The Linking Pathogen in Neurosystemic Diseases
Several strains of mycoplasma
have been "engineered" to become more dangerous. They are now being blamed for AIDS, cancer, CFS, MS, CJD and other neurosystemic
I - PATHOGENIC MYCOPLASMA
A Common Disease Agent Weaponised
There are 200 species of Mycoplasma. Most are innocuous and do no harm; only four or five are pathogenic. Mycoplasma
fermentans (incognitus strain) probably comes from the nucleus of the Brucella bacterium. This disease agent is
not a bacterium and not a virus; it is a mutated form of the Brucella bacterium, combined with a visna virus, from
which the mycoplasma is extracted.
The pathogenic Mycoplasma used to be very innocuous, but biological warfare research conducted between 1942 and
the present time has resulted in the creation of more deadly and infectious forms of Mycoplasma. Researchers extracted
this mycoplasma from the Brucella bacterium and actually reduced the disease to a crystalline form. They "weaponised"
it and tested it on an unsuspecting public in North America.
Dr Maurice Hilleman, chief virologist for the pharmaceutical company Merck Sharp & Dohme, stated that this disease
agent is now carried by everybody in North America and possibly most people throughout the world.
Despite reporting flaws, there has clearly been an increased incidence of all the neuro/systemic degenerative diseases
since World War II and especially since the 1970s with the arrival of previously unheard-of diseases like chronic fatigue
syndrome and AIDS.
According to Dr Shyh-Ching Lo, senior researcher at The Armed Forces Institute of Pathology and one of America's top mycoplasma
researchers, this disease agent causes many illnesses including AIDS, cancer, chronic fatigue syndrome, Crohn's colitis, Type
I diabetes, multiple sclerosis, Parkinson's disease, Wegener's disease and collagen-vascular diseases such as rheumatoid arthritis
Dr Charles Engel, who is with the US National Institutes of Health, Bethesda, Maryland, stated the following 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
I have all the official documents to prove that mycoplasma is the disease agent in chronic fatigue syndrome/fibromyalgia
as well as in AIDS, multiple sclerosis and many other illnesses. Of these, 80% are US or Canadian official government documents,
and 20% are articles from peer-reviewed journals such as the Journal of the American Medical Association, New England
Journal of Medicine and the Canadian Medical Association Journal. The journal articles and government documents
complement each other.
How the Mycoplasma Works
The mycoplasma acts by entering 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 the mycoplasma 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 bacterium, it doesn't have any organelles to process its own nutrients, so it
grows by uptaking pre-formed sterols from its host cell and it literally kills the cell; the cell ruptures and what is left
gets dumped into the bloodstream.
II - CREATION OF THE MYCOPLASMA
A Laboratory-Made Disease Agent
Many doctors don't know about this mycoplasma disease agent because it was developed by the US military in biological warfare
experimentation and it was not made public. This pathogen was patented by the United States military and Dr Shyh-Ching Lo.
I have a copy of the documented patent from the US Patent Office.(1)
All the countries at war were experimenting with biological weapons. In 1942, the governments of the United States, Canada
and 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. While they researched
a number of disease pathogens, they primarily focused on the Brucella bacterium and began to weaponise it.
From its inception, the biowarfare program was characterised by continuing in-depth review and participation by the most
eminent scientists, medical consultants, industrial experts and government officials, and it was classified Top Secret.
The US 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 weaponising these diseases. These are diseases that have existed for thousands of
years, but they have been weaponised--which means they've been made more contagious and more effective. And they are spreading.
The Special Virus Cancer Program, created by the CIA and NIH to develop a deadly pathogen for which humanity had no natural
immunity (AIDS), was disguised as a war on cancer but was actually part of MKNAOMI.(2) Many members
of the Senate and House of Representatives 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", and couldn't find it. Somehow they heard I had it, called me and asked me to mail it to them. Imagine:
a retired schoolteacher being called by the United States Senate and asked for one of their secret documents! The US Senate,
through the Government Reform Committee, is trying to stop this type of government research.
The title page of a genuine US Senate Study, declassified on February 24, 1977, shows that George Merck, of the pharmaceutical
company, Merck Sharp & Dohme (which now makes cures for diseases that at one time it created), reported in 1946 to the
US Secretary of War that his researchers had managed "for the first time" to "isolate the disease agent in crystalline form".(3)
They had produced a crystalline bacterial toxin extracted from the Brucella bacterium. The bacterial toxin could be removed
in crystalline form and stored, transported and deployed without deteriorating. It could be delivered by other vectors such
as insects, aerosol or the food chain (in nature it is delivered within the bacterium). But the factor that is working in
the Brucella is the mycoplasma.
Brucella is a disease agent that doesn't kill people; it disables them. But, according to Dr Donald MacArthur of the Pentagon,
appearing before a congressional committee in 1969,(4) researchers found that if they had mycoplasma at a
certain strength--actually, 10 to the 10th power (1010)--it would develop into AIDS, and the person would die from it within
a reasonable period of time because it could bypass the natural human defences. If the strength 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 very interested in life; they would waste away.
Most of us have never heard of the disease brucellosis because it largely disappeared when they began pasteurising milk,
which was the carrier. One salt shaker of the pure disease agent in a crystalline form could sicken the entire population
of Canada. It is absolutely deadly, not so much in terms of killing the body but disabling it.
Because the crystalline disease agent goes into solution in the blood, ordinary blood and tissue tests will not reveal
its presence. The mycoplasma will only crystallise at 8.1 pH, and the blood has a pH of 7.4 pH. So the doctor thinks your
complaint is "all in your head".
Crystalline Brucella and Multiple Sclerosis
In 1998 in Rochester, New York, I met a former military man, PFC Donald Bentley, who gave me a document and told me: "I
was in the US Army, and I was trained in bacteriological warfare. We were handling a bomb filled with brucellosis, only it
wasn't brucellosis; it was a Brucella 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 US military when he was discharged from the service. They linked brucellosis with multiple
sclerosis, and stated in one section: "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 Brucella, and we will give you a pension.
Don't go raising any fuss about it." In these documents, the government of the United States revealed evidence of the cause
of multiple sclerosis, but they didn't make it known to the public--or to your doctor.
In a 1949 report, Drs Kyger and Haden suggested "the 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 Brucella.(5) We have a document from a medical journal, which concludes that one out of 500 people
who had brucellosis would develop what they call neurobrucellosis; in other words, brucellosis in the brain, where the Brucella
settles in the lateral ventricles--where the disease multiple sclerosis is basically located.(6)
Contamination of Camp Detrick Lab Workers
A 1948 New England Journal of Medicine report titled "Acute Brucellosis Among Laboratory Workers" shows us how actively
dangerous this agent is.(7) The laboratory workers were from Camp Detrick, Frederick, Maryland, where they
were developing biological weapons. Even though these workers had been vaccinated, wore rubberised 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
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 Brucella
into a more effective biological weapon.
III - COVERT TESTING OF MYCOPLASMA
Testing the Dispersal Methods
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 Brucella would cause disease in humans. Now they needed to determine how it
would spread and the best way to disperse it. They tested dispersal methods for Brucella suis and Brucella melitensis
at Dugway Proving Ground, Utah, in June and September 1952. Probably, 100% of us now are infected with Brucella suis
and Brucella melitensis.(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 US Government to cooperate in testing weaponised Brucella,
and Canada cooperated fully with the United States. The US Government wanted to determine whether mosquitoes would carry the
disease and also if the air would carry it. A government report stated that "open-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".(9)
Testing via Mosquito Vector in Punta Gorda, Florida
A report from The New England Journal of Medicine reveals that one of the first outbreaks of chronic fatigue syndrome
was in Punta Gorda, Florida, back in 1957.(10) 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. The truth is that
those mosquitoes were infected in Canada by Dr Guilford B. Reed at Queen's University. They were bred in Belleville, Ontario,
and taken down to Punta Gorda and released there.
Within a week, the first five cases ever of chronic fatigue syndrome were reported to the local clinic in Punta Gorda.
The cases kept coming until finally 450 people were ill with the disease.
Testing via Mosquito Vector in Ontario
The Government of Canada had established the Dominion Parasite Laboratory in Belleville, Ontario, where it raised 100 million
mosquitoes a month. These were shipped to Queen's University and certain other facilities to be infected with this crystalline
disease agent. The mosquitoes were then let loose in certain communities in the middle of the night, so that the researchers
could determine how many people would become ill with chronic fatigue syndrome or fibromyalgia, which was the first disease
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 hundreds of millions of infected mosquitoes. Over 700 people in the next four or five weeks developed myalgic
encephalomyelitis, or chronic fatigue syndrome.
IV - COVERT TESTING OF OTHER DISEASE AGENTS
Mad Cow Disease/Kuru/CJD in the Fore Tribe
Before and during World War II, at the infamous Camp 731 in Manchuria, the Japanese military contaminated prisoners of
war with certain disease agents.
They also established a research camp in New Guinea in 1942. There they 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" or
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, Dr Ishii Shiro--the medical doctor who was commissioned as a General in the Japanese Army so he
could take command of Japan's biological warfare development, testing and deployment--was captured. He was given 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
US military to demonstrate how the Japanese had created mad cow disease in the Fore Indian tribe.
In 1957, when the disease was beginning to blossom in full among the Fore people, Dr Carleton Gajdusek of the US National
Institutes of Health headed to New Guinea to determine how the minced-up brains of the visna-infected sheep affected them.
He spent a couple of years there, studying the Fore people, and wrote an extensive report. He won the Nobel Prize for "discovering"
kuru disease in the Fore tribe.Testing Carcinogens over Winnipeg, Manitoba
In 1953, the US Government asked the Canadian Government if it could test a chemical over the city of Winnipeg. It was
a big city with 500,000 people, miles from anywhere. The American military sprayed this carcinogenic 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 the chemical had been used at full strength.
We located evidence that the Americans had indeed tested this carcinogenic chemical--zinc cadmium sulphide--over Winnipeg
in 1953. We wrote to the Government of Canada, explaining that we had solid evidence of the spraying and asking that we be
informed as to how high up in the government the request for permission to spray had gone. We did not receive a reply.
Shortly after, the Pentagon held a press conference on May 14, 1997, where they admitted what they had done. Robert Russo,
writing for the Toronto Star(11) from Washington, DC, reported the Pentagon's admission that in 1953 it had
obtained permission from the Canadian Government to fly over the city of Winnipeg and spray out this chemical--which 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 Pentagon got its statistics, which indicated that if the chemical
released had been full strength, approximately a third of the population of Winnipeg would have developed cancers over the
next five years.
One professor, Dr Hugh Fudenberg, MD, twice nominated for the Nobel Prize, wrote a magazine article stating that the Pentagon
came clean on this because two researchers in Sudbury, Ontario--Don Scott and his son, Bill Scott--had been revealing this
to the public. However, the legwork was done by other researchers!
The US Army actually conducted a series of simulated germ warfare tests over 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
A report commissioned by US Congress, chaired by Dr Rogene Henderson, lists 32 American towns and cities used as test sites
as well.V - BRUCELLA MYCOPLASMA AND DISEASE
The AIDS pathogen was created out of a Brucella bacterium 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,
In the previously mentioned US congressional document of a meeting held on June 9, 1969,(12) the Pentagon
delivered a report to Congress about biological weapons. 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.
In laboratories throughout the United States and in a certain number in Canada including at the University of Alberta,
the US Government provided the leadership for the development of AIDS for the purpose of population control. After the scientists
had perfected it, the government sent medical teams from the Centers for Disease Control--under the direction of Dr Donald
A. Henderson, their investigator into the 1957 chronic fatigue epidemic in Punta Gorda--during 1969 to 1971 to Africa and
some countries such as India, Nepal and Pakistan where they thought the population was becoming too large.(13)
They gave them all a free vaccination against smallpox; but five years after receiving this vaccination, 60% of those inoculated
were suffering from AIDS. They tried to blame it on a monkey, which is nonsense.
A professor at the University of Arkansas made the claim that while studying the tissues of a dead chimpanzee she found
traces of HIV. The chimpanzee that she had tested was born in the United States 23 years earlier. It had lived its entire
life in a US military laboratory where it was used as an experimental animal in 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 analyse 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 HIV in it. That virus was acquired by that chimpanzee in the laboratories where it was tested.(14)Chronic
Fatigue Syndrome/ Myalgic Encephalomyelitis
Chronic fatigue syndrome is more accurately called myalgic encephalomyelitis. The chronic fatigue syndrome nomenclature
was given by the US National Institutes of Health because it wanted to downgrade and belittle the disease.
An MRI scan of the brain of a teenage girl with 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 been replaced by scar tissue. This caused
cognitive impairment, memory impairment, etc. And what was the cause of the scarring? 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 Pensions
Plan Review Tribunal will be turned down because they cannot prove that they are ill. During 1999 I conducted several appeals
to Canada Pensions and the Workers Compensation Board (WCB, now the Workplace Safety and Insurance Board) on behalf of people
who have been turned down. I provided documented evidence of these illnesses, and these people were all granted their pensions
on the basis of the evidence that I provided.
In March 1999, for example, I appealed to the WCB on behalf of a lady with fibromyalgia who had been denied her pension
back in 1993. The vice-chairman of the board came 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 that 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 MYCOPLASMA IN YOUR BODY
Polymerase Chain Reaction Test
Information is not generally available about this agent because, first of all, the mycoplasma is such a minutely small
disease agent. A hundred years ago, certain medical theoreticians conceived that there must be a form of disease agent smaller
than bacteria and viruses. This pathogenic organism, the mycoplasma, is so minute that normal blood and tissue tests will
not reveal its presence as the source of the disease.
Your doctor may diagnose you with Alzheimer's disease, 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 the polymerase chain reaction (PCR) test was developed,
in which a sample of your blood is examined and damaged particles are removed and subjected to a polymerase chain reaction.
This causes the DNA in the particles to break down. The particles are then placed in a nutrient, which causes the DNA to grow
back into its original form. If enough of the substance is produced, the form can be recognised, so it can be determined whether
Brucella or another kind of agent is behind that particular mycoplasma.Blood Test
If you or anybody in your family has myalgic encephalomyelitis, fibromyalgia, multiple sclerosis or Alzheimer's, you can
send a blood sample to Dr Les Simpson in New Zealand for testing.
If you are ill with these diseases, your red blood cells will not be normal doughnut-shaped blood cells capable of being
compressed and squeezed through the capillaries, but will swell up like cherry-filled doughnuts which cannot be compressed.
The blood cells become enlarged and distended because the only way the mycoplasma can exist is by uptaking pre-formed sterols
from the host cell. One of the best sources of pre-formed 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 and 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 are 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. The mycoplasma 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 this causes the lateral ventricles to deteriorate
and die. This leads to multiple sclerosis, which will progress until these people are totally disabled; frequently, they die
prematurely. The mycoplasma will get into the lower bowel, parts of which will die, thus causing colitis. All of these diseases
are caused by the degenerating properties of the mycoplasma.
In early 2000, a gentleman in Sudbury phoned me and told me he had fibromyalgia. He applied for a 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 Simpson 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.ECG Test
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 heartbeat and 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 heartbeat. At various periods during the 24 hours,
the heart, instead of working happily away going "bump-BUMP, bump-BUMP", every now and again goes "buhbuhbuhbuhbuhbuhbuhbuhbuh".
The T-wave (the waves are called P, Q, R, S and 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 from Sudbury had this test done and, lo and behold, the results stated: "The shape of T and S-T suggests 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 analysed the report of this patient who had been turned down by Canada Pensions and sent it back to them. They
wrote back, saying: "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.Blood Volume Test
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 other
illnesses 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 5 cc, putting a tracer in it and then putting it
back into the body. One hour later, take out 5 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 alright and should just
take up line dancing and get over it? They would rush you to the nearest hospital and start transfusing you with blood. These
tragic people with these awful diseases are functioning with anywhere from 7% to 50% less blood than their body needs to function.VII - UNDOING THE DAMAGE
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 that disease process. It is one of the tetracycline antibiotics,
but it is not bactericidal; it is bacteriostatic--it stops the growth of the mycoplasma. And if the mycoplasma growth can
be stopped for long enough, then the immune system takes over.
Doxycycline treatment is discussed in a paper by mycoplasma expert Professor Garth Nicholson, PhD, of the Institute for
Molecular Medicine.15 Dr Nicholson is involved in a US $8-million mycoplasma research program funded by the US military and
headed by Dr Charles Engel of the NIH. The program is studying Gulf War veterans, 450 of them, because there is evidence to
suggest that Gulf War syndrome is another illness (or set of illnesses) caused by mycoplasma.
- "Pathogenic Mycoplasma", US Patent No. 5,242,820, issued September 7, 1993. Dr Lo is listed as the "Inventor" and the
American Registry of Pathology, Washington, DC, is listed as the "Assignee".
- "Special Virus Cancer Program: Progress Report No. 8", prepared by the National Cancer Institute, Viral Oncology, Etiology
Area, July 1971, submitted to NIH Annual Report in May 1971 and updated July 1971.
- US Senate, Ninety-fifth Congress, Hearings before the Subcommittee on Health and Scientific Research of the Committee
on Human Resources, Biological Testing Involving Human Subjects by the Department of Defense, 1977; released as US Army
Activities in the US Biological Warfare Programs, Volumes One and Two, 24 February 1977.
- Dr Donald MacArthur, Pentagon, Department of Defense Appropriations for 1970, Hearings before Subcommittee of the Committee
on Appropriations, House of Representatives, Ninety-First Congress, First Session, Monday June 9, 1969, pp 105-144, esp. pp.
- Kyger, E. R. and Russell L. Haden, "Brucellosis and Multiple Sclerosis", The American Journal of Medical Sciences
- Colmonero et al., "Complications Associated with Brucella melitensis Infection: A Study of 530 Cases", Medicine 1996;75(4).
- Howell, Miller, Kelly and Bookman, "Acute Brucellosis Among Laboratory Workers", New England Journal of Medicine
- "Special Virus Cancer Program: Progress Report No. 8", ibid., table 4, p. 135.
- US Senate, Hearings before the Subcommittee on Health and Scientific Research of the Committee on Human Resources, March
8 and May 23, 1977, ibid.
- New England Journal of Medicine, August 22, 1957, p. 362.
- Toronto Star, May 15, 1997.
- Dr Donald MacArthur, Pentagon, Department of Defense Appropriations for 1970, Hearings, Monday June 9, 1969, ibid., p.
- Henderson, Donald A., "Smallpox: Epitaph for a Killer", National Geographic, December 1978, p. 804.
- Blum, Deborah, The Monkey Wars, Oxford University Press, New York, 1994.
- Nicholson, G. L., "Doxycycline treatment and Desert Storm", JAMA 1995;273:618-619.
- Horowitz, Leonard, Emerging Viruses: Aids and Ebola, Tetrahedron Publishing, USA, 1996.
- Johnson, Hillary, Osler's Web, Crown Publishers, New York, 1996.
- Scott, Donald W. and William L. C. Scott, The Brucellosis Triangle, The Chelmsford Publishers (Box 133, Stat. B.,
Sudbury, Ontario P3E 4N5), Canada, 1998 (US$21.95 + $3 s&h in US).
- Scott, Donald W. and William L. C. Scott, The Extremely Unfortunate Skull Valley Incident, The Chelmsford Publishers,
Canada, 1996 (revised, extended edition available from mid-September 2001; US$16.00 pre-pub. price + US$3 s&h in US).
- The Journal of Degenerative Diseases (Donald W. Scott, Editor), The Common Cause Medical Research Foundation (Box
133, Stat B., Sudbury, Ontario, P3E 4N5), Canada (quarterly journal; annual subscription: US$25.00 in USA, $30 foreign).
About the Author:
- Ms Jennie Burke, Australian Biologics, Level 6, 383 Pitt Street, Sydney NSW 2000, Australia tel +61 (0)2 9283 0807, fax
+61 (0)2 9283 0910. Australian Biologics does tests for mycoplasma.
- Consumer Health Organization of Canada, 1220 Sheppard Avenue East #412, Toronto, Ontario, Canada M2K 2S5, tel +1 (416)
490 0986, website www.consumerhealth.org/.
- Professor Garth Nicholson, PhD, Institute for Molecular Medicine, 15162 Triton Lane, Huntington Beach, CA, 92649-1401,
USA, tel +1 (714) 903 2900.
- Dr Les Simpson, Red Blood Cell Research Ltd, 31 Bath Street, Dunedin, 9001, New Zealand, tel +64 (0)3 471 8540, email
email@example.com. (Note: Dr Simpson directs his study to red cell shape analysis, not the mycoplasma hypothesis.)
- The Mycoplasma Registry for Gulf War Illness, S. & L. Dudley, 303 47th St, J-10 San Diego, CA 92102-5961, tel/fax
+1 (619) 266 1116, fax (619) 266 1116, email firstname.lastname@example.org.
Donald Scott, MA, MSc, is a retired high school teacher and university professor. He is also 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. He
is currently President of The Common Cause Medical Research Foundation, a not-for-profit organisation devoted to research
into neurosystemic degenerative diseases. He is also Adjunct Professor with the Institute for Molecular Medicine and he produces
and edits the Journal of Degenerative Diseases. 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.
Extracted from Nexus Magazine, Volume 8, Number 5 (August-September 2001)
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© by Donald W. Scott, MA, MSc © 2001
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