Persecuted Heroes




Gaston Naessens invented a 30,000X dark-field microscope that allows living tissue to be seen at much higher levels of magnification. Hidden within the blood plasma he found tiny bodies he named “somatids”. These somatids were observed to change from one form to another in regular cycles. In a healthy person the somatids have a three stage cycle. In an unhealthy person the somatids have a 16 stage cycle. The critical stage between stage three and stage four is fermentation. Fermentation is the result of sub-cellular trauma that is produced by exposure to chemical pollution, radiation, accidents, shocks, depression, etc.

The 13 unhealthy somatid stages include a bacterial stage. Bacteria comes from external sources or are internally generated, and usually do not cause disease. Bacteria is usually the result of disease, and the disease actually exists on the somatids level and this biological imbalance allows the unhealthy forms of somatids to thrive. Studying the blood of healthy people and people with various diseases, Naessens found that he could predict the diseases the healthy people were going to get, based on the condition of their somatids. In traumatized animals, the somatids become highly active and begin to destroy the bodies of their hosts. Naessens has become famous for treating diseases by monitoring the somatids to determine the effectiveness of the treatment. He has successfully treated thousands of cases of cancers and other diseases. Somatids are electrical in nature. Their nuclei is positively charged and their exterior membrane coating is negatively charged. Somatids are actually the smallest living condensers of energy ever found.

The optical microscope developed by Dr. Royal Raymond Rife in the 1920s and 1930s also magnified living tissue around 30,000X. With his microscope, Rife observed tiny organisms smaller than the bacteria that he isolated from cancer tumors. He studied the effect of various frequencies of light on these organisms until he was able to find a frequency that killed them. Cancer patients were exposed to light of a certain frequency for three minutes every third day. After three months, 14 out of 16 terminal cancer patients fully recovered. Using only light, he was able to cure cancer and many other diseases including tuberculosis, typhoid, leprosy, and hoof-and-mouth disease. If a person understands what causes cancer, every cancer cell in a person’s body can be reverted into a normal cell within 24 hours. In the 1930s, researcher Dr. Royal Rife cured cancer within minutes because he understood what causes cancer. The American Medical Association (A.M.A.) offered to buy Dr. Royal Rife’s technology (they intended to “bury” the technology), but Dr. Rife refused to sell. The FDA then destroyed his equipment. Mr. R. Webster Kehr, researcher, President and member of the Board of Directors of the Independent Cancer Research Foundation, Inc., a non-profit corporation organized in the state of Nevada, has an article on the Internet discussing the overall treatment of advanced cancer: Treatment For Stage IV Patients.

The cancer causing organisms could be isolated from tumors, cultured, injected into healthy animals where new tumors would form, and then be isolated once again from the new tumors. When placed onto plant tissue, it developed into fungus. Under certain circumstances, the cancer-causing organisms would transform themselves into bacillus coli, a common intestinal bacteria. The ability of an organism to change from one shape or size to another is called pleomorphism.

Guenther Enderlein developed remedies that were based on the blood pH getting off balance causing microbes in the blood to grow into pathogenicity (pathogens). If the blood’s pH balance, mineral balance, etc. shifts, the elemental forms, the colloidal particles known as the protits or somatids, will change their shape to adapt to the new environment. What they change into can be pathogenic to the body. When Professor Enderlein was doing his research in this area, he understood the developmental life cycle of the internal parasite. He knew that disease was brought about by a shift in the internal metabolic balance. To get well, you had to rebalance the metabolism. The way to rebalance your metabolism (pH) is through diet. But in severe situations, you could accelerate the process biologically. Enderlein understood that if you have a microbe at a late developmental stage in the body that is causing problems, you could introduce the earlier stage of that same type of microbe and they would combine and become a lesser form.

This is how his isopathic remedies work. The protit is a colloid of life. It is the progenitor to later stages of development if the pH of the blood gets thrown off. To de-evolve the later pathogenic stages, you can re-introduce new cultured young protits back into the blood, and the pathogenic forms will become lesser, apathogenic forms. Professor Enderlein re-introduced the small colloids of life (protits) back into the body to combine with the pathogenic forms so they would de-evolve back into a non-pathogenic state. The colloids in your blood are protits (somatids) and are very small particles, unfilterable by the kidneys. When you consume your own urine, you are receiving a dose of these pure colloids. These colloids proceed to support the immune function, taking the pathogenic microbes in the blood back to the apathogenic state.