Other views on BACTERIA - what are they?

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Some trong possibilities that ring true and possible to me

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http://www.newtreatments.org/Basics/ga/503/Synthesis%20of%20the%20Work%20of%

20Enderlein,%20Bechamps%20and%20other%20Pleomorphic%20Researchers

Synthesis of the Work of Enderlein, Bechamps and other Pleomorphic

Researchers

©Copyright 1997 by Dr. Karl Horst Poehlman, Australia

(Explore Issue: Volume 8, Number 2)

All mammals and most likely all other animals have two parasites. They are

in a particular relationship and supplement each other.

Those two parasites or endobionts are called Mucor racemosus Fresen and

Aspergillus niger van Tiegham.

Bechamp, Rife and Naessens could demonstrate that they are virtually

indestructible. Neither carbonizing temperatures nor radioactive radiation

can harm them.

Enderlein believed that they entered the cells of higher differentiated

cell colonies as parasites while Antoine Bechamp believed that they

are the

essence of life in the cell.

The endobiont is always present and cannot be removed from the living

cell;

the clinical symptoms of a disease depend on the stadium of its

development. This " fungal parasite " can be present in all tissues and

organs.

Today's mainstream medicine is governed by consent of opinions rather than

hard scientific evidence. This is the reason why false and fraudulent

teachings can survive even though the truth has been known for a long

time.

There are basically three dogmas that are still adhered to:

The first and probably most disastrous error originates from Ferdinand

Cohn, who in 1870 proclaimed that all microbes and bacteria have only one

form (Monomorphism). This was also taught by Louis Pasteur. This teaching

was opposed to the teaching of Antoine Bechamp who, roughly at the same

time, could demonstrate that microbes can alter their form and appear as

different germs (pleomorphism). Enderlein basically confirmed this and

many

other researchers after him.

All microbes that permanently live in our organism go through the same

stages of their development. According to Enderlein they are as follows:

Colloid -- microbe (primitive phrase), bacteria (middle phase), fungus

(end

phase). Royal Rife could show that with increased toxicity the

transformation goes into non-filterable forms, not visible with ordinary

light microscopes (viruses). This also disproves Pasteur's infection

theory

as the " pathogenic bacteria " do not have to come from outside and in fact

hardly ever do. The state of development depends on the medium the germ

lives in:

Primitive phases live in a strong alkaline pH

Bacterial phases live in mild alkaline pH

Fungal forms live in a medium acid pH

Viral forms live in a strong acid pH

In order to keep the right environment, every microbe produces an organic

acid:

Mucor racemosus -- lactic acid,

Aspergillus niger -- citric acid.

The pathogenity of a particular germ lies only in one phase of its

development. Our " constant tenants " are the only exemption where all but

the very early stages are pathogenic. Only what Enderlein termed

protit and

chondrite are completely avirulent and play an important regulatory

role in

reducing higher virulent forms to primitive forms by copulating with them.

Those phases can be easily seen in living blood under the microscope, but

only in " darkfield " as the small primitive forms are invisible in

" brightfield. "

Even Louis Pasteur said in the last minutes of his life: " Bernard is

right;

it is the soil and not the germ, that makes the plant grow. "

The second major error originates from Harvey who stated in 1651

(!!) that the cell is the smallest unit of life. This statement can be

easily understood considering the very limited magnification and

resolution

of the microscopes of his time. Enderlein demonstrated and published in

1921 and 1925 that the smallest unit of life is not the cell but the

protit, named microzyma by Bechamp and somatid by Gaston Naessens.

The third error came again from Pasteur who claimed that the blood is

sterile, a piece of nonsense still taught by modern bacteriologists. A

look

through a high power darkfield microscope quickly disproves this theory

(provided one wants to see). Pasteur had the talent of teaching the

biggest

nonsense and of making people believe it. It is now well known that he

even

falsified the results of his research when it did not show the results he

wanted. He was also quite ready to plagiarize the results of others. The

vaccination fraud is based on his manipulated " research " . Whole

generations

of researchers followed his example. Modern " scientific medicine " became a

collection of long disproven theories (blood clot and obstruction

theory of

coronary heart disease, germ theory and infection theory, single cell

theory of cancer, etc.).

Microbes follow the same basic urges as other living beings:

a) Urge for survival;

Urge for sex and multiplication;

c) Urge for power.

a) The urge for survival shows in the urge to eat. Our " endobiont " eats

protein. Naturally it also has a typical metabolism which produces lactic

acid (Mucor racemosus) and citric acid (Aspergillus niger) as mentioned

before.

The urge for sexual multiplication can be seen in the strong attraction

in all stages of development from the very first stages, even when

they are

within blood cells. This leads to the formation of " clots " (called

symplasts) which can block our blood vessels with the relevant

consequences. Symplasts can be made out of colloids or symprotids,

thrombocytes, erythrocytes, leukocytes or a mixture of all.

c) The urge for power is seen in the urge to combine with other cells to

form a higher, more stable form. In this combination (systatogenesis), all

stages of development can be involved as this is not a sexual combination.

But it is strictly within the same kind. This combination stops all forms

in further development. On the other hand those formations are a major

obstacle for the circulation. (They can be impressively demonstrated by

staining and are often misdiagnosed as fungus structures.)

All those structures can be easily observed in the living blood, and from

the observed stages we can draw conclusions regarding the health of our

patients.

We have to finally stop believing in long disproven theories and stick to

the old principles of science: when reality shows results different from

the theory, the theory is wrong, not reality. Medicine has to change

from a

religion with popes and dogmas into a real science.

The most important terms created by Prof. Enderlein

Ascit Name for all phases of bacterial development. The nuclei are in a

row (katatakt)

Chondrit Name for the very first primitive phases

Cystit a Mychit with polydynamic nucleus

Dioekothecit a Colloidthecit, filled with very small nuclei

Filum linear unification of several Protits

Kolloidthecit a cell without nucleus

Mych the symprotit in its function as nucleus in a cell

Mychit the first bacterial cell; it has only one nucleus

Protit the most primitive form of every microbe

Spermi the sexual cell = 1 Filum and 1 Symprotit

Symplast the unification of all different phases in order to copulate

Symprotit the three-dimensional unification of several protits (spherical

shape)

Synascit name for all bacterial phases with multiple nuclei in all

directions

Systatogenie the desire of primitive units to get together and form a

more

stable form

Thecit a Mychit with more than 8 nuclei

Thrombocyte a Mychit with 2 to 8 nuclei

Enderlein could find the following errors in the official teachings:

Bacterium paracoli is not a " degenerated " Bacterium coli but the Phytit of

the endobiont.

The cause for the infectivity of filtrates from tuberculous material

is the

chondrit of mycobacterium tuberculosum. This was already proven in 1910 by

Fontes (Brasil) -- (cf. Mem. Instit. Oswaldo Cruz, I, 2, 1910, pg. 186).

Dostal could demonstrate that it is easily possible to convert

mycobacterium tuberculosum into a spherical form (Basit) -- (Wien. Med.

Wochenschr., 60 Jahrg., 1910, pg. 2098-2100 and 63. Jahrg. 1913)

Fibrin is not the result of precipitation of protein but Thecits of the

endobiont.

Megacariocytes (Metschnikov) are not " normal " cell elements but a mass

infestation with primitive forms of the endobiont which disabled the

ability of the cell and nucleus to divide. They do not originate from a

leukocyte but from an erythrocyte!

The megaloblasts in anaemia perniciosa are not erythrocytes with

nuclei but

erythrocytes which have a colony of endobiont chondrites (pseudonucleus)

inside them which causes the abnormal size.

Normoblasts are erythrocytes that do not have a nucleus but a

pseudonucleus

made out of colonies of endobiont-chondrites.

Macrocytes are enlarged erythrocytes without nucleus. This is also caused

by a massive invasion of endobiont-chondrites.

Reticulocytes (Heilmeyer) are not erythrocytes with special organellae but

erythrocytes that have a little " tree " of endobiont-chondrites inside.

The Round- and Spindlecells of sarcomas do not contain round-and spindle-

cells of the host but (round) cells and (spindle) cells of mycelias of the

endobiont.

Royal R. Rife stated that there are only about ten different germs.

All the

various appearances that are classified in bacteriology are adaptations

(pleomorphic changes) to the toxicity (or varying pH) of the medium they

live in. He describes the pleomorphic development of E. coli as follows:

E. coli

salmonella typhi

mycobacterium tuberculosum

yeast forms

BX (bacterium X)

BY (bacterium Y)

Rife could isolate BX from all cancerous tumors, the BY he found in

sarcomas. The change from one form into another happens in about 36 hours.

BX and BY pass readily through 000 ceramic filters and cannot be seen

in an

ordinary light microscope.

Antibiotics severely increase the toxicity of the host organism,

especially

when highly toxic halogenated antibiotics are used. The " disappearance " of

a particular germ from the culture does not mean that the germ is dead; it

only became invisible due to its transformation into an invisible form.

That means, that the host organism is now in a cancerous state.