The Germ Theory of Disease Refuted by Many Researchers

All mammals and most likely all other animals have two parasites. They are in a particular relationship and supplement each other.

Those two parasites (endobionts) are called Mucor racemosus Fresen and Aspergillus niger van Tiegham.

Béchamp, 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 Béchamp 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 Béchamp 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.

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 (not infective) 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."

The second major error originates from William 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 Béchamp 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.).

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 Professor Gunther 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 (white blood cells) but from an erythrocyte (red blood cells)! See All Human Blood Is Infected With Bacteria, by Alan Cantwell, M.D.

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

1. E. coli
2. salmonella typhi
3. mycobacterium tuberculosum
4. yeast forms
5. BX (bacterium X)
6. 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. 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.