THE LINKING PATHOGEN IN NEURO-SYSTEMIC DISEASES: CHRONIC FATIGUE,

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THE LINKING PATHOGEN IN NEURO-SYSTEMIC DISEASES: CHRONIC FATIGUE,

ALZHEIMER'S, PARKINSON'S & MULTIPLE SCLEROSIS

by: Scott, Donald W., M.Sc.

 

 

 

Donald Scott is a retired high school teacher and university professor

who is currently president of the Common Cause Medical Research

Foundation and adjunct professor of the Institute of Molecular

Medicine. 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. Donald Scott is 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.

 

I - THE MYCOPLASMA

 

A COMMON PATHOGENIC MYCOPLASMA There are 200 species of mycoplasmas.

Most are innocuous and do no harm; only four or five are pathogenic.

The Mycoplasma fermentans (incognitus strain) probably comes from the

nucleus of the brucellosis bacteria. This disease agent is not a

bacteria, and not a virus; it is a mutated form of the brucellosis

bacteria, mutated with a visna virus, from which the mycoplasma, is

extracted. Dr. Maurice Hilleman, chief virologist for the

pharmaceutical company of Merck, Sharp and Dohme, stated that this

disease agent is now carried by everybody in North America and

possibly most people throughout the world. The mycoplasma used to be

very innocuous. Only one person out of 500,000 would get multiple

sclerosis; one out of 300,000 would develop Alzheimer's; one out of

1,000,000 would develop Creutzfeldt-Jakob disease. Before the early

1980's, nobody ever died of AIDS because it didn't exist. The

mycoplasma is also the disease agent in AIDS, and I have all the

documentation to prove it.

 

BIOWARFARE RESEARCH Between 1942 and the present time, biological

warfare research has resulted in a more deadly and infectious form of

the mycoplasma. They extracted this mycoplasma from the brucellosis

bacteria, weaponized it and actually reduced the disease to a

crystalline form. According to Dr. Shyh-Ching Lo, one of America's

top, top researchers, this disease agent, the mycoplasma, causes among

other things, AIDS, chronic fatigue syndrome, multiple sclerosis,

Wegener's disease, Parkinson's disease, Crohn's colitis, Type I

diabetes, and collagen-vascular diseases such as rheumatoid arthritis

and Alzheimer's. The mycoplasma enters 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 it 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 bacteria, it doesn't have any organelles to process

its own nutrients, so it grows by uptaking preformed sterols from its

host cell, literally kills the cell, and the cell ruptures and what is

left gets dumped into the blood stream.

 

DOCUMENTED EVIDENCE My conclusions are entirely based upon official

documents: 80% are United States or Canadian official government

documents, and 20% are articles from peer-reviewed journals, such as

the Journal of the American Medical Association, The New England

Journal of Medicine, and The Canadian Medical Association Journal. The

journal articles and government documents complement each other. We

also have a document from Dr. Shyh-Ching Lo which names the mycoplasma

as a cause of cancer. Dr. Charles Engel who is with the National

Institutes of Health, Bethesda, Maryland, stated 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 " .

 

II - CREATION OF THE MYCOPLASMA

 

MYCOPLASMA PATENT Many doctors don't know about this mycoplasma

because it was developed by the U.S. military in biological warfare

experimentation, and it was not made public. This pathogenic

mycoplasma disease agent was patented by the United States military by

Dr. Shyh-Ching Lo, who was the top researcher for the military

biological warfare research facility. I have the documented patent

from the U.S. patent office.

 

A LABORATORY-CREATED PATHOGEN BY THE U.S. MILITARY Researchers in the

United States, Canada and Britain were doing biowarfare research with

the brucellosis bacteria as well as with a number of other disease

agents. 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 top secret. The U.S. 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 which have existed for thousands of

years, but they have been weaponized which means they were made more

contagious and more effective. And they are spreading. A program

developed by the CIA and NIH to develop a deadly lethal pathogen for

which humanity had no natural immunity (AIDS) was disguised as a war

on cancer and was part of MKNAOMI (ref. Special Virus Cancer Program:

Progress Report 8, prepared by National Cancer Institute, Viral

Oncology, Etiology Area, July, 1971 and submitted to NIH Annual Report

in May, 1971 and updated July, 1971).

 

COMMITTEE ON GOVERNMENT REFORM Many members of the Senate and House of

Represent-atives 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 mentioned above and couldn't find

it. Somehow they heard I had it, called me and asked me to mail it to

them. Imagine. A retired school teacher being called by the United

States Senate and asked for one of their secret documents! The United

States Senate through their government reform committee is trying to

stop this type of government research.

 

BIOLOGICAL WARFARE RESEARCH AGREEMENT All the countries at war were

experimenting with biological weapons. In 1942, the governments of the

United States, Canada and Great 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. They primarily

focused on brucellosis, and they began to weaponize the brucellosis

bacteria.

 

CRYSTALLINE BRUCELLOSIS In a genuine U.S. Senate Study unclassified on

February 24, 1977, the title page of this government record reports

that George Merck, of the pharmaceutical company, Merck, Sharp and

Dohme (which now makes cures for diseases they at one time created),

in 1946, reported to the Secretary of War in the United States that

his researchers had produced in isolation for the first time, a

crystalline bacterial toxin extracted from brucellosis bacteria. The

bacterial toxin could be removed in crystalline form and delivered by

other vectors (in nature they are delivered within the bacteria). But

the factor that is working in the brucellosis is the mycoplasma.

Brucellosis is a disease agent that doesn't kill people; it disables

them. But they found that if they had mycoplasma at a certain

strength, actually ten to the tenth power, it would develop into AIDS,

and the person would die from it within a reasonable period of time

because it could bypass our natural human defenses. If it 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 that interested in

life, they would waste away (ref. Dr. Donald MacArthur of the Pentagon

appearing before a Congressional Committee, June 9, 1969, Department

of Defense Appropriations, p.114, 129). Most of us have never heard of

brucellosis because it largely disappeared when they began

pasteurizing milk, which was the carrier. One salt shaker of this pure

disease in a crystalline form could sicken the entire population of

Canada. It is absolutely deadly, not in terms of killing the body, but

in terms of disabling the body. The advantage of this crystalline

disease agent is that it does not show up in blood and tissue tests

because the bacteria has disappeared and only the pure disease agent

remains. So the doctor thinks that it's all in your head.

 

CRYSTALLINE BRUCELLOSIS AND MULTIPLE SCLEROSIS About three years ago

in Rochester, New York, a gentleman gave me a document and told me, " I

was in the U.S. Army, and I was trained in bacteriological warfare. We

were handling a bomb filled with brucellosis, only it wasn't

brucellosis; it was a brucellosis 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 U.S. military when he was discharged from the service. It

linked brucellosis with multiple sclerosis and stated: " 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

brucellosis and we will give you a pension. Don't go raising any fuss

about it. " The government of the United States, in this official

document revealed evidence of the cause of multiple sclerosis, but

they didn't make it known to the public, or to your doctor. In a 1958

report, Drs. Kyger and Haden suggest " …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 brucellosis. We have a document

from a medical journal which concludes that one out of 500 people who

had brucellosis would develop what they called neurobrucellosis, in

other words, brucellosis in the brain which settles in the lateral

ventricles where the disease multiple sclerosis is basically located.

 

CONTAMINATION OF CAMP DETRICK LAB WORKERS A report from the New

England Journal of Medicine, 1948, Vol.236, p.741 called " Acute

Brucellosis Among Laboratory Workers " shows us how actively dangerous

this agent is. The laboratory workers were from Camp Detrick,

Frederick, Maryland where they were developing biological weapons.

Even though these laboratory 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 brucellosis into a more effective biological weapon.

 

III - COVERT TESTING OF THE MYCOPLASMA

 

TESTING BRUCELLOSIS UPON AN UNSUSPECTING PUBLIC 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 brucellosis would cause disease

in humans. Now they needed to determine how it spread, and the best

way to disperse it. They tested dispersal methods for Brucella suis

and Brucella melitensis at Dugway Proving Ground, Utah, June and

September 1952. Probably, 100% of us now are infected with Brucella

suis and Brucella melitensis. (ref. p.135, table 4 of Special Virus

Cancer Program: Progress Report 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 government of the United States

to cooperate in testing weaponized brucellosis, and Canada cooperated

fully with the government of the United States. They wanted to

determine (i) if mosquitoes will carry the disease and (ii) if the air

will 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 " .

 

TESTING BRUCELLOSES VIA MOSQUITO VECTOR IN PUNTA GORDA A report from

The New England Journal of Medicine, August 22, 1957, p.362 reveals

that one of the first outbreaks of chronic fatigue syndrome was in

Punta Gorda, Florida, back in 1957. 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. When the forest fire broke out, the mosquitoes all said, " Well,

let's go over to Punta Gorda - there will be a bunch of people over

there, we can have a picnic, and then we will go home " . The truth is

that those mosquitoes were infected in Canada by Dr. J.B. Reed at

Queen's University. They were bred in Belleville, Ontario, and taken

down and released in Punta Gorda. Within a week, the first five cases

ever of chronic fatigue syndrome were reported to the local clinic in

Punta Gorda, and it continued until finally 450 people were ill with

the disease.

 

TESTING BRUCELLOSIS VIA MOSQUITO VECTOR IN ONTARIO The government of

Canada established the Dominion Parasite Laboratory in Belleville,

Ontario, and raised 100 million mosquitoes a month which were shipped

to Queen's University and certain other facilities to be infected with

this disease agent. The mosquitoes were then let loose in certain

communities in the middle of the night so they 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 absolutely

hundreds of millions of infected mosquitoes. Over 700 people in the

next four or five weeks developed myalgic encephalomyelitis, or

chronic fatigue syndrome.

 

IV - OTHER SECRET GOVERNMENT TESTING

 

MAD COW DISEASE IN THE FORE INDIAN TRIBE At the infamous Japanese Camp

731 in Manchuria, they contaminated prisoners of war with certain

disease agents. They also established a research camp in New Guinea in

1942, and 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 (Creutzfeldt-Jakob

disease which is known to you as mad cow disease, but which was known

to the Fore Indian tribe as kuru). 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, the Japanese General Doctor who was in charge

of biological warfare experimentations in Japan, Dr. Ishii Shiro, was

captured. They gave him 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 United States military to demonstrate how they

had created mad cow disease in the Fore Indian tribe. In 1957, when

the disease was beginning to blossom in full among these Fore Indian

people, Dr. Carleton Gajdusek of the National Institutes of Health of

the U.S. headed down to New Guinea to to determine how the minced-up

brains of the visna-infected sheep affected these people. He spent a

couple of years in New Guinea studying the Fore tribe, wrote an

extensive report on it, and won the Nobel Prize for " discovering " kuru

disease (also known as mad cow or Creutzfeldt-Jakob disease) in the

Fore Indian tribe in New Guinea.

 

TESTING CARCINOGENS IN RUSSIA In 1953, the Americans developed a

carcinogenic chemical which they wanted to test, but they didn't want

to test it in the United States so they flew over Russia, accidentally

wandered off course, and sprayed this stuff. Many people started

getting cancer. And the U.S. had some jokes about this. One American

researcher, Dr. Maurice Hilleman of Merck, Sharp and Dohme, joked, " We

are going to win the next Olympics because all the Russians are going

to turn up with 40-pound tumours. " They thought it was a big joke.

 

TESTING CARCINOGENS IN WINNIPEG Next they said, " How about testing it

in Canada? " In 1953, the U.S. asked the government of Canada if they

could test this carcinogenic chemical over the city of Winnipeg. It

was a big city with 500,000 people, miles from anywhere. They sprayed

the 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 it had been full strength. When we located

evidence that the Americans had tested this carcinogenic chemical over

the city of Winnipeg in 1953, and informed the government that we had

this evidence, they denied it. However, finally, on May 15, 1997, a

story out of the Canadian Press in Washington, D.C. by Robert Russo,

published in the Toronto Star, stated that the Pentagon of the United

States admitted that in 1953 they had obtained permission from the

government of Canada to fly over the city of Winnipeg and spray this

crap out, and it 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 chemical used was zinc cadmium sulfide, a carcinogen. They

got their statistics, which indicated that if it had been full

strength, approximately a third of the population of Winnipeg would

have developed cancers over the next five years. The Pentagon called a

press conference to admit what they had done. One professor, Dr. Hugh

Fudenberg, MD, who was nominated twice for the Nobel Prize wrote a

magazine article which stated that the Pentagon has come clean on this

because two researchers up in Sudbury, Ontario, Don Scott and his son

Bill Scott had been revealing this to the public. The US Army actually

conducted a whole series of simulated germ warfare tests in 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 - BRUCELLOSIS MYCOPLASMA AND DISEASE

 

AIDS The AIDS pathogen was created out of a brucellosis bacteria

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 a

United States congressional document of a meeting held June 9, 1969,

the Pentagon delivered a report to Congress about biological weapons

(described on page 129 of the document). 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 a certain number in Canada, including the

University of Alberta, the U.S. government provided the leadership for

the development of the AIDS virus for the purpose of population

control. After they had it perfected, they sent medical teams from the

Centers for Disease Control to Africa and other mid-eastern countries

where they thought the population was becoming too large. They gave

them all a free vaccination for smallpox. Five years after receiving

this smallpox vaccination, 60% of them were suffering from AIDS. They

tried to blame it on a monkey, which is nonsense. There was a report

in the newspapers a while back about a professor at the University of

Arkansas who claimed that while studying the tissues of a dead

chimpanzee, she found the HIV virus. The chimpanzee that she had

tested was born in the United States 23 years earlier. It had lived

its entire life in a U.S. military laboratory where it was used as an

experimental animal for 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 the HIV

virus in it. That virus was acquired by that chimpanzee in the

laboratories where it was tested.

 

CHRONIC FATIGUE Chronic fatigue syndrome is more accurately called

myalgic encephalomyelitis, not chronic fatigue syndrome. That

nomenclature was given by the National Institutes of Health in the

United States because they wanted to downgrade and belittle the

disease. An MRI of the brain of a teenage girl who had 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 had been replaced by scar tissue. This caused cognitive

impairment, memory impairment, etc. And what was the cause of the

scars? 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

 

APPEALS TO CANADA PENSION Many people with chronic fatigue syndrome,

myalgic encephalo-myelitis and fibromyalgia who apply to the Canada

Pension Plan will be turned down because they cannot prove that they

are ill. Over the past year I have conducted several appeals to Canada

Pension and Workers Compensation on behalf of people who have been

turned down. I provided documented evidence of these illnesses, and

they were all granted their pensions on the basis of the evidence that

I provided. In March of last year, for example, I appealed to the

Workers' Compensation on behalf of a lady with fibromyalgia who had

been denied her pension back in 1993. The vice-chairman of the board

came up 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 which 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 THE PRESENCE OF MYCOPLASMA IN YOUR BODY

 

THE POLYMERASE CHAIN REACTION TEST Information is not generally

available about this agent, because first of all, the mycoplasma is

such an infinitely small disease agent. A hundred years ago certain

medical theoreticians conceived that there must be something smaller

than the bacteria and the virus, which are the most common living

forms of disease agents. This pathogenic organism is so infinitely

small that normal blood and tissue tests will not reveal the source of

the disease. Your doctor may diagnose you with Alzheimer's 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 they developed the

polymerase chain reaction test in which they examine a sample of your

blood, remove damaged particles, and subject that damaged particle to

a polymerase chain reaction. This causes the DNA in the particle to

break down. Then they place it in a nutrient which causes the DNA to

grow back into its original form. If they get enough of it they can

recognize what it is, and determine whether brucellosis or another

kind of agent is behind that particular mycoplasma.

 

THE BLOOD TEST If anybody in your family has myalgic

encephalomyelitis, fibromyalgia, multiple sclerosis, or Alzheimer's,

you can send a blood test to Dr. Les Simpson in New Zealand. If you

are ill with these diseases, your red blood cells will not be normal

donut-shaped blood cells capable of being compressed and squeezed

through the capillaries, but will swell up like cherry-filled donuts,

which cannot be compressed. The blood cells become enlarged and

distended because the only way the mycoplasma can exist is by uptaking

preformed sterols from the host cell. One of the best sources of

preformed 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, 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 is 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. It 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 it causes

the lateral ventricles to deteriorate and die and this leads to

multiple sclerosis which will progress until they are totally disabled

and frequently die prematurely. It will get into the lower bowel and

parts of the lower bowel will die and cause colitis. All of these

diseases are caused by the degenerating properties of the mycoplasma.

 

About two months ago a gentleman in Sudbury phoned me and told me he

had fibromyalgia. He applied for Canada 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. Les Simpson of New Zealand 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.

 

THE 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 heart beat, which 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 heart

beat. At various periods of time, during the 24 hours, the heart,

instead of working happily away, going " bump-BUMP, bump-BUMP " , every

now and again, it will go " buhbuhbuhbuhbuhbuhbuhbuhbuh " . The T-wave

(the waves are called P, Q, R, S, and the last one is 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 did this test, and lo and behold, the test results stated: " The

shape of T and S-T suggest 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 analyzed the report of the patient

who had been turned down by Canada Pension and sent it back to them.

They wrote back and said, " 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 others

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 five cc, putting a

tracer in it, and then putting it back in the body. One hour later

take out five 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 all right, just take up line dancing and you will get over it?

They would rush you to the nearest hospital and start infusing you

with blood transfusions. These tragic people with these awful diseases

are functioning with anywhere from 7 to 50% less blood than their

bodies need to function.

 

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 the disease. It is one of the

tetracycline antibiotics, but it is not bactericidal; it is

bacteriostatic. It stops the growth of the mycoplasma, and if it is

stopped long enough, then the immune system takes over. (Nicholson,

G.L., Doxycycline treatment and Desert Storm, JAMA, 1995, 273: 618-619),

 

GULF WAR RESEARCH Professor Garth Nicholson, Ph.D., of the Institute

for Molecular Medicine is one of the top experts on mycoplasma. He has

been given an $8 million grant to study 450 Gulf War veterans, because

Gulf War illness is caused by the mycoplasma. Dr. Les Simpson has done

most of the research in detecting the disease by the polymerase chain

reaction blood test. You may contact Dr. Nicholson at 15162 Triton

Lane, Huntington Beach, Ca, 92649-1401, tel 714-903-2900.

 

In summary, there is a disease agent that is called a mycoplasma. All

of these neurodegenerative systemic diseases are caused by a particle

of a bacterial DNA, a mycoplasma, that enters into the cells of living

organisms and takes the cells apart, sterol by sterol, leaving scar

tissue, and causing all the range of symptoms that you see in people

with these diseases. The military and the National Institutes of

Health and the government are all dedicated to keeping this mycoplasma

as covert as they possibly can.

 

For more information and references, please refer to The Brucellosis

Triangle and The Extremely Unfortunate Skull Valley Incident by Don

Scott and William Scott, both available at Consumer Health Organization.

Other recommended reading is Osler's Web by Hillary Johnson and

Emerging Viruses: Aids and Ebola by Leonard Horowitz. Don Scott also

produces The Journal of Degenerative Diseases.

 

You may contact Donald Scott at: 190 Mountain St., Ste. 405, Sudbury,

Ontario, Canada P3B 4G2. 705-670-0180.

 

Note: Dr. David Webster at Sudbury General Hospital, a wonderful

person, with whom I have had conversations about these awful diseases

can tell your doctor about the Blood Volume test.

 

Recommended Books

 

The Brucellosis Triangle

SCOTT, Donald, MD, & William