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The argument about the nature of disease became more
divided in the 19th century France. Louis Pasteur was a French chemist who
lived between 1822-1895. He described the scientific basis for fermentation,
the process used to make beer and wine, showing that it is carried out by
microorganisms, called germs. Pasteur learned that these germs are also
responsible for spreading contagious disease, at least infectious disease,
that came from outside the body as an invader. |
Louis Pasteur
(1822 -- 1895) |
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Claude Bernard was a French physiologist who first discovered that the
body makes every effort to maintain a steady internal state (the internal
environment). He included the immune system as part of that system.
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| Claude Bernard (1813-1878) |
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Claude Bernard
(1813-1878) |
Antoine Be`champ was a French microbiologist and medical
school professor who was often at odds with Pasteur. Pasteur believed that
bacteria were the significant players in infectious diseases. Be`champ believed
that the internal environment described by Bernard was the significant player.
He attempted to prove this at a medical meeting by drinking a glass of water
containing a large quantity of cholera germs. He was not effected by the deadly
cholera, proving that his system was more important than his encounter with the
bacteria.
In addition to his debate with Pasteur about the internal or external cause of
infectious disease, Be'champ identified tiny biological particles which he
called microzymes. He found microzymes in all cells, dead or alive, and in
ancient chalk deposits.
He found that these fundamental biological units could change into pathological
bacteria. This was the beginning of the concept of pleomorphism (many forms,
described below). This means that something can change into many different
things.
On his deathbed, Pasteur conceded that he was wrong and Be'champ was correct.
However this had very little effect on Pasteur's disciples. The concept of
Pasteur that infectious diseases were caused by coming into contact with
pathogenic bacteria became the standard belief of most physicians today. Lost
for many years, the concept of Be'champ (pleomorphism) was that the pathogen
came from within the body when the internal environment was out of balance.
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Gunther Enderlein |
Be'champ's pleomorphism description that a basic building unit of the universe which he
called microzymes was ignored for many years. German physician and
bacteriologist, Gunther Enderlein described the life cycle of bacteria in 1916.
He found tiny particles in blood, which he called protits. Under normal
conditions, he found the protits to work symbiotically with the immune system.
However, when the pH of the blood changed the protits changed into pathogenic
bacteria. The protit merge to form rudimentary nuclei called symprotits. The
symprotits then add a tail to form a sperm shaped unit called a spermit The
spermits enter the red blood cells (RBC) and one can see multiple tails sticking
out of the cells as they enter. Once inside the red blood cells they begin to
multiply and mature. They consume the red blood cells as they grow. As the
volume of red blood cells decreases, the maturing forms look like barnacles on a
ship. However, the forms are really inside the transparent cell membrane of the
red blood cell. The form gradually mature and then exit the red blood cells as
bacteria without cell walls =mycoplasma. When mycoplasma enter other cells, they
are called rickettsia. Mycoplasma and rickettsia are the major cause of chronic
diseases.
One of the forms that can exit the RBC's
is Proprionbacteria acne. This bacterial form is often found in the mouth around
the teeth. It is also the precursor of the fungus which is present in all cancer
= Mucor Racemos fresen.
It is likely that the microzyme of
Be'champ and the protit of Enderlein are the same thing. Certainly they both
reached the same startling conclusion. They discovered that an element normally
present in all cells could become pathogenic bacteria from inside the body. Thus
it is not necessary that the body be externally exposed to pathogenic bacteria
to become ill. Enderlein discovered that all cancer cells contain the same
fungus, Mucor racemos fresen
In the 1940's and early 1950's Enderlein
developed biological remedies from plants and fungal extracts, which he found
capable of changing pathogenic bacteria back into harmless protits by changing
the tissues` pH back to normal. In the 1920`s and 1930`s Royal Raymond Rife, a
bacteriologist in Los Angeles, was trying to find the cause for cancer. He
discovered that a cancer causing organism was found to have four forms which he
called the BX (associated with carcinoma), Virus BY (associated with sarcomas)
Monoccoid forms (found in more than 90% of cancer patients) and crytomices
fungi. He found that these forms could change in the laboratory from one form to
another in 36 hours. Note the finding of those similar to Enderlein. Rife
discovered that these pathogens could be killed with a radio frequency of 2127
or 2128 Hz was used at the University of California School of Medicine with
documented success. All 16 terminal cancer patients were successfully treated
under the observance of a team of doctors from various universities. However, he
was later accused of quackery and taken to court. He was found not guilty, but
his work had been burned and his equipment destroyed by politics.
In 1946 a French scientist named Gaston
Naessen noted some unusual particles in blood samples he was studying. Because
they are barely visible with standard light microscopes, he set out to develop a
different type of microscope. He developed a special type of "Dark Field"
microscope in which one could see the interior of living cells in their live
state. (Light microscopes require that the tissues be killed and dyed with stain
to reveal their internal parts). Using this high powered dark-field microscope,
he defined the particles which he called somatids (small bodies) Naessen found
that these somatids were capable of pleomorphism. They could change from
particles the sizes of viruses to bacteria, yeast and fungal forms! He also
noted that chronic diseases such as rheumatoid arthritis, multiple sclerosis,
lupus and cancer showed fungal forms in the blood cells.
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