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
[Special Note for readers who are reading this page from an electronic translation in your native language. Since you are already reading this page within the electronic translator, when you click on any of the articles linked below, the article will go to a translated page, allowing you to read the article in your native language. Ken Adachi]
by Donald W. Scott, MA, MSc
President, The Common Cause Medical Research Foundation
To post this article on Facebook, link to the TinyUrl seen below. Facebook will remove any article identified as coming from educate-yourself.org https://tinyurl.com/y7d5jfs4
[Update, July 24, 2012. I was informed by e-mail that Donald Scott had passed away on Dec. 7, 2011. He was 87 years old. God bless him for his efforts to aid humanity. .Ken Adachi]
Extracted from Nexus Magazine, Volume 8, Number
5 (August-September 2001)
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
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 the mycoplasma..."
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
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
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 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 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,
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
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 Creutzfeldt&endash;Jakob disease.
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
Star11 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 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 – 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, etc. 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. AIDS.
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
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
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.
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.
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 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
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
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.
1. "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".
2. "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.
3. 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.
4. 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&endash;144, esp. pp. 114, 129.
5. Kyger, E. R. and Russell L. Haden, "Brucellosis and Multiple Sclerosis",
The American Journal of Medical Sciences 1949:689-693.
6. Colmonero et al., "Complications Associated with Brucella melitensis
Infection: A Study of 530 Cases", Medicine 1996;75(4).
7. Howell, Miller, Kelly and Bookman, "Acute Brucellosis Among Laboratory
Workers", New England Journal of Medicine 1948;236:741.
8. "Special Virus Cancer Program: Progress Report No. 8", ibid.,
table 4, p. 135.
9. US Senate, Hearings before the Subcommittee on Health and Scientific
Research of the Committee on Human Resources, March 8 and May 23, 1977,
10. New England Journal of Medicine, August 22, 1957, p. 362.
11. Toronto Star, May 15, 1997.
12. Dr Donald MacArthur, Pentagon, Department of Defense Appropriations
for 1970, Hearings, Monday June 9, 1969, ibid., p. 129.
13. Henderson, Donald A., "Smallpox: Epitaph for a Killer",
National Geographic, December 1978, p. 804.
14. Blum, Deborah, The Monkey Wars, Oxford University Press, New York,
15. Nicholson, G. L., "Doxycycline treatment and Desert Storm",
¥ 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).
¥ 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
¥ Professor Garth Nicholson, PhD, Institute for Molecular Medicine,
15162 Triton Lane, Huntington Beach, CA, 92649-1401, USA, tel +1 (714)
¥ Dr Les Simpson, Red Blood Cell Research Ltd, 31 Bath Street, Dunedin,
9001, New Zealand, tel +64 (0)3 471 8540, email firstname.lastname@example.org.
(Note: Dr Simpson directs his study to red cell shape analysis, not the
¥ 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 email@example.com.
About the Author:
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.
Web posted at: http://www.nexusmagazine.com/mycoplasma.html
Extracted from Nexus Magazine, Volume 8, Number
5 (August-September 2001)
PO Box 30, Mapleton Qld 4560 Australia. firstname.lastname@example.org
Telephone: +61 (0)7 5442 9280; Fax: +61 (0)7 5442 9381
From our web page at: www.nexusmagazine.com
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