The apathogene development stage develops only if the accord

Enderlein's system of the Bacterium cyclogeny, which I contrary to E. K l i e n e b e r g e r less than complicates, but than logical product of its comparatively morphologic, bacteriological and zoo-logical studies regards, most likely as theoretical construction due to of single observations developed. Whether however its teachings correspond to the reality, should not be by any means said thereby. Read more

The progressive degenerative development can lead the Enderlein to different symptoms

The progressive degenerative development can lead the Enderlein to different symptoms as the "complex of the Endobiosis" designated. All these illness forms against-placed always the largest difficulties to the medical art and resistances.

In addition belong among other things: chronic illnesses, container wall changes, pathological coagulating procedures, Gelosen, Rheumatism, Arthritis, Spondylose, Tonsillitis, Diabetes, Lymphogranulomatose, charge, Tumors of all kinds (also good-like as well as their preliminary states), Anemia, Leukemia, Bronchitis, Cerebral scleroses, paralyses, allergies etc. Read more

The two most important Symbionts are:

A) the Mucor Racemosus Fresen and b) the Aspergillus the Niger van Thieghem; in all their stages from the virus to the mushroom. The appropriate bacteria forms of these Cyklod are A) Leptotrichia buccalis Robin and b) Mycobakterium tuberculosis. Read more

as soon as the equilibrium of blood serum between mineral salts (Base, alkalis) and acids longer time is disturbed by wrong

Professor Dr. Enderlein says:

"as soon as the equilibrium of blood serum between mineral salts (Base, alkalis) and acids longer time is disturbed by wrong, no biologic nutrition toward the sour side, sets an endless reproduction of these Endobionten and at the same time the ascent of these to parasites transformed Urkluempchen into the large development series of the parasites. The more highly the Endobiont in its development series rises, the more increases its injurious character and the more largely is the disturbance of the acid Base of equilibrium, thus in a mutually increasing changing relations." Continue Reading >>

Enderlein recognized, which results the formation of Blood clots from sticking together red blood corpuscles

Enderlein recognized, which results the formation of Blood clots from sticking together red blood corpuscles. In a cascade of the Pathogen development a Filit (threads) develops, again able is further threads to be formed from a Symprotit (in the darkfield visibly as bright protein ball). These can be connected to a net, which includes the blood corpuscles which a thickening of the blood and thus a Thrombose building as well as a less blood circulation of the fabric and the organs to the consequence has. Continue Reading >>

For millions of years colloids of the mushroom trunks Mucor live racemosus Fresen and Aspergillus the Niger van Tieghem

For millions of years colloids of the mushroom trunks Mucor live racemosus Fresen and Aspergillus the Niger van Tieghem, who live as Endobiont in symbiosis with humans and mammals. Under adverse circumstances they can form transitions to higher forms, which lead to humoralpathologischen changes and thus to diseases. Continue Reading >>

The therapy covers thus an adjustment of the environment and basic regulations of body

The therapy covers thus an adjustment of the environment and basic regulations of body, whereby pathogenen valences the base of life is extracted. The-obtained result is thus a healing process.
With the dark field microscopy we can judge singularly the blood environment and experience important notes to the following topics:

• Shifts in the acid - alkaline household
• Lack of the protein processing
• Cell and degeneration tendencies
• Chron. Inflammations and disturbances of the protein admission
• Dysbiose or Endobiosis
• Accelerated cell purge
• Tumor tendencies Continue Reading >>

into physiological saline solution germinates at the outstanding edges the so called Pseudo crystals low valence Chondrite

The all-last unit of the living substance are the colloids. Colloids are not only to be formed in a the position other organisms, them can also into a drying protein form purge, into one so called for fright position, which can be caused by the smallest effects.It concerns a sudden retreat into the drying protein form, which even temperatures of 310°C bears, without losing the vitality. Spengler observed even still higher temp. One brings these into physiological saline solution germinates at the outstanding edges the so called Pseudo crystals low valence Chondrite. Continue Reading >>

Prof.Enderlein - Pleomorphism

The method involves generating images, outputting the images, comparing specific patterns of an image with known patterns, determining deviations and/or agreements and outputting the results regarding which type of fungus is involved. The generated dark field images are placed in a memory and image data and/or additional information are transmitted by a data transmission device. AN Independent claim is also included for the following: (a) an arrangement, especially for implementing the inventive method.

SANUM Therapy: Puzzling Medicine putting the pieces together

by Kirk R. Dr. Slagel

Since the time that German Professor Dr. Guenther Enderlein stood behind the eyepiece of his darkfield microscope, much has changed in the world of Isopathic/Homeopathic medicine. Dr. Enderlein studied blood, live blood, via a darkfield microscope; a specially designed microscope that angles the light through the viewing plane as compared to a bright field microscope that points the light directly upward through the viewing plane. The difference: bright field light washes out objects that may be seen with a darkfield scope. This darkfield difference however, allows minute microscopic objects to be visible to the human eye that otherwise would be lost in the sea of light normally flowing through the eyepiece of a bright field scope. Much like the disappearance of stars in the light of day that become visible by the absence of light when the sun sets, darkfield microscopy sets free the hidden forms that exist deeper in the universe of a drop of blood.

Dr. Enderlein spent thousands of hours, culminating many years of his life studying this microscopic universe. He based his initial work on Antoine Bechamp, the French researcher who while performing his own research on the microbiological world coined the term "Microzymas" for the minute forms he found. The first real point in time noted for Dr. Enderlein was during his work in 1916 when he was studying typhoid. He cited the observance of objects and forms, moving structures in the blood besides those mobile scavengers, the white blood cells. But of particular interest was that these structures appeared to change form; they underwent a pleomorphic process. Bechamp's Microzymas did the same.

Dr. Enderlein was not the only researcher during that time that noted these pleomorphic structures. There were a number of other medical health professionals in the late 1800's and early 1900's who had also observed various pleomorphic microbe forms in the body. Lida Mattman, PhD in her book Cell Wall Deficient Forms: Stealth Pathogens mentions similar findings in research conducted by Willibald Winkler, MD, Ernest B. Almquist, MD, Emmy Klieneberger, Nobel Prize winner in 1950, and many others. In addition, Dr. Mattman states that Louis Dienes, Honorary Member of the American Society for Microbiology, developed an incubator to grow cell wall deficient forms. As her book indicates he may very well be the person who shed light on these multi-formed pathogens to the US investigators. However, different than the other researchers, Dr. Enderlein expanded his work to include the resultant medicines he developed from those many hours of darkfield assessment. Continue Reading >>

IS BLOOD STERILE?

For a long time many researchers and doctors believed, and many still do, that blood is sterile. Professor Dr. Gunter Enderlein after numerous years of research, proved otherwise. He showed using darkfield microscopy, that the serum of all people and warm-blooded animals are alive with many moving 'particles'. He called these particles ENDOBIONTS (from the Greek "endon" = internal and "bios" = life). When you first look at a live blood sample under a microscope or on a monitor you cannot fail to see a multitude of moving, living particles. These are the Endobionts, and are an important part of health.

There are a wide variety of different Endobionts in the blood. In fact, from the simplest apathogenic (non-disease forming) PROTIT, they can change forms into pathological (disease causing) species, depending on how much the pH (acidity-alkalinity) of the blood is changed. The higher the acidity, the more pathogenicity, and the more likelihood of developing a chronic, degenerative disease process over time. The wonderful world of Live Blood Analysis can enable you to see the different forms in the blood, and to therefore determine how far ahead you are in the disease process.

Prof. Enderlein discovered that these Endobionts change into different forms as the internal milieu changes. The more the metamorphosis (different changes), the greater the probability of disease. The pH of our blood is determined by the food we eat, and the nutrients we take in daily, as well as other factors such as stress and pollutants. Fast and refined foods and concentrated protein foods all lead to acidic blood which triggers the Endobiont to change to more pathogenic forms. All microbes partake in a natural developmental cycle, that begins with the PRIMITIVE PHASE which is microscopically invisible; this changes into the BACTERIAL PHASE; and finally culminates in the FUNGAL PHASE, which is the most pathogenic stage. This is the theory of PLEOMORPHISM (many forms), as opposed to monomorphism (one form). Continue Reading >>

Günther Enderlein - The Father of the Pleomorphism

Günther Enderlein (1872-1968) of Germany is the researcher who will forever be inseparable from pleomorphism, isopathy and homeopathy.

Dr. Enderlein built upon the research of Antoine Béchamp and proved that blood is not sterile, and that a microorganism can appear in various developmental stages and in diverse forms, without the loss of its specific characteristics.

Through intensive research, Dr. Enderlein came to the conclusion that the monomorphistic perspective of disease conditions favored by Dr. Louis Pasteur and others could no longer be maintained, and that a pleomorphic perspective more accurately reflected the disease process.

Dr. Enderlein discovered in 1916 that primitive microorganic forms prepared in a remedy, when combined with a change in the biological terrain (or milieu) of the body, can cause virulent forms to return to their original avirulent condition, bringing healing to the host body.

He found that when the tiniest, mobile living forms of bacteria, which he called “spermits,” exchanged genetic material with higher developmental organisms, the highly developed organisms became suddenly invisible, having been broken down to their primitive, avirulent forms. Using this knowledge, he developed homeopathic and isopathic remedies from fungal cultures. When these living remedies contact virulent microbial masses, the masses are induced to return to their avirulent form, and then leave the body through the natural organs of elimination. Continue Reading >>

Dr Bigelsen Protocol - Cancer - Mold

The Truth as I See It: What Is IT?
Beating Cancer With the "Bigelsen Protocol"

©Copyright 1999 by Harvey Bigelsen, MD, USA
(Explore Issue: Volume 9, Number 2)

For the past five years I have been working as a consultant at the Instituto de Medicina Biologica in Mexico, where most of the patients have cancer. I have been asked, how can you beat cancer and all the U.S. researchers and physicians cannot? My answer is that in the U.S. there are approximately 600,000 physicians, who are some of the brightest, most intelligent people in our society. The problem is that they are not allowed to think for themselves.

All standards are set by academicians who are funded by pharmaceutical companies, to prove that their new drug works. These physicians, who only treat rats in laboratories, set the standards for the physicians who are out there in practice. Cancer is the Sacred Cow of the Medical-Industrial-Complex. To cure cancer would destroy their industry.

Also, frankly, they have no idea what cancer is all about. They remind me of the moron, who lost a dime on a dark night, and was looking 2 blocks down the street because that where the street-lamp was. On the other hand, Mexico has offered all the freedoms that a physician should have. The Medical Community in Mexico will totally cooperate with me. If I asked a Radiologist for 25 Rads, he says "Sure". In the U.S. I would be reported to the Medical Authorities for such a request. With this kind of cooperation, results improve greatly. It makes no difference what treatments I use, as long as the patient improves everyone is happy. If this cooperation and care were used the U.S., cancer would have been cured long ago.

First of all, let us examine what is cancer? Albert Szvent-Giorgi, Nobel Prize winner, father of modern biochemistry, stated "They will never find the answer to cancer unless they understand the meaning of life". All modern cancer therapies, whether they are alternative, or traditional, are based on the magic bullet concept. Everyone is looking for the single treatment to kill cancer, but it will never work! Cancer is not a mutation of one cell gone wild. Mutations are rare, and cancer is epidemic. Those of you who are involved in Terrain understand that cancer is a mold of the human body just like a mold of cream cheese.

Cancer spreads like a mold. If there is a green mold on the cream cheese and we cut it out, the next day there will be 12 more spots. The mold is not metastasizing; the whole cream cheese is rotten. There are no blood vessels or lymphatic vessels in a cream cheese. As a point of scientific fact, there never has been found a cancer cell in a lymphatic vessel. The lymphatic system drains waste products. If you have an infected tooth, the lymph node under the jaw will get enlarged. A woman with breast cancer gets enlarged lymph nodes in her armpit. The node is draining the waste mold growing in the lymph node that contains human garbage. If I throw seeds to asphalt, nothing grows. But, if I throw seeds in manure, they will grow.

Also, why does breast cancer go to bones, first? A woman can develop 20 spots in the bones and yet none in the lungs, liver, etc. There are a billion miles of blood vessels the human body. Just by the law of chance, if cancer traveled through the blood, some spots would develop in other places and not all in the bones. Breast cancer goes to the bones first, because the mold of breast cancer feeds on calcium. Therefore, the spread of cancer is not random. The mold can only grow in certain pHs and chemistry of the cells. Cancer can only grow when the cells are acid, the blood is alkaline, and there is poor oxygenation.

Now that we know what cancer is and how it spreads, the next of important thing to understand is how does the body fight cancer? Every day old cells die and new cells are being created. The natural death of the old cell is called apoptosis. As the old cell becomes weakened, its DNA and RNA start to break up. The body contains proteins, called cytokines. These are analogous to hormones of the immune system. One of these cytokines' key purpose is to seek out and destroy those cells with weakened DNA. Knowing these facts, I have developed over several years a multi-dimensional plan of attack against cancer. With the following 4-step program I have had some extraordinary results.

"Bigelsen Protocol"
Step 1: The Use of chemotherapy and/or radiation
This may seem repugnant to many purists, but let me explain. I will use anything to help my patient. Cancer cells have a faster metabolism than normal cells. The traditional system uses some of the strongest poisons in huge doses to kill the cancer before they kill the person. I use only the mildest forms of chemotherapy in very low doses.

The purpose is to not kill the cancer cell but just to weaken the DNA of the cancer cell and not to harm the normal cell. Traditional medicine also uses radiation. The standard dose is 300-500 Rads a day, five days a week, for five to seven weeks. I use no more than 75-150 Rads for 3 to 5 days. Again, just to weaken the DNA of the cancer cell. I monitor the dose by using my Darkfield Microscope and BTA. This procedure of chemotherapy and /or radiation is repeated every 4 to 8 weeks. If the patient is monitored closely, I have seen virtually no side effects using this method.

Step 2: The use of cytokines
I have been using a product which is a multi-cocktail of cytokines and probably various other molecules. The B-Lymphocyte is grown in culture and the supernatant extracted. This extract contains multiple different molecules, most of which is still unknown. The key cytokine produced by the B-lymphocyte is TNF-Beta or Tumor- Necrosis- Factor Beta. The purpose of this cytokine is to cause apoptosis of the cell that has damaged DNA. The dose that I use is measured in nanograms. The most familiar cytokines belong to the Interferon and Interleukin families. The exact effects and impact of many of these cytokines on human body still are not fully understood. Overdosage will cause a toxic shock syndrome. The dose that is used by traditional medicine is billions of times stronger than the dose that the normal human body possesses. Also, cytokines always work in a balance, and the use of massive doses of only one type of cytokine can cause many serious negative effects.

Step 3: This part of the treatment program is based on the philosophies of Professor Enderlein.
Now that we have killed the cancer cells that are present, we must prevent the cancer from returning. The daily treatments that I use are designed to stabilize the pHs and slowly bring the fungus/mold back to a normal symbiotic state by using the Isopathic remedies. It took many years for the mold of cancer to grow and, therefore, you must take your time step by step to slowly return the terrain back to a healthy symbiosis. If I can keep the pH of the blood at 7.35 and under each day, then the cancer will not grow that day. Most of cancer therapy is done in a state of panic. But, if you have patience, and daily monitor the case, your results will improve. By using the Isopathic remedies developed by Professor Enderlein and by understanding the BTA and Darkfield Microscope, the Terrain can be manipulated on a daily basis. I also use Homeopathics, Cell therapy (not the whole cell, only cytoplasmic products), and the philosophy of Homotoxolgy in order to strengthen and follow my patients closely. By using these remedies I can prevent the mold from spreading by increasing the vital force of each specific organ system. Mold will not grow in tissue that has good vital force.

Step 4: The life style and the stresses of the patient must be addressed and changed.
This is an extremely important step as it is the life style of the patient that created the disease. Hammer in Germany has demonstrated that there are specific emotions and stresses associated with each disease. Every single disease has its pattern, like a fingerprint or snowflake (I like to call it a BIOGRAM). For example, John Wayne, Steve McQueen, Yul Brynner, Gary Cooper, Humphrey Bogart, etc., all had cancer of the lungs. The lungs de-tox themselves by crying. These macho men would smoke cigarettes instead of crying, thereby setting the terrain to become cancerous. Every single disease known to man has its own personality or BIOGRAM. In order to change the disease picture, we must change the personality (BIOGRAM) of each disease. This is an extremely important point to understand. There is only one cause of disease and that is "Consciousness". Diet, chemicals, poisons, etc. do not cause disease. Linda McCartney, wife of the "Beatles" Paul McCartney, died of breast cancer, and she wrote many books on vegetarianism. We are all exposed to noxious agents, yet, only some get ill and others do not. This concept of specific disease patterns (BIOGRAMS) I will write about in future articles.

A former teacher of mine stated "Miracles only happen when you know what you are doing. By the time that you see cancer the size of a pinky nail, the whole body is too far gone just to use only natural therapy". In order to treat cancer, you must have all of your weapons available in your arsenal that you can use. It will usually, take from 6 months to 1 year, at least, to be able to completely reverse a Stage 4 cancer into total " remission". Then, it will take me at least another year, to totally change the "Biogram" of the patient. The major problem, I believe, is that it is virtually impossible to treat cancer in the U. S. Since, the results that I have achieved thus far in prostate cancer have been so astounding and so easily reproducible, that I would like to propose a research project without walls. *Any physician who would like to join me in this project, please contact my office for further information @602-581-2988. (Prostate cancer is so easy, that I would like to be able to publish 50 cases of cure, over the next few years. That would really make the establishment stop, look and listen! I do well with other cancers, also, but prostate cancer is such a "gimme". My results have been 100%).

Finally, I would like to express my gratitude and appreciation at this time to the Country and People (who are absolutely delightful to work with) of Mexico, for allowing me to be free to work and search for answers, without any restrictions. Also, my partner and dear friend Salvador Vargas M.D., who has worked with me side by side to create this "Protocol". I have often been asked, "Would you come back to work in the U. S.?" (I was thrown out.) I would equate this as if I would be Jewish in 1938 Germany and I moved to London, would I move back to Germany in 1942? Why would I ever return to the U.S.? I feel like I am in Heaven, already. I will only come back to work in the U.S. if they make me Surgeon General.

About the Author
Dr. Bigelsen is the first medical doctor to practice Isopathy or Biological Medicine in North America. He is a trained MD, was a trauma surgeon in Vietnam and helped author the law that made Arizona Homeopathy what it is today. As the first president of the Arizona Homeopathic Medical Board, he drafted guidelines and standards for the practice of "Holistic" Medicine that were precedent setting in U.S. History. He believes his successful political effort in Arizona, led to the Medical Establishment finding him guilty of defrauding the U.S. Government and its taxpayers of $70.00. For this "grave" crime, he was banned from practicing medicine in the U.S. and its territories. He now works in "exile" and in freedom in Tijuana, Mexico at the Instituto de Medicina Biologica.

http://www.explorepub.com/articles/bigelson3.html

Man lives with the Endobiont

Man lives with the Endobiont, i.e. a plant microorganism, symbiotically. Every single human being acquires this Endobiont diaplacentally and harbors at least its primitive stages in cells and body fluids throughout life. They are even present in human sperm and egg cells, i.e. from impregnation on, in the earliest developmental stages of the new being, according to Leschke. It is thus nothing new for Gerlach to declare that the fetus in the mother's body already contains what he termed "myoplasma". In the Endobiontic developmental series, the lower stages, Protit and Chondrit, are apathogenic.

In the Chondrit stage, they can be used therapeutically as remedies. All the higher valences of the Endobiont can encourage or cause diseases, whereby they appear not only in the blood and blood cells, but also - from certain stages on - also in tissue cells, exerting a degenerative influence on them.

The upward development of the Endobiont is caused or favored, among other things, by the continual harmful influences of our civilization (artificial fertilizers, chlorinated water, polluted air, etc.) but primarily by a false diet that outright "fattens up" the Endobiont with its too-high protein and sugar content.

According to Enderlein, the diseases of the Endobiosis complex are based on the upward development of the Endobiont to higher-valence, parasitic growth forms with a characteristic metabolism that poisons the human body fluids (highly potentiated lactic acid production). This reduces the regulatory equilibrium in the mutual relationship with the vegetative centers in the diencephalon, which brings about the failure of its shape and formative function.

• Disease means disturbed symbiosis
  The plant symbiont spreads throughout the warm-blooded body, either numerically by means of simple reproduction or through the formation of higher developmental forms, which clog up circulatory organs (prethrombosis, capillary thrombosis).
• Disturbed symbiosis is detected in the darkfield from the absence of certain growth forms of the Endobiont (Diecothecit) As bioregulators, these maintain symbiotic equilibrium. At the same time, various pathogenic cell elements appear.
• Restoration of symbiotic equilibrium
  (Disease healing) is only possible when the body is once again given what it has lost (the bioregulators, which - by means of nonviolent restructuring processes - dismantle higher parasitic developmental forms and excrete them via the kidneys, skin, etc.).
• Issues of health exclusively concern life-processes
  They can therefore only be resolved through the science of biology.

From the orthodox side, Enderlein has been accused of refusing to use the generally-accepted nomenclature. How is it possible to use accepted scholarly terminology if one is describing things that don't even exist in the standard doctrine? Continue Reading >>

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. Guenther Enderlein, pg. 77, 1993, Compiled by Dr. med. Maria M-Bleker) Continue Reading >>

Book's recommendation's on the topic Live Blood Cell Dar kfield Microscopy

Here some book’s recommendations on the topic Live Blood Cell Analysis Dark field Microscopy:
· Introduction Into Darkfield Diagnostics by Prof. Dr. Gunther Enderlein
· A Comprehensive Guide to Sanum Therapy by Guenther Enderlein
· BIOLOGICAL MEDICINE: THE FUTURE OF NATURAL HEALING by Dr. Thomas Rau
· The Swiss Secret to Optimal Health: Dr. Rau's Diet for Whole Body Healing by Thomas Rau and Susan Wyler
· The Blood and Its Third Element by Antoine Bechamp
· Bechamp or Pasteur? by Ethel, D Hume
· An Introduction to Antoine Bechamp by Douglas Hume
· Blood and its Third Anatomical Element by A. Bechamp
· Bechamp or Pasteur: A Lost Chapter in the History of Biology by Douglas Hume
· The Mystery of Fermentation by Douglas Hume
· Praxis der SANUM-Therapie by Harald Krebs
· Praxisleitfaden SANUM-Therapie nach Prof. Enderlein by Günter WeigelPraxisleitfaden Dunkelfeld-Vitalblutuntersuchung by Günter Weigel more info about this topic Live Blood Cell Analysis Dark field Microscopy at Live Blood Course: Dark field Course Blog and Live Blood Blog.

Detoxification

The most commonly overlooked aspect of nutritional approaches is detoxification. Most doctors fall into the habit of only detoxifying the organ or system that is evident from superficial diagnostic techniques. We often stop before asking how and why the body acquired and maintains an abundance of toxins or pathological organisms.

This relates back to the functional tests and the biological terrain. The most lucid explanation of biological terrain is derived from the work of Enderlein, M.D. using darkfield microscopy. The insight gained from understanding his approach gives you an idea of the severity of the condition and estimates not only the types of therapy that will need to be employed, but also the duration one can expect before health is rejuvenated. The stages of health are outlined into 6 progressive "Reckeweg" phases. Continue Reading >>

Germs and Viruses. Part 4

In 1898, Guenther Guenther Enderlein (1872-1968) graduated with honors in natural sciences, physics and zoology from Leipzig University, and in 1914 he became a bacteriologist and serologist at the German military hospital at Stettin.

Enderlein had studied the findings of Antoine Bechamp and had further studied under Rudolph Leuckart, the zoologist who initiated the modern science of parasitology, and also under Otto Schmidt, the doctor who in 1901 reported the discovery of parasites in the blood of cancer patients. (Schmidt was not the first to discover cancer parasites. As early as 1890 Scottish pathologist William Russell reported on widely variegated microbes present in all cancer tissue, which microbes were referred to as "Russell bodies".) Continue Reading >>

Synthesis of the Work of Enderlein, Bechamps and other Pleomorphic 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 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. Continue Reading >>

Cancer is not an infectious disease like tuberculosis, typhoid, cholera, pneumonia, etc.

Cancer is not an infectious disease like tuberculosis, typhoid, cholera, pneumonia, etc. It does not spread by contact. It is not caused by any germs coming from outside. However, certain viruses are known to cause cancer in experimental animals. Virus is an extremely small germ, smaller than bacteria, which can not be seen under regular microscope. Virus can be studied only under high power microscope or electron microscope.

Electron microscope were developed recently, in the past few decades. Some viruses are demonstrated to produce breast cancers and other tumours in monkeys, rabbits and mice. In human, Burkitt’s lymphoma a type of lymph node cancer, and some malignant papilloma are linked with certain viruses. In general, if we are exposed to chronic infection, injury, pollution, unhealthy food, water air, tobacco and drug abuse, etc over many years, our risk of developing cancer increases markedly. We are all actually swimming in the sea of germs all through our life. Only few of us get the disease while others resist the germs successfully.

Dr. Royal Rife had a very novel approach for his time. Rife was a true researcher and a genius. In early 1920s, he developed a special microscope, which could magnify objects to around 25,000 times or more. The common microscopes we see in our clinical laboratories magnify only up to 3000 times. At high power of magnification at 25000 or more, very small viruses could be easily studied. He then studied blood and tissue cells from a number of cancer patients.

He found that very small living particles were present within the cells of cancer patients. He termed this as BX virus. On studying a large number of patients and healthy individuals over a long period, he concluded that these viruses did not come from outside the body. These virus developed within the cells. He proved transformation of pre-existing harmless bacteria into disease causing bacteria and viruses. This, he thought, was in response to accumulation of toxic waste products within tissues.

As per the earlier work of Prof. Enderlein of Germany, all the living cells in body always have such small living harmless particles, which Dr. Enderlein named as protids. We all are born with protids within the cells, which sit quietly and harmlessly till something goes wrong. Then these protids change their harmless form and are converted into disease producing microorganism.

It was shown, by Rife that, under toxic unhealthy conditions, certain harmless bacteria assumed different forms and converted themselves to harmful viruses, bacteria, fungi, etc leading to different disease conditions. Under microscope, Rife observed conversion was due to accumulated toxins and waste products in the cells in different parts of body.

He came to the conclusion that exposure to carcinogens slowly alters the constitution and makes body ready for cancer. BX viruses then grow within the body and invade the cells to cause cancer. Continue Reading >>