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MYCOPLASMA
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 diseases.
Donald W.
Scott MA, MSc.
?
2001
Nexus Magazine Aug 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 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 and Alzheimer’s.
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 thepathogen 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 or 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.
Crystalline Brucella
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—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 10
to 8, the person would manifest with chronic fatigue syndrome or
fibromyalgia. If it was l0 to 7, 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 ventrides—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, 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 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 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 Creutzfeldt—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 AIDS
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 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 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 flbromya1gia 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 or 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
"buhbuhbuhbuhbubbuhbuhbuhbuh". 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 way 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 allright 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, doxycydine 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." 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.
Endnotes
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—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, ibid.
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, 1994.
15. Nicholson, G. 1., "Doxycycline treatment and Desert Storm",
JAMA 1995;273:61 8-619.
Recommended Reading
•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 1. 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).
Additional Contacts
• 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 255, 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
rbc.research.limited@xtra.co.nz . (Note: Dr Simpson directs
his study to red cell shape analysis, not the mycoplasrna
hypothesis.)
• The Mycoplasma Registry for Gulf War Illness, S. & 1. Dudley,
303 47th St, J-10 San Diego, CA 92102-5961, tel/fax +1(619) 266
1116, fax (619) 266 1116, email
mycoreg@juno.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.
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.
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