart disease, arteriosclerosis,
Alzheimers’s disease, most major psychiatric
diseases, Hashimoto’s thyroiditis, cerebral
palsy, polycystic ovarian disease, and perhaps
obesity and certain eating disorders. Multiple
sclerosis has been linked to the human herpes
virus 6, the agent of Roseola infantum, a very
mild disease of childhood” (ibid.)
***
Where do these bacteria come from…?
To modern science, this is still an unanswered
question.
***
Regarding stomach ulcers;
In 1981 Barry J. Marshall became interested in
incidences of spiral bacteria in the stomach
lining. The bacteria were assumed to be
irrelevant to ulcer pathology, but Marshall and J.
R. Warren noticed, serendipitously, that when
one patient was treated with tetracycline for
unrelated reason, his pain vanished, and in
endoscopy, revealed the ulcer was gone.
An article by Marshall and Warren on their
culturing of “unidentified curved bacilli”
appeared in the British medical journal,The
Lancet in 1984. No one listened until finally
Marshall personally ingested a batch of the
spiral bacteria and came down with painful
gastritis, thereby fulfilling all of Koch’s
postulates.
There is now little doubt that Helicobacter pylori,
found in the stomachs of a third of adults in the
United States, cause inflammation of the
stomach lining. In 20 percent of infected people
it produces and ulcer, Nearly everyone with a
duodenal ulcer is infected. H. pylori infections
can be readily diagnosed with endoscopic
biopsy tests, a blood test for antibodies, or a
breath test. In 90 percent of cases the infections
can be cured in less than a month with
antibiotics.
***
Where do these bacteria come from?
You don’t “catch” them, so infectious is not the
correct word.
***
Regarding arteriosclerosis;
It has recently been discovered that
arteriosclerosis is also a bacterial process.
Notice I did not say, ’caused by bacteria’. The
plaques of 99% of patients with hardening of the
arteries have the bacteria Chlamydia
pneumoniae in them.
According to The Atlantic Monthly, Feb. 1999,
Chlamydia pneumoniae is a newly discovered
bacterium that causes pneumonia and
bronchitis. The germ is a relative of Chlamydia
trachomatis, which cause trachoma, a leading
cause of blindness in parts of the Third World.
C. trachomatisis perhaps more familiar to us as
a sexually transmitted disease that, left
untreated in women, can lead to scarring of the
fallopian tubes.
Pekka Saikku and Maija Leinonen of Finland
discovered the new type of chlamydial infection
in 1985 though its existence was not officially
recognized until 1989. Saikku and Leinonen
found that 68 percent of Finnish patients who
had suffered heart attacks had high levels of
antibodies to C. pneumoniae, as did 50 percent
of patients with coronary heart disease, in
contrast to 17 percent of the healthy controls.
While examining coronary-artery tissues at
autopsy in 1991, Allan Shor, a pathologist in
Johannesburg, saw “pear-shaped bodies” that
looked like nothing he had seen before. Cho-
Chou Kuo, of the University of Washington
School of Public Health, found that the clogged
arteries were full of C. pneumoniae. Everywhere
the bacterium lodges, it appears to precipitate
the same grim sequence of events: a chronic
inflammation, followed by a buildup of plaque
that occludes the opening of the artery (or, in
the case of venereal Chlamydia, a buildup of
scar tissue in the fallopian tube).
Recently a team of pathologists at MCP-
Hahnemann School of Medicine, found the
same bacterium in the diseased section of the
autopsied brains of seventeen out of nineteen
Alzheimer’s patentsand in only one of nineteen
controls.
Whether antibiotics help any of these diseases
or not remains to be seen. The first major
clinical trial is under way in the United States,
sponsored by the National Institutes of Health
and the Pfizer Corporation: 4000 heart patients
at twenty-seven clinical centers will be given
either the antibiotic azithromycin or a placebo
and followed for four years to gauge whether
the antibiotic affects the incidence of further
coronary events.
Whether the antibiotic helps coronary heart
disease or not does not explain where these
bacteria come from and thereby how to effect a
causalor real cure. That this issue of Chlamydia
in the tissues, is still being pursued by the
modern pharmaceutical firms as “infectious” in
nature, amenable to the treatment with
antibiotics and/or vaccines, is an another
example of how entrenched Pasteur’s and
Koch’s ideas are in the whole of medicine from
the 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 have
antibodies to C. pneumoniae, and even if
colonies of the bacteria are found living and
breeding in diseased coronary arteries, is it
certain that the germ caused the damage?
Perhaps it is there as an innocent bystander, as
some critics have proposed.”
As will be shown, the above bacteria,
Chlamydia pneumoniae andHelicobacter pylori
come out the red blood cells themselves The
blood is teaming with microorganisms,
especially if it sits on the microscope slide for a
few hours. You can watch this process under
any microscope, anywhere, anytime.
***
This is a funny situation really. Modern,
allopathicly trained physicians <can’t see these
things, literally. You can see all these organisms
in the blood with any microscope, so its not a
matter of “seeing is believing”. More, it’s a mater
of “believing is seeing<”, so you can even
dareto take a look in the first place.

In summary:
1. The blood is not sterile, as we were led to
believe after the Second World War with
Hitler’s ideology of the creation of a ‘pure’
blooded race.

2. The cell is not the

smallest living thing.
3. Organisms come of the blood and tissues to
decompose those tissues when they can no
longer live and support their own metabolism
within the environment they find themselves in,
in their internal milieu.
4. These same organisms can also come out of
the blood and regenerate new tissues and
organs; depends on which way we want to go.
One needs a source of Protits in the diet, organ
meats provide these, organ specific
Protits/Somatides. (See Live Cell Therapy )
Continue on to: The Hystory of the
Monomorphism Pleomorphism Debate
http://www.euroamericanhealth.com/hysty.html
THE HISTORY OF THE PLEOMORPHISM/
MONOMORPHISM DEBATE
WHY PLEOMORPHISM IS UNKNOWN TO
MODERN MEDICINE
A dichotomy in medical speculation, an
unresolved philosophical conflict, has existed
from ancient times to the present. This conflict is
between two theories known traditionally as
Empiricism and Rationalism.
“While this conflict can be discerned in the
earliest writings of the Hippocratic Corpus, from
the fifth century BC, the names Empirical and
Rationalist became current in Rome at the
beginning of the Christian era - designating
groups of physicians competing with one
another ideologically and economically.”
(Divided Legacy, Harris Counter, pg. xv.)
The main form of medicine practiced today is of
the Rationalist or Rationalist/Methodist point
of view. Rationalism involves a mechanistic or
chemical understanding of the human organism.
It maintains that life itself can be explained by
physics and chemistry, or, more generally
speaking, by mechanics. Rationalism maintains
that there is no essential difference between the
structural chemistry of life and that of inanimate
nature.
This idea of the body viewed as a machine
composed of many little machines is contrary to
the Empirical view that the laws governing the
living organism differ from those of lifeless
matter. This concept is called Vitalism.
The person as a whole is something different
from a collection of viscera; the wholeness gives
some extra, if undeniable, quality to the
individual organs. Today we pay for our
knowledge of the parts in ignorance of the
whole.
Vitalism maintains that;
“the organism is reactive, at all times coping
with, and attempting to overcome, the stresses
which impinge upon it from outside. It behaves
purposively, the nature and form of its reaction
being determined by the specific environmental
stress encountered. It responds to challenge,
which no aggregate or assembly of non-living
substances can ever do”. (Divided Legacy,
Harris Counter, pg. xvii.)
In 1946, the quantum physicist Erwin
Schroedinger pointed out…
“that biological material has a totally different
character from all other states of matter density
of life - that is, the information stored per unit
volume - and that of any inorganic system that
has not been produced by living forms…The
silicon chip must use many orders of magnitude
more atoms to store the same amount of
information as a gene.”
This is vitalism, Quantum Vitalism.
According to Harris Coulter, no perfect
Rationalist therapeutic doctrine has ever been
devised. Even Galen, who of all physicians in
history worked hardest at theoretical
consistency, left a few loose ends. But the
formulation which emerged in the late
nineteenth century - the specific bacterial
disease treated by the ‘contrary’ medicine -
seemed to its devotees an almost unblemished
depiction of the Rationalistic reality. The above
is what is what ‘modern’, allopathic medicine
has become.
The microbe and the Germ Theory of Disease
became a new organizing principle in medicine,
bringing much scattered clinical data together
into a series of new specific entities with some
cures, specific cures. The ‘germ theory’ was
bolstered by the doctrine of ‘monomorphism’ -
meaning again that microbial genera and
species are fixed and eternal, that the form of
each microorganism associated with a specific
disease always stays the same and always
causes that same disease.
“Monomorphism was above all, a practical
response to an emergency situation in
bacteriology. This concept of disease, emerged
in a context of intense anxiety over the social
depredations inflicted in every country in Europe
and the United States by a series of diseases
whose very names - tuberculosis, diphtheria,
typhus, cholera–were chilling reminders of
human mortality,” (Divided Legacy, Harris
Coulter, pg. 37)
More to the point;
“involved in the concept of Pleomorphism was
the role and importance of the host organism -
THE PATIENT! Microbes altered their forms in
response 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 organism
or patient was an active participant in
infection and disease - in contrast to Koch and
Pasteur and the monomorphists who held the
microbe to be all-powerful, the host organism a
passive victim. Pleomorphism meant
downgrading the microbe, since the host, by
resisting the latter’s onslaught, could alter its
characteristics and make it return to a normal
form as again. The patient had control over
the bacteria, not the other way around. The
microbes are the result, not the cause of
disease.
Even the common “communicable” diseases,
e.g. strep throat or chickenpox, can not take
hold, grow, if the internal milieu is not conducive
to their reproduction. This is what base powder
does. As stated before, one third of people in
Europe did not get bubonic plague. In treating
cancer with isopathic medicine, for example,
one does not attack the tumor at all, instead one
changes the environment, the internal milieu
that caused the cancer in the first place.
What this all means then, this
pleomorphism/monomorphism controversy, is
that at its most fundamental level it has
socioeconomic dimensions that still effect us
profoundly today.
“Accepting Pleomorphism meant acknowledging
the host organism’s, the patient’s capacity to
defend itself (him or her) against, and
dominate, the microbe.
Monomorphism, on the contrary, enhanced the
role of the microbe in disease, and
consequently that of the physician who combats
the microbe. This is the principal reason for
the instinctive hostility of the majority of
physicians to Pleomorphism and
Whoistic/Alternative Medicine in
general.“(Ibid. pg. 39)
***
This gives the responsibility for health back
to the patient…
 if they want it !
***
Pleomorphism has been a great threat to this
“control” factor. This control factor means;
“control of the disease with poisons that need monitored
and controlled, controlling therefore, the patient and their
pocket book.”(Ibid, pg.39)
The phenomena are forced into categories
which can be manipulated to make a living from
the practice of medicine. The monomorphists
have identified their doctrine with science itself,
as science itself, that Monomorphism is a law of
nature, which it is not. This viewpoint has,
through the years, taken on such an aspect of
truth that to question it now seems a scientific
sacrilege.
The followers of Koch proclaimed
Monomorphism with ‘religious fanaticism’,
stated Max Gruber in 1885. F. Loehnis stated in
1922 that the intransigence and verbal violence
displayed by the various factions in this conflict
resembled certain historic theological quarrels.
This battle has been going on for a long time!
For all these reasons, Monomorphism was at
first excessively rigid, even dogmatic. Rene
Dubious states that Koch and Pasteur;
“overestablished” the doctrine of the specificity
of disease causes and that blind acceptance by
several generations of bacteriologist of the
dogma of constancy of cell forms and
immutability of cultural characteristics
discouraged for many years the study of the
problems of morphology, inheritance, and
variation in bacteria.
“Upon clear contemplation, not only the cancer
problem but the entire pathology, as taught by
school medicine, have become unsustainable.
In any case, it is extremely revealing of the
insight that Prof. Sauerbruch, in following a
series of cancer patients he treated isopathically
(with pleomorphic medicines) in his hospital at
the Charite and who, subsequently, in the
closing years of his life again and again had
pointed out that:
“IF ENDERELEIN, AND NASSONS ET AL, ARE CORRECT,
THEN WE CAN THROW OUT OUR ENTIRE LITERATURE”.
(Blutuntersuchung im Dunkelfeld, nach Prof. Dr.
Günther Enderlein, pg. 77, 1993, Compiled by
Dr. med. Maria M-Bleker)
The consequences of this are profound.
***
Also, there are many problems that
monomorphism has not been able to explain.
Bacterial resistance to antibiotics is one that is
becoming quite critical in today’s world. The
bacteria don’t ‘mutate’ into a drug resistant form,
they just change, evolve, de-volve. There is a
big difference between the two forms of change.
Mutation occurs rarely, Pleomorphism occurs all
the time.
Another problem has been microbiology’s
inability to classify microorganisms in proper
families and the like, genera and species
because the organisms do change form.
Despite the inability of a century of
bacteriological research to define the
boundaries of these supposed genera and
species, the suggestion is never heard that the
search for them should be abandoned. The
monomorphist conviction that genera and
species do exist somewhere still retains a
peculiarly tenacious hold.
In school we only cultured bacteria on very
particular growth media. For example, all the
strep “germs” in hospital microbiology labs
anywhere are grown on blood agar (sterile
human or rabbit blood mixed with agar).
Therefore all the germs grow the same way, all
streptococcal bacteria look like little round balls
in strings, if they are grown on blood agar, at a
very specific pH’s, pH 7.6 - 7.8, and
temperatures. Change any of these conditions,
the pH etc. and the germs change form.
According to Enderlein’s formulations, the
protits which are used as medicine actually are
grown on a culture medium composed of a
broth made of asparagus and agar.
In medical school
we never grew anything on an asparagus/agar broth so,
we never saw protits!!!
What you see
is determined by how you look at something.
 Is this science?
***
The thing is, that to classify all the different
forms that bacteria can and do assume, in the
terms of contemporary microbiology would be a
taxicological (taxonomy- the science of
classification) nightmare. We knew in school
that syphilis microbes could grow as fungal
forms, on old culture plates. These plates were
just ignored and thrown away.
To say that the above syphilis organism began
as a protit, somewhere, sometime, in some
other generation even, and then went through
all the stages that it would take to end up on an
old culture plate in some microbiology lab,
would require an impossible classification
system, if done in the mono-morphistic way.
This begs a quantum system of
classification, like the definition of vitalism
given by Schroedinger above.
(As an aside, when these organisms do change
form, for example when the protit changes into a
virus, well, it just changes, instantaneously - as
if it made a quantum jump. You have to watch
awhile though, through the microscope, to see
this.)
“If Pleomorphism were correct, scientific
investigation of bacteria would be an
impossibility. One grasps one’s head to make
sure it is still on the shoulders. The whole
structure of our science threatens to collapse.”
(F. Loehnis, 1922)
Winogradsky in (1930) called pleomorphism;
“chaotic…truly, the whole of a researcher’s
lifetime would hardly be sufficient to follow
directly all of the transformations indicated by
[Felix Loehnis].”
Hans Zinsser in 1932 stated that;
“If the pleomorphic surmise is a correct one,
acid base–the entire structure of our attitude
toward the biology of disease must be
changed…If these conclusions are correct, this
will bring about a revolution in biology…At the
present time it is dangerous for the progress of
bacteriology to accept this work until it has been
satisfactorily demonstrated…Nothing short of
absolute proof should be accepted or we may
risk making research more difficult than it
already is.”
To this end, the French microscopist and
bacteriologist, Gaston Naessens has described
the whole cycle of the Somatid/Protit,
maintaining that all bacteria are derived from a
single Somatid/Protit.
“Naessens demonstrates and describes each
such stage, with return to the starting point, thus
meeting an earlier objection as to the idea of a
bacterial life cycle. In effect this view rejects all
bacterial classification. The French have a
proclivity for Pleomorphism, are more radical,
and also more theoretical, and contend that the
whole of the earth’s microbial life constitutes a
single collection of genetic material,
“GENOME”, (the self reproducing portion of a
cell), adequate to supply every microbial genus
and species.” (Divided Legacy, Harris Coulter,
pg. 197)
Sonea and Panisset, representing the French
view, maintain that;
“each microorganism has access to this
genome (genetic pool) and borrows from it
genes as needed - employing conjugation,
transformation, transduction, and other
mechanisms of gene transfer which are still
incompletely known. Genes are relinquished
when environmental circumstances no longer
require their use for survival.”(Ibid pg. 196)
The German view represented by Günther
Enderlein is not much different. Enderlein finds
that all microorganisms originate from a Protit
that, in its culminant and most degenerative
phase, turns into the fungus Mucor racemosis.
In going from the original Protit to the fungal
form, all known bacteria are manifested, if the
conditions for their manifestation, are right. This
fungus then, Mucor racemosis, is the end, of the
beginning. After it has decayed all the organic
matter present it disintegrates back into the
Protit it came from. Acid Base
***
Of all the impediments to the acceptance of
Pleomorphism: Rationalism vs. Empiricism; the
need for Magic Bullets, specific cures and
disease entities in the face of the epidemic type
diseases prevalent at the end of the last
century; the “control” factor consisting of the
contradiction between the patient healing his or
herself and the doctor doing the job with
allopathic, potentially dangerous drugs; the
religious fanaticism and intransigence of the
monomorphists; the inability of modern science
to classify microorganisms into families etc. and
the other inconsistencies contained in the
monomorphist ’science’ including drug
resistance; of all these impediments I feel the
most important one is the so called
“complexity” factor.
“The phenomena are forced into categories
which can be manipulated and named, to make
a living from the practice of medicine, as easily
as possible.” (Harris Coulter)
It isn’t complex.
You just need to know more than one form of
medicine.
[The link bar feature is not available in this web]
Tags: colloids of life
Prev: ATP LIQUID MINERALS- Product Brochure (FREE to the Poorest of
the Poor)
Next: What is the Importance of pH? By - ATP Global Foundation. Source:
http://www.zeolifeasia.com/hrq.php
reply share
audio reply video reply
Add a Comment
Top of Form
U2FsdGVkX19b8 reply 1

reply 8595:U2FsdGV kX

F
o
r
:
Add a comment to this blog entry, for everyone
Send atpcoop a personal message

S
u
b
j Re: Colloids of
e
c
t
:

Quote original message

Submit Preview & Spell Check

submitted
Bottom of Form

© 2009 Multiply, Inc. About · Blog · Terms · Privacy · Corporate · Advertise · Contact · Help