Fw: [asthma] Weaponised Mycoplasma the desease that will eventually disable and effect all!

[Guest guest]

- walt

asthma

Tuesday, December 02, 2003 10:31 AM

[asthma] Weaponised Mycoplasma the desease that will eventually disable and effect all!

Folks: Its time to wake up! The people incharge are NOT playing with a fulldeck. Today its survivial of the SMARTEST. Be that as it may. Those whostill care about you are trying to get you to see things are not as youwould believe. Everyone now has this in them! How long before it rears itsugly face and destroys your life? Nows the time to treat it and rid yourbody of it! Not after it disables you. Took me eight years to find out whatwas destroying my life. I'm now on the cure, and after years of going downfeel i am winning back my health! All this posted for your benifit not mine!I already know how to get well.WaltI - PATHOGENIC MYCOPLASMAA Common Disease Agent WeaponisedThere are 200 species of Mycoplasma. Most are innocuous and do no harm; onlyfour or five are pathogenic. Mycoplasma fermentans (incognitus strain)probably comes from the nucleus of the Brucella bacterium. This diseaseagent is not a bacterium and not a virus; it is a mutated form of theBrucella bacterium, combined with a visna virus, from which the mycoplasmais extracted.The pathogenic Mycoplasma used to be very innocuous, but biological warfareresearch conducted between 1942 and the present time has resulted in thecreation of more deadly and infectious forms of Mycoplasma. Researchersextracted this mycoplasma from the Brucella bacterium and actually reducedthe disease to a crystalline form. They "weaponised" it and tested it on anunsuspecting public in North America.Hilleman, chief virologist for the pharmaceutical company Merck Sharp & Dohme, stated that this disease agent is now carried by everybody in NorthAmerica and possibly most people throughout the world.Despite reporting flaws, there has clearly been an increased incidence ofall the neuro/systemic degenerative diseases since World War II andespecially since the 1970s with the arrival of previously unheard-ofdiseases 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, thisdisease agent causes many illnesses including AIDS, cancer, chronic fatiguesyndrome, Crohn's colitis, Type I diabetes, multiple sclerosis, Parkinson'sdisease, Wegener's disease and collagen-vascular diseases such as rheumatoidarthritis 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 fatiguesyndrome and fibromyalgia is the mycoplasma..."I have all the official documents to prove that mycoplasma is the diseaseagent in chronic fatigue syndrome/fibromyalgia as well as in AIDS, multiplesclerosis and many other illnesses. Of these, 80% are US or Canadianofficial government documents, and 20% are articles from peer-reviewedjournals such as the Journal of the American Medical Association, NewEngland Journal of Medicine and the Canadian Medical Association Journal.The journal articles and government documents complement each other.How the Mycoplasma WorksThe 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 cellsin your brain, or you may develop Crohn's colitis if thepathogen invades anddestroys cells in the lower bowel.Once the mycoplasma gets into the cell, it can lie there doing nothingsometimes for 10, 20 or 30 years, but if a trauma occurs like an accident ora vaccination that doesn't take, the mycoplasma can become triggered.Because it is only the DNA particle of the bacterium, it doesn't have anyorganelles to process its own nutrients, so it grows by uptaking pre-formedsterols from its host cell and it literally kills the cell; the cellruptures and what is left gets dumped into the bloodstream.II- CREATION OF THE MYCOPLASMAA Laboratory-Made Disease AgentMany doctors don't know about this mycoplasma disease agent because it wasdeveloped by the US military in biological warfare experimentation and itwas not made public. This pathogen was patented by the United Statesmilitary and Dr Shyh-Ching Lo. I have a copy of the documented patent fromthe US Patent Office.(1)All the countries at war were experimenting with biological weapons. In1942, the governments of the United States, Canada and Britain entered intoa secret agreement to create two types of biological weapons (one that wouldkill, and one that was disabling) for use in the war against Germany andJapan, who were also developing biological weapons. While they researched anumber or disease pathogens, they primarily focused on the Brucellabacterium and began to weaponise it.From its inception, the biowarfare program was characterised by continuingin-depth review and participation by the most eminent scientists, medicalconsultants, industrial experts and government officials, and it wasclassified Top Secret.The US Public Health Service also closely followed the progress ofbiological warfare research and development from the very start of theprogram, and the Centers for Disease Control (CDC) and the NationalInstitutes of Health (NIH) in the United States were working with themilitary in weaponising these diseases. These are diseases that have existedfor thousands of years, but they have been weaponised-which means they'vebeen made more contagious and more effective. And they are spreading.The Special Virus Cancer Program, created by the CIA and NIH to develop adeadly pathogen for which humanity had no natural immunity (AIDS), wasdisguised as a war on cancer but was actually part of MKNAOMI.2 Many membersof the Senate and House of Representatives do not know what has been goingon. For example, the US Senate Committee on Government Reform had searchedthe archives in Washington and other places for the document titled "TheSpecial 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 Senateand asked for one of their secret documents! The US Senate, through theGovernment Reform Committee, is trying to stop this type of governmentresearch.Crystalline BrucellaThe 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".3They had produced a crystalline bacterial toxin extracted from the Brucellabacterium. The bacterial toxin could be removed in crystalline form andstored, transported and deployed without deteriorating. It could bedelivered by other vectors such as insects, aerosol or the food chain (innature it is delivered within the bacterium). But the factor that is workingin 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 acongressional committee in 1969,(4) researchers found that if they hadmycoplasma at a certain strength-actually, 10 to the 10th power-it woulddevelop into AIDS, and the person would die from it within a reasonableperiod of time because it could bypass the natural human defences. If thestrength was 10 to 8, the person would manifest with chronic fatiguesyndrome 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 veryinterested in life; they would waste away.Most of us have never heard of the disease brucellosis because it largelydisappeared when they began pasteurising milk, which was the carrier. Onesalt shaker of the pure disease agent in a crystalline form could sicken theentire population of Canada. It is absolutely deadly, not so much in termsof 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 mycoplasmawill only crystallise at 8.1 pH, and the blood has a pH of 7.4 pH. So thedoctor thinks your complaint is "all in your head".Crystalline Brucella and Multiple SclerosisIn 1998 in Rochester, New York, I met a former military man, PFC DonaldBentley, who gave me a document and told me: "I was in the US Army, and Iwas trained in bacteriological warfare. We were handling a bomb filled withbrucellosis, only it wasn't brucellosis; it was a Brucella toxin incrystalline form. We were spraying it on the Chinese and North Koreans."He showed me his certificate listing his training in chemical, biologicaland radiological warfare. Then he showed me 16 pages of documents given tohim by the US military when he was discharged from the service. They linkedbrucellosis with multiple sclerosis, and stated in one section: "Veteranswith multiple sclerosis, a kind of creeping paralysis developing to a degreeof 10% or more disability within two years after separation from activeservice, may be presumed to be service-connected for disabilitycompensation. Compensation is payable to eligible veterans whosedisabilities are due to service." In other words: "If you become ill withmultiple sclerosis, it is because you were handling this Brucella, and wewill give you a pension. Don't go raising any fuss about it." In thesedocuments, the government of the United States revealed evidence of thecause of multiple sclerosis, but they didn't make it known to the public-orto your doctor.In a 1949 report, Drs Kyger and Haden suggested "the possibility thatmultiple sclerosis might be a central nervous system manifestation ofchronic brucellosis". Testing approximately 113 MS patients, they found thatalmost 95% also tested positive for Brucella.(5) We have a document from amedical journal, which concludes that one out of 500 people who hadbrucellosis would develop what they call neurobrucellosis; in other words,brucellosis in the brain, where the Brucella settles in the lateralventrides-where the disease multiple sclerosis is basically located.6Contamination of Camp Detrick Lab WorkersA 1948 New England Journal of Medicine report titled "Acute BrucellosisAmong Laboratory Workers" shows us how actively dangerous this agent is.7The laboratory workers were from Camp Detrick, Frederick, Maryland, wherethey were developing biological weapons. Even though these workers had beenvaccinated, wore rubberised suits and masks and worked through holes in thecompartment, many of them came down with this awful disease because it is soabsolutely and terrifyingly infectious.The article was written by Lt Calderone Howell, Marine Corps Captain EdwardMiller, Marine Corps, Lt Emily Kelly, United States Naval Reserve; andCaptain Henry Bookman. They were all military personnel engaged in makingthe disease agent Brucella into a more effective biological weaponIII - COVERT TESTING OF MYCOPLASMATesting the Dispersal MethodsDocumented evidence proves that the biological weapons they were developingwere tested on the public in various communities without their knowledge orconsent.The government knew that crystalline Brucella would cause disease in humans.Now they needed to determine how it would spread and the best way todisperse it. They tested dispersal methods for Brucella suis and Brucellamelitensis at Dugway Proving Ground, Utah, in June and September 1952.Probably, 100% of us now are infected with Brucella suis and Brucellamelitensis.(8)Another government document recommended the genesis of open-airvulnerability tests and covert research and development programs to beconducted by the Army and supported by the Central Intelligence Agency.At that time, the Government of Canada was asked by the US Government tocooperate in testing weaponised Brucella, and Canada cooperated fully withthe United States. The US Government wanted to determine whether mosquitoeswould carry the disease and also if the air would carry it. A governmentreport stated that "open-air testing of infectious biological agents isconsidered essential to an ultimate understanding of biological warfarepotentialities because of the many unknown factors affecting the degradationof micro-organisms in the atmosphere".9Testing via Mosquito Vector in Punta Gorda, FloridaA report from The New England Journal of Medicine reveals that one of thefirst outbreaks of chronic fatigue syndrome was in Punta Gorda, Florida,back in 1957.(10) It was a strange coincidence that a week before thesepeople came down with chronic fatigue syndrome, there was a huge influx ofmosquitoes.The National Institutes of Health claimed that the mosquitoes came from aforest fire 30 miles away. The truth is that those mosquitoes were infectedin Canada by Dr Guilford B. Reed at Queen's University. They were bred inBelleville, Ontario, and taken down to Punta Gorda and released there.Within a week, the first five cases ever of chronic fatigue syndrome werereported to the local clinic in Punta Gorda. The cases kept coming untilfinally 450 people were ill with the disease.Testing via Mosquito Vector in OntarioThe Government of Canada had established the Dominion Parasite Laboratory inBelleville, Ontario, where it raised 100 million mosquitoes a month. Thesewere shipped to Queen's University and certain other facilities to beinfected with this crystalline disease agent The mosquitoes were then letloose in certain communities in the middle of the night, so that theresearchers could determine how many people would become ill with chronicfatigue 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 ofmillions of infected mosquitoes. Over 700 people in the next four or fiveweeks developed myalgic encephalomyelitis, or chronic fatigue syndrome.IV - COVERT TESTING OF OTHER DISEASE AGENTSMad Cow Disease/Kuru/CJD in the Fore TribeBefore and during World War II, at the infamous Camp 731 in Manchuria, theJapanese military contaminated prisoners of war with certain disease agents.They also established a research camp in New Guinea in 1942. There theyexperimented upon the Fore Indian tribe and inoculated them with a minced-upversion of the brains of diseased sheep containing the visna virus whichcauses "mad cow disease" or Creutzfeldt-Jakob disease.About five or six years later, after the Japanese had been driven out, thepoor people of the Fore tribe developed what they called kuru, which wastheir word for "wasting", and they began to shake, lose their appetites anddie. 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 wascommissioned as a General in the Japanese Army so he could take command ofJapan's biological warfare development, testing and deployment-was captured.He was given the choice of a job with the United States Army or execution asa war criminal. Not surprisingly, Dr Ishii Shiro chose to work with the USmilitary to demonstrate how the Japanese had created mad cow disease in theFore Indian tribe.In 1957, when the disease was beginning to blossom in full among the Forepeople, Dr Carleton Gajdusek of the US National Institutes of Health headedto New Guinea to determine how the minced-up brains of the visna-infectedsheep affected them. He spent a couple of years there, studying the Forepeople, and wrote an extensive report. He won the Nobel Prize for"discovering" kuru disease in the Fore tribe.Testing Carcinogens over Winnipeg, ManitobaIn 1953, the US Government asked the Canadian Government if it could test achemical over the city of Winnipeg. It was a big city with 500,000 people,miles from anywhere. The American military sprayed this carcinogenicchemical in a 1,000%-attenuated form, which they said would be so watereddown that nobody would get very sick; however, if people came to clinicswith a sniffle, a sore throat or ringing in their ears, the researcherswould be able to determine what percentage would have developed cancer ifthe chemical had been used at full strength.We located evidence that the Americans had indeed tested this carcinogenicchemical-zinc cadmium sulphide-over Winnipeg in 1953. We wrote to theGovernment of Canada, explaining that we had solid evidence of the sprayingand asking that we be informed as to how high up in the government therequest for permission to spray had gone. We did not receive a reply.Shortly after, the Pentagon held a press conference on May 14, 1997, wherethey admitted what they had done. Robert Russo, writing for the TorontoStar11 from Washington, DC, reported the Pentagon's admission that in 1953it had obtained permission from the Canadian Government to fly over the cityof Winnipeg and spray out this chemical-which sifted down on kids going toschool, housewives hanging out their laundry and people going to work. USArmy planes and trucks released the chemical 36 times between July andAugust 1953. The Pentagon got its statistics, which indicated that if thechemical released had been full strength, approximately a third of thepopulation of Winnipeg would have developed cancers over the next fiveyears.One professor, Dr Hugh Fudenberg, MD, twice nominated for the Nobel Prize,wrote a magazine article stating that the Pentagon came clean on thisbecause two researchers in Sudbury, Ontario-Don Scott and his son, BillScott-had been revealing this to the public. However, the legwork was doneby other researchers!The US Army actually conducted a series of simulated germ warfare tests overWinnipeg. The Pentagon lied about the tests to the mayor, saying that theywere testing a chemical fog over the city, which would protect Winnipeg inthe event of a nuclear attack.A report commissioned by US Congress, chaired by Dr Rogene Henderson, lists32 American towns and cities used as test sites as well.V - BRUCELLA MYCOPLASMA AND DISEASE AIDSThe AIDS pathogen was created out of a Brucella bacterium mutated with avisna virus; then the toxin was removed as a DNA particle called amycoplasma. They used the same mycoplasma to develop disabling diseases likeMS, Crohn's colitis, Lyme disease, etc.In the previously mentioned US congressional document of a meeting held onJune 9, 1969, (12) the Pentagon delivered a report to Congress aboutbiological weapons. The Pentagon stated: "We are continuing to developdisabling weapons." Dr MacArthur, who was in charge of the research, said:"We are developing a new lethal weapon, a synthetic biological agent thatdoes not naturally exist, and for which no natural immunity could have beenacquired."Think about it. If you have a deficiency of acquired immunity, you have anacquired immunity deficiency. Plain as that. AIDS.In laboratories throughout the United States and in a certain number inCanada including at the University of Alberta. the US Government providedthe leadership for the development of AIDS for the purpose of populationcontrol. After the scientists had perfected it, the government sent medicalteams from the Centers for Disease Control-under the direction of Dr DonaldA. Henderson, their investigator into the 1957 chronic fatigue epidemic inPunta Gorda-during 1969 to 1971 to Africa and some countries such as India,Nepal and Pakistan where they thought the population was becoming toolarge.13 They gave them all a free vaccination against smallpox; but fiveyears after receiving this vaccination, 60% of those inoculated weresuffering 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 studyingthe tissues of a dead chimpanzee she found traces of HIV. The chimpanzeethat she had tested was born in the United States 23 years earlier. It hadlived its entire life in a US military laboratory where it was used as anexperimental animal in the development of these diseases. When it died, itsbody was shipped to a storage place where it was deep-frozen and stored incase they wanted to analyse it later. Then they decided that they didn'thave enough space for it, so they said, "Anybody want this dead chimpanzee?"and this researcher from Arkansas said: "Yes. Send it down to the Universityof Arkansas. We are happy to get anything we can get." They shipped it downand she found HIV in it. That virus was acquired by that chimpanzee in thelaboratories where it was tested.14Chronic Fatigue Syndrome/ Myalgic EncephalomyelitisChronic fatigue syndrome is more accurately called myalgicencephalomyelitis. The chronic fatigue syndrome nomenclature was given bythe US National Institutes of Health because it wanted to downgrade andbelittle the disease.An MRI scan of the brain of a teenage girl with chronic fatigue syndromedisplayed a great many scars or punctate lesions in the left frontal lobearea where portions of the brain had literally dissolved and been replacedby scar tissue. This caused cognitive impairment, memory impairment, etc.And what was the cause of the scarring? The mycoplasma. So there is veryconcrete physical evidence of these tragic diseases, even though doctorscontinue to say they don't know where it comes from or what they can doabout it.Many people with chronic fatigue syndrome, myalgic encephalo-myelitis andfibromyalgia who apply to the Canada Pensions Plan Review Tribunal will beturned down because they cannot prove that they are ill. During 1999 Iconducted several appeals to Canada Pensions and the Workers CompensationBoard (WCB, now the Workplace Safety and Insurance Board) on behalf ofpeople who have been turned down. I provided documented evidence of theseillnesses, and these people were all granted their pensions on the basis ofthe evidence that I provided.In March 1999, for example, I appealed to the WCB on behalf of a lady withflbromya1gia who had been, denied her pension back in 1993. Thevice-chairman of the board came to Sudbury to hear the appeal, and I showedhim a number of documents which proved that this lady was physically illwith fibromyalgia. It was a disease that caused physical damage, and thedisease agent was a mycoplasma. The guy listened for three hours, and thenhe said to me: "Mr Scott, how is it I have never heard of any of thisbefore? I said: "We brought a top authority in this area into Sudbury tospeak on this subject and not a single solitary doctor came to thatpresentation."VI-TESTING FOR MYCOPLASMA IN YOUR BODYPolymerase Chain Reaction TestInformation is not generally available about this agent because, first ofall, the mycoplasma is such a minutely small disease agent. A hundred yearsago, certain medical theoreticians conceived that there must be a form ordisease agent smaller than bacteria and viruses. This pathogenic organism,the mycoplasma, is so minute that normal blood and tissue tests will notreveal 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 yourbrain begins to deteriorate, cells rupture, the myelin sheath around thenerves dissolves, and so on." Or if you have chronic fatigue syndrome, thedoctor will not be able to find any cause for your illness with ordinaryblood and tissue tests.This mycoplasma couldn't be detected until about 30 years ago when thepolymerase chain reaction (PCR) test was developed, in which a sample ofyour blood is examined and damaged particles are removed and subjected to apolymerase chain reaction. This causes the DNA in the particles to breakdown. The particles are then placed in a nutrient, which causes the DNA togrow back into its original form. If enough of the substance is produced,the form can be recognised, so it can be determined whether Brucella oranother kind of agent is behind that particular mycoplasma.Blood TestIf you or anybody in your family has myalgic encephalomyelitis,fibromyalgia, multiple sclerosis or Alzheimer's, you can send a blood sampleto Dr Les Simpson in New Zealand for testing.If you are ill with these diseases, your red blood cells will not be normaldoughnut-shaped blood cells capable of being compressed and squeezed throughthe capillaries, but will swell up like cherry-filled doughnuts which cannotbe compressed. The blood cells become enlarged and distended because theonly way the mycoplasma can exist is by uptaking pre-formed sterols from thehost cell. One of the best sources of pre-formed sterols is cholesterol, andcholesterol is what gives your blood cells flexibility. If the cholesterolis taken out by the mycoplasma, the red blood cell swells up and doesn't gothrough, and the person begins to feel all the aches and pains and all thedamage it causes to the brain, the heart, the stomach, the feet and thewhole body because blood and oxygen are cut off.And that is why people with fibromyalgia and chronic fatigue syndrome havesuch a terrible time. When the blood is cut off from the brain, punctatelesions appear because those parts of the brain die. The mycoplasma will getinto portions of the heart muscle, especially the left ventricle, and thosecells will die. Certain people have cells in the lateral ventricles of thebrain that have a genetic predisposition to admit the mycoplasma, and thiscauses the lateral ventricles to deteriorate and die. This leads to multiplesclerosis, which will progress until these people are totally disabled;frequently, they die prematurely. The mycoplasma will get into the lowerbowel, parts of which will die, thus causing colitis. All of these diseasesare caused by the degenerating properties of the mycoplasma.In early 2000, a gentleman in Sudbury phoned me and told me he hadfibromyalgia. He applied for a pension and was turned down because hisdoctor said it was all in his head and there was no external evidence. Igave him the proper form and a vial, and he sent his blood to Dr Simpson tobe tested. He did this with his family doctor's approval, and the resultsfrom Dr Simpson showed that only 4% of his red blood cells were functioningnormally and carrying the appropriate amount of oxygen to his poor body,whereas 83% were distended, enlarged and hardened, and wouldn't go throughthe capillaries without an awful lot of pressure and trouble. This is thephysical evidence of the damage that is done.ECG TestYou can also ask your doctor to give you a 24-hour Holter ECG. You know, ofcourse, that an electrocardiogram is a measure of your heartbeat and showswhat is going on in the right ventricle, the left ventricle and so on. Testsshow that 100% of patients with chronic fatigue syndrome and fibromyalgiahave an irregular heartbeat. At various periods during the 24 hours, theheart, instead of working happily away going "bump-BUMP, bump-BUMP", everynow and again goes "buhbuhbuhbuhbubbuhbuhbuhbuh". The T-wave (the waves arecalled P, Q, R, S and T) is normally a peak, and then the wave levels offand starts with the P-wave again. In chronic fatigue and fibromyalgiapatients, the T-wave flattens off, or actually inverts. That means the bloodin the left ventricle is not being squeezed up through the aorta and aroundthrough the body.My client from Sudbury had this test done and, lo and behold, the resultsstated: "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 theT-wave was not working properly. I analysed the report of this patient whohad been turned down by Canada Pensions and sent it back to them. They wroteback, saying: "It looks like we may have made a mistake. We are going togive 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 theheart. The left ventricle muscles do show scarring.That is way many people are diagnosed with a heart condition when they firstdevelop fibromyalgia, but it's only one of several problems because themycoplasma can do all kinds of damage.Blood Volume TestYou can also ask your doctor for a blood volume test. Every human beingrequires a certain amount of blood per pound of body weight, and it has beenobserved that people with fibromyalgia, chronic fatigue syndrome, multiplesclerosis and other illnesses do not have the normal blood volume their bodyneeds 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 hourlater, take out 5 cc again and look for the tracer. The thicker the bloodand the lower the blood volume, the more tracer you will find.The analysis of one of my clients stated: "This patient was referred for redcell mass study. The red cell volume is 16.9 ml per kg of body weight. Thenormal range is 25 to 35 ml per kg. This guy has 36% less blood in his bodythan the body needs to function." And the doctor hadn't even known the testexisted.If you lost 36% of your blood in an accident, do you think your doctor wouldtell you that you are allright and should just take up line dancing and getover it? They would rush you to the nearest hospital and start transfusingyou with blood. These tragic people with these awful diseases arefunctioning with anywhere from 7% to 50% less blood than their body needs tofunction.VII- UNDOING THE DAMAGEThe body undoes the damage itself. The scarring in the brain of people withchronic fatigue and fibromyalgia will be repaired. There is cellular repairgoing 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 diseaseprocess. It is one of the tetracycline antibiotics, but it is notbactericidal; it is bacteriostatic-it stops the growth of the mycoplasma.And if the mycoplasma growth can be stopped for long enough, then the immunesystem takes over.Doxycycline treatment is discussed in a paper by mycoplasma expert ProfessorGarth Nicholson, PhD, of the Institute for Molecular Medicine." Dr Nicholsonis involved in a US$8 million mycoplasma research program funded by the USmilitary and headed by Dr Charles Engel of the NIH. The program is studyingGulf War veterans, 450 of them, because there is evidence to suggest thatGulf War syndrome is another illness (or set of illnesses) caused bymycoplasma.Endnotes1. "Pathogenic Mycoplasma", US Patent No. 5,242,820, issued September 7,1993. Dr Lo is listed as the Inventor" and the American Registry ofPathology, Washington, DC, is listed as the "Assignee".2. "Special Virus Cancer Program: Progress Report No. 8", prepared by theNational 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 onHealth 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 for1970, Hearings before Subcommittee of the Committee on Appropriations, Houseof 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 melitensisInfection: A Study of 530 Cases", Medicine 1996;75(4).7. Howell, Miller, Kelly and Bookman, "Acute Brucellosis Among LaboratoryWorkers", 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 ScientificResearch 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 for1970, Hearings, Monday June 9, 1969, ibid., p.129.13. Henderson, Donald A., "Smallpox: Epitaph for a Killer", NationalGeographic, 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", JAMA1995;273:61 8-619.Recommended Reading.Horowitz, Leonard, Emerging Viruses: Aids and Ebola, TetrahedronPublishing, USA, 1996.. Johnson, Hillary, Osler's Web, Crown Publishers, New York, 1996.. Scott, Donald W. and William L. C. Scott, The Brucellosis Triangle, TheChelmsford 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 SkullValley Incident, The Chelmsford Publishers, Canada, 1996 (revised, extendededition available from mid-September 2001; US$16.00 pre-pub. Price + US$3s & h in US)..The journal of Degenerative Diseases (Donald W. Scott, Editor), The CommonCause Medical Research Foundation (Box 133, Stat B., Sudbury, Ontario, P3E4N5), Canada (quarterly journal; annual subscription: US$25.00 in USA, $30foreign).Additional Contacts. Ms Jennie Burke, Australian Biologics, Level 6, 383 Pitt Street, SydneyNSW 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, websitewww.consumerhealth.org/.. Professor Garth Nicholson, PhD, Institute for Molecular Medicine, 15162Triton 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, emailrbc.research.limited . (Note: Dr Simpson directs his study to redcell 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 AuthorDonald Scott, MA, MSc, is a retired high school teacher and universityprofessor. He is also a veteran of WWII and was awarded the North AtlanticStar, the Burma Star with Clasp, the 1939-1945 Volunteer Service Medal andthe Victory Medal. He is currently President of The Common Cause MedicalResearch Foundation, a not-for-profit organisation devoted to research intoneurosystemic degenerative diseases. He is also Adjunct Professor with theInstitute for Molecular Medicine and he produces and edits the journal ofDegenerative Diseases. He has extensively researched neurosystemicdegenerative diseases over the past five years and has authored manydocuments on the relationship between degenerative diseases and a pathogenicmycoplasma called Mycoplasma fermentans. His research is based upon solidgovernment evidence.