Walt on mycoplasma

[Guest guest]

Hi Walt,

I have a bunch of info on mycoplasma, I will go ahead and post it on HH and

if you would like pick and chose and repost it in your group, you are

welcome to advertise your group in any of my groups. (Here is one that Walt

posted a couple of years ago) Your group is going to be terrific!

Elaine

___________________

 

 

MYCOPLASMA The Linking Pathogen in Neurosystemic Diseases

 

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.

 

Donald W. Scott MA, MSc. Ó 2001

 

Nexus Magazine Aug 2001

 

I - PATHOGENIC MYCOPLASMA 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 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 thepathogen 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 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 or 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-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 10 to 8, the person would manifest with chronic fatigue

syndrome or fibromyalgia. If it was l0 to 7, 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

ventrides-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 - 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 infamous Camp 731 in Manchuria, the Japanese military contaminated

prisoners of war with certain disease agents.

 

They also established a research camp in New Guinea in 1942. There they

experimented upon the Fore Indian tribe and inoculated them with a minced-up

version of the brains of diseased sheep containing the visna virus which

causes " mad cow disease " or Creutzfeldt-Jakob disease.

 

About five or six years later, after the Japanese had been driven out, the

poor people of the Fore tribe developed what they called kuru, which was

their word for " wasting " , and they began to shake, lose their appetites and

die. The autopsies revealed that their brains had literally turned to mush.

They had contracted " mad cow disease " from the Japanese experiments.

 

When World War II ended, Dr Ishii Shiro-the medical doctor who was

commissioned as a General in the Japanese Army so he could take command of

Japan's biological warfare development, testing and deployment-was captured.

He was given the choice of a job with the United States Army or execution as

a war criminal. Not surprisingly, Dr Ishii Shiro chose to work with the US

military to demonstrate how the Japanese had created mad cow disease in the

Fore Indian tribe.

 

In 1957, when the disease was beginning to blossom in full among the Fore

people, Dr Carleton Gajdusek of the US National Institutes of Health headed

to New Guinea to determine how the minced-up brains of the visna-infected

sheep affected them. He spent a couple of years there, studying the Fore

people, and wrote an extensive report. He won the Nobel Prize for

" discovering " kuru disease in the Fore tribe.

 

Testing Carcinogens over Winnipeg, Manitoba In 1953, the US Government asked

the Canadian Government if it could test a chemical over the city of

Winnipeg. It was a big city with 500,000 people, miles from anywhere. The

American military sprayed this carcinogenic chemical in a 1,000%-attenuated

form, which they said would be so watered down that nobody would get very

sick; however, if people came to clinics with a sniffle, a sore throat or

ringing in their ears, the researchers would be able to determine what

percentage would have developed cancer if the chemical had been used at full

strength.

 

We located evidence that the Americans had indeed tested this carcinogenic

chemical-zinc cadmium sulphide-over Winnipeg in 1953. We wrote to the

Government of Canada, explaining that we had solid evidence of the spraying

and asking that we be informed as to how high up in the government the

request for permission to spray had gone. We did not receive a reply.

 

Shortly after, the Pentagon held a press conference on May 14, 1997, where

they admitted what they had done. Robert Russo, writing for the Toronto

Star11 from Washington, DC, reported the Pentagon's admission that in 1953

it had obtained permission from the Canadian Government to fly over the city

of Winnipeg and spray out this chemical-which sifted down on kids going to

school, housewives hanging out their laundry and people going to work. US

Army planes and trucks released the chemical 36 times between July and

August 1953. The Pentagon got its statistics, which indicated that if the

chemical released had been full strength, approximately a third of the

population of Winnipeg would have developed cancers over the next five

years.

 

One professor, Dr Hugh Fudenberg, MD, twice nominated for the Nobel Prize,

wrote a magazine article stating that the Pentagon came clean on this

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

Scott-had been revealing this to the public. However, the legwork was done

by other researchers!

 

The US Army actually conducted a series of simulated germ warfare tests over

Winnipeg. The Pentagon lied about the tests to the mayor, saying that they

were testing a chemical fog over the city, which would protect Winnipeg in

the event of a nuclear attack.

 

A report commissioned by US Congress, chaired by Dr Rogene Henderson, lists

32 American towns and cities used as test sites as well.

 

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 as India,

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 to blame 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 analyse 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 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 and

fibromyalgia 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 with

flbromya1gia 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 or 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 recognised, 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 or Alzheimer'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.

 

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 heartbeat

and 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 heartbeat. At various periods during the 24

hours, the heart, instead of working happily away going " bump-BUMP,

bump-BUMP " , every now and again goes " buhbuhbuhbuhbubbuhbuhbuhbuh " . The

T-wave (the waves are called P, Q, R, S and 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 from Sudbury had this test done and, lo and behold, the results

stated: " The shape of T and S-T suggests 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 analysed the report of this patient who

had been turned down by Canada Pensions and sent it back to them. They wrote

back, saying: " 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 way 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 other illnesses 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 5 cc,

putting a tracer in it and then putting it back into the body. One hour

later, take out 5 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 allright and should just take up line dancing and get

over it? They would rush you to the nearest hospital and start transfusing

you with blood. These tragic people with these awful diseases are

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

function.

 

VII- 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, doxycydine may reverse that disease

process. It is one of the tetracycline antibiotics, but it is not

bactericidal; it is bacteriostatic-it stops the growth of the mycoplasma.

And if the mycoplasma growth can be stopped for long enough, then the immune

system takes over.

 

Doxycycline treatment is discussed in a paper by mycoplasma expert Professor

Garth Nicholson, PhD, of the Institute for Molecular Medicine. " Dr Nicholson

is involved in a US$8 million mycoplasma research program funded by the US

military and headed by Dr Charles Engel of the NIH. The program is studying

Gulf War veterans, 450 of them, because there is evidence to suggest that

Gulf War syndrome is another illness (or set of illnesses) caused by

mycoplasma.

 

Endnotes

1. " Pathogenic Mycoplasma " , US Patent No. 5,242,820, issued September 7,

1993. Dr Lo is listed as the Inventor " and the American Registry of

Pathology, Washington, DC, is listed as the " Assignee " .

2. " Special Virus Cancer Program: Progress Report No. 8 " , prepared by the

National Cancer Institute, Viral Oncology, Etiology Area, July 1971,

submitted to NIH Annual Report in May 1971 and updated July 1971.

3. US Senate, Ninety-fifth Congress, Hearings before the Subcommittee on

Health and Scientific Research of the Committee on Human Resources,

Biological Testing Involving Human Subjects by the Department of Defense,

1977; released as US Army Activities in the US Biological Warfare Programs,

Volumes One and Two, 24 February 1977.

4. Dr Donald MacArthur, Pentagon, Department of Defense Appropriations for

1970, Hearings before Subcommittee of the Committee on Appropriations, House

of Representatives, Ninety-First Congress, First Session, Monday June 9,

1969, pp 105-144, esp. pp. 114, 129.

5. Kyger, E. R. and Russell L. Haden, " Brucellosis and Multiple Sclerosis " ,

The American journal of Medical Sciences 1949:689-693.

6. Colmonero et al., " Complications Associated with Brucella melitensis

Infection: A Study of 530 Cases " , Medicine 1996;75(4).

7. Howell, Miller, Kelly and Bookman, " Acute Brucellosis Among Laboratory

Workers " , New England Journal of Medicine 1948;236:741.

8. " Special Virus Cancer Program: Progress Report No. 8 " , ibid., table 4, p.

135.

9. US Senate, Hearings before the Subcommittee on Health and Scientific

Research of the Committee on Human Resources, March 8 and May 23, 1977,

ibid.

10. New England journal of Medicine, August 22, 1957, p. 362.

11. Toronto Star, May 15, 1997.

12. Dr Donald MacArthur, Pentagon, Department of Defense Appropriations for

1970, Hearings, Monday June 9, 1969, ibid., p. 129.

13. Henderson, Donald A., " Smallpox: Epitaph for a Killer " , National

Geographic, December 1978, p. 804.

14. Blum, Deborah, The Monkey Wars, Oxford University Press, New York, 1994.

15. Nicholson, G. 1., " Doxycycline treatment and Desert Storm " , JAMA

1995;273:61 8-619.

 

Recommended Reading

 

..Horowitz, Leonard, Emerging Viruses: Aids and Ebola, Tetrahedron

Publishing, USA, 1996. . Johnson, Hillary, Osler's Web, Crown Publishers,

New York, 1996. . Scott, Donald W. and William L. C. Scott, The Brucellosis

Triangle, The Chelmsford Publishers (Box 133, Stat. B., Sudbury, Ontario P3E

4N5), Canada,

1998 (US$21.95 + $3 s & h in US). . Scott, Donald W. and William 1. C. Scott,

The Extremely Unfortunate Skull Valley Incident, The Chelmsford Publishers,

Canada, 1996 (revised, extended edition available from mid-September 2001;

US$16.00 pre-pub. Price + US$3 s & h in US). .The journal of Degenerative

Diseases (Donald W. Scott, Editor), The Common Cause Medical Research

Foundation (Box 133, Stat B., Sudbury, Ontario, P3E

4N5), Canada (quarterly journal; annual subscription: US$25.00 in USA, $30

foreign).

 

Additional Contacts . Ms Jennie Burke, Australian Biologics, Level 6, 383

Pitt Street, Sydney NSW 2000, Australia tel +61 (0)2 9283 0807, fax +61 (0)2

9283 0910. Australian Biologics does tests for mycoplasma. . Consumer Health

Organization of Canada, 1220 Sheppard Avenue East #412, Toronto, Ontario,

Canada M2K 255, tel +1 (416)490 0986, website www. consumerhealth. org/. .

Professor Garth Nicholson, PhD, Institute for Molecular Medicine, 15162

Triton Lane, Huntington Beach, CA, 92649-1401, USA, tel +1(714) 903 2900. .

Dr Les Simpson, Red Blood Cell Research Ltd, 31 Bath Street, Dunedin,

9001, New Zealand, tel +64 (0)3 471 8540, email

rbc.research.limited . (Note: Dr Simpson directs his study to red

cell shape analysis, not the mycoplasrna hypothesis.) . The Mycoplasma

Registry for Gulf War Illness, S. & 1. Dudley, 303 47th St, J-10 San Diego,

CA 92102-5961, tel/fax +1(619) 266 1116, fax (619) 266 1116, email

mycoreg.

 

About the Author Donald Scott, MA, MSc, is a retired high school teacher and

university professor. He is also 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. He is currently President of The Common Cause

Medical Research Foundation, a not-for-profit organisation devoted to

research into neurosystemic degenerative diseases. He is also Adjunct

Professor with the Institute for Molecular Medicine and he produces and

edits the journal of Degenerative Diseases. 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.