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Mycoplasmas - Stealth Pathogens

Mycoplasmas - Stealth Pathogens

By Leslie Taylor, ND January, 2001  


Mycoplasmas are a specific and unique species of bacteria - the smallest free-living organism known on the planet. The primary differences between mycoplasmas and other bacteria is that bacteria have a solid cell-wall structure and they can grow in the simplest culture media. Mycoplasmas however, do not have a cell wall, and like a tiny jellyfish with a pliable membrane, can take on many different shapes which make them difficult to identify, even under a high powered electron microscope. Mycoplasmas can also be very hard to culture in the laboratory and are often missed as pathogenic causes of diseases for this reason.    


The accepted name was chosen because Mycoplasmas were observed to have a fungi-like structure (Mycology is the study of fungi - hence "Myco") and it also had a flowing plasma-like structure without a cell wall - hence "plasma". The first strains were isolated from cattle with arthritis and pleuro-pneumonia in 1898 at the Pasteur Institute. The first human strain was isolated in 1932 from an abscessed wound. The first connection between mycoplasmas and rheumatoid diseases was made in 1939 by Drs. Swift and Brown. Unfortunately, mycoplasmas didn't become part of the medical school curriculum until the late 1950's when one specific strain was identified and proven to be the cause of atypical pneumonia, and named Mycoplasma pneumonia. The association between immunodeficiency and autoimmune disorders with mycoplasmas was first reported in the mid 1970s in patients with primary hypogammaglobulinemia (an autoimmune disease) and infection with four species of mycoplasma that had localized in joint tissue. Since that time, scientific testing methodologies have made critical technological progress and along with it, more mycoplasma species have been identified and recorded in animals, humans and even plants.    


While Mycoplasma pneumonia is certainly not the only species causing disease in humans, it makes for a good example of how this stealth pathogen can move out of it's typical environment and into other parts of the body and begin causing other diseases. While residing in the respiratory tract and lungs, Mycoplasma pneumonia remains an important cause of pneumonia and other airway disorders, such as tracheobronchitis, pharyngitis and asthma. When this stealth pathogen hitches a ride to other parts of the body, it is associated with non-pulmonary manifestations, such as blood, skin, joint, central nervous system, liver, pancreas, and cardiovascular syndromes and disorders. Even as far back as 1983, doctors at Yale noted:    


"Over the past 20 years the annual number of reports on extrapulmonary symptoms during Mycoplasma (M.) pneumoniae disease has increased. Clinical and epidemiological data indicate that symptoms from the skin and mucous membranes, from the central nervous system, from the heart, and perhaps from other organs as well are not quite uncommon manifestations of M. pneumoniae disease." (15)


This single stealth pathogen has been discovered in the urogenital tract of patients suffering from inflammatory pelvic disease, urethritis, and other urinary tract diseases (8) It has been discovered in the heart tissues and fluid of patients suffering from cardititis, pericarditis, tachycardia, hemolytic anemia, and other coronary heart diseases.(9, 10, 14) It has been found in the cerebrospinal fluid of patients with meningitis and encephalitis, seizures, ALS, Alzheimer's and other central nervous system infections, diseases and disorders.(11-13) It has even been found regularly in the bone marrow of children with leukemia.(16- 18) It is amazing that one single tiny bacteria can be the cause of so many seemingly unrelated diseases in humans. But as with all mycoplasma species, the disease is directly related to where the mycoplasma resides in the body and which cells in the body it attaches to or invades.  


Today, over 100 documented species of mycoplasmas have been recorded to cause various diseases in humans, animals, and plants. Mycoplasma pneumonia as well as at least 7 other mycoplasma species have now been linked as a direct cause or significant co-factor to many chronic diseases including, rheumatoid arthritis, Alzheimer's, multiple sclerosis, fibromyalgia, chronic fatigue, diabetes, Crohn's Disease, ALS, nongonoccal urethritis, asthma, lupus, infertility, AIDS and certain cancers and leukemia, just to name a few.(1-6)    


 In 1997, the National Center for Infectious Diseases, Centers for Disease Control and Prevention's journal, Emerging Infectious Diseases, published the article, Mycoplasmas: Sophisticated, Reemerging, and Burdened by Their Notoriety, by Drs. Baseman and Tully who stated:


"Nonetheless, mycoplasmas by themselves can cause acute and chronic diseases at multiple sites with wide-ranging complications and have been implicated as cofactors in disease. Recently, mycoplasmas have been linked as a cofactor to AIDS pathogenesis and to malignant transformation, chromosomal aberrations, the Gulf War Syndrome, and other unexplained and complex illnesses, including chronic fatigue syndrome, Crohn's disease, and various arthritides."


Mycoplasmas, unlike viruses, can grow in tissue fluids (blood, joint, heart, chest and spinal fluids) and can grow inside any living tissue cell without killing the cells, as most normal bacteria and viruses will do. Mycoplasmas are frequently found in the oral and genito-urinary tracts of normal healthy people and are found to infect females four times more often than males, which just happens to be the same incidence rate in rheumatoid arthritis, fibromyalgia, Chronic Fatigue and other related disorders.(7)


Mycoplasmas are parasitic in nature and can attach to specific cells without killing the cells and thus their infection process and progress can go undetected. In some people the attachment of mycoplasmas to the host cell acts like a living thorn; a persistent foreign substance, causing the host's immune defense mechanism to wage war. This allergic type of inflammation often results in heated, swollen, and painful inflamed tissues, like those found in rheumatoid diseases, fibromyalgia and many other autoimmune disorders like lupus and MS, Crohn's and others. In such cases the immune system begins attacking itself and/or seemingly healthy cells. Some species of mycoplasmas also have the unique ability to completely evade the immune system. Once they attach to a host cell in the body, their unique plasma and protein coating can then mimic the cell wall of the host cell and the immune system cannot differentiate the mycoplasma from the body's own host cell.    


Mycoplasmas are parasitic in nature because they rely on the nutrients found in host cells including cholesterol, amino acids, fatty acids and even DNA. They especially thrive in cholesterol rich and arginine-rich environments. Mycoplasmas can generally be found in the mucous membrane in the respiratory tract. They need cholesterol for membrane function and growth, and there is an abundance of cholesterol in the bronchial tubes of the respiratory tract. Once attached to a host cell, they then begin competing for nutrients inside the host cells. As nutrients are depleted, then these host cells can begin to malfunction, or even change normal functioning of the cell, causing a chain reaction with other cells (especially within the immune and endocrine systems). Mycoplasmas can even cause RNA and DNA mutation of the host cells and have been linked to certain cancers for this reason. Mycoplasmas can also invade and live inside host cells which evade the immune system, especially white blood cells. Once inside a white blood cell, mycoplasmas can travel throughout the body and even cross the blood/brain barrier, and into the central nervous system and spinal fluid.    



Baseman, Joel,, Mycoplasmas: Sophisticated, Reemerging, and Burdened by Their Notoriety, CDC, Journal of Infectious Diseases, Vol 3, No.1, Feb 1997    

S-C. Mycoplasmas and AIDS. In: Maniloff J, McElhaney RN, Finch LR, Baseman JB, editors. Mycoplasmas: molecular biology and pathogenesis. Washington (DC): American Society for Microbiology, 1992:525-45.    

Nicolson G, Nicolson NL. Diagnosis and treatment of mycoplasmal infections in Gulf War illness-CFIDS patients. Intl J Occup Med Immunol Toxicol 1996;5:69-78.    

Wear DJ, Mycoplasmas and oncogenesis:persistent infection and multistage malignant transformation. Proc Natl Acad Sci USA 1995;92:10197-201.    

Ekbom A, Daszak P, Kraaz W, Wakefield AJ. Crohn's disease after in-utero measles virus exposure. Lancet 1996;348:516-7.    

Taylor-Robinson D. Mycoplasmas in rheumatoid arthritis and other human arthritides. J Clin Pathol 1996;49:781-2.    

Dr.Harold Clark, The Intercessor, June 1993, The Road Back Foundation, Delaware OH.    

Goulet M,, Isolation of Mycoplasma pneumoniae from the human urogenital tract. J Clin Microbiol 1995;33:2823-5    

Daxbock F,, Severe hemolytic anemia and excessive leukocytosis masking mycoplasma pneumonia. Ann Hematol. 2001 Mar;80(3):180-2.    

Higuchi ML,, Detection of Mycoplasma pneumoniae and Chlamydia pneumoniae in ruptured atherosclerotic plaques. Braz J Med Biol Res. 2000 Sep;33(9):1023-6.    

Socan M, Neurological symptoms in patients whose cerebrospinal fluid is culture- and/or polymerase chain reaction-positive for Mycoplasma pneumoniae. Clin Infect Dis. 2001 Jan 15;32(2):E31-5.    

Bencina D,, Intrathecal synthesis of specific antibodies in patients with invasion of the central nervous system by Mycoplasma pneumoniae. Eur J Clin Microbiol Infect Dis. 2000 Jul;19(7):521-30    

Smith R,, Neurologic manifestations of Mycoplasma pneumoniae infections: diverse spectrum of diseases. A report of six cases and review of the literature. Clin Pediatr (Phila). 2000 Apr;39(4):195-201.    

Umemoto M, Advanced atrioventricular block associated with atrial tachycardia caused by Mycoplasma pneumoniae infection. Acta Paediatr Jpn. 1995 Aug;37(4):518-20.    

Lind K. Manifestations and complications of Mycoplasma pneumoniae disease: a review.Yale J Biol Med. 1983 Sep-Dec;56(5-6):461-8.    

Alexander FE. Is Mycoplasma Pneumonia associated with childhood acute lymphoblastic leukemia? Cancer Causes Control. 1997 Sep;8(5):803-11.    

Hall JE, Mycoplasma pneumonia in acute childhood leukemia. Pediatr Pulmonol. 1985 Nov-Dec;1(6):333-6.    

Murphy WH, Gullis C, Dabich L, Heyn R, Zarafonetis CJD. Isolation of Mycoplasma from leukemic and nonleukemia patients. J Nat Cancer Inst 1970;45:243-51.    


How Mycoplasmas Interact in the Body


To understand how mycoplasmas can cause widespread disease, we must first look at the species' unique properties and interactions with host cells. Unlike viruses and bacteria, mycoplasmas are the smallest free-living and self-duplicating microorganisms, as they don't require living cells to replicate their DNA and growth.  


Mycoplasmas are able to hide inside the cells of the host (patient) or to attach to the outside of host cells. Whether they live inside or outside the host cell, they depend on host cells for nutrients such as cholesterol, amino acids, etc. They compete with the host cells for these nutrients which can interfere with host cell function without killing the host cell.  


A mycoplasma has very little DNA of its own, but is capable of using DNA from a host cell. When a mycoplasma takes over the DNA of the host cell, anything can happen - including causing that cell to malfunction in many different ways and/or die, or can cause DNA mutation of the host cell. Mycoplasmas attach to host cells with a tiny arm coated in protein which attaches to the protein coating of host cells. For this reason, antibiotics like tetracycline, which are classified as "protein synthesis inhibitors" are often used against mycoplasma infections. While these antibiotics may block this protein attachment and very slowly starve it from the nutrients it needs from host cells to thrive and replicate, it still takes a healthy immune system to actually kill the mycoplasma for good.    


Mycoplasmas are highly adaptable to changing environments and can move anywhere in the body, attaching to or invading virtually any type of cell in the body. The mycoplasma adhesion proteins are very similar to human proteins. Once adhered to the host cell, the mycoplasma can completely mimic or copy the protein cell of the host cell. This can cause the immune system to begin attacking the body's own cells; an event that happens in all autoimmune diseases.


Certain Mycoplasma species can either activate or suppress host immune systems, and they may use these activities to evade host immune responses. Mycoplasmas can turn on the chain reaction called an immune system response. This includes the stimulation of pro-inflammatory cytokines (chemical messengers of the immune system) which is generally found in most autoimmune and inflammatory diseases and disorders. Mycoplasma can also attach to or invade immune system cells, like the very phagocytes (natural killer cells) that are supposed to kill them. Inside these phagocytes, they can be carried to new locations of inflammation or disease - hidden away like a spy who has infiltrated the defending army. When a mycoplasma attaches to a host cell, it generates and releases hydrogen peroxide and superoxide radicals which cause oxidative stress and damage to the surrounding tissues.    


The Main Human Mycoplasma Pathogens

Pathogen / Implicated Disease (1-6)  

Mycoplasma genitalium    

Arthritis, chronic nongonococcal urethritis, chronic pelvic inflammatory disease, other urogenital infections and diseases, infertility, AIDS/HIV    

Mycoplasma fermentans    

Arthritis, Gulf War Syndrome, Fibromyalgia, Chronic Fatigue Syndrome, Lupus, AIDS/HIV, autoimmune diseases, ALS, psoriasis and Scleroderma, Crohn's and IBS, cancer, endocrine disorders, Multiple Sclerosis, diabetes    

Mycoplasma salivarium    

Arthritis, TMJ disorders, Eye and ear disorders and infections, gingivitis, periodontal diseases including even cavities.    

Mycoplasma hominis and Ureaplasma urealyticum    

Pelvic inflammatory disease, infertility, non-gonococcal urethritis, vaginitis, cervicitis, amnionitis, pyelonephritis, post-partum septicemia, neonatal pneumonia, neonatal conjunctivitis, Reiter's syndrome, peritonitis, wound infections (C-section), low birth weight infants, and premature rupture of membranes.    

Mycoplasma pneumonia    

Pneumonia, asthma, upper and lower respiratory diseases, heart diseases, leukemia, Steven-Johnson syndrome, polyarthritis or septic arthritis, CNS disorders and diseases, urinary tract infections, Crohn's and Irritable Bowel Syndrome, Guillain-Barr syndrome, polyradiculitis, encephalitis, and septic meningitis, autoimmune diseases.    

Mycoplasma incognitus and
Mycoplasma penetrans  

AIDS/HIV, urogenital infections and diseases, Autoimmune disorders and diseases    

Mycoplasma pirum    

Urogenital infections and diseases, AIDS/HIV    

Mycoplasma faucium, M. lipophilum and M. buccale    

Diseases of the gingival crevices and respiratory tract    


Krause DC, Taylor-Robinson D. Mycoplasmas which infect humans. In: Maniloff J, McElhaney RN, Finch LR, Baseman JB, editors. Mycoplasmas: molecular biology and pathogenesis. Washington (DC): American Society for Microbiology, 1992:417-44.    

Murray HW, Masur H, Senterfit LB, Roberts RB. The protean manifestations of Mycoplasma pneumoniae infection in adults. Am J Med 1975;58:229-42.    

Baseman, Joel,, Mycoplasmas: Sophisticated, Reemerging, and Burdened by Their Notoriety. CDC, Journal of Infectious Diseases, Vol 3, No.1, Feb 1997    

Blanchard, A.,, AIDS-associated mycoplasmas. Ann.Rev.Microbiol. 1994; 48:687-712.    

Hawkins,, Association of mycoplasma and human immunodeficiency virus infection: detection of amplified mycoplasma fermentans DNA in blood. J.Infec.Dis. 1992: 165:581-585    

Hussain AI,, Mycoplasma penetrans and other mycoplasmas in urine of human immunodeficiency virus-positive children. J Clin Microbiol. 1999 May;37(5):1518-23.    


(Plus other health disorders, including auto-immune disorders)
by: Scott, Donald W., M.Sc.


Donald Scott is a retired high school teacher and university professor who is currently president of the Common Cause Medical Research Foundation and adjunct professor of the Institute of Molecular Medicine. He has extensively researched neurosystemic degenerative diseases over the past five years and has authored many documents on the relationship between degenerative diseases and a pathogenic mycoplasma called Mycoplasma fermentans. His research is based upon solid government evidence. Donald Scott is a veteran of WWII and was awarded the North Atlantic Star, the Burma Star with Clasp, the 1939-1945 Volunteer Service Medal and the Victory Medal.    


I - The Mycoplasma a Common Pathogenic Mycoplasma


There are 200 species of mycoplasmas. Most are innocuous and do no harm; only four or five are pathogenic. The Mycoplasma fermentans (incognitus strain) probably comes from the nucleus of the brucellosis bacteria. This disease agent is not a bacteria, and not a virus; it is a mutated form of the brucellosis bacteria, mutated with a visna virus, from which the mycoplasma, is extracted. Dr. Maurice Hilleman, chief virologist for the pharmaceutical company of Merck, Sharp and Dohme, stated that this disease agent is now carried by everybody in North America and possibly most people throughout the world. The mycoplasma used to be very innocuous. Only one person out of 500,000 would get multiple sclerosis; one out of 300,000 would develop Alzheimer's; one out of 1,000,000 would develop Creutzfeldt-Jakob disease. Before the early 1980's, nobody ever died of AIDS because it didn't exist. The mycoplasma is also the disease agent in AIDS, and I have all the documentation to prove it.    


BIOWARFARE RESEARCH Between 1942 and the present time, biological warfare research has resulted in a more deadly and infectious form of the mycoplasma. They extracted this mycoplasma from the brucellosis bacteria, weaponized it and actually reduced the disease to a crystalline form. According to Dr. Shyh-Ching Lo, one of America's top, top researchers, this disease agent, the mycoplasma, causes among other things, AIDS, chronic fatigue syndrome, multiple sclerosis, Wegener's disease, Parkinson's disease, Crohn's colitis, Type I diabetes, and collagen-vascular diseases such as rheumatoid arthritis and Alzheimer's. The mycoplasma enters into the individual cells of the body depending upon your genetic predisposition. You may develop neurological diseases if the pathogen destroys certain cells in your brain, or you may develop Crohn's colitis if the pathogen invades and destroys cells in the lower bowel. Once it gets into the cell, it can lie there doing nothing sometimes for 10, 20 or 30 years, but if a trauma occurs like an accident, or a vaccination that doesn't take, the mycoplasma can become triggered. Because it is only the DNA particle of the bacteria, it doesn't have any organelles to process its own nutrients, so it grows by uptaking preformed sterols from its host cell, literally kills the cell, and the cell ruptures and what is left gets dumped into the blood stream.    


DOCUMENTED EVIDENCE My conclusions are entirely based upon official documents: 80% are United States or Canadian official government documents, and 20% are articles from peer-reviewed journals, such as the Journal of the American Medical Association, The New England Journal of Medicine, and The Canadian Medical Association Journal. The journal articles and government documents complement each other. We also have a document from Dr. Shyh-Ching Lo which names the mycoplasma as a cause of cancer. Dr. Charles Engel who is with the National Institutes of Health, Bethesda, Maryland, stated at an NIH meeting on February 7, 2000, "I am now of the view that the probable cause of Chronic Fatigue Syndrome and fibromyalgia is the mycoplasma".    


II - Creation of the Mycoplasma Patent


Many doctors don't know about this mycoplasma because it was developed by the U.S. military in biological warfare experimentation, and it was not made public. This pathogenic mycoplasma disease agent was patented by the United States military by Dr. Shyh-Ching Lo, who was the top researcher for the military biological warfare research facility. I have the documented patent from the U.S. patent office.  A LABORATORY-CREATED PATHOGEN BY THE U.S. MILITARY Researchers in the United States, Canada and Britain were doing biowarfare research with the brucellosis bacteria as well as with a number of other disease agents. From its inception, the biowarfare program was characterized by continuing in-depth review and participation by the most eminent scientists, medical consultants, industrial experts and government officials, and it was top secret. The U.S. Public Health Service also closely followed the progress of biological warfare research and development from the very start of the program, and the Centers for Disease Control (CDC), and the National Institutes of Health (NIH) in the United States were working with the military in weaponizing these diseases. These are diseases which have existed for thousands of years, but they have been weaponized which means they were made more contagious and more effective. And they are spreading. A program developed by the CIA and NIH to develop a deadly lethal pathogen for which humanity had no natural immunity (AIDS) was disguised as a war on cancer and was part of MKNAOMI (ref. Special Virus Cancer Program: Progress Report 8, prepared by National Cancer Institute, Viral Oncology, Etiology Area, July, 1971 and submitted to NIH Annual Report in May, 1971 and updated July, 1971).    


COMMITTEE ON GOVERNMENT REFORM Many members of the Senate and House of Represent-atives do not know what has been going on. For example, the US Senate Committee on Government Reform had searched the archives in Washington and other places for the document titled The Special Virus Cancer Program: Progress Report No.8 mentioned above and couldn't find it. Somehow they heard I had it, called me and asked me to mail it to them. Imagine. A retired school teacher being called by the United States Senate and asked for one of their secret documents! The United States Senate through their government reform committee is trying to stop this type of government research.    

BIOLOGICAL WARFARE RESEARCH AGREEMENT All the countries at war were experimenting with biological weapons. In 1942, the governments of the United States, Canada and Great Britain entered into a secret agreement to create two types of biological weapons (one that would kill and one that was disabling) for use in the war against Germany and Japan, who were also developing biological weapons. They primarily focused on brucellosis, and they began to weaponize the brucellosis bacteria.    


CRYSTALLINE BRUCELLOSIS In a genuine U.S. Senate Study unclassified on February 24, 1977, the title page of this government record reports that George Merck, of the pharmaceutical company, Merck, Sharp and Dohme (which now makes cures for diseases they at one time created), in 1946, reported to the Secretary of War in the United States that his researchers had produced in isolation for the first time, a crystalline bacterial toxin extracted from brucellosis bacteria. The bacterial toxin could be removed in crystalline form and delivered by other vectors (in nature they are delivered within the bacteria). But the factor that is working in the brucellosis is the mycoplasma. Brucellosis is a disease agent that doesn't kill people; it disables them. But they found that if they had mycoplasma at a certain strength, actually ten to the tenth power, it would develop into AIDS, and the person would die from it within a reasonable period of time because it could bypass our natural human defences. If it was 108, the person would manifest with chronic fatigue syndrome or fibromyalgia. If it was 107, they would present as wasting; they wouldn't die, and they wouldn't be disabled, but they would not be that interested in life, they would waste away (ref. Dr. Donald MacArthur of the Pentagon appearing before a Congressional Committee, June 9, 1969, Department of Defence Appropriations, p.114, 129). Most of us have never heard of brucellosis because it largely disappeared when they began pasteurizing milk, which was the carrier. One salt shaker of this pure disease in a crystalline form could sicken the entire population of Canada. It is absolutely deadly, not in terms of killing the body, but in terms of disabling the body. The advantage of this crystalline disease agent is that it does not show up in blood and tissue tests because the bacteria has disappeared and only the pure disease agent remains. So the doctor thinks that it's all in your head.    


CRYSTALLINE BRUCELLOSIS AND MULTIPLE SCLEROSIS About three years ago in Rochester, New York, a gentleman gave me a document and told me, "I was in the U.S. Army, and I was trained in bacteriological warfare. We were handling a bomb filled with brucellosis, only it wasn't brucellosis; it was a brucellosis toxin in crystalline form. We were spraying it on the Chinese and North Koreans." He showed me his certificate listing his training in chemical, biological, and radiological warfare. Then he showed me 16 pages of documents given to him by the U.S. military when he was discharged from the service. It linked brucellosis with multiple sclerosis and stated: "Veterans with multiple sclerosis, a kind of creeping paralysis developing to a degree of 10% or more disability within two years after separation from active service may be presumed to be service-connected for disability compensation. Compensation is payable to eligible veterans whose disabilities are due to service." In other words, "If you become ill with multiple sclerosis, it is because you were handling this brucellosis and we will give you a pension. Don't go raising any fuss about it." The government of the United States, in this official document revealed evidence of the cause of multiple sclerosis, but they didn't make it known to the public, or to your doctor. In a 1958 report, Drs. Kyger and Haden suggest "Öthe possibility that multiple sclerosis might be a central nervous system manifestation of chronic brucellosis". Testing approximately 113 MS patients, they found that almost 95% also tested positive for brucellosis. We have a document from a medical journal which concludes that one out of 500 people who had brucellosis would develop what they called neurobrucellosis, in other words, brucellosis in the brain which settles in the lateral ventricles where the disease multiple sclerosis is basically located.    


CONTAMINATION OF CAMP DETRICK LAB WORKERS A report from the New England Journal of Medicine, 1948, Vol.236, p.741 called "Acute Brucellosis Among Laboratory Workers" shows us how actively dangerous this agent is. The laboratory workers were from Camp Detrick, Frederick, Maryland where they were developing biological weapons. Even though these laboratory workers had been vaccinated, wore rubberized suits and masks, and worked through holes in the compartment, many of them came down with this awful disease because it is so absolutely and terrifyingly infectious. The article was written by Lt. Calderone Howell, Marine Corps, Captain Edward Miller, Marine Corps, Lt. Emily Kelly, United States Naval Reserve and Captain Henry Bookman. They were all military personnel engaged in making the disease agent brucellosis into a more effective biological weapon.    


III - Covert Testing of the Mycoplasma Testing Brucellis upon an Unsuspecting Public


Documented evidence proves that the biological weapons they were developing were tested on the public in various communities without their knowledge or consent. The government knew that crystalline brucellosis would cause disease in humans. Now they needed to determine how it spread, and the best way to disperse it. They tested dispersal methods for Brucella suis and Brucella melitensis at Dugway Proving Ground, Utah, June and September 1952. Probably, 100% of us now are infected with Brucella suis and Brucella melitensis. (ref. p.135, table 4 of Special Virus Cancer Program: Progress Report 8) . Another government document recommended the genesis of open air vulnerability tests, and covert research and development programs to be conducted by the army and supported by the Central Intelligence Agency. At that time, the government of Canada was asked by the government of the United States to cooperate in testing weaponized brucellosis, and Canada cooperated fully with the government of the United States. They wanted to determine (i) if mosquitoes will carry the disease and (ii) if the air will carry it. A government report stated that "Öopen air testing of infectious biological agents is considered essential to an ultimate understanding of biological warfare potentialities because of the many unknown factors affecting the degradation of micro-organisms in the atmosphere".    




A report from The New England Journal of Medicine, August 22, 1957, p.362 reveals that one of the first outbreaks of chronic fatigue syndrome was in Punta Gorda, Florida, back in 1957. It was a strange coincidence that a week before these people came down with chronic fatigue syndrome, there was a huge influx of mosquitoes. The National Institutes of Health claimed that the mosquitoes came from a forest fire 30 miles away. When the forest fire broke out, the mosquitoes all said, "Well, let's go over to Punta Gorda - there will be a bunch of people over there, we can have a picnic, and then we will go home". The truth is that those mosquitoes were infected in Canada by Dr. J.B. Reed at Queen's University. They were bred in Belleville, Ontario, and taken down and released in Punta Gorda. Within a week, the first five cases ever of chronic fatigue syndrome were reported to the local clinic in Punta Gorda, and it continued until finally 450 people were ill with the disease.    

TESTING BRUCELLOSIS VIA MOSQUITO VECTOR IN ONTARIO The government of Canada established the Dominion Parasite Laboratory in Belleville, Ontario, and raised 100 million mosquitoes a month which were shipped to Queen's University and certain other facilities to be infected with this disease agent. The mosquitoes were then let loose in certain communities in the middle of the night so they could determine how many people would become ill with chronic fatigue syndrome, or fibromyalgia, which was the first disease to show. One of the communities they tested it on was the St. Lawrence Seaway valley all the way from Kingston to Cornwall in 1984. They let out absolutely hundreds of millions of infected mosquitoes. Over 700 people in the next four or five weeks developed myalgic encephalomyelitis, or chronic fatigue syndrome.    


IV - Other Secret Government Testing Mad Cow Disease in the Fore Indian Tribe


At the infamous Japanese Camp 731 in Manchuria, they contaminated prisoners of war with certain disease agents. They also established a research camp in New Guinea in 1942, and experimented upon the Fore Indian tribe, and inoculated them with a minced-up version of the brains of diseased sheep containing the visna virus which causes mad cow disease (Creutzfeldt-Jakob disease which is known to you as mad cow disease, but which was known to the Fore Indian tribe as kuru). About five or six years later, after the Japanese had been driven out, the poor people of the Fore tribe developed what they called kuru which was their word for wasting, and they began to shake, lose their appetites, and die. The autopsies revealed that their brains had literally turned to mush. They had contracted mad cow disease from the Japanese experiments. When World War II ended, the Japanese General Doctor who was in charge of biological warfare experimentations in Japan, Dr. Ishii Shiro, was captured. They gave him the choice of a job with the United States army or execution as a war criminal. Not surprisingly, Dr. Ishii Shiro chose to work with the United States military to demonstrate how they had created mad cow disease in the Fore Indian tribe. In 1957, when the disease was beginning to blossom in full among these Fore Indian people, Dr. Carleton Gajdusek of the National Institutes of Health of the U.S. headed down to New Guinea to to determine how the minced-up brains of the visna-infected sheep affected these people. He spent a couple of years in New Guinea studying the Fore tribe, wrote an extensive report on it, and won the Nobel Prize for "discovering" kuru disease (also known as mad cow or Creutzfeldt-Jakob disease) in the Fore Indian tribe in New Guinea.    



 In 1953, the Americans developed a carcinogenic chemical which they wanted to test, but they didn't want to test it in the United States so they flew over Russia, accidentally wandered off course, and sprayed this stuff. Many people started getting cancer. And the U.S. had some jokes about this. One American researcher, Dr. Maurice Hilleman of Merck, Sharp and Dohme, joked, "We are going to win the next Olympics because all the Russians are going to turn up with 40-pound tumours." They thought it was a big joke.    



 Next they said, "How about testing it in Canada?" In 1953, the U.S. asked the government of Canada if they could test this carcinogenic chemical over the city of Winnipeg. It was a big city with 500,000 people, miles from anywhere. They sprayed the chemical in a 1,000% attenuated form, which they said would be so watered down that nobody would get very sick. However, if people came to clinics with a sniffle, a sore throat, or ringing in their ears, the researchers would be able to determine what percentage would have developed cancer if it had been full strength. When we located evidence that the Americans had tested this carcinogenic chemical over the city of Winnipeg in 1953, and informed the government that we had this evidence, they denied it. However, finally, on May 15, 1997, a story out of the Canadian Press in Washington, D.C. by Robert Russo, published in the Toronto Star, stated that the Pentagon of the United States admitted that in 1953 they had obtained permission from the government of Canada to fly over the city of Winnipeg and spray this crap out, and it sifted down on kids going to school, housewives hanging out their laundry, and people going to work. US Army planes and trucks released the chemical 36 times between July and August 1953. The chemical used was zinc cadmium sulfide, a carcinogen. They got their statistics, which indicated that if it had been full strength, approximately a third of the population of Winnipeg would have developed cancers over the next five years. The Pentagon called a press conference to admit what they had done. One professor, Dr. Hugh Fudenberg, MD, who was nominated twice for the Nobel Prize wrote a magazine article which stated that the Pentagon has come clean on this because two researchers up in Sudbury, Ontario, Don Scott and his son Bill Scott had been revealing this to the public. The US Army actually conducted a whole series of simulated germ warfare tests in Winnipeg. The Pentagon lied about the tests to the mayor, saying that they were testing a chemical fog over the city, which would protect Winnipeg in the event of a nuclear attack. A report commissioned by US Congress, chaired by Dr. Rogene Henderson, lists 32 American towns and cities used as test sites as well.    


V - Brucellosis Mycoplasma & Disease


AIDS The AIDS pathogen was created out of a brucellosis bacteria mutated with a visna virus; then the toxin was removed as a DNA particle called a mycoplasma. They used the same mycoplasma to develop disabling diseases like MS, Crohn's colitis, Lyme disease etc. In a United States congressional document of a meeting held June 9, 1969, the Pentagon delivered a report to Congress about biological weapons (described on page 129 of the document). The Pentagon stated, "We are continuing to develop disabling weapons." Dr. MacArthur, who was in charge of the research said, "We are developing a new lethal weapon, a synthetic biological agent that does not naturally exist, and for which no natural immunity could have been acquired." Think about it. If you have a deficiency of acquired immunity, you have an acquired immunity deficiency. Plain as that. AIDS. In laboratories throughout the United States and a certain number in Canada, including the University of Alberta, the U.S. government provided the leadership for the development of the AIDS virus for the purpose of population control. After they had it perfected, they sent medical teams from the Centers for Disease Control to Africa and other mid-eastern countries where they thought the population was becoming too large. They gave them all a free vaccination for smallpox. Five years after receiving this smallpox vaccination, 60% of them were suffering from AIDS. They tried to blame it on a monkey, which is nonsense. There was a report in the newspapers a while back about a professor at the University of Arkansas who claimed that while studying the tissues of a dead chimpanzee, she found the HIV virus. The chimpanzee that she had tested was born in the United States 23 years earlier. It had lived its entire life in a U.S. military laboratory where it was used as an experimental animal for the development of these diseases. When it died, its body was shipped to a storage place where it was deep-frozen and stored in case they wanted to analyze it later. Then they decided that they didn't have enough space for it, so they said, "Anybody want this dead chimpanzee?" and this researcher from Arkansas said, "Yes. Send it down to the University of Arkansas. We are happy to get anything that we can get." They shipped it down and she found the HIV virus in it. That virus was acquired by that chimpanzee in the laboratories where it was tested.    


CHRONIC FATIGUE Chronic fatigue syndrome is more accurately called myalgic encephalomyelitis, not chronic fatigue syndrome. That nomenclature was given by the National Institutes of Health in the United States because they wanted to downgrade and belittle the disease. An MRI of the brain of a teenage girl who had chronic fatigue syndrome displayed a great many scars or punctate lesions in the left frontal lobe area where portions of the brain had literally dissolved and had been replaced by scar tissue. This caused cognitive impairment, memory impairment, etc. And what was the cause of the scars? The mycoplasma. So there is very concrete physical evidence of these tragic diseases even though doctors continue to say they don't know where it comes from or what they can do about it    



Many people with chronic fatigue syndrome, myalgic encephalo-myelitis and fibromyalgia who apply to the Canada Pension Plan will be turned down because they cannot prove that they are ill. Over the past year I have conducted several appeals to Canada Pension and Workers Compensation on behalf of people who have been turned down. I provided documented evidence of these illnesses, and they were all granted their pensions on the basis of the evidence that I provided. In March of last year, for example, I appealed to the Workers' Compensation on behalf of a lady with fibromyalgia who had been denied her pension back in 1993. The vice-chairman of the board came up to Sudbury to hear the appeal, and I showed him a number of documents which proved that this lady was physically ill with fibromyalgia. It was a disease which caused physical damage, and the disease agent was a mycoplasma. The guy listened for three hours and then he said to me, "Mr. Scott, how is it I have never heard of any of this before? I said, "We brought a top authority in this area into Sudbury to speak on this subject and not a single solitary doctor came to that presentation."    


VI - Testing for the Presence of Mycoplasma in your Body - the Polymerase Chain Reaction Test


Information is not generally available about this agent, because first of all, the mycoplasma is such an infinitely small disease agent. A hundred years ago certain medical theoreticians conceived that there must be something smaller than the bacteria and the virus, which are the most common living forms of disease agents. This pathogenic organism is so infinitely small that normal blood and tissue tests will not reveal the source of the disease. Your doctor may diagnose you with Alzheimer's and he will say, "Golly, we don't know where Alzheimer's comes from. All we know is that your brain begins to deteriorate, cells rupture, the myelin sheath around the nerves dissolves, and so on." Or if you have chronic fatigue syndrome, the doctor will not be able to find any cause for your illness with ordinary blood and tissue tests. This mycoplasma couldn't be detected until about 30 years ago when they developed the polymerase chain reaction test in which they examine a sample of your blood, remove damaged particles, and subject that damaged particle to a polymerase chain reaction. This causes the DNA in the particle to break down. Then they place it in a nutrient which causes the DNA to grow back into its original form. If they get enough of it they can recognize what it is, and determine whether brucellosis or another kind of agent is behind that particular mycoplasma.    



If anybody in your family has myalgic encephalomyelitis, fibromyalgia, multiple sclerosis, or Alzheimer's, you can send a blood test to Dr. Les Simpson in New Zealand. If you are ill with these diseases, your red blood cells will not be normal donut-shaped blood cells capable of being compressed and squeezed through the capillaries, but will swell up like cherry-filled donuts, which cannot be compressed. The blood cells become enlarged and distended because the only way the mycoplasma can exist is by uptaking preformed sterols from the host cell. One of the best sources of preformed sterols is cholesterol, and cholesterol is what gives your blood cells flexibility. If the cholesterol is taken out by the mycoplasma, the red blood cell swells up, doesn't go through and the person begins to feel all the aches and pains, and all the damage it causes to the brain, the heart, the stomach, the feet and the whole body because blood and oxygen is cut off. And that is why people with fibromyalgia and chronic fatigue syndrome have such a terrible time. When the blood is cut off from the brain, punctate lesions appear, because those parts of the brain die. It will get into portions of the heart muscle, especially the left ventricle, and those cells will die. Certain people have cells in the lateral ventricles of the brain that have a genetic predisposition to admit the mycoplasma, and it causes the lateral ventricles to deteriorate and die and this leads to multiple sclerosis which will progress until they are totally disabled and frequently die prematurely. It will get into the lower bowel and parts of the lower bowel will die and cause colitis. All of these diseases are caused by the degenerating properties of the mycoplasma.    


About two months ago a gentleman in Sudbury phoned me and told me he had fibromyalgia. He applied for Canada Pension and was turned down because his doctor said it was all in his head and there was no external evidence. I gave him the proper form and a vial, and he sent his blood to Dr. Les Simpson of New Zealand to be tested. He did this with his family doctor's approval, and the results from Dr. Simpson showed that only 4% of his red blood cells were functioning normally and carrying the appropriate amount of oxygen to his poor body, whereas 83% were distended, enlarged and hardened, and wouldn't go through the capillaries without an awful lot of pressure and trouble. This is the physical evidence of the damage that is done.    



You can also ask your doctor to give you a 24-hour Holter ECG. You know, of course, that an electrocardiogram is a measure of your heart beat, which shows what is going on in the right ventricle, the left ventricle, and so on. Tests show that 100% of patients with chronic fatigue syndrome and fibromyalgia have an irregular heart beat. At various periods of time, during the 24 hours, the heart, instead of working happily away, going "bump-BUMP, bump-BUMP", every now and again, it will go "buhbuhbuhbuhbuhbuhbuhbuhbuh". The T-wave (the waves are called P, Q, R, S, and the last one is T) is normally a peak, and then the wave levels off and starts with the P-wave again. In chronic fatigue and fibromyalgia patients, the T-wave flattens off, or actually inverts. That means the blood in the left ventricle is not being squeezed up through the aorta and around through the body. My client did this test, and lo and behold, the test results stated: "The shape of T and S-T suggest left ventricle strain pattern, although voltage and so on is normal". The doctor had no clue as to why the T-wave was not working properly. I analyzed the report of the patient who had been turned down by Canada Pension and sent it back to them. They wrote back and said, "It looks like we may have made a mistake. We are going to give you a hearing and you can explain this to us in more detail." So it is not all in your imagination. There is actual physical damage to the heart. The left ventricle muscles do show scarring. That is why many people are diagnosed with a heart condition when they first develop fibromyalgia, but it's only one of several problems because the mycoplasma can do all kinds of damage.    



You can also ask your doctor for a blood volume test. Every human being requires a certain amount of blood per pound of body weight, and it has been observed that people with fibromyalgia, chronic fatigue syndrome, multiple sclerosis and others do not have the normal blood volume their body needs to function properly. Doctors aren't normally aware of this. This test measures the amount of blood in the human body by taking out five cc, putting a tracer in it, and then putting it back in the body. One hour later take out five cc again and look for the tracer. The thicker the blood and the lower the blood volume, the more tracer you will find. The analysis of one of my clients stated: "This patient was referred for red cell mass study. The red cell volume is 16.9 ml per kg of body weight. The normal range is 25 to 35 ml. per kg." This guy has 36% less blood in his body than the body needs to function". And the doctor hadn't even known the test existed. If you lost 36% of your blood in an accident, do you think your doctor would tell you that you are all right, just take up line dancing and you will get over it? They would rush you to the nearest hospital and start infusing you with blood transfusions. These tragic people with these awful diseases are functioning with anywhere from 7 to 50% less blood than their bodies need to function.    



The body undoes the damage itself. The scarring in the brain of people with chronic fatigue and fibromyalgia will be repaired. There is cellular repair going on all the time. But the mycoplasma has moved on to the next cell. In the early stages of a disease, doxycycline may reverse the disease. It is one of the tetracycline antibiotics, but it is not bactericidal; it is bacteriostatic. It stops the growth of the mycoplasma, and if it is stopped long enough, then the immune system takes over. (Nicholson, G.L., Doxycycline treatment and Desert Storm, JAMA, 1995, 273: 618-619),    



Professor Garth Nicholson, Ph.D., of the Institute for Molecular Medicine is one of the top experts on mycoplasma. He has been given an $8 million grant to study 450 Gulf War veterans, because Gulf War illness is caused by the mycoplasma. Dr. Les Simpson has done most of the research in detecting the disease by the polymerase chain reaction blood test. You may contact Dr. Nicholson at 15162 Triton Lane, Huntington Beach, Ca, 92649-1401, tel 714-903-2900.


In summary, there is a disease agent that is called a mycoplasma. All of these neurodegenerative systemic diseases are caused by a particle of a bacterial DNA, a mycoplasma, that enters into the cells of living organisms and takes the cells apart, sterol by sterol, leaving scar tissue, and causing all the range of symptoms that you see in people with these diseases. The military and the National Institutes of Health and the government are all dedicated to keeping this mycoplasma as covert as they possibly can.    


For more information and references, please refer to The Brucellosis Triangle and The Extremely Unfortunate Skull Valley Incident by Don Scott and William Scott, both available at Consumer Health Organization.  

Other recommended reading is Osler's Web by Hillary Johnson and Emerging Viruses: Aids and Ebola by Leonard Horowitz. Don Scott also produces The Journal of Degenerative Diseases.  

You may contact Donald Scott at: 190 Mountain St., Ste. 405, Sudbury, Ontario, Canada P3B 4G2. 705-670-0180. Note: Dr. David Webster at Sudbury General Hospital, a wonderful person, with whom I have had conversations about these awful diseases can tell your doctor about the Blood Volume test.    


Colloidal Silver may be the answer. By John Claydon D.Hom


M.S. patients, taking  colloidal silver (typically one pint a day) have made excellent improvements in their symptoms. One such person, Nadine A Wooley, had brain scans taken before and after one years use of the colloidal silver. Before, showed typical white areas in the brain showing typical M.S. lesions. A year after taking one pint of silver daily a subsequent scan showed no lesions.  


It may be that mycoplasma can be eliminated with colloidal silver. We also recommend the use of a product called Zell-Oxygen. This is a live cell very small, nutritional yeast (helps fight pathogenic fungi in the body including Candida Albicans, and is extremely well tolerated by persons who have allergic reactions to other forms of yeast (usually cooked or sterilised).    


The Zell yeast provides enzymes that repair the structure and function of the mitochondria of every cell. The DNA of cellular mitochondria are damaged very easily by virus, bacteria, mycoplasma, toxins etc. One of the roles of the mitochondria is to act as a Ďbiological spark plugí to get all the cells processing nutrients and, especially, oxygen. Most of the energy required for day to day functioning, including a proper activity of the immune system rests upon sufficient cellular metabolism. It is for these reasons that the administration of Zell-Oxygen proves so effective in improving the immune system, aids detoxification, and helps improve many chronic health disorders especially M.E. I also recommend a protein digesting enzyme that targets Ďdeadí cells and scars, called Serrapeptase. M.S. sufferers are finding that this helps to promote healing of scar tissue internally and promote a healing process. This has the effect of helping to improve mobility. Serrapeptase has a wide role clinically and is perfectly safe to take long term. It may also help regenerate any tissue ravaged by mycoplasma.  


It is also interesting to note that the damaged red blood cells referred to earlier in the above mycoplasma article, can be corrected with the use of Zell Oxygen.  Until we know more, I will be encouraging the use of Zell-Oxygen, and colloidal silver, and Serrapeptase for all the diseases mentioned in the above mycoplasma article.    


Excerpt from the book: HOW TO BEAT MULTIPLE SCLEROSIS    

by Nadine A Wooley.    


Colloidal Silver is a suspension of extremely fine sub- microscopic particles (0.15-.001 microns) of pure silver suspended in water by a positive electric charge on each particle. A powerful germicidal, silver is an exceptional metal in that it is non-toxic to the human body, but lethal to over 650 disease-causing bacteria, viruses, fungi, parasites, and moulds; while conventional pharmaceutical antibiotics are typically effective against only 6 or 7 types of bacteria. Some new strains of bacteria classified as MDR (Multiple Drug Resistant) have proven to be resistant to ALL pharmaceutical antibiotics, but NOT to Colloidal Silver due to different germicidal mechanisms of deactivation.


The function of our immune system is to respond to invading micro organisms by producing and or sensitizing lymphocytes that will recognize and destroy the invaders. Autoimmune disorders occur when these reactions unexplainably start fighting our body's own cells and tissues, producing a variety of disorders, like MS.


Many scientists believe that the MS immune response is triggered by a virus. Recently, certain bacteria also have been associated with MS. According to the scientific research, there is no bacteria, fungus or virus that silver does not kill. Consequently, it seems very likely it will kill the MS "trigger." As Sais points out: Regular ingestion of Colloidal Silver can act as a second immune system by assisting the body in the war against invading micro-organisms. Unlike pharmaceutical antibiotics, which destroy beneficial enzymes. Colloidal Silver leaves these tissue cell enzymes intact. Colloidal Silver, if used sensibly, is completely non-toxic and will not harm the immune system in any way. The Environmental Protection Agency's Poison Control Centre reports no toxicity listing for Colloidal Silver.


In testing by the UCLA Medical Research Centre, silver has not been found to interact with any of more than 400 drugs. This is significant for MS patients, who are often taking a number of drugs. I began drinking purified water fortified with Colloidal Silver on March 12,1999, and I have not felt this good in ten years. My neurologist, Dr. Grimm, is amazed and dumbfounded. He commented that "Never has a chronic/progressive patient walked into my office and announced that she will be walking soon without a cane. Never has a chronic patient of mine anticipated not having another exacerbation."    


When I began drinking the Colloidal Silver on March 12,1 could not walk a city block without holding someone's arm with one hand and a cane with my other hand. In fact, unassisted, I could only walk between my kitchen counters. The first week I began drinking Colloidal Silver, I quit using the walker in my house. The second week I walked 4/lOths of a mile up my street holding Les' arm and without a cane. I have continued to increase the distance I can walk. On the graph of improvement, I continue to go up.    


How does silver work? (According to Sais:)


There are three mechanisms of deactivation that silver utilizes to incapacitate disease-causing organisms. They are: Catalytic Oxidation; Reaction with Cell Membranes; and Binding with the DNA of disease organisms to prevent unwinding. Catalytic Oxidation: in its atomic state, silver has the capacity to absorb oxygen and act as a catalyst to bring about oxidation. Atomic (nascent) oxygen absorbed onto the surface of silver ions in solution will readily react with the sulfhydryl (-S-H) groups surrounding the surface of bacteria or viruses to remove the hydrogen atoms (as water), causing the sulfur atoms to form an R-S-S-R bond, blocking respiration and causing the bacteria to expire. Employing a simple catalytic reduction/oxidation reaction, Colloidal Silver will react with any negative charge presented by the organism's transport or membrane proteins and deactivate them.    


Reaction with Bacterial Cell Membrane: there is evidence that silver ions attach to membrane surface radicals of bacteria, impairing their cell respiration and blocking their energy transfer system. One explanation is based on the nature of enzyme construction: specific enzymes are required for a given biochemical activity to take place. Enzyme molecules usually require a specific metallic atom as part of the molecular matrix in order to function. A metal of lower valance in the enzyme complex will prevent the enzyme from functioning normally. Silver, with a valance of plus 2, can replace many metals with a lower or equal valance. Binding with DNA: studies with Pseudomonas aeruginosa, a tenacious bacteria that is difficult to treat, demonstrated that as much as 12 percent of silver is taken up by the organism's DNA without destroying the hydrogen bonds holding the lattice together but this nevertheless prevents the DNA from unwinding, an essential step for cellular replication to occur.


Silver is not new to MS. Its antibiotic qualities were first investigated in regards to MS during the 1930s. At that time, spirochetal bacteria were observed in Syphilis and MS patients. Silver kills the bacteria and was used topically in a salve to treat Syphilis. Research on MS in conjunction with silver then began. Following Penicillin's use as a Syphilis treatment in the 1940s, MS research with silver was unfortunately halted because of silver's great expense. The original research was never concluded, and no further research occurred for decades. In the last several decades, the process of creating Colloidal Silver has been developed and refined. During the manufacturing process, electricity passes through the purified water as the silver particles are being introduced and causes the silver to break into a microscopic "dust" Lightning actually passes through the water. My nickname for it is "liquid lightning." The result is water with electrically charged, antiviral, antibacterial, and antifungal properties.    


Sais explains that Colloidal Silver may be taken orally or topically (applied directly to the skin). It can be taken vaginally or anally, atomized or inhaled into the nose or lungs or dropped into the eyes. Liquid silver, as well as new gel formations, may be applied directly to the skin. A few drops on a Q-tip or Band-Aid may be used to disinfect any wound or sore. Liquid silver can also be injected. Colloidal Silver does not affect any of the body's friendly bacteria.


It does not have any negative effects on the natural flora in the bowels. It kills disease-causing organisms very quickly upon contact. It is both a remedy for illness and a preventative treatment. So why haven't we heard about this before? One reason is that although we have known about silver's medical properties for some time, the process of manufacturing a good quality, drinkable silver water was not developed until a few decades ago. Another reason may be that Colloidal Silver does not offer the profit possibilities major American companies are seeking. Silver cannot be patented. The manufacturing process for Colloidal Silver cannot be patented. I drink one 16 ounce bottle per day.    


Dr. Grimm has warned me to wait until the results are in from a scientific study regarding silver and specifically MS. I can't. You have to know about this. As I write this, I have been using the silver solution for just under three months and I can walk further than I have in seven years. This is too exciting. Study results will come in over the course of the next two years. However, that is too long to wait. It is my recommendation that MS patients begin using Colloidal Silver on a daily basis. As noted, I drink one bottle, 16 ounces per day. That may be excessive, but it has worked for me. Do not use less than 4. ounces per day. A maintenance program is figured at 1 ounce per 100 pounds of body weight. But you are not looking for maintenance.    


You want to boost your immune system so it can fight the invading virus or bacteria. Colloidal Silver works in your body like a second immune system, and that is what we MS patients need! And remember, we are not waiting for FDA approval; this stuff is sold "over-the-counter" Try the amount I take. (Remember, your body will pass what it does not use. Colloidal Silver is not addictive, and you will not build up a resistance.) What have you got to lose?  A few dollars? Health is wealth. When test results come in positive for Colloidal Silver helping MS patients, we can only hope that our insurance agencies will encourage its use and decide to pick up the cost.


Taken from ĎHOW TO BEAT MULTIPLE SCLEROSIS (and the things your doctors didnít tell you)í By Nadine A Wooley, Self published, MS UPBEAT, Portland, Oregon. USA. c2000    


Colloidal silver cured M.S. By Nancy Delise


What follows is the story of Nancy Delise, who, over the years, has utilized retail colloidal silver, colloidal silver made with a basic generator, basic colloidal silver enhanced with H2O2 ( orally ), and finally IV Silver ( Argentyn 23 by Natural-Immunogenics - Available only to MD's ).    


Condition: MS Before silver    

I have been on Betaseron since it came on the marketófor 6 or 7 years? I would say it did as promised; I have had no exacerbation since I began the injections. However, everyday I hate to get up to see what additional symptom I have to add to my list to get used to.

My right had is numb, my feet, especially my toes are numb. When I get hot or tired my right leg does not lift well. It drags when I walk. After a day at work, I practically have to crawl to my car. I must hold on to a wall at all times. I really should use a cane. I cannot even go up a curb without holding on to someone or something. No way can I climb a ladder. When I sit for any length of time, my legs stiffen and get spasms and I have to wait awhile before I can walk. It appears that I have had too much to drink. I really should use a cane, but usually I can take my companionís arm to get to my car.


If I sit on the floor for any reason, like play with my grandchildren, I must first get on my knees, then on all fourís, then finally I can get up. Just like a cow. I cannot use help getting up from the floor, I need more control. I sit on the floor as little as possible. When it is hot, I must wear a cold pack vest or I cannot walk. My feet are hot all the time, and I cannot sleep unless my feet are uncovered. I have night paralysis. I must throw my body in order to turn to another side. My legs are locked in the foetal position and it is a real chore to get them unlocked and able to walk. I must use a cane to get to the bathroom during the night. It is about ten feet from my bed.

Jane Wyman has become my good friend with the Poise pads. I cannot go out without the Ultra Poise pads. If I know I will be away from a bathroom for any length of time, I must use Depends. It goes without saying, I must use the pads at night, also.  

Colloidal silver oral use


I drank 2 oz of Silver water twice a day - in the morning & at three PM. Day four I begin to drink 8 oz of Silver water two times per day. I seem to have more energy and the end of the day seems to come a little later. I do not drag as much to my car.

Day 12 The night paralysis seems to be easing. I can get out of bed with more ease Day 14 thru Day 18 My fingers and toes are tingling more and more. My toes are aching. As the days go by my fingertips seem to be aching, also. Day 20 I seem to have surreal feelings in my fingers. Itís like a far away out of body feeling. They still ache.

Day 21, I am getting out of bed much easier and quicker. I climbed a ladder at work, and I am not nearly so tired when I leave work. I can actually walk to my car without holding on to the wall. I did some things on the floor at work, and was able to get up without too much trouble.

Week four, the bottom of my feet are tingling, and I could feel whiskers on Mikeís face (a surreal feeling). I could feel cool bathroom tile on bottom of my feet. My legs ached all night. It was very painful, I wanted to scream out. My legs hurt a great deal. The next morning I was able to walk further than I had in years. Mike and I walked about four blocks that morning. I feel stronger and stronger every day.

Week five, more and more feeling in both fingers and toes every day, less surreal and more natural. Both toes and fingesr get cold.

Week 10, Seem to have small changes every day. Again my toes ached for several days, then I had more feeling in my toes. Itís as though I have a non feeling pad at the bottom of my feet, but feeling all the way around. Like an animalís paw with the padded bottom. It seems I hurt for a few days, then something feels better.

Week 12, I feel like a caterpillar in a cocoon. I wonder if they have pain during the metamorphosis. The bottom of my feet are no longer numb, the fingers on my right hand tingle only at the very tips. I donít even think about lifting a heavy container with my right hand. For years, I wouldnít dare lift, or I would drop whatever I was holding. I poured coffee from a pot without even thinking about it, until I noticed myself. Doing it. There is NO WAY I could be working the hours I have this Christmas, if not for the water. Last year, I had to wear my cooling vest all day every day, and when I went home I could barely walk to my car. Some days I literally dragged my right leg to get to my car. I had to hold on to the building to get around the corner and into my car. When I got home I actually crawled on my hands and knees to get up the steps. This year I never once had to wear my cooling vest. I walk normally to my car at the end of the day, and the steps are not too much of a problem. I still go up one leg only, but it is stronger. The fatigue is minimized, also. Iíve worked many more hours this year than last.

Week 14: I started making my own water about three weeks ago, and Iíve had to send samples to San Antonio for testing. It seems the probe they sent me was not working to full potential, and for about a week I was drinking water with very minimal amounts of silver. After the week I KNEW IT!!! I was regressing. Things were not working so well, again. I was regressing. Thankfully we figured out the problem and within a couple of days I was back on track. Thank God. This set back has convinced me even more. As if that were possible. I have my life back. I will never give up silver water. Week 20: Christmas Week. I had 16 people for dinner Christmas eve. I had 7 people for dinner Christmas day, I worked 11 hours the day after Christmas, and I had 14 people for dinner the next day. That is four days out of four I entertained at my house. I canít remember when I did something like that. I still have night paralysis, but not nearly as bad as it used to be, and I have a lot of stiffness still when I sit a long time, but nothing near as bad as it used to be. My energy level is very high.

August 2002
My MS Update This is the second anniversary of my long, but wonderful journey with colloidal silver (CS). I am a 59-year-old female who had relapsing remitting MS for 31 years. About 1995 it changed to secondary progressive MS. Thus began my long road of decline. Everyday I got worse. When I discovered CS I could barely walk. I was beginning to use a cane. I could not even go up on the curb without aid. My prognosis was grim. I had some knowledge of the great properties of silver, so the idea of CS intrigued me. I researched CS. What did I have to loose?

I began drinking 16 oz per day. In about three weeks I began to notice a difference. You already have a log of my first yearís progress. I seemed to reach a plateau about this time. I did not improve, BUT I never got worse.

I have since had an MRI and it showed that at this time Aug 2001, I no longer had MS. I have had no new lesions for well over a year. What I was working on at the time is to now repair the damage. Since the damage is to the myelin and not the central nervous system, I was quite confident I could improve.  

1 year- 6 months Hydrogen Peroxide Added.
I have researched adding hydrogen peroxide to the CS. One drop of H2O2 per 2 oz. of CS. I learned this would cause the tiny silver particles to break up into even more minute particles. After 15 minutes, the peroxide was evaporated out of the CS, so it is not harmful to the body, but the tinier particles of silver got into the blood stream quicker. All this time it was a slow process because by the time the silver got to the myelin where it was needed, it was so diluted, it couldnít penetrate the lesions and kill the mycoplasma (MS virus). Within a week I began to feel old symptoms again. This is what I call a healing crisis: I would get symptoms of the MS as the virus was dying and the dying pathogen aggravated the nerves, so for 2-4 days I would feel like I was having varying degrees of exacerbation. After a short period, it would end and I was improved again. If I had known about this earlier, I am convinced my recovery time would have decreased a great deal.

1 year-9 months: I am sure there is a way to go even quickerÖÖÖ I began to research IV drips. There are cases of HIV-AIDS infected patients going into complete remission after three infusions. I worked on this project for about six weeks. I finally found someone with a protocol of infusing CS intravenously. I also found a doctor willing to work with me and give this a try.


1 year-11 months: Colloidal Silver IV Administered
First IV: I had my first IV. By that evening I had my first healing crisis; my legs became extremely heavy (like they were 2 years ago). My fingers tips were still numb, but the numbness was extremely exaggerated. All was better at day four.

Second IV a week later: My legs are again aching a great deal, the numbness in my fingers is very intense. It almost feels like they are not attached to me. All better by day three.

Third, fourth, fifth IV: Each time I experienced a reverse of some symptoms I had either forgotten about over the last 40 years, or didnít realize over the years were actually MS symptoms. Iíve practically no problems at all. I feel better then I have in 15 years. I will have no more IVís, but I will NEVER stop drinking CS.

If I had known about the IVís I probably would have had full recovery even sooner. I am quite sure the old lesions are going away. I am anxious for another MRI to prove this also.

TWO YEAR ANNIVERSARY: No more MS, no more symptoms. Most myelin repaired.

PS: My friend, also an MS patient is on the IV drip. She also no longer has MS (By her MRI), but she was worse than me, and not able to get out of her wheel chair. Since IVís she has given up all her spasm medication and has begun to take STEPS ON HER OWN.

I would be happy to share what I've learned with anyone. Call me, Nancy Delise, @ 708-442-6229


Disclaimer: Regenerative Nutrition advocates a holistic approach to natural health and wellbeing.   The body's ability and power to heal depends upon the totality of diet, nutrition, lifestyle and environmental factors.  No claims for the cure of any disease is intended, or implied.  Always consult a health care practitioner when combating disease states.   The statements in this article have not been approved by the FDA.


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Disclaimer: Regenerative Nutrition advocates a holistic approach to natural health and wellbeing. The body's ability and power to heal depends upon the totality of diet, nutrition, lifestyle and environmental factors. The information provided in our article is for information purposes only, it in no way constitutes a medical consultation, or medical advice, nor is it intended to be taken as a solicitation to purchase our products.

Always consult a health care practitioner when combating disease states.

No claim for the cure of any disease is intended, or implied nor do we claim that our products will treat, cure or prevent any disease.