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.
Extracted from Nexus Magazine, Volume 8, Number 5 (August-September 2001)
PO Box 30, Mapleton Qld 4560 Australia.
editor@nexusmagazine.com
Telephone: +61 (0)7 5442 9280; Fax: +61 (0)7 5442 9381
http://www.nexusmagazine.com/articles/mycoplasma.html
© by Donald W. Scott, MA, MSc © 2001
President
The Common Cause
Medical Research Foundation
190 Mountain Street, Suite 405
Sudbury, Ontario, Canada P3B 4G2
Tel/fax: +1 (705) 670 0180
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 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.
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.
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 (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 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&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
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 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.
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. L., "Doxycycline treatment
and Desert Storm", JAMA 1995;273:618-619.
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 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).
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 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 rbc.research.limited@xtra.co.nz.
(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 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.
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Mycoplasma
n. Any of numerous parasitic, pathogenic
microorganisms of the genus Mycoplasma
that lack a true cell wall, are gram-negative, and need sterols such as
cholesterol for growth. In humans, one species is a primary cause of
nonbacterial pneumonia. Also called pleuropneumonia-like
organism.
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In general, Blacks throughout the world give credibility
to a thing when a White person has given their blessings to it. All the
same, there are those of us who are the watchers and tell you as it is long
before the “great White savior” bring his or her blessings within your
mind. We also have those Blacks who
ignorantly reject things just for the hell of “fighting the power that be”, knowing little about what they fight
against and when it is appropriate to use tact and diplomacy. When you know the victory is already yours,
it is easier to use diplomacy. It is
without a doubt that African people have been targeted for extermination and
this includes African Americans. Yes,
extermination, just as you would exterminate termites. Another way of saying this is, EXTINCTION.
Those Blacks who have
assimilated in their minds and moved on to physical assimilation most often
think Blacks have become better in America. However,
here is a short snippet from the New York Times:
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Nicole Bengiveno/The New York Times
Janice
Johnson, a social worker, is seated at left next to Eunice Brown. Ms.
Brown’s mother stands at right.
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In
Turnabout, Infant Deaths Climb in South
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HOLLANDALE, Miss. — For decades, Mississippi and neighboring states with
large black populations and expanses of enduring poverty made steady
progress in reducing infant death. But, in what health experts call an
ominous portent, progress
has stalled and in recent years the death rate has risen in Mississippi and
several other states……. The
setbacks have raised questions about the impact of cuts in welfare and
Medicaid and of poor access to doctors, and, many doctors say, the growing
epidemics of obesity,
diabetes
and hypertension
among potential mothers, some
of whom tip the scales here at 300 to 400 pounds.
http://www.nytimes.com/2007/04/22/health/22infant.html?_r=1&hp=&adxnnl=1&oref=slogin&adxnnlx=1177254335-T8B33omAVLHerIq50eWzkQ
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The solution is the CART Vision/Objectives, not more
American welfare in America and Aid in Africa. Our people have been given AIDS for aid. The food has even poisoned millions causing
excessive obesity, diabetes and other ailments.
Biggest Problem Demands Biggest
Attention
It is important to be
able to see and respond to the unseen.
Police brutality is more often that which is seen. Blacks in America place a great deal of attention on police
brutality targeted at Blacks. However,
little attention has been placed on how White America and elements of Europe are killing far more Blacks than police could ever kill. Attention must be placed on the
politicians, corporate and business leaders who long ago decreed that a free African shall be a dead
African.
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Merck At Center of Forced HPV Vaccination of All
Girls
These critical "Special Virus Cancer Program" documents, that must be brought to world attention,
include the National Institute of Health contracts numbered NIH-71-2025 and
NIH-71-2059, to Litton Bionetics and the Merck pharmaceutical company. U.S.
Congressional Records show both of these companies were linked, during the
1960s and early 1970s, to each other as well as to biological weapons
programs administered by the CIA and U.S.
military contractors under National Security Agency oversight. Bionetics employed the world's leading primate cancer
virus investigating team. The viruses they manufactured en masse at that
time, using comparatively crude, by today's standards, laboratory methods,
included viruses that were functionally and descriptively identical to HIV.
The evidence for this seemingly outrageous claim is astonishingly certain.
Leonard
G. Horowitz, D.M.D, M.A., M.P.H.
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This mass murder is
accomplished via HIV/AIDS. Some of you
thought and assumed all of those “brothers” coming out of prison were simply
“down low brothers”. You should think
again. They, like rats in a
laboratory, are introduced to HIV in prisons via what they eat, vaccines and
it is even possible to contract it via the centralized controlled air
breathed within prisons. What about the White prisoners?
Before I answer that,
take a look at what Dr. Maurice Hilleman had to say
about what you have been inundated with in some of these CART Analysis.
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Dr. Maurice Hilleman
Died in April 2005
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Much of modern
preventive medicine is based on his work, and his contributions have helped
extend human life expectancy and improve the economies of many countries.
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….. That these vaccine related
studies likely triggered AIDS is further implied by Merck's leading vaccine
expert, Dr. Maurice Hilleman, President Clinton's
1998 Sabin Gold Medal of Honor awardee. Dr. Hilleman went on record, during a
1986 interview, that he brought the AIDS virus
into North
America in contaminated monkeys destined for vaccine research and testing
at Merck. This admission alone, deserves a US
Congressional, United Nations, if not World Court
inquiry…..
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We
are talking about an “ethnic specific weapon”, an ethnic bomb. Recently, someone asked me, with the
birthrate of Mexicans being so high and with so many arriving across the
American southern border by the millions, why haven’t they been targeted for
HIV? The reason is because they are
too closely related to many of the Whites genetically. For example, there are two main groups in Mexico, the Criollos (pure
White Spanish “blood”), and the Mestizos (of mixed
Spanish “blood”). More than 90 percent
of the native people of Mexico were exterminated by the Spanish, French and
other minor European groups. The 10
percent that remained mixed with the replacement population of
Europeans. The Mexican genome is too
closely related to most Europeans and would endanger too many Whites if HIV
was targeted at them.
Many
White prisoners would not be affected by certain foods, vaccines and other
vectors used to deliver this “mycoplasm” that is
decimating Blacks all around the world while “the band played on”.
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Dr. Leonard Horowitz’s October 2007 Letter
to South African President, Thabo Mbeki
…….Despite the largely false
and misleading arguments that the gene sequences of Bionetics's
bioengineered retroviruses differed substantially from HIV-1 and HIV-2, an
argument that Dr. Robert Gallo gave me which is echoed by leading AIDS
researchers today, it is clear a virtual "smoking gun" exists
with these contracts that show the unique
immune-suppression/leukemia/lymphoma/sarcoma cancer complex, arguably
non-existent on plant earth prior to the first cases of HIV/AIDS seen
around 1978,
was precisely what Dr. Gallo, leading the Bionetics
team for the National Cancer Institute, spent most of his time and money
researching, developing, and testing during the late 1960s and early 1970s.
This was precisely timed for the first simultaneous HIV/AIDS outbreaks on
two far removed continents in two demographically distinct, and unique,
populations…..
Leonard
G. Horowitz, D.M.D, M.A., M.P.H.
http://www.tetrahedron.org/news/nr20001019.html
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Notice
that Dr. Horowitz stated that this killer virus was, reportedly, first seen
in 1978. This was 8 years after
American congressional representatives discussed the funding and creation of
this killer virus as discussed in Public Law 91-171.
How
could Bayer’s keep the HIV/AIDS virus alive in Aspirins that it intentionally
sold to hemophiliacs? Read the
following:
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Keeping Their Killer Alive
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.
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