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
• 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 agentbecause  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  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 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 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, 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  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.

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  infamousCamp 731 in  Manchuria, the Japanese military contaminated prisoners of  war with  certain disease agents.

They also established a research camp  in New Guinea in 1942. There  they experimented upon the Fore Indian tribe and inoculated them  with a minced-up version of the brains of diseased sheep containing  the visna virus which causes “mad cow disease” or  Creutzfeldt-Jakob  disease.

About five or six years later, after the Japanese  had been driven  out, the poor people of the Fore tribe developed what they called  kuru, which was their word for “wasting”, and they began to  shake,  lose their appetites and die. The autopsies revealed that their  brains had literally turned to mush. They had contracted “mad cow  disease” from the Japanese experiments.

When World War II  ended,  Dr Ishii Shiro –the medical doctor who was  commissioned as a General in the Japanese Army so he could take  command of Japan’s biological warfare development, testing and  deployment– was captured. He was given the choice of a job with the  United States Army or execution as a war criminal. Not surprisingly,  Dr Ishii Shiro chose to work with the US military to demonstrate how   the Japanese had created mad cow disease in the Fore Indian  tribe.

In 1957, when the disease was beginning to blossom in full among  the  Fore people, Dr Carleton Gajdusek of the US National Institutes of  Health headed to New Guinea to determine how the minced-up brains of  the visna-infected sheep affected them. He spent a couple of  years  there, studying the Fore people, and wrote an extensive report.

He  won the Nobel Prize for “discovering” kuru disease in  the Fore  tribe.

Testing  Carcinogens over Winnipeg, Manitoba In 1953, the US Government asked the  Canadian Government if it could  test a chemical over the city of Winnipeg. It was a big city with  500,000 people, miles from anywhere. The American military sprayed  this carcinogenic chemical in a 1,000%-attenuated form, which they  said would be so watered down that nobody would get very sick;  however, if people came to clinics with a sniffle, a sore throat or  ringing in their ears, the researchers would be able to determine  what percentage would have developed cancer if the chemical had been  used at full strength.

We located evidence that the Americans  had indeed tested this  carcinogenic chemical –zinc cadmium sulphide– over Winnipeg in  1953.  We wrote to the Government of Canada, explaining that we had solid  evidence of the spraying and asking that we be informed as to how  high up in the government the request for permission to spray had  gone. We did not receive a reply.

Shortly after, the  Pentagon held a press conference on May 14, 1997,  where they admitted what they had done. Robert Russo, writing for  the Toronto Star¹¹ from Washington, DC, reported the  Pentagon’s  admission that in 1953 it had obtained permission from the Canadian  Government to fly over the city of Winnipeg and spray out this  chemical –which sifted down on kids going to school, housewives  hanging out their laundry and people going to work.

US Army planes  and trucks released the chemical 36 times between July and August  1953. The Pentagon got its statistics, which indicated that if  the  chemical released had been full strength, approximately a third of  the population of Winnipeg would have developed cancers over the  next five years.

One professor, Dr Hugh Fudenberg, MD, twice  nominated for the Nobel  Prize, wrote a magazine article stating that the Pentagon came  clean  on this because two researchers in Sudbury, Ontario –Don Scott and  his son, Bill Scott– had been revealing this to the public. However,   the legwork was done by other researchers!

The US Army  actually conducted a series of simulated germ warfare  tests over Winnipeg. The Pentagon lied about the tests to the  mayor,  saying that they were testing a chemical fog over the city, which  would protect Winnipeg in the event of a nuclear attack.

A  report commissioned by US Congress, chaired by  Dr Rogene  Henderson, lists 32 American towns and cities used as test sites as  well.

V – BRUCELLA MYCOPLASMA AND DISEASE

AIDS The  AIDS pathogen was created out of a Brucella bacterium  mutated  with a visna virus; then the toxin was removed as a DNA particle  called a mycoplasma. They used the same mycoplasma to  develop  disabling diseases like MS, Crohn’s colitis, Lyme disease, etc.

In the previously mentioned US congressional document of a  meeting  held on June 9, 1969, ¹² the Pentagon delivered a report  to Congress  about biological weapons. The Pentagon stated: “We are  continuing to  develop disabling weapons.” Dr MacArthur, who was in charge of the  research, said: “We are developing a new lethal weapon, a synthetic  biological agent that does not naturally exist, and for which no  natural immunity could have been acquired.”

Think about it. If  you have a deficiency of acquired immunity, you  have an acquired immunity deficiency. Plain as that. AIDS.

In laboratories throughout the United States and in a certain  number  in Canada including at the University of Alberta, the US Government  provided the leadership for the development of AIDS for the purpose  of population control. After the scientists had perfected it, the  government sent medical teams from the Centers for Disease  Control–under the direction of Dr Donald A. Henderson, their  investigator into the 1957 chronic fatigue epidemic in Punta  Gorda – during  1969 to 1971 to Africa and some countries such asIndia, 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 toblame 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 analyze 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 andfibromyalgia 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 withfibromyalgia 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 recognized,  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 orAlzheimer’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.