CureZone   Log On   Join
Yoga Prayer Ayurveda Vibrational healing. Vaccine A history Squalene, Mycoplasma Lyme. STD as VTD? Gulf war, illness etc... Heal now.
 
CHESTA Views: 15,659
Published: 9 years ago
 

Yoga Prayer Ayurveda Vibrational healing. Vaccine A history Squalene, Mycoplasma Lyme. STD as VTD? Gulf war, illness etc... Heal now.


 

                                               http://www.facebook.com/#!/OneAnswerToCancerMovie
================================================================
by Bruce Fife and Jon J. Kabara. Coconut oil for health benefit.
================================================================
Note that antibiotics only work against bacteria and not other disease causing organisms like mycoplasma, bad yeasts, viruses, parasites.
Saints, Christ, Cleopatra, pharaohs’, kings, queens, common folk, and healers have used pure essential oils for many millennia. Cultures throughout the world regard them as some of the most powerful medicines created by Mother Nature under the guidance of the Supreme Personality of Godhead. Essential oils are good enough for them, and they are good enough for you, your family, and everyone on Mother Earth..
Therapeutic pure essential oils never go bad. They are practical, portable, easily be shared, excellent medicine, & great conversation piece. Get creative & mix your own natural perfumes.
Pure essential oils immediately raise your bodies natural immune system, and body frequency / vibration. Microscopic hooligans that seek to do you harm, intentionally or not are immediately are stopped in their tracks whether they like it or not. Best security and insurance policy is prevention.”

Bruce Tainio of Tainio Technology in Cheney, Washington, developed new
equipment to measure the biofrequency of humans and foods. He used this
biofrequency monitor to determine the relationship between frequency and disease.

Distilled water with 2 drops peppermint has the frequency of 78MHz, With lemon is 76MHz,
Tap water 32MHz, Chlorinated water is worse than coffee

Measuring in megahertz, it was found that processed foods.
Canned food had a 0 to 15 MHz
Dry herbs from 12 to 22 MHz;
Fresh produce measured up to 15 to 22 MHz
Fresh herbs from 20 to 27 MHz.
Essential Oils started at 47 MHz and went as high as 320 MHz, which is the frequency of
rose oil.

Our body and all the organs have their own frequency, here are a few listed.
Normal Brain wave frequency is 72-78 MHz
Visionary Range 120 MHz
Bone 38-43 MHz
From the neck down 62-68 MHz this is a healthy body normal frequency

If the frequency drops just 4 points this is when a headache will start.
58 MHz. Disease begins, Like the cold symptoms
57 MHz Flu invades the body
55 MHz when more serious problems come about like pneumonia, Epstein Barr and etc.
48 MHz is when tissue breaksdown from disease
42 MHz is when cancer can set in
20 MHz death

Clinical research shows essential oils, having the highest frequency of any natural
substance known to man, can create an environment in which microbes, disease,
bacteria, virus, fungus, etc., cannot live
. Truly, the chemistry and frequencies of
essential oils have the ability to help man maintain an optimal health frequency.

One drop of pure essential oils applied to skin can be detected in every cell of the body within 20 minutes.
Note: antibiotics only work against bacteria and not other disease causing organisms like mycoplasma, bad yeasts, viruses, parasites. Even diabetics that suffer from foot complications including gane green still suffer and even die because antibiotics are not powerful enough to get the job done. Natural doctors are turning to PEO pure essential oils, colloidal silver, activated biocharcoal and herbal poultices with great success. Prebiotics and probiotics aka friendly bacteria like that found in raw yogurt are far better at healing than that of antibiotics also.

It is wonderful to discover that essential oil frequencies are several times
greater than frequencies of herbs and foods. For years, research has been
conducted on the use of electrical energy to reverse disease. Scientists in the
field of natural healing have believed there has to be a more natural way to
increase the body's electrical frequency. This led to the research and subsequent
discovery of electrical frequencies in essential oils.

The more results that have been seen, the more research has been initiated. Unhealthy Substances Cause Frequency Changes.

In one test, the frequency of two individuals - the first a 26 year old male and the second a 24 year old male - was measured at 66 MHz each.
The first individual held a cup of coffee (without drinking any), and his frequency dropped to 58 MHz in 3 seconds. He put the coffee down and inhaled an aroma of essential oils. Within 21 seconds, his frequency had returned to 66 MHz.
The second individual took a sip of coffee and his frequency dropped to 52 MHz in the same 3 seconds. However, no essential oils were used during the recovery time, and it took 3 days for his frequency to return to its initial 66 MHz.
Another young many with the frequency of 65 MHz put a cigarette in his hand and his
frequency dropped to 56 and when he put it between his lips without lighting it, his frequency dropped to 48 MHz. (Remember what happens when the body's frequency
drops to 48? Tissue breakdown from disease.
Do you really want to put your body in that kind of jeopardy?
One surprising aspect of this study measured the influence that thoughts have on the body's electrical frequency.
Negative thoughts lowered the measured frequency by 12 MHz and positive thoughts raised the measured frequency by 10 MHz.
It was also found that prayer and meditation increased the measured frequency levels by 15 MHz.
================================================================
More evidence that animals are amazing teachers -

"Elizabeth's research into the cat's purr has brought her a great deal of support from many sources, including veterinarians. She has also received support from a professor emeritus in England who is known as the "grandfather of bones." He is the foremost authority on bone density. She doesn't want to give his name since she doesn't have his permission.

Interestingly, he writes that optimal frequency for bone stimulation is 50 hertz. The dominant and fundamental frequency for three species of cats' purrs is exactly 25 to 50 hertz: the best frequencies for bone growth and fracture healing.

The cat's purr falls well within the 20 — 50 hertz anabolic range, and extends up to 140 hertz. All members of the cat family except cheetahs have a dominant or strong harmonic at 50 hertz. The harmonics of three cat species fall exactly on, or within, 2 points of 120 hertz, a frequency which has been found to repair tendons.

A few veterinarians have said that the purr is only a vocalization of contentment, and most people believe that. But Elizabeth's research analysis shows it's not true. Cats will purr when they are injured and in pain as well as when they are content. In one case, a cat had broken its femur and the femur was sticking out. But it was purring, so it can be assumed that purring is not always a sign of contentment.

Some people claim that cats purr when they're injured because they're humming to make themselves feel better. That makes absolutely no sense. If you've ever broken your leg or an arm and you find yourself in the emergency room, are you whistling "Dixie"?

Purring takes a lot of energy. It's created by both the diaphragm and the larynx. Getting a diaphragm to move for something other than breathing is difficult, it takes energy. When there is pain and suffering, our bodies are traumatized and they shut down non-essential activity. Since cats purr when they are severely injured or dying, it has to be survival-related.

According to Elizabeth, that statement is an old veterinarian's adage and it's still taught in veterinary schools to this day. That's the first thing she came across when she started out with this research. But no one has done any studies on it.

The type of frequencies that are found in the cat's purr are good for healing muscle, tendon, and ligament injuries, as well as for muscle strengthening and toning. They are good for any type of joint injury, wound healing, reduction of infection and swelling, pain relief, and relief of chronic pulmonary disease.

Authors of the veterinarians' surgery manual say that what it basically comes down to is that, compared to other animals, cats simply don't get chronic pulmonary disease, muscle and tendon injuries, bone diseases, and a lot of other things that dogs get. The purr seems to be a constant strengthener and toner for the muscles.

The average health of cats is considered to be greater than that of dogs. An actual case study was done where they took 52,000 animals and found that lameness in dogs occurred 3.6 percent and in cats only .26 percent. In another study arthritis in dogs was listed as 2.4 percent of the population, and was not reported at all in cats. The prevalence of lameness in dogs occurred 3.1 percent of the time, and again, in cats it was not even mentioned. The overall incidence of primary lung tumors in the dog is 1.24 percent, and in the cat, .38 percent. This basically says that cats are in fact healthier than dogs are."
------------------------------------------------------------------------------------------------
There are so many reports of a cat's purr being therapeutic; even to the point of helping you mend your broken bones. I read a report, last year, of a study regarding people with broken bones and holding a cat on their laps. Apparently, it helped them to heal much faster than normal.

Here's an interesting report:
http://www.bksv.com/2798.asp

"Cats do not have near the prevalence of orthopedic disease or ligament & muscle traumas as dogs have. Also, non-union of fractures in cats is rare. Researchers believe that self-healing is the survival mechanism behind the purr. There is extensive documentation that suggests that low frequencies, at low intensity, are therapeutic. These frequencies can aid bone growth, fracture healing, pain relief, tendon & muscle strength & repair, joint mobility, the reduction of swelling, & the relief of dyspnea, or breathlessness."
================================================================
How to distinguish material sound from spiritual sound.
Creation via sound
============================================================================================
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 & other neurosystemic diseases.

http://www.nexusmagazine.com/articles/mycoplasma.html original document

15. Nicholson, G. L., "Doxycycline treatment and Desert Storm", JAMA 1995;273:618-619. http://Immed.org/

Extracted from Nexus Magazine, Volume 8, Number 5 (August-September 2001)
PO Box 30, Mapleton Qld 4560 Australia.
editor@nexusmagazine.com
Telephone: +61 (0)7 5442 9280; Fax: +61 (0)7 5442 9381
From our web page at:
www.nexusmagazine.com

© by Donald W. Scott, MA, MSc © 2001
President
The Common Cause
Medical Research Foundation
190 Mountain Street, Suite 405
Sudbury, Ontario, Canada P3B 4G2
Tel/fax: +1 (705) 670 0180

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 (dangerous). 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 the pathogen invades and destroys cells in the lower bowel.

Once the mycoplasma gets into the cell, it can lie there doing nothing sometimes for 10, 20 or 30 years, but if a trauma occurs like an accident or a vaccination that doesn't take, the mycoplasma can become triggered.

Because it is only the DNA particle of the bacterium, it doesn't have any organelles to process its own nutrients, so it grows by uptaking pre-formed sterols from its host cell and it literally kills the cell; the cell ruptures and what is left gets dumped into the bloodstream.

II & CREATION OF THE MYCOPLASMA

A Laboratory-Made Disease Agent

Many doctors don't know about this mycoplasma disease agent because it was developed by the US military in biological warfare experimentation and it was not made public. This pathogen was patented by the United States military and Dr Shyh-Ching Lo. I have a copy of the documented patent from the US Patent Office. *1*

All the countries at war were experimenting with biological weapons. In 1942, the governments of the United States, Canada and Britain entered into a secret agreement to create two types of biological weapons (one that would kill, and one that was disabling) for use in the war against Germany and Japan, who were also developing biological weapons. While they researched a number of disease pathogens, they primarily focused on the Brucella bacterium and began to 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, then stored, transported and deployed without deteriorating. It could be delivered by other vectors such as insects, aerosol or the food chain (in nature it is delivered within the bacterium). But the factor that is working in the Brucella is the mycoplasma.

Brucella is a disease agent that doesn't kill people; it disables them. But, according to Dr Donald MacArthur of the Pentagon, appearing before a congressional committee in 1969, *4* researchers found that if they had mycoplasma at a certain strength--actually, 10 to the 10th power (1010)--it would develop into AIDS, and the person would die from it within a reasonable period of time because it could bypass the natural human defences. If the strength was 108, the person would manifest with chronic fatigue syndrome or fibromyalgia. If it was 107, they would present as wasting; they wouldn't die and they wouldn't be disabled, but they would not be very interested in life; they would waste away.

Most of us have never heard of the disease brucellosis because it largely disappeared when they began 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 ventricles--where the disease multiple sclerosis is basically located. *6*

Contamination of Camp Detrick Lab Workers, Detrick = the trick

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 thata 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.

Ticks are now carrying many more illnesses. As a result of being tested upon & released among tick populations.

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&endash;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 Star *11* 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 (mad cow 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 that we can get." They shipped it down and she found HIV in it. That virus was acquired by that chimpanzee in the laboratories where it was tested. *14*

Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis

Chronic fatigue syndrome is more accurately called myalgic encephalomyelitis. The chronic fatigue syndrome nomenclature was given by the US National Institutes of Health because it wanted to downgrade and belittle the disease.

An MRI scan of the brain of a teenage girl with chronic fatigue syndrome displayed a great many scars or punctate lesions in the left frontal lobe area where portions of the brain had literally dissolved and been replaced by scar tissue. This caused cognitive impairment, memory impairment, etc. And what was the cause of the scarring? The mycoplasma. So there is very concrete physical evidence of these tragic diseases, even though doctors continue to say they don't know where it comes from or what they can do about it.

Many people with chronic fatigue syndrome, myalgic encephalo-myelitis 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 fibromyalgia who had been denied her pension back in 1993. The vice-chairman of the board came to Sudbury to hear the appeal, and I showed him a number of documents which proved that this lady was physically ill with fibromyalgia. It was a disease that caused physical damage, and the disease agent was a mycoplasma. The guy listened for three hours, and then he said to me: "Mr Scott, how is it I have never heard of any of this before? I said: "We brought a top authority in this area into Sudbury to speak on this subject and not a single solitary doctor came to that presentation."

VI & TESTING FOR MYCOPLASMA IN YOUR BODY

Polymerase Chain Reaction Test

Information is not generally available about this agent because, first of all, the mycoplasma is such a minutely small disease agent. A hundred years ago, certain medical theoreticians conceived that there must be a form of disease agent smaller than bacteria and viruses. This pathogenic organism, the mycoplasma, is so minute that normal blood and tissue tests will not reveal its presence as the source of the disease.

Your doctor may diagnose you with Alzheimer's disease, and he will say: "Golly, we don't know where Alzheimer's comes from. All we know is that your brain begins to deteriorate, cells rupture, the myelin sheath around the nerves dissolves, and so on." Or if you have chronic fatigue syndrome, the doctor will not be able to find any cause for your illness with ordinary blood and tissue tests.

This mycoplasma couldn't be detected until about 30 years ago when the polymerase chain reaction (PCR) test was developed, in which a sample of your blood is examined & damaged particles are removed & 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 24-hour Holter ECG

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 "buhbuhbuhbuhbuhbuhbuhbuhbuh". 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 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 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 alright 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 some of 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 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. *15* 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. WWW.IMMED.ORG

U.S. military & VA facilities only test for 4 out of over 200 versions of mycoplasma. VA does not test for mycoplasma incognitus.

A sperm clinic in L.A. stopped testing for mycoplasma for cost reasons. They declared they were finding most people to have mycoplasma at varying levels.

Endnotes / FootNotes *##*
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&endash;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. L., "Doxycycline treatment and
Desert Storm", JAMA 1995;273:618-619.
http://immed.org/

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 L. 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 2S5, 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@xtra.co.nz. (Note: Dr Simpson directs his study to red cell shape analysis, not the mycoplasma hypothesis.)

¥ The Mycoplasma Registry for Gulf War Illness, S. & L. Dudley, 303 47th St, J-10 San Diego, CA 92102-5961, tel/fax +1 (619) 266 1116, fax (619) 266 1116, email mycoreg@juno.com.

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.

 
============================================================================================
IF THE U.N. MAGAZINE CAN PROMULGATE THE AIDS CURE, WHY CAN'T THE U.N.?
in real terms "u.n." means "not".
The U.N. is NOT going to further the double blind AIDS CURE trials so desperately needed. The U.S. is NOT. The PEOPLE must.
Boyd Ed Graves   www.boydgraves.com
Boyd Graves <boyded2003@yahoo.com> wrote:
Dear Mr. Secretary General:
Your proclamation that AIDS is a weapon (of mass destruction) is consistent with the prevailing view amongsy AIDS experts around the world. It is also the view of the informed public from sheriffs and police officers in Tenessee to soccer moms in Colorado.
The synthetic HIV/AIDS is the designer virus of the mostly secret, U.S. Special Virus program (1948 - 1978). On May 15, 2000) the United States' Dr. VICTORIA CARGILL located the program's 1971 flowchart www.boydgraves.com/flowchart.
Additonally, the following African American professionals now agree that HIV/AIDS is a laboraotry product, Dr. William Richardson, M.D. of Atlanta, GA , Dr. Randy Taylor, M.D., Los Angeles, CA, Dr. Attorney David Whitaker, Esq., Cleveland, OH, Dr. Attorney Shaune Arnold, Esq., Los Angeles. CA, Dr. Owen Ellington, M.D., Houston, YX.
We also believe that we have made contact with concerned doctors at the Centers for Disease Control.and Prevention.
The implementation of the one time injection AIDS CURE will assist the world in stabilizing itself to continue a path built on turth and fact. We have also provided information to the U.S. Project on Government Secrecy of the Federation of American Scientists, Steven Aftergood, Director.
On December 1, 2003, your independent magazine editor, Paul Rafferty, the U.N. Observer and International Report published the fact that a CURE for AIDS exists (www.unobserver.com (War of the Shadows section). You are now on record as is Dr. Peter Piot, Executive Director, UNAIDS, who also believes that HIV/AIDS is a laboratory creation.
A review of the U.S. Special Virus-Cancer Program will solve AIDS. I am certain. Boyd Ed Graves, J.D., DIRECTOR-AIDS CONCERNS, the Common Cause Medical Research Foundation, Sudbury, Ontario, Canada
Boyd Ed Graves,
Method of curing AIDS with tetrasilver tetroxide molecular crystal devices
Abstract
The diamagnetic semiconducting molecular crystal tetrasilver tetroxide (Ag.sub.4 O.sub.4) is utilized for destroying the AIDS virus, destroying AIDS synergistic pathogens and immunity suppressing moieties (ISM) in humans. A single intravenous injection of the devices is all that is required for efficacy at levels of about 40 PPM of human blood. The device molecular crystal contains two mono and two trivalent silver ions capable of "firing" electrons capable of electrocuting the AIDS virus, pathogens and ISM. When administered into the bloodstream, the device electrons will be triggered by pathogens, a proliferating virus and ISM, and when fired will simultaneously trigger a redox chelation mechanism resulting in divalent silver moieties which chelate and bind active sites of the entities destroying them. The devices are completely non-toxic. However, they put stress on the liver causing hepatomegaly, but there is no loss of liver function.
==================================================================================
 

Dr. Clark through exhaustive research documented the resonant frequencies of over 250 different microorganisms ranging from parasites and fungi to bacteria and viruses. While they range from 81,000 to 878,000 hertz, the majority of these frequencies lie between the values of 400,000 and 500,000 hertz.
The difficulty with this frequency range is that it is too high to be effectively transmitted electrically through the skin, and it is too low to be effectively transmitted through an antenna. Many people mistakenly confuse the resonant frequency that was identified with the frequency that will destroy it. They are not the same. Crane machines (currently known as Rife machines) can effectively transmit frequencies from 0 to 2500 thought the skin electrically. True Rife machines can effectively transmit frequencies from 7 to 14 million through an antenna. The Clark range misses both of these biological windows.
The solution is to raise a Hulda Clark frequency up 4 or 5 octaves until it reaches the Rife range and then transmit it through an antenna. For example, the Fasciolopsis buskii adult parasite which is listed by Hulda Clark as having a frequency of 434,000 when multiplied by 32 (2x2x2x2x2, the fifth octave up) yields 13,888,000 hertz. This frequency is very effectively transmitted through the air from an antenna.
A device is now available which can transmit all three sets of frequencies, Crane, Clark and Rife. The unlocking of Hulda Clarks frequencies represents a milestone in the reversal of disease.
Want more Information? frequencies@road-to-health.com

© Copyright 2002- 2006 road-to-health.com Coaching Link
Similar to Royal Raymond Rife frequencies. 
The QXCI & SCIO triquarter technologies bases on similar principles.
Hulda Clark's Frequencies From "The Cure For All Diseases"
 
Note: The formatting of this document has been reworked in Windows Notepad text editor, so that the tabs display into collumns properly
 
Also note that, in the book, data values seemed to have been placed in the wrong cells in the tables / spreadsheet that was in my copy- 1995 Copyright, 10th printing. I've tried to move the data to the apropriate places as well as possible now. Much of this data was scanned, run through an OCR program, then reformatted.
 
My sincere thanks to Hulda Clark for giving permission in her book to pass on this information!
++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++
Re-edited December 20th, 1998
 
Editor's Note: three extra frequencies have been added into this list, with a " ** "in front of the entry, for the "Adenovirus"; recently, some cold- like symptoms are being found to not be responsive to use of the 393KHz, which has so often done the job in the past. These are added into this list as other possible experimental frequencies.
 
 
PLEASE UNDERSTAND THAT THESE FREQUENCIES ARE THE PRIMARY RESONANT FREQUENCIES, LISTED IN KHZ!
These primary frequencies were detected directly by Hulda Clark in her research. To relate these to "Rife Frequencies", which are limited to much lower audio range frequencies due to the technical limitations of the equipment, or to translate these higher frequencies into a frequency which can be set on the EMEM2, EMEM2+, or the Rife/ Bare Radiant Plasma systems, divide the CLARK frequency found here by 512. If this result is still beyond the generation range of your device, try dividing these CLARK Frequencies by 256. Our Thanks to Brian McInturff and others for their input on this frequency translation process.
 
When these primary CLARK frequencies are known, it may be most effective to work with a device capable of generating these frequencies *AS A PULSED DC SQUARE WAVE* with a waveform rise time of 100nS or faster for optimum effect, according to many researchers. The Zapper HFA-4AV and HFA-4AVR models have a 75nS rise time on the output waveform, and can generate frequencies from below 8 Hz to typically 1.3+ MHz, with an adjustable outputvoltage amplitude of from 5 volts to 14 volts. This may be the only device available in any price range that has this capability, especially in a portable rechargable format.
+++++++++++++++++++++++++++++++++++++++++++++++++++++++++
HULDA CLARK'S FREQUENCIES
Mold, Mold Toxin Frequencies
Slime Molds                             KHz
Agyfla                                     81
Lycogala                                126
Stemonius                               211
 
Other molds and mold toxins        KHz 
Aflatoxin                                 177, 188 
Cytochalasin B                          77, 91   
Ergot                                        295
Griseofulvin                                288
Sorghum syrup                           277
Sterigmatocystin                        88, 96, 133, 126
Zearalenone                              100
 
BACTERIA AND VIRUSES         Low Freq   High Freq     Use (KHz)            
Acetobacter aceti
Adenovirus                                  393             393             393
Adenovirus (2nd range)                371.45         386.90         (375?)
*   Adenovirus (3rd range)                                             371 KHz
*   Adenovirus (4th range)                                             334 KHz
*   Adenovirus? (5th range- much higher)                         568 KHz
Agrobacterium tumefaciens
Alcaligenes faecalis
Alpha streptococcus                       369.75         385.4          380, 375
Azobacter chroococcum
Bacillus anthracis                            393.5          398.05         395
     causes anthrax in cattle (tooth)
Bacillus anthracis (2nd range)           363.2          365.3          364
Bacillus anthracis (3rd range)           359.4          370.5          368
Bacillus anthracis spores                391.45         386.95         388
Bacillus cereus                              373.65         375.85         374.5
Bacillus megaterium
Bacillus sterothennophilus
Bacillus subtilis spores
Bacillus subtilis var. niger                371.85         387.1      385, 380, 375
Bacteria capsules                           416.05         418.75         417.5
        (capsular strain)
Bacterial capsules                           362.4          357.6          360
Bacteroides fragilis found with           324.3          325.0          325
     common roundworm Ascaris
Bacteroides fragilis (2nd range)         325.7          326.0
Beta streptococcus (tooth)                380~6          387.4           385
Blepharisma                                    405.65         407.45         406.5
Bordetella pertussis                          329.85          332.25         331
     "whooping cough" (tooth)
Borellia burgdorferi Lyme disease    378.95     382.0          380
Branhamella (Neisseria) catarrhalis        394.9      396.7          396
                                                (has hole at 398)
Brucella abortus
Cabbage Black Rot
Campylobacterfetus smear        365.3          370.6          368
Campylobacter pyloridis            352.0          357.2          355
Candida albicans (pure powder) 384.2          388.4          386
     common yeast
Caulobacter vibrioides
Central spores (bacillus smear) 372.45         378.65         376
Chlamydia trachomatis             379.7          383.95         381
Clostridium acetobutylicum       382.8          391.15         389, 384
 
BACTERIA AND VIRUSES        Low Freq       High Freq       Use for
Continued                                 (Khz)          (Khz)              3 min
 
Clostridium botulinum (tooth)    361.0          364.55          362
     causes food poisoning
Clostridium pedringens
Clostridiurn perrringens spores  394.2          393.1           396
Clostridiurn septicum               362.05         3656             364
Clostridium sporogenes
Clostridium tetani
     (tooth) causes tetanus
Corynebacterium diptheriae        340             344             342
     (tooth) causes diphtheria
Corrynebacterium pseudodiphthericum
Corynebacterium xerosis           3l5.65         316.8            316.0
Coxsackie virus B-I                   360.5          366.1           364
     found with Bacteroides fragilis
Coxsackievirus B4                     361.45         363.7           362.5
     found with Bacteroides fragilis
Coxsackie virus BA (2nd range)   363.9          364.9
Crithidia fasciculata
Cytomegalovirus (CMV) antigen   403.35         410.75          409
Cytophaga rubra                        428.1          432.2           430
Diplococcus diphtheriae            357.95         364.0           361
Diplococcus pneumoniae         351.65         368.45          365, 360
Elkanella corroderis                379.5          384.3           382
Enterobacter aerogenes          374             374             374
    intestinal bacterium
Epstein Barre virus (EBV)       372.5          382.35          380, 375
Erwinia amylovora                  347.2          352.1           350
Erwinia carotovora                 363.1          377.0           373
Escherichia coli (E. coli)         356             356             356
intestinal bacterium
Escherichia coil                     392             393             393
        (E. coli) (2nd range)
Gaffkya tetragena                   344.85         352.5           350
        causes respiratory infections
Gardnereila vaginalis               333.0          342.55          340
        ovarian and genital tract infection
Haemophilus influenzae           336.41         336.41          336
        bacterial meningitis, infects joints
Hepatitis B antigen                  414.55         420.8           418
Herpes simplex I                      291.25         293.05          292
Herpes simplex 1(2nd range)     345.35         345.76          345.5
Herpes simplex 2 (fresh smear) 353.9          362.9           360, 355
Herpes Zoster "shingles"          416.6          420.2           418
Histomonas meleagridis (liver)  376.55         373.7           377
Histoplasma capsulatum          293.3          304.35          302
HlV                                        365             365             365
Influenza A and B (flu shot)     313.35         323.9           320, 315
Iron Bacterium Sphaerotilus
Klebsiella pneumoniae           393.45         404.66          401
     causes pneumonia
klebsiella pneumoniae           416.9          421.9           419
        (2nd range)      
Lactobacillus acidophilus       346.05         351.65         349
        (tooth)      
Leptospira interrogans          397.05         401.1           399
        Spirochete
Lumpy Jaw
Measles antigen                 369.5          373.0           371
Micrococcus luteus
Micrococcus roseus
 
BACTERIA AND VIRUSES       Low Freq       High Freq      Use for
Continued                                  (Khz)          (Khz)            3 min
 
Mumps antigen                        377.6          384.65         382
Mycobacterium para TB
Mycobacterium phlei                409.65         410.65         410.0
Mycobacterium smegmatis
Mycobacterium tuberculosis      430.55         434.2          432
        (infec nodule) causes tuberculosis
Mycoplasma                           322.85         323.9          323.5
Mycoplasma (range 2)             342.75         349.3          346
Neisseria gonorrhea                333.85         336.5          334
        causes gonorrhea 
Neisseria sicca
Nocardiaasteroides                  354.95         355.35         355.1
     found in Parkinson's Disease
Norcardia asteroides                363.7           370             368
        (2nd range)
Propionobacterium acnes         383.75         389.0          387
Proteus mirabilis                      320.55         326.0          324
Proteus mirabilis (2nd range)     345.95         352.1          349
Proteus vulgaris                        408.75         416.45         413
        urinary tract pathogen
Proteus vulgaris (2nd range)        333.75         339.15
Proteus vulgaris (3rd range)        327.2          329.5
Pseudomonas aeruginosa          331.25         334.6          333
        found in open wounds   
Pseudomonas fluonescens
Respiratory syncytial virus          378.95         383.15         380
Rhizobium leguminosarum
Salmonella enteriditis                   329            329             329
        intestinal infection
Salmonella paratyphi                  365.05         370.1          368
Salmonella typnimurium              382.3          386.55         385, 386
        food poisoning, nenvousness, apathy
Serratia marcescens                   349.45         352.1          351
Shigella dysenteriae                  390.089         390.089         390.089
        intestinal problem
Shigella flexneri depression             394           394             394
Shigella sonnei invades tumors        318           318             318
Sphaerotilus natans                        388.4         393.45         391
Spirillum itersonil
Spirillum serpens                            378.35        382.8          380
Spirillum sinuosum
Spirillum volutans
Spores in bacteria spore stain
Staphylococcus aureus (culture)       376.27        380.85          378
Staphylococcus aureus (slide)          381           381             381
     source is tooth infection, causes abscesses, heart disease, invades tumors
Staphylococcus epidenmidis; infects skin & mucous membranes
Streptococcus lactis:                        382          387             385
        occurs in milk
Streptococcus mitis :                        313.8        321.1          318
     lung infection, tooth infection abscesses,causes stiff knees
Streptococcus pneumoniae causes    366.85       370.2          368
     pneumonia and inner ear disease
Streptococcus pyogenes (tooth)      360.5        375.3          373
Streptococcus sp. group G (tooth)   368.15       368.85         368
Sub terminal spores bac. smear      385.15       385.95
Terminal spores bacillus smear
Tobacco mosaic virus (tobacco)      427.15       429.55         428
 
BACTERIA AND VIRUSES           Low Freq       High Freq       Use for
Continued                                       (Khz)          (Khz)          3 min
 
Treponema pallidum:             346.85         347.4           347                 causes syphilis       
Troglodytella abrassari          377.75         385.2          383
Troglodytella abrassari          416.9          422.2          419
        (2nd range)
Veillonella dispar                  401.75         405.2          403
Vibrio (photobacterium) fischeri
 
Roundworms, Flatworms, One-celled Animals
 
                                              Low Freq       High Freq       kill use
                                                (KHz)         (Khz)          for 3   min
 
Acanthocephala
Anaplasma marginale                    386.4       388.0           387
Anaplasma rnarginale (2nd range)   415.3       424              422
Ancylostoma braziliense (adult)      397.6       403.25          401
Ancylostoma caninum                   383.1       402.9       400, 393, 386
Ancylostoma duodenale male
Anguillula aceti
Ascaris larvae in lung                    404.9        409.15         408
     common roundworm of cats and dogs
Ascaris lumbricoides (m and f)  same
Ascaris megalocephala (male)       403.85       409.7          408
Babesia bigemina
Babesia canis smear
Balantidium coli cysts                    458.8        462.9          460
Balantidium sp. trophozoites (from
     guinea pig) parasitic ciliate
Besnoitia (lung sect.) protozoan      352.8        361.4          358
Capillaria hepatica (liver sect)          424.25       430.65         428
Chilomastix cysts (rat)                   388.95       390.7          389
ChiIomastix cysts (rat) (2nd range)  425.2        427.3          426
Chilomastix mesnili   (trophozoite)same
Chilomonas, whole mount                393.75         400             398
Clinostomum metacercaria
Clonorchis metacercariae
Clonorcnis sinensis                       425.7          428.75         427
Clonorchis sinensis eggs
Cryptocotyle lingua (adult)             409.95         416.0          414
Didinium
Dientamoeba fragilis                      401.35         406.05         404
Dipetalonema perstans (microfilaria
human blood)
Dirofilaria immitis dog heartworm     408.15        411.15         409
Echinoporyphium recurvatum          418.55         423.9           421
Echinostoma revolutum                  425.5          429.65         428
Eimeria stiedac
Eimeria tenella
Endamoeba gingivalis trophozoite    433.8          441.0          438
Endolimax nana trophozoites          394.25         397.1          396
& cysts    
Endolimax nana trophozoites           430.5          433.35         432
& cysts(2nd range)
Entamoeba coil cysts
Entamoeba coil trophozoites            397.0          400.35         396
 
 
Roundworms, Flatworms,         Low Freq       High Freq       To kill,  use
One-celled Animals, Continued         (KHz)          (Khz)          for 3 min
 
Entamoeba histolytica trophozoite     381.1         367.8           385
Enterobius vernicularis                     420.95         425.3          423
Eurytrema pancreaticum                  420.35         422.3          421
Eurytrema pancreaticum stages
Fasciola hepatica                            421.35         427.3          425
Fasciola hepatica cercariac              423.8          430.6          427
Fasciola hepatica eggs                    422.0          427.6           425
Fasciola hepatica metacercariae
Fasciola hepatica miracidia              421.75         424.7          423
Fasciola hepatica rediae                   420.6          427.5          425
Fasciolopsis buskii adult                  427.7          435.1          434
Fasciolopsis buskil eggs                  427.35         435.45         434
Fasciolopsis buskii eggs unincubated
Fasciolopsis cercariae                    429.5          435.25         434
Fasciolopsis miracidia                    427.35         435.2          434
Fasciolopsis rediae                         427.3          433.0          432
Fischoedrius elongatus                   441.75         443.2          442
Gastrothylax elongatus                   451.9          457.1          455
Giardia lamblia (trophozoites)          421.4          426.3          424
Giardia lamblia cysts
Gyrodactylus                                 378.75         381.8          380
Haemonchus contortus                   386.8          395.5          393
Haemoproteus
Hasstile sig. tricolor (adult)              448.05         455.1           453
Heterakis
Hypodereum conoideum                  424.45         429.55         427
lodamoeba butschlii trophozclles      437.85         448.5          445
     & cysts
lodamoeba butschlii trophozoites      398.15        404.75         402
     & cysts (2nd range)
Leishmania braziliensis                    400.05         405.1          403
Leishmania donovani                        398.0          402.65         400
Leishmania mexicana                       400.2          403.8          402
Leishmania tropica                           402.1          407.4          405
Leucocytozoon                                397.46         402.55         400
Loa Ioa                                            360.551         360.551         361
Macracanthorhynchus                      438.85         442.8          440
Metagonimus Yokogawai                  437.35         442.1          440
Monocystis agilis
Myxosoma                                       409.6          416.95         414
Naegleria fowleri                               356.9          354.35         362
Naegleria fowleri (brain sec.)
Necator americanus (infect larvae)
Notocotylus quinqeserialis
Onchocerca volvulus (tumor)             435.3          442.1          440
Paragonimus Westermanil adult       437.8          454.2          452, 447
Passalurus ambiguus                      428.8          444.15         441, 437
Pelomyxa carolinensis
Plasmodium cynomolgi                    417.3          424.5          422
Plasmodium falciparum smear          372.3          373.8          373.0
Plasmodium vivax smear                  438.15         445.1          442
Platynosomum fastosum adult
Pneumocystis carnil (lung)               405.75         409.15         407
Prostnogonimus macrorchis(eggs)    396.85         404.75         401
 
 
Roundworms, Flatworms,         Low Freq       High Freq      To kill, use
One-celled Animals, Continued      (KHz)           (Khz)           for 3  min
 
Sarcina lutea
Sarcocystis                                   450.55         454.95         452
Schistosoma haematobium             473             473             473
Schistosoma japonicum eggs
Schistosoma mansoni                    353             353             353
Stephanurus dentalus (ova)             467.35         463.1          461
Stigeoclonium                                404.25         415.25         412, 407
Strongyloides (filariform larva)          398.4          402.0          400
Strongyloides parasitic females
Toxocara (eggs)
Toxoplasma (human strain)           395.0          395.0          395
Trichinella spiralis (muscle)           403.85         405.57         404.5
Trichomonas muris
Trichomonas vaginalis                   378.0          383.6          381
Trichuris sp. (male)                       388.3          408.9          406
Trypanosoma brucel                     423.2          431.4          429
Trypanosoma cruzi (brain tissue)   460.2          465.65         463
Trypanosoma equiperdum             434.6          451.25         443. 442, 436
Trypanosoma gambiense              393.75         393-7          396
Trypanosoma lewisi (blood smear) 424.5          426.0          425
Trypanosoma rhodesiense            423.5          423.55         426
Urocleidus                                   442.35         450.0          447
 
 
Wart Frequencies    (Most of these are from homemade slides.)
                                        (Low Freq)       (High Freq)     To kill,
                                                                                  use for
                                             (KHz)           (Khz)          3 minutes
Wart BS                                   402             406             404
Wart CC                                   426             432.35         430
Wart FR                                   459.3          464.75         462
Wart HA                                   434.3          444.1          442, 437
Wart HRCm                              436.9          443.55         446, 441
Wart human papilloma planar     404.7          406.75         405
Wart human papilloma virus       402.85         410.7          407
Wart JB                                    418.75         422.4          420
Wart L arm                               343.65         345.95         344
Wart papilloma cervix smear      404.05         404.6          404.3
       
 
Tapeworms
     Tapeworms are segmented. The first segment is the head, called the scolex. Tapeworms grow by adding a new segment to their body.
     Tapeworms can have very large bandwidths (range of frequencies), and it varies by the length of the specimen! It is as if each new segment has a unique, and slightly lower, frequency.
     Do not use a frequency generator to kill tapeworms. If you accidentally kill middle segments instead of working your way up from the bottom, you may conceivably ~rom0te dispersion! Use only a zapper.
 
(Editor's Note: By this, Hulda means to use only a device producing a pulsed DC square wave output.)
 
 
TAPEWORM FREQUENCIES                         Low Freq.(KHz)   High Freq.(KHz)
 
Cysticercus fasciolaris                                    436.4           440.05
Diphyllobothrium erinacei(Mansoni)(scolex)       467.25         487.55
Diphyllobothrium erinacei eggs
Diphyllobothrium latum (scolex)                        452.9           472.3
Dipylidium caninum (proglottid composite)         439.55         444.3         
Dipylidium caninum (scolex)                            451.95         472.15
Echinococcus granulosus                               451.6           461.5
Echinococcus granulosus (cysts)                    441.15          446.5
Echinococcus granulosus (eggs)
Echinococcus multilocularis                            455.85         458.35
Heterophytesa heterophytes             
Hymenolepsis cysticercoides                          478.0           481.75
Hymenolepsis diminuta                                   445             481.15
Hymenolepsis diminuta ova
Hymenolepsisnana eggs
Moniezia (scolex)                                          430.35         465.2
Moniezia expansa (composite)                       430.35         465.2
Moniezia expansa eggs
Multiceps serialis                                          453.6           457.8
Pigeon tapeworm
Taenia pisiformus (cysticercus)                      475.2           482.1
Taenia pisiformus eggs (ova)                          465.2           469.7
Taenia saginata (cysticercus)                        476.5           481.05
Taenia saginata eggs                   
Taenia solium (cysticercus)                           475            475
Taenia solium (scolex)                                  444.0           448.9
Taenia solium eggs
 
MITE FREQUENCIES :These are the organisms that cold viruses ride in with!
 
MITE                                                  Freq. In Khz
Demodex folliculorum : folicle mite                682
Dermatophagoides : dust mite                      707
Meal Mite                                                  718
Ornithonyssus : bird mite                         877, 878
Scarcoptes scabei : itch                             735
 
Miscellaneous Frequencies
 
Blue-green Algae                                  256
Bryozoa cristatalla                               396
Mucor mucedo                                      288
Rhizobium meliloti                                330
Rotifer                                               1151
 
UNIDENTIFIED PATHOGENS                   Low(Khz)       High(KHz)
A Cold Virus HRC                                     395.8          395.8
Fungus EW                                              362.0          364.9
Fungus JWB                                            397.2          400.75
Tooth Decay                                         384.3          387.2
Tooth Decay (N)                                        367.9          375.05
Tooth Decay (N) (2nd range)                       326.95         331.5
Tooth Decay (N) (3rd Range)                       293.2          297.4
Tooth Plaque I                                           378.8          383.05
Tooth Plaque I (2nd Range)                        294.7          298.05
Tooth Plaque I (3rd Range)                        233.1          238.2
Tooth Plaque II                                         384.95         387.05
Tooth Plaque II (2nd Range)                       278.75         284
Tooth Plaque II (3rd Range)                       212.15         218
Tooth Plaque II (4th Range)                       340.15         344.8
Tooth Plaque II (5th Range)                       305.5          310.35             
 
 
NOTE: The previous frequency table data is reproduced from Hulda Regehr Clark, Ph.D., N.D.'s Book, "THE CURE FOR ALL DISEASES", Copyright 1995, and are included for free for your information.
 
On the title page of this book, just inside the front cover, is the following:
 
"Permission is hereby granted to make copies of any part of this document for non-commercial purposes provided this page with the original copyright notice is included".
 
As stated in the review of the book, I recommend that you buy this book!
============================================================================================
Dr. Rima Laibow goes on: "Squalene, a response enhancer or adjuvant, is present in many modern vaccines and is highly irritating to the immune system. . . . (used in) Anthrax vaccine in Gulf War I soldiers is believed by many to be a primary cause, along with depleted uranium, of the devastating condition known as Gulf War Syndrome".
Squalene
Mycoplasma and Squalene Discussion
Military Vaccine Resource Directory.
There is a lot of controversy about what is actually going on in the anthrax vaccine - about the actual causes of such severe reactions that six deaths are admitted to on the current vaccine label, and at least one more death attributable to military vaccines (Rachel Lacy) has occurred since. In addition, uncounted troops and veterans have become permanently incapacitated.
Those of us who run The Military Vaccine Resource Directory are not trained scientists or medical professionals. But we do have access to a great deal of research and to various professionals and physicians who kindly provide us with their insights and views.
Mycoplasma are the smallest of free-living organisms, and can reproduce outside of living cells. They can cause chronic inflammatory diseases of the respiratory system, urogenital tract, & joints. The most common human illnesses caused by mycoplasma are due to infection with M. pneumoniae, which is responsible for 10-20% of all pneumonias. This type of pneumonia is also called atypical pneumonia, walking pneumonia, or community-acquired pneumonia. Infection moves easily among people in close contact because it is spread primarily when infected droplets circulate in the air (that is, become aerosolized), usually due to coughing, spitting, or sneezing. (Source: Gale Encyclopedia of Medicine online)
In his Jan. 29, 2002 Congressional testimony, Dr. Garth Nicolson writes: "...the types of infection caused by Mycoplasma and Brucella species that have been found in GWI patients, can cause complex problems found in GWI [reviews: 23,40,41]. These microorganisms are now considered important emerging pathogens in causing chronic diseases as well as being important cofactors in some illnesses, including AIDS and other immune dysfunctional conditions [23,40,41]."
"Historically, mycoplasmal infections were thought to produce relatively mild diseases limited to particular tissues or organs, such as urinary tract or respiratory system [23,40,41]. However, the mycoplasmas detected in GWI patients with molecular techniques are highly virulent, colonize a wide variety of organs and tissues, and are difficult to treat [23,45,46]. The mycoplasma most commonly detected in GWI, Mycoplasma fermentans (found in >80% of those GWI patients positive for any mycoplasma), is found intracellularly. It is unlikely that this type of infection will result in a strong antibody response, which may explain the DoD's lack of serologic evidence for these types of intracellular infections [47]."
Squalene, an orgamic polymer which occurs naturally in the human body, is, in remanufactured form, an adjuvant, or vaccine "booster," used in several experimental vaccines. The purpose of such an adjuvant is to boost the immune system's reaction to the vaccine. It is illegal for use on human beings in the United States and Great Britain. There is evidence that when injected, squalene is responsible for arthritic conditions and pain. Squalene appears to be highly reactive when injected, although not as reactive when ingested orally.
Although the Dept. of Defense denied the presence of Squalene in the anthrax vaccine for many years, the FDA tested several lots for the presence of the adjuvant, and found it - in varying levels. Those lots are (ppb=parts per billion):
·         AVA 020 - 11 ppb squalene
·         AVA 030 - 10 ppb squalene
·         AVA 038 - 27 ppb squalene
·         AVA 043 - 40 ppb squalene
·         AVA 047 - 83 ppb squalene
Squalene has also been found in the vaccine administered in Great Britain, although the Ministry also denied its presence. See MOD (Ministry of Defense - UK - ANTHRAX VACCINE CONTAINS SQUALENE)
Recent research by Pamela B. Asa, Russell B. Wilson, and Robert F. Garry links the anthrax vaccine to Gulf War Syndrome through the presence of squalene antibodies, as noted in the introduction to their report:
"Date: 2002-07-15 Received August 15, 2001, and in revised form October 26, 2001"

"We previously reported that antibodies to squalene, an experimental vaccine adjuvant, are present in persons with symptoms consistent with Gulf War Syndrome (GWS) (P. B. Asa et al., Exp. Mol. Pathol 68, 196-197, 2000). The United States Department of Defense initiated the Anthrax Vaccine Immunization Program (AVIP) in 1997 to immunize 2.4 million military personnel. Because adverse reactions in vaccinated personnel were similar to symptoms of GWS, we tested AVIP participants for anti-squalene antibodies (ASA). In a pilot study, 6 of 6 vaccine recipients with GWS-like symptoms were positive for ASA. In a larger blinded study, only 32% (8/25) of AVIP personnel compared to 15.7% (3/19) of controls were positive (P 0.05). Further analysis revealed that ASA were associated with specific lots of vaccine. The incidence of ASA in personnel in the blinded study receiving these lots was 47% (8/17) compared to an incidence of 0% (0/8; P 0.025) of the AVIP participants receiving other lots of vaccine. Analysis of additional personnel revealed that in all but one case (19/20; 95%), ASA were restricted to personnel immunized with lots of vaccine known to contain squalene. Except for one symptomatic individual, positive clinical findings in 17 ASA-negative personnel were restricted to 4 individuals receiving vaccine from lots containing squalene. ASA were not present prior to vaccination in pre-immunization sera available from 4 AVIP personnel. Three of these individuals became ASA positive after vaccination. These results suggest that the production of ASA in GWS patients is linked to the presence of squalene in certain lots of anthrax vaccine. 2002 Elsevier Science (USA)"
-----------------------------------------------------------------------------
Resource for Iraqi freedom vets to find assistance
Tuesday, November 09, 2004
Tainted Lot numbers
If you know you have been given anthrax from any of these lots please contact me. I am here to help and your info remains confidential.

To All: Based on data from Tulane University Medical School, and medical records submitted by military personnel to Dr. Asa, this the complete list the vaccine lot numbers that Tulane considers problematic (I forgot to mention three of them in earlier postings):

Squalene-Positive [per FDA and SRI]:
FAV 008, FAV 020, FAV 030, FAV 038, FAV 043, FAV 047

Have Induced Anti-Squalene Antibodies [per Tulane Med School]:
FAV 041, FAV 070 and FAV 071

Associated with Autoimmune-Related Symptoms or Fullly Diagnosed Autoimmune Diseases in Troops [per Tulane]:
FAV 017, FAV 048b, FAV 066, FAV 068, FAV 069, FAV 073, FAV 074, FAV 075, FAV 078

I recommend directing any questions concerning this data to either Dr. Pamela B. Asa or Dr. Robert F. Garry.
-------------------------------------------------------------------------------------------
Anthrax vaccine blamed for illness
Book claims Gulf War GIs were guinea pigs


By Bartholomew Sullivan
sullivanb@snhs.com
November 17, 2004
http://www.commercialappeal.com/mca/local_news/article/0,1426,MCA_437_3334125... (must register to view original article)

WASHINGTON -- Mark Ammend of Collierville can't talk about it now.

The former fire chief for the 164th Air National Guard unit based at Memphis International Airport got vaccinated against anthrax five years ago. Now, as he lies in a specially designed bed, the only thing he can move is his left eye.

Fully conscious and aware, Ammend, 55, is a quadriplegic with amyotrophic lateral sclerosis (ALS), or Lou Gehrig's disease.

A new book suggests he and many other soldiers immunized against anthrax during the 1991 Gulf War and since are suffering auto-immune diseases after receiving an illegal chemical adjuvant -- a chemical designed to boost the immune system -- called squalene.

The Pentagon adamantly disagrees and insists that the vaccine is safe.

In his just-published "Vaccine A: The Covert Government Experiment That's Killing Our Soldiers and Why G.I.'s Are Only the First Victims," author Gary Matsumoto suggests Memphis was the key to the immunological puzzle.

"The whole idea originated in Memphis," he said in an interview.

That idea came from Pamela B. Asa, a former Memphis immunologist now living in Tupelo who collaborates with Robert F. Garry, a professor of microbiology at the Tulane University Medical School in New Orleans. Asa and Garry made the connection between squalene, which has not been authorized for use in humans in the United States, and what has been called Gulf War Syndrome in an article in Experimental and Molecular Pathology in 2002.

Auto-immune diseases such as ALS, lupus and rheumatoid arthritis are chronic and increasingly debilitating. They occur when the body can't distinguish between itself and foreign substances it's supposed to attack. Thirty years of scientific literature has shown squalene and other oil adjuvants have induced auto-immune-like illnesses in four species of lab animals. Squalene has never been licensed for use in humans in this country, although it is an element of a variety of experimental drugs.

Asa began looking into the connection between the constellation of symptoms associated with the soldiers' syndrome in 1994, and went to the Pentagon with her concerns. She said she found that many of the soldiers complaining of rashes, fatigue, blackouts, seizures, and joint and muscle pain looked like they had systemic lupus erythematosus, a multi-symptomatic auto-immune disease.

She monitored discussions on Gulf War Syndrome chat rooms, and recommended medical tests that those who were suspicious about their health might take. Word got around, and some shared seriology data with her.

Matsumoto wrote about her suspicions for the first time in 1999, in Vanity Fair magazine, prompting some soldiers in bases around the country to protest taking their anthrax shots. Many others soldiered on, and took them.

At least four members of the 164th Air Guard unit in Memphis quit in 1999 rather than take the shots. But more than 800 took them, according to unit officials at the time.

Ammend, the Air Guard fire chief in Memphis for 11 years and a soldier since 1972, took his first anthrax shot in 1999. He took the last one in April 2000. In 2002, he could still walk, his wife, Mary, said Tuesday. He now lies, mouth open, in his living room, on a respirator 24 hours a day.

"I understand why it was done, or why it was needed," Mary Ammend said. "But I just feel it could -- there should have been more care taken for the FDA to study it before they started dishing it out to the guys."

Three members of the 164th ANG unit in Memphis approached Asa after the Vanity Fair article and asked her to test their blood for antibodies to squalene before they were administered their mandatory anthrax shots. Before the shots, they had no antibodies to the substance. Afterward, two did.

One of them was Sgt. Serge Trullet of Ripley, Miss. A naturalized citizen from Argentina, Trullet wouldn't disobey an order to take the shot, but he wanted to take precautions, he told Matsumoto. When he tested positive for the antibodies to squalene, then started getting a rash and swelling, he didn't blame Uncle Sam. He blamed the unknown people "somewhere along the line," who let it happen.

"I don't know what to think about my commanders," Matsumoto quotes him saying. "I think that they're just ignorant -- you know, 'follow the leader' types that absolutely question nothing that their superiors tell them. I feel that some of them would have probably done the same things that the Nazis did to the Jews with the excuse that they were just following orders." Trullet did not respond to phone calls from The Commercial Appeal Tuesday.

"This (squalene) has not been out in the public forum because the Department of Defense has sort of blown it off and tried to portray people who spoke about it as conspiracy nuts," Asa said in an interview Tuesday.

"Had they (soldiers) not been given this stuff, we would not be finding antibodies to it in people who are sick with auto-immune diseases that squalene has been chronicled to cause for decades."

It's complicated science, but Asa and Matsumoto maintain that the squalene was used experimentally to boost the immune response to a very weak vaccine prepared to ward off a bio-chemical attack of weaponized anthrax spores known to have been developed by Saddam Hussein before the first Gulf War.

Over the years, symptoms of Gulf War illness have been blamed on stress or nerve gas exposure, flea collar insecticides and other factors, but anthrax vaccine has usually been among them. More than $100 million has been spent to find its cause.

James Turner, a Department of Defense spokesman specializing in health matters, said Tuesday that he was familiar with Matsumoto's book but called the concerns it raises "an old, old issue" being pushed by his publisher. Turner directed specific questions about anthrax and squalene to a department Web site. The site acknowledges that the Food and Drug Administration found squalene in some vaccines for anthrax, but says the amount was probably from fingerprint contamination by lab technicians and too small to cause concern.

Before ending the call, Turner added: "The fact is that we do not put squalene in our vaccines and never have. ... The notion that we're using military people as guinea pigs without their knowledge is absurd."

Absurd or not, it is Gary Matsumoto's most explosive claim, and it's backed by Asa. He says in the book "Vaccine A" that FDA tests show that the amounts of squalene found in different "lots" or batches of the vaccine administered to some troops shows a pattern. That pattern establishes someone was trying to determine the response to a progression of different doses, he claims.

"This is an experiment," Asa said Tuesday. "This is a dose-range experiment."

Perhaps the strangest set of facts revealed in his exhaustive history of anthrax's use as a potential weapon is Matsumoto's claim that the vaccine administered to soldiers might protect against anthrax encountered by contact, but would never work effectively against inhaled anthrax spores such as the threat foreseen from Saddam.

Asa agrees, and so does a federal judge in Washington. U.S. Dist. Judge Emmett Sullivan ruled Oct. 27 that the mandatory use of anthrax vaccine on soldiers is illegal and must stop because authorities can't prove it actually works against the inhaled anthrax expected to be used as a weapon in wartime.

Since the mid-1980s, the FDA had never found the vaccine effective in other than occupational settings, such as for protection of workers exposed to infested animal hides. But in December 2003, after the mandatory inoculations had been under way for five years, the FDA found that the vaccine was effective for inhaled anthrax. Sullivan said the agency failed to follow its own protocols in reaching that conclusion and ruled the vaccine can be used only in the case of informed consent or a presidential waiver.

Asked Tuesday why the Pentagon would want to vaccinate soldiers with a shot that couldn't accomplish its purpose, Asa said she doesn't know. But in her decades of research, she knows the Department of Health and Human Services has been looking for an oil adjuvant to boost potential anti-AIDS vaccines. She says agency researchers are trying to "make the science fit their wish list."

Contact Washington correspondent Bartholomew Sullivan at (202) 408-2726.
 
============================================================================================
Death by Vaccine - A Time Line        http://curezone.com/forums/fm.asp?i=1647231
The following is a history of virology, bacteriology, mycology and vaccination that has lead to many of the out-breaks and/or epidemics from the Spanish Flu Epidemic to Polio to HIV/AIDS to the Gulf War Syndrome and now to our latest epidemics of prostate and breast cancer, diabetes, obesity and the rise of autism in children.

Dr. Young has stated that the use of vaccinations, antibiotics and antifungals will only poison the body leading to the one sickness and one disease - latent tissue acidosis and then death.

All vaccinations, antibiotics and antifungals are the acids of morbid fermentation of plant, animal and human matter and when ingested or injected, it only proves that you can poison the body and then hopefully live through it.

The day will soon come when scientists will proclaim that the use of vaccinations, antibiotics and antifungals were and are harmful to the human body and should not be used under ANY circumstances.

In the words of Thomas Edison, 'The Doctor of the Future will give no medicine, but will involve the patient in the proper use of food, fresh air, and exercise.'

The future that Thomas Edison speaks is here and now! Read on to understand and to see for yourself the course we have been walking for the last several centuries and how things must change before it is to late.

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

1798 General vaccine programs against cowpox instituted in the US.

1801 First widespread experimentation with vaccines begins.

1802 The British government gives Edward Jenner £10,000 for continued experimentation with 'smallpox vaccine.' The paradigm that vaccines provide 'lifetime immunity' is abandoned, and the concept of 'revaccination' is
sanctioned.

1822 The British government advances Edward Jenner another £20,000 for 'smallpox vaccine' experimentation. Jenner suppresses reports which indicate his concept is causing more death than saving lives.

1844 Fredrich Loeffler isolated the diphtheria bacillus from the throats of patients.

1881 Sternberg in his own lab isolated the pneumococcus

1882 Robert Koch isolates the tubercle bacillus

1883 Robert Koch isolates the cholera bacillus.

1883 Max Von Pettenkofer suggested that Koch's bacteria were only one of the many factors in the causation of cholera. He prepared test tubes thick with lethal cholera bacteria and he and several of his students drank them down with no side affects.

1888 Bacteriological Institute opens in Paris for experimentation with animals and production of vaccines and sera. Other institutes open around the world modeled after the Paris Institute.

1888 Bacteriological Institute in Odessa, Russia tries its hand at a vaccine for anthrax. Over 4500 sheep are vaccinated; 3,700 of them die from the vaccination.

1909 New York Press, January 26, 1909 publishes a report by W.B. Clark which states, 'cancer was practically unknown until cowpox vaccination began to be introduced. I have seen 200 cases of cancer, and I never saw a case of cancer in an unvaccinated person.' Scientific evidence begins to mount that where human lymph is employed in a vaccine, syphilis, leprosy and TB soon follow. Where calf lymph is employed in the creation of a vaccine, TB and cancer soon follow. (Cancer and Vaccination by Esculapius).

1911 The head of French Public Health for the French Army said that germs alone were 'powerless to create an epidemic.'

1912 First whooping cough (Pertussis) vaccine created by two French bacteriologists, Jules Bordet and Octave Gengou, who wanted to use it in Tunisia. After they grew Pertussis bacteria in large pots, they killed it with heat, mixed it with formaldehyde (used to embalm bodies) and injected it into children.

'Vaccinations, Not a Virus, Is Responsible for Spanish Flu - 1918'
Dr. Robert O. Young


1933 a British science team to identify the first filterable bacteria in man, yet propaganda says that the virus of Spanish flu killed millions of civilians and soldiers during the pandemic from 1918 to 1920.

Many would have us believe that all those American soldiers who died from non-combatant causes died from Spanish flu. However, U.S. Army records show that seven men died after being vaccinated.

A report from U.S. Secretary of War Henry L Stimson, the deaths were not only verified but also there had been 63 deaths and 28,585 cases of hepatitis reported as a direct result of yellow fever vaccination during only six months of the war. Plus, the yellow fever vaccination was only one of the 14 to 25 shots given to recruits.

1911 vaccinations became a requirement in the U.S. Army. Cases of typhoid and vaccinal diseases increased rapidly, according to Army records.

1917 The death rate from typhoid reached the highest point in the history of the U.S. Army after America entered the war.

In 1917, 19,608 men were admitted into army hospitals due to antityphoid inoculation and vaccinia, according to a report of the Surgeon-General of the U.S. Army; and this doesn't take into account others whose symptoms were attributed to other causes. The army doctors knew all these cases of disease and death were due to vaccination and were honest enough to admit it in their medical reports. Army doctors tried to suppress the symptoms of typhoid with a stronger vaccine, however it caused a worse form of typhoid, paratyphoid. They then concocted an even stronger vaccine to suppress the previous one and created an even worse disease--Spanish flu.

After the war, this was one of the vaccines used to protect a panic-stricken world from the soldiers returning from WWI battle fronts infected with dangerous diseases.

The rest is history.

1918 Great influenza epidemic attributed to widespread use of vaccines that killed up to 100 million people.

1921 BCG tuberculosis vaccine developed.

1922 A study by Samuel Torrey Orton connects emotional disturbance with neurological problems. This insight was lost after World War II when psychology, psychiatry and psychoanalysis became popular, breaking the connection. The emotional disturbances caused by vaccines then became financial fodder for the new psych-industries. With the causes suppressed, a new industry was born.

1925 Danish researcher Thorvald Madsen tries a modified Pertussis vaccine during an epidemic in the Faroc Islands. It did not prevent Pertussis. (See 1933).

1925 General vaccine programs against tuberculosis began in the United States.

1927 British government appoints a committee to inquire into 'vaccine lymph', as it is noticed that the 'glycerinated calf lymph' used in vaccinations causes deaths from 'sleepy sickness'. Two London professors bring notice of the problem to the government in 1922. It takes 5 years before the government responds.

1930 Max Theiler develops a yellow fever vaccine.

1931 Roosevelt endorses polio 'immune serum', precursor to vaccines in 1950's.

1932 Diptheria vaccines injure 171 and kill 1 in Charolles, France.

1933 Danish researcher Thorvald Madsen discovers the Pertussis vaccines ability to kill infants without warning (SIDS). He reports that two babies vaccinated immediately after birth died in a few minutes.

1933 American researchers report that children react to Pertussis vaccine with fever, convulsions and collapse.

1936 Pertussis vaccine introduced in the United States. Autism begins to appear in children shortly thereafter.

1936 Diptheria vaccine injures 75 in France.

1943 American vaccine researcher Pearl Kendrick reports that adding a metallic salt seemed to heighten the capacity of the Pertussis vaccine to produce anti-bodies. (Metal salt is an 'adjuvant' in this way). Some metallic salts used are those of aluminum (alum). Pearl Kendrick is the researcher that urged that Pertussis vaccine be combined with Diptheria vaccine. Later the Tetanus vaccine was added, producing the nefarious DPT Vaccine.

1943 General vaccine program against influenza begins in the US.

1944 Health Practitioners Journal, June 1944, reports Dr. S.S. Goldwater, the New York Commissioner of Hospitals states 'as a result of the drugs, vaccines and other suppressive treatments used to check diseases, chronic diseases are growing at such a rate that America may become a nation of invalids.'

1945 Japan surrenders twice, followed by US bombing of Hiroshima/Nagasaki and a third and final surrender. The Allies mandate compulsory vaccination in Japan. The first cases of autism follow pertussis vaccine introduction.

1946 US Government Pertussis vaccine expert Margaret Pittman and FDA's Charles Kendrick decide to test Pertussis vaccine by injecting it into the brains of mice and see how many survive.

1946 Werne and Garrow describe the deaths of identical twins within 24 hours of their second Pertussis shot.

1947 Matthew Brody at the Brooklyn Hospital gives detailed descriptions of two cases of brain damage leading to death in children receiving Pertussis shots.

1947 Charles Posner of the Harvard Medical School Department of Neurology writes, 'almost any vaccination can lead to noninfectious inflammatory reaction involving the nervous system. The common denominator consists of vasculopathy that is often associated with demyelination.' (demyelination is the stripping of the insulation away from the nerves).

1947 The British Medical Research Council begins testing 50,000 children in Britain with the Pertussis vaccine. All children tested are more than 14 months old (not newborns). Eight infants had convulsions within 72 hours of the shot, 34 had convulsions within 28 days of the shot. British doctors denied a connection between the vaccine and the convulsions, declaring the tests a success and began administering it to all British children.

Despite the fact that none of the tests were conducted on children under 14 months old (newborns & babies), the United States holds the tests in evidence that the vaccine is safe for newborns as young as 6 weeks of age. The testing would continue until 1957.

1948 Randolph K. Byers and Frederick C. Moll of the Harvard Medical School publish an article describing children who had suffered brain damage after receiving Pertussis vaccine. The findings provided the first clear evidence that the vaccine caused the serious neurological complications in children.

1948 Randolph Byes and Frederick Moll of Harvard Medical School validate that severe neurological disorders follow the administration of DPT vaccine. The research was performed at Children's Hospital in Boston and published in Pediatrics magazine. Nothing was done by physicians to halt the use of DPT vaccine.

1948 A study on Pertussis vaccine reaction is done by Randolph K. Byers and Frederick C. Moll of the Harvard Medical School. They examine 15 children who had reacted violently within 72 hours of a Pertussis vaccination. All the children were normal before the shot. None had ever had a convulsion before. One of the children became blind, deaf, spastic and helpless after being given the Pertussis shot. Out of the 15 children, 2 died and 9 suffered from damage to their nervous system. Physicians were displeased by these results.

1948 England bans smallpox vaccine.

1948 North Carolina polio cases number 2,498. See 1949.

1948 Louis Sauer makes an interesting observation at an AMA meeting where Pertussis vaccination was discussed. Louis Sauer points out that 'the neurological damage caused by Pertussis vaccine is the same as the damage caused by Pertussis (whooping cough -- Which is logical, because they use the bacteria in the vaccine). According to Sauer, 'a customary prophylactic dose of Pertussis vaccine seems to illicit a chain of nervous system reactions and in some cases irreversible pathological changes in the brain. These findings resemble those encountered in cases of severe whooping cough (Pertussis).' In other words, the vaccine is causing the disease condition.

1949 US Public Health Service Division of Biologics Standards establish a national potency test for Pertussis vaccine, and modify it in 1953 to establish potency limits. Despite this, the Pertussis vaccine that is pronounced 'safe' still causes minimal brain damage (MBD) in humans.

1951 Theiler wins Nobel for work on yellow fever vaccine.

1952 Formulation of the polio vaccine begins. Tens of millions of doses of polio vaccines produced from virus grown in monkey cells infected with SV-40 (Simian Virus #40). Scientists 'perform experiments in laboratories to determine the correct doses of antigen and supplementary chemicals to use in the polio
vaccine. (Ironically, since the scientific premise of vaccination is faulty, a 'correct dose of antigen and chemicals' does not exist).
SIVS Simian Immunodeficiency Virus Syndome had been tested upon paving the way for HIV Human Immunodefiency Virus.

1953 At the University of Zurich, Dr. S.Kong of the Pediatric Clinic compiles a list of 82 cases of Pertussis vaccine damage from world literature.

1953 The Swedish conduct a study on the Pertussis vaccine. Anna L. Annell, a Swedish researcher, writes a major work on Pertussis which indicates that 'pertussis vaccine may be associated with the most varying kinds of cerebral complications which may be cortical, subcortical or peripheral.'

Encephalitis after vaccination is known to produce the same range of disabilities and impairment. Annel also wrote, 'during the past few decades certain of the epidemic children's disease, measles in particular, have shown an increased tendency to attack the central nervous system. After the 1920's a large number of cases involving CNS damage were reported.

1954 Salk vaccine begins to be given to school children in Philadelphia.

1954 Parke-Davis pharmaceutical company combines the DPT shot with Polio vaccine. The new combination of four vaccines is called Quadrigen. (See 1959).

1954 Reward of $30,000 offered to anyone who proves polio vaccine not a fraud. Not one person was able to claim the reward.

1954 Mrs. Oveta Culp Hobby, Secretary of Health, Education and Welfare, allows a press photo to be taken during a ceremony declaring Salk vaccine safe.

1954 Polio rate caused by the vaccine accelerates ten-fold in Massachusetts.

1954 Eli Lilly company begins renovation of a five-story building in Indianapolis in July 1954 for the production of Salk vaccine. It is in full production by October of

1954. Wyeth, Parke-Davis and others follow suit.

1954 A study on 'neurologic sequelae of prophylactic innoculation' summarized state-of-the-art knowledge in noting that the common factor in the pathologyof encephalitis from vaccination is 'anaphlactic hypersensitivity'.

1955 Georgia State public health officers meet in Atlanta (May 1955) to discuss
what was going wrong with the Salk vaccine program. A U.S. Public Health scientist at the meeting told the group that 'he was not permitted to disclose what had happened because it would jeopardize the investment of the pharmaceutical firms in the vaccine program.'

1955 Measles death rate has naturally declined, without vaccines, to .03 per
100,000 by 1955.

1955 At the University of Illinois School of Medicine, Department of Neurology, Niels Low shows that the EEG of infants is sometimes altered by a DPT shot,concluding that significant cerebral reactions and neurological changes occur.

1955 American Cancer Society advertising circular states 'cancer will strike one of every four persons now living. More children from 3 to 15 years of age die of cancer than from any other disease.' (50 years before, cancer was unheard of in children). According to the ACS, they are predicting 6.4 million deaths from cancer, compared with 128,000 in 1933--an increase of 6.2 million cases in 22 years. Vaccination, pesticide use and chemical pollution are the main factors that have increased since 1933.

1955 Despite the sky rocketing cases of vaccine-induced polio, the AMA, NFIP and USPHS claim a reduction of 40-50%.

1955 Idaho brings its Salk vaccination program to a halt on July 1, 1955.

Utah does the same on July 12, 1955.

1955 Boston Herald newspaper reports on April 18, 1955, features an article entitled 'Drug Companies Expecting Big Profit on Salk Vaccine', which stated. 'A spokesman for Parke-Davis, which made 50% of the Salk vaccine, said 'now that it has been declared safe, we can get back the millions we invested in the development of the Salk vaccine and make a profit out of it. Our company will made over $10 million on Salk vaccine in 1955.'

1955 Rhodes and Company, Wall Street brokers specializing in drug securities, estimate that the gross revenue of the six vaccine houses licensed to produce and sell Salk vaccine would be about $60 million, with profits of $20 million.

1955 The CIA conducts a biological warfare experiment in the Tampa Bay area in Florida with agents withdrawn from an Army CBW center. A sharp rise in whooping cough (Pertussis) cases occurs, including 12 deaths, following the test.

1955 Washington Bureau of the Detroit Free Press reports, on June 3, 1955, that 'The USPHS reported that more children who received Salk shots made by the Wyeth Labs suffered polio more than could normally be expected;'

1955 AMA Conference in Atlantic City, New Jersey. Article by James C. Spaulding who covered the conference was published in the AMA Journal, June 19,

1955, 'A policy of secrecy and deception has been followed by the National Foundation for Infantile Paralysis and the US Public Health Service in the polio vaccine programs. The nation's physicians were prevented from learning vital information about the trouble with Salk vaccine. The US Public Health Service had an advisory group made up almost entirely of scientists who were receiving money from the National Foundation of Infantile Paralysis, which was exerting pressure to go ahead with the program even after Salk vaccine was found to be dangerous.' Spaulding further said, 'the Infantile Paralysis Foundation kept secret the fact that live virus was detected in four out of six supposedly 'finished and safe' lots of vaccine.'

1955 Salk Polio Vaccine again used in the US. Cases of polio skyrocket again in the United States.

1955 Reported that doctors on the staff of the National Institutes for Health are avoiding vaccination of their children with the Salk vaccine, and that after experimenting with 1200 monkeys, they declared the Salk vaccine worthless as a preventative and a danger to take.

1955 First vaccinated generation become adolescents.

1955 Massachusetts reports 642% increase in polio since vaccinations began in 1954 with vaccination of 130,000 children. In response, the National Foundation for Infantile Paralysis states that the increase in cases was due to the fact that 'no children were vaccinated there.'

1955 Massachusetts bans the sale of Salk vaccine.'

1955 Dr. Graham W. Wilson, director of Britain's Public Health Laboratory Service, who knew about the NIH Salk vaccine trials, says 'I do not see how any vaccine prepared by Salk's method can be guaranteed safe.'

1955 US Surgeon General Scheele admits in a closed session of the AMA that 'Salk polio vaccine is hard to make and no batch can be proven safe before given to children'. Despite this fact, the public is told that the vaccine is safe. The government announces that it has the intention to vaccinate 57 million people before August 1955.

1955 Surgeon General Scheele (who never practiced medicine a day in his life!) goes on public radio saying 'I have complete confidence in the Salk vaccine. I urge doctors to continue vaccinations.'

1956 Seventeen states in the United States reject their government-supplied Salk polio vaccine.

1956 US government appropriates $53.6 million to 'aid states in providing free vaccine to people under 20 years of age'.

1956 Idaho health director Peterson states that polio only struck vaccinated children in areas where there had been no cases of polio since the preceding autumn. In 90% of the cases, the paralysis occurred in the arm in which the vaccine had been injected.

1956 American Public Health Service announces 168 cases of polio and 6 deaths among those vaccinated. Censorship is then imposed on the reporting of reactions to Salk vaccine.

1956 Oral polio vaccine developed further by Sabin.

1956 The US Public Health Service and the National Foundation for Infantile Paralysis (Rockefeller) put on a drive to 'sell' Salk polio vaccine to the public.

1957 Governor Knight of California asks the legislature for $3 million in order to insure vaccination for all those under 40 years old with Salk polio vaccine. The newspapers report that corporate profits from the Salk vaccine will be in excess of $5 billion. (Feb 6, 1957). Governor Knight notes there are 4 million Californians under 40 and signs the bill.

1957 Pertussis vaccination programs exist in all industrialized nations, with the US leading the way. The vaccine is promoted as 'risk free'.

1957 Scientists isolate a series of Simian (monkey) viruses and discover that these same viruses contaminate polio vaccines. SV-40 found in both Sabin and Salk polio vaccines. (made since early '50s), Information not made public. The same vaccines continued to be used until the early 1960's.

1958 World literature now contains 107 cases of severe reaction to Pertussis vaccine (93 of those cases were in the US). At the Fountain Hospital in London, Dr. J.M. Berg analyzed the 107 cases and found that 31 of them showed signs of permanent brain damage. Berg calls attention to the danger of mental retardation as an effect of the Pertussis vaccine and emphasizes that 'any suggestion of a neurological reaction to a Pertussis vaccination should be an absolute contraindication to further inoculation.' The United States medical establishment ignores and suppresses the data. American physicians maintain that the damage caused is small compared to 'lack of 'serious' reactions in children vaccinated.' No data has ever been found to justify a basis for this conclusion.

1958 Verdict of $147,000 rendered against Cutter Laboratories in California for the crippling of two children with the Salk polio vaccine. Cutter Labs was the only vaccine manufacturer not part of the Rockefeller Trust.

1959 The United States never conducts its own clinical trials on Pertussis vaccine, but instead relies (as it still does today) on data collected by Britain's Medical Research Council in clinical trials in England in the 1950's for 'proof of vaccine safety and effectiveness in newborns and children.' Interestingly, Britain's trials on 50,000 British children were performed on children more than 14 months old. None of the children were newborns.

1959 National Institutes of Health (NIH) approves licensing of Quadrigen vaccine for children, containing Pertussis, Diptheria, Tetanus and Polio vaccines. The new combination vaccine was found to be highly reactive and was withdrawn from the market in 1968 after parents started filing lawsuits against Parke- Davis for vaccine damaged children.

1959 Pertussis vaccine found to have allergenic effect on animals.

1960 British Medical Journal publishes an article by Swedish vaccine researcher Justus Strom, who stated that the neurological complications from the disease Pertussis are less than that in the Pertussis vaccine. Strom also pointed out that 'whooping cough (Pertussis) had changed and had become a milder disease, making it questionable whether universal vaccination against it is justified.'

1960 General vaccination program for measles begins in the United States.

1960 It is estimated in 1960 that over 1,000,000 children have vaccine-caused disabilities, including learning difficulties and school behavioral problems, behavioral disturbances, allergies, speech difficulties, visual problems, and problems in adjustment and coping.

1961 A senior school medical officer in Northern England, J.M. Hooper, finds that parents are beginning to refuse to bring children for a Pertussis booster shot, based on earlier violent reaction to the 'vaccination.' Children were suffering from collapse, vomiting, and uncontrollable screaming. No one paid attention to these warnings.

1961 Sabin polio vaccine immunization campaign.

1963 American researcher John F. Enders creates a measles vaccine. Mass inoculations begin.

1963 Children vaccinated with killed measles vaccine between 1963 and 1967 develop Atypical Measles Syndrome (AMS). Studies suggest the children's reshponse to the 'wild' measles virus is 'altered' and that the severity and persistence of symptoms suggests encephalopathy (brain damage.) See 1967.

1964 Reward of $30,000 offered to prove polio vaccine was not fraud. No takers.

1965 US Government's leading Pertussis vaccine specialist, Margaret Pittman, (until 1971) states, 'Bordetella Pertussis is unique among infectious bacteria in its marked ability to modify biological processes.'

1965 Congress passes the Immunization Assistance Act. More states made their vaccination programs mandatory/obligatory.

1967 The FDA stops the use of an experimental cancer vaccine which was producing significant results. Developed by James Rand and Eernest Ayre, a recognized cancer specialist. The Rand vaccine produced significant improvement in terminal patients in over 30% of patients. It cured tumors and breast cancer in four to six months, without radiation, surgery or chemotherapy. The FDA Commissioner was James L. Goddard, the same man who persecuted the use of DMSO. Goddard used the DMSO issue in 1966 in an attempt to foster a medical dictatorship in the US in collusion with the medical and pharmaceutical industries, and remove viable treatments from public access.

1967 At the Bland-Sutton Institute of Middlesex Hospital in London, George Dick writes, 'it has been long known that increasing the number of Pertussis bacteria per dose of vaccine increases the frequency of reactions. It would be surprising if decreasing the size of the infants receiving a particular vaccine did not also increase the reactions.' A violation of a standard axiom in medicine, which matches the size and weight to an amount of substance. (Why are newborns getting the same dosage as an adult?).

1967 Dr. Vicent Fulginiti, M.D., former chairman of the American Academy of Pediatrics Committee on Infectious Diseases, asserts that inactivated measles vaccine should no longer be administered. See 1963.

1967 Killed measles vaccine is discontinued in the United States.

1967 General vaccination program for Mumps begins in the United States.

1967 Science magazine (10/20/67) features article on Joshua Lederberg of the Department of Genetics, Stanford University School of Medicine. Lederberg notifies the scientific world that 'live viruses (as in vaccines) are genetic messages used for the purpose of programming human cells' and 'we already practice biological engineering on a rather large scale by use of live viruses in mass immunization campaigns'

1970 Due to the increasingly mild nature of whooping cough (Pertussis), infant deaths cease from naturally acquired Pertussis in Sweden. Deaths associated with vaccine continue. Sweden stops Pertussis vaccination in 1970.

1970 A study by Pittman reveals Pertussis vaccine can induce hypoglycemia due to increased production of insulin. (Ref: DPT shots). Study is corroborated in 1978 by Hannick and Cohen and by Hennessen and Quast in West Germany. Result: Pertussis and DPT vaccines can cause diabetes.

1972 British Journal of Psychiatry #120 reveals that 'psychotic disorders may be caused by viral infections.' (Ref: viruses induced by vaccines).

1973 The field of genetic engineering is opened by advances in scientific research, making way for creation of recombinent micro-organisms and new viral structures in the laboratory. The U.S. military applies the technology to its chemical and biological weapons program, claiming overtly that such work is 'to develop defensive vaccines'.

1974 British researcher George Disk estimates that there are 80 cases of severe neurological complications from Pertussis vaccine annually. Over 33% of these children died and another 33% were left with brain damage. Dick maintains he is not convinced that the community benefit from the vaccine outweighs the damage.

1974 The Association of Parents of Vaccine Damaged Children is formed in Britain, & pressures the government to study adverse reactions to Pertussis vaccine.

1975 Federal Drug Administration Bureau of Biologics concludes that Diptheria toxoid (vaccine) is 'not as effective an immunizing agent as might be anticipated.' They admit that Diptheria may occur in vaccinated people, and note that 'the permanence of immunity induced by the toxoid is open to question.'

1975 Japan stops using Pertussis vaccine following publicity about vaccine-related deaths.

1976 FDA Pertussis vaccine specialist Charles Manclark comments 'Pertussis vaccine is one of the most troublesome products to produce and assay. It has one of the highest failure rates of all products submitted to the Bureau of Biologics for testing and release. Approximately 15-20% of all lots which pass manufacturer tests fail to pass the tests of the Bureau.'

1976 According to a letter from the British Association for Parents of Vaccine Damaged Children, published in the British Medical Journal of February 1976, 'two years ago we started to collect details from parents of serious reactions suffered by their children to immunizations of all kinds. In 65% of the cases referred to us, reactions followed 'triple' vaccinations. The children in this group total 182 to date. All are severely brain damaged, some are paralyzed, and 5 have died during the past 18 months. Approximately 60% of reactions (major convulsions, collapse, screaming) happened within 3 days and all within 12 days.

1976 Dr. Jonas Salk, creator of the polio vaccine, says that analysis indicates that the live virus vaccine in use since the 1960's is the principle, if not sole cause of all polio cases since 1961.

1976 More than 500 people receiving flu vaccinations become paralyzed with Guilain-Barre Syndrome.

1977 A Blue Ribbon Panel is convened to investigate the reason for the drop in the general IQ of the United States. Seventy-nine theories were advanced, but none of them satisfactorily explained the drop in mental capacity of the US population. The idea that vaccines could be part of the problem was not brought up. Y.L. Warten, 1977. (The Prussian education system is also part of the problem, for those volkschuelen).

1977 The British government is pressured by the publicity following the new data about Pertussis and DPT vaccinations.

1977 The University of Glasgow in Scotland, Department of Community Medicine, Dr. Gordon Stuart, publishes a study analyzing 160 cases of adverse reaction and neurotoxicity following DPT vaccination. In 65 of those cases, reactions to DPT shots included convulsions, hyperactivity and severe mental defect. In a stern statement, Stuart says, 'it seems likely that most adverse reactions are unreported and/or overlooked.'

1977 The British government conducts the National Childhood Encephalopathy Study (NCES) which tests the connection between vaccinations and neurological disease.

1977 (Mar) Jonas and Darrell Salk warn live virus vaccines produce same disease.

1978 According to Charlotte Parker of the University of Texas Department of Microbiology, the nature of the organism Bordetella Pertussis means that different lots of vaccine made from the same strains sometimes show different properties.

1978 In the United States, the FDA finances and conducts a study at UCLA from January 1, 1978 to December 15, 1979 called 'Pertussis Vaccine Project: Rates, Nature and Etiology of Adverse Reactions Associated with DPT Vaccine'. The results of the study were published in Pediatrics in November.

1978 In England, Griffith studies pertussis vaccine reactions in children, noting a case in which a boy experiences brain damage 3 days after vaccination and dies 27 days later due to injection of triple vaccine.

1981 The unpublished contractors 'Final Report' was submitted to the FDA on March 18, 1980 (a year earlier) and contained revealing data. The study found a higher incidence of adverse reactions to the DPT shot than any previously reported in literature. After the study had run nine months, the FDA convened a Pertussis Symposium, at which it was revealed that 'the most striking finding in this preliminary analysis is the high frequency of persistent crying, episodes of convulsions and collapse following DPT immunization.' Because of these findings, the study was curtailed from the planned examination of 50,000 vaccinations to only 17,000. The UCLA FDA study also found that systemic reactions in the central nervous system were present in 50% of the vaccinations. Because of this potentially damaging information, the FDA placed an arbitrary time limit of 48 hours within which reactions had to occur, despite ongoing data which indicates that serious reactions occur after that time
limit, in order to limit the statistical data and conceal the extent of the problem from the population. (See 1981).

In 1988, an FDA-sponsored follow-up study of the '18' children with neurological reactions concluded 'no significant neurological impairment.'

A 1988 re-examination of those same children by an independent researcher, pediatric neurologist Ronald Gabriel, not associated with the FDA, proved that the FDA lied--only 4 of the 18 were normal. The results were presented at a May 1980 meeting of the Institute of Medicine. Results indicate that encephalopathy is followed by subtle learning, behavioral and neurological problems. (Note: See the book Vaccination, Social Violence and Criminality: the Medical Assault on the American Brain, by Harris Coulter,1990. The FDA is continuously involved in criminal conspiracy and racketeering along with pharmaceutical and chemical companies in the United States.)

1978 Trials of Hepatitis B vaccine in New York City on non-monogamous males between 20 and 40 years old. Homosexuals receive a different vaccine.

1979 Two pediatricians in California report brain swelling associated with DPT vaccine administration.

1979 New rubella vaccine introduced. See 1988.

1979 The US Food and Drug Administration (FDA) funds a study which represents the first significant 'attempt' to evaluate reactions to the DPT shot. The study is conducted at the University of California (UCLA) and was published in Pediatrics in

1981. After studying 16,000 DPT and DT vaccination cases, they concluded that the Pertussis (P) element of the DPT shot was the element causing reactions. They also found that the incidence of all DPT reactions was much higher in the population than had been suspected or reported in the scientific literature. Despite these results, even in 1994 physicians promote Pertussis vaccine with confidence, pay little attention to identification of high risk children, and do not carefully observe contraindications. Parents are legally required to vaccinate their children with Pertussis before entering them in school. (See 1982)

1980 Estimated 2 million American children with vaccine-caused disabilities.

1981 At the headquarters of the Occupational Safety and Health Administration (OSHA), the director of the OSHA office of carcinogenic identification, Dr. Peter Infante, pointed out that a Current Intelligence Bulletin (CIB) on formaldehyde was 'an important document assessing formaldehyde's cancer causing potential'. The top bureaucracy at OSHA were embarrassed at the release of the truth, and tried to dismiss Infante. On July 27th, Infante writes Dr. John Higginson, director of the International Agency for Research on Cancer (IARC), disagreeing with the IARC decision to conceal the carcinogenic nature of the substance. Formaldehyde is a common component of vaccines.

1981 Britain conducts the National Childhood Encephalopathy Study, and finds that there exists a significant correlation between serious neurological illness and Pertussis vaccination occurring within 7 days of the shot. In the US, the FDA limits statistical data to 48 hours in order to conceal damaging data and eliminate data on deaths and damage occurring after that period of time.

1981 Japan begins use of a new childhood Pertussis vaccine, recommended to be given as 4th and 5th dose. US vaccine used for 1st,2nd,3rd doses. 1981 In Britain, Dr. D.L. Miller reports to the NCES on an analysis of the first 1,000 cases of neurological illness. He reported 'a significant association was shown between serious neurological illness and Pertussis (also DPT) vaccine.'

1981 New England Journal of Medicine (11/26/81) publishes a study showing that tetanus vaccines cause T-cell ratios to drop below normal, with the greatest decrease after two weeks. The altered ratios were found to be similar to those found in AIDS victims.

1982 A reporter at WRC-TV in Washington, DC breaks a story on Pertussis vaccine reactions in the documentary 'DPT: Vaccine Roulette', which generally informs the American public that their children are at risk from Pertussis vaccinations. (See 1988)

1982 Homosexuals in Chicago, St. Louis, Denver, Los Angeles and San Francisco get Hepatitis B vaccine.

1983 Bellman, Ross and Miller publish a study of 269 cases of infantile spasms which returns to the establishment position that 'DPT vaccines do not cause infantile spasms, but may trigger their onset in those children in whom the disorder is 'destined to develop'. (Note: Using this logic, if one can
)

1983 Stanford University Study on Pertussis Vaccine. Lawrence Steinman and colleagues at Stanford University School of Medicine perform a study which reveals that children with allergies may overreact to Pertussis vaccine.

1984 - The 1984 Connaught Laboratory package insert for DPT vaccine cites a 1978 Scandinavian study linking the vaccine to the development of hemolytic anemia and warns that this is a contraindication. By 1991, they would remove this warning from their package inserts in order to conceal this data. This kind of anemia is typified by weakness and periodic loss of consciousness.

1984 A complaint was filed by a group of US physicians with the UN Center for Human Rights in Geneva, entitled 'A Complaint Against Medical Tyranny As Practiced in the United States of America: American Medical Genocide'; the existence of the report was suppressed by the Bush Administration and the media. Reprinted in The Leading Edge in Oct/Nov 1994.

1984 Shaywitz Study at Yale Medical School Pediatrics revealed that 'minimal brain damage is perhaps the most common and time-consuming problem in current pediatric practice.'

1984 Wyeth Laboratories package insert for DPT vaccine states, 'The occurrence of Sudden Infant Death Syndrome (SIDS) has been reported following administration of DTP vaccine' and that 'approximately 85% of SIDS cases occur in the period 1 through 6 months of age, with the peak incidence at age 2 to 4 months.'

Two years later in 1986, the Wyeth insert stated, 'SIDS has occurred in infants following administration of DPT' but went on to state that 'one study showed that there was no causal connection'. (Note: One wonders who paid for and did that specific study.)

1984 CDC acknowledges that 60% of those receiving hepatitis vaccine are HIV +.

1985 Tests developed to detect simian viruses in vaccines.

1985 The Assistant Secretary of Health, Edward Brandt, Jr., M.D, testifies before a Senate Committee, 'every year 35,000 children suffer neurological complications because of DPT vaccine.' (May 3, 1985).

1985 Hemophilus Influenza type B (HIB) vaccine approved for general use in US. The HIB vaccine is often referred to as the 'meningitis' vaccine, but meningitis has several causes.

1986 150 lawsuits pending against DPT vaccine makers.

1986 National Childhood Vaccine Injury Act. Administered by the US Claims Court in Washington, DC, which does recognize an association between the DPT shot and infantile spasms. The court awarded $2 million to a body in 1989 relative to a reaction to DPT vaccine.

1986 National Health Survey finds that between 1969 and 1981, the prevalence of 'activity-limiting chronic conditions' in children increased by 44%, from 2.9 million children to 3.8 million children. Almost all of the increase happened between 1969 and 1975. Most of these conditions are readily associated with post-encephalitic syndrome. Childhood respiratory disease during this period increased 47%, childhood asthma increased 65% (with deaths from asthma increasing), mental and nervous system disorders increased 80%, personality and other non-psychotic disorders (behavior disorders, drug abuse and hyperactivity) increased 300%, diseases of the eyes and ears (especially otitis media) rose 120%, and cases of hearing loss in the ears rose 129%. All of these increases were identical in both high and low income groups. For the same period of time, levels of disease not associated with vaccine damage remained unchanged.

1986 Connaught Laboratory, manufacturer of DPT vaccine, changes the product info sheet to warn against 'allergies' and 'anaphylactic sensitivity'.

1986 Connaught Laboratories package insert for their DPT vaccine reads 'some data suggests that fever is more likely to happen in those who have had local reactions, and that local reactions are more likely to occur with increasing numbers of doses of DPT.'

1987 Centers for Disease Control (CDC) releases a study indicating that the Hib vaccine shows an efficacy (effectiveness) rate of 41%. Children were found to be 5 times more likely to contract the disease than those not vaccinated.

1987 66 Japanese victims of Pertussis vaccine receive huge damage awards from the Japanese government.

1988 Lederle Laboratories package insert for DPT vaccine reads 'Pertussis vaccine has been associated with a greater proportion of adverse reactions than many other childhood vaccinations. Local reactions are common after administration of DTP, occurring in 35-50% of recipients. Febrile [feverish] reactions are more likely to occur in those who have experienced such responses after prior doses.'

1988 Two scientific studies find that new rubella vaccine introduced in 1979 was found to be the cause of Chronic Fatigue Syndrome (Epstein-Barr virus), an immune disorder first reported in 1982.

1988 Robert S. Mendelsohn M.D, publishes material indicating that Dr. John Seal of the National Institute of Allergy and Infectious Disease believes that 'any and all flu vaccines are capable of causing Guillain-Barre.'

1988 New 'conjugated' [joined together] HIB vaccine approved for use in children at least 18 months old in the United States. HIB = Hemophilus Influenza Type B.

1990 Health Consciousness magazine features article entitled 'Live Virus Vaccines and Genetic Mutation' by H.E.Buttram, M.D, in which it is determined that 'the physical invasion of the human body by foreign genetic material may have the immediate effect of permanently weakening the immune system, setting in motion a new era of autoimmune diseases.'

1990 The US Public Health Service Immunization Practices Advisory Committee (ACIP) and the American Academy of Pediatrics considers high-pitched screaming after a Pertussis (DPT) vaccination an absolute contraindication to further Pertussis vaccine.

1990 Pediatric neurologist Dr. John H. Menkes, professor emeritus at UCLA, reports on 46 children experiencing neurological adverse reaction within 72 hours of a DPT shot. Over 87% of the children reacted with a seizure, 2 children died and most surviving children became retarded, with 72% having uncontrollable seizure disorders. Menkes conclude, 'Pertussis vaccine encephalopathy (brain damage) is not a myth but rather a serious complication of immunization.'

1990 U.S. Claims Court, as of October 31, 1990, indicates that 'several thousand claims for compensation from injuries or death caused by vaccines have already been filed.' National Vaccine Information Center.

1990 Estimated 3 million in US with vaccine-caused disabilities.


1990 In December of 1990, a federal regulation was adopted permitting the FDA to circumvent US and International laws forbidding medical experimentation on unwilling subjects. This regulation permits the FDA to inject American military with unapproved experimental drugs or vaccines without informed consent. The FDA merely needs to deem it 'not feasible' to obtain the soldiers permission. See Health Letter, Washington, DC. Public Citizens Health Research Group '400,000 Human Guinea Pigs in the Persian Gulf', Feb 12, 1991. See 1991 Gulf War Entry.

1991 Operation Desert Storm. Bush stops war after 100 hours at preserve Iraq as a threat. American troops are given experimental vaccines against biological agents. Within months thousands of troops sicken with the acids that cause cancer. Disease deemed 'Gulf War Syndrome'. Government denies responsibility. Over 8,000 troops were vaccinated with Botulism, over 150,000 troops were given anthrax vaccine, and all 500,000 troops were given Pyristigimine, an experimental nerve agent. All drugs were experimental.

1991 New York Times, Mar 17th, 1991 'US Vaccine Plan Uses Welfare Offices' indicates the Federal government has considered denying welfare and nutritional benefits to families who refuse vaccinations.

1991 The US Public Health Service Advisory Committee on Immunization Practices (ACIP) drafts new guidelines which eliminate most contraindications to Pertussis vaccine. Essentially, this results in a denial or cover-up of most reactions on the grounds that 'there is no proof the vaccine causes brain ' They base their position on several studies financed by vaccine manufacturers conducted in the late 1980's by vaccine policymakers such as Dr. James Cherry and Dr. Edward Mortimer, who sit on the ACIP Committee and are also paid consultants to US Pertussis vaccine manufacturers, resulting in biased and flawed studies in order to prove 'no cause and effect' between the Pertussis vaccine and permanent brain damage. US vaccine policymakers are the CDC and the American Academy of Pediatrics. All this, despite decades of experience indicating the opposite conclusion. (Note: This policy constitutes criminal neglect, racketeering and conspiracy!).

1991 The 'conjugated' HIB vaccine introduced in 1988 is extended for use in infants as young as two months. It becomes mandated in 44 states in the US.
--The Olympian, Nov 23, 1994. Pertussis also can cause Sudden Infant Death. SIDS.


1991 The CDC begins the process of mandating Hepatitis B vaccinations for all infants in the United States. Many infants receive multiple doses from birth.

1992 Lancet, Journal of the British Medical Association, reports (3/7/92) that the oral polio vaccine used in the mid 1970's to treat recurrent herpes was contaminated with a number of potentially dangerous retroviruses, and may have seeded HIV among Americans'.

1992 Article in the Washington Post, Nov 2, 'On Vaccinating Safely' and Dec 14th press release by the National Vaccine Information Center indicate release by the FDA of a report acknowledging more than 17,000 adverse events-- including more than 350 deaths--following vaccination, all in a 20 month period ending July 31,

1992. Reported events number far less than actual events, so number is actually larger, perhaps 170,000 or more. 1992 From 1988 to 1992, over $249 million has already been awarded due to hundreds of deaths and injuries caused by mandated vaccines. Thousands of cases are still pending. The permanent injuries from vaccines include, but are not limited to, learning disabilities, seizure disorders, mental retardation, and paralysis. Many of the awards for pertussis vaccine deaths were initially (and wrongfully) misclassified as Sudden Death Syndrome (SIDS).

1992 Centers for Disease Control (CDC) reports that 87% of all cases of polio in the United States between 1973 and 1983 were caused by the vaccine. The CDC also said that every case from 1980 to 1989 was caused by vaccine.

1993 Clinton administration announces plans for a National Childhood Vaccination Program. 103rd Congress introduces S732,S733,HR1460, legislation that would attempt to vaccine all children in the United States, while severely limiting exemptions parents could claim. The bills also seek to set up a national vaccine registry to track down parents who resist.

1993 Seattle Times reports that all polio in the US is caused by vaccines. (6/10/93).

1993 The US Army directs Walter Reed Army Institute of Research to sign an agreement with MicroGeneSys in Meridan, Connecticut for a 'large scale clinical evaluation' of an AIDS vaccine designed to block destruction of the immune system. The VaxSyn vaccine uses a genetically engineered protein that matches a protein called (gp160) that covers the surface of the HIV virus. (Note: That the HIV virus is harmless and does not 'cause AIDS' is known, illustrating that the military is in on the AIDS scam). See Duesberg material.

1994 Researchers at the Gladstone Institute of Virology and Immunology use genetic engineering to alter a Polio virus (Sabin type) to allow it to carry two key genes from the HIV virus, plus proteins from both cholera bacteria and influenza virus, in a misguided attempt to create an 'AIDS vaccine' by induction of immune reaction to foreign proteins. (San Francisco Chronicle 9/2/94)

1994 Sweden reports the testing of a 'new safer Pertussis vaccine' to combat whooping cough (what is now a relatively mild disease). According to an article in The Olympian, Olympia, Washington, it 'could be available in the United States, according to federal health officials.' According to the article 'the vaccine could mean the end of rare, severe side effects associated with the Pertussis/whooping cough vaccine.' (Note: On the contrary, the evidence proves the Pertussis organism found in Pertussis 'vaccine', whether bred in live tissue ('live' virus) or dead tissue ('killed virus'), causes brain damage and other pathology in humans).

1889 Protégé's of Louis Pasteur, Emile Rouz & Alexandre Yersin grew a broth thick with diphtheria bacteria and used compressed air to force the broth through a filter of unglazed porcelain.

NO bacteria or solids could pass through the porcelain - only liquid.

They then sterilized the liquid.

They took the sterilized liquid of diphtheria toxin and injected into animals.

The liquid killed the animals not the bacteria!

According to Dr. Young, this early scientific test showed that a liquid toxic acid kills, not a bacteria or fungi. The major contributors to an acidic body that leads to irritation, inflammation, induration, ulceration and degeneration are as follows:

1) Nitric, sulphuric, phosphoric and uric acids from animal proteins including eggs.

2) Lactic acids from dairy products.

3) All sugars including herbal sugars which are all acids including glucose and ethanol alcohol.

4) Vinegar which is diluted acetylaldehyde an acid that destroys brain cells.

5) All mushrooms and algae which breakdown dead bodies.


6) Peanuts and corn which produce exotoxins and mycotoxins.

7) All fermented foods including soy sauce.

8) Antibiotics which are mycotoxins.

9) Antifungals which are stronger mycotoxins.

10) All vaccinations which are full of exotoxins and mycotoxins.

1994 Dr. Robert O. Young discovers the (potential hydrogen 1-14) pH factor in triggering biological transformation of the red blood cells into bacteria and yeast.

1994 Dr. Robert O. Young discovers that there is only one sickness and one disease and that is the over-acidification of the blood and tissues due to an inverted way of living eating and thinking.

1994 to the present the increase of Autism is at epidemic proportions - 1 in 90 boys and 1 in 150 girls are affected. Dr. Young has suggested that this is a result of congestion of the bowels from eating animal proteins and dairy as well as vaccinations and antibiotics that destroys the root system or intestinal villi of the small intestine - the focal point where new blood is produced.

1994 to the present the increase of breast cancers is now 1 in 3 and the increase of prostate cancers in men is now 1 in 2. Dr. Young has suggested that this is a result of antibiotic and anti-fugal use, vaccination and an acidic lifestyle and diet.

2008 A formal investigation has been launched by French authorities against two managers from drug companies GlaxoSmithKline and Sanofi Pasteur. A second investigation for manslaughter has also been opened against Sanofi Pasteur MSD.

The investigations are in response to allegations that the companies failed to fully disclose side effects from an anti-hepatitis B drug used between 1994 and 1998.

During this time, close to two-thirds of the French population, and almost all newborn babies, received a hepatitis B vaccine. The vaccination campaign was halted after concerns rose over the shot's side effects.

Thirty plaintiffs, including the families of five people who died after the vaccination, have launched a civil action in the case against the drug companies. Source: Reuters February 1, 2008

For more information on viruses, bacteria, yeast and vaccines read Sick and Tired, Reclaim Your Inner Terrain, or A Second Thought About Viruses, Vaccines and the HIV AIDS Hypothesis, both by Dr. Robert O. Young.

I would also recommend reading
Antione BeChamp's books, The Blood The Third Anatomical Element and The Origin of Organic Beings.

You can find these books at:

http://www.phmiracleliving.com/books.htm

As someone that looks to improve their health we are pleased to offer you this free audio, an excerpt of a powerful two hour interview with Dr Robert O. Young and Anthony Robbins. (it is free to listen!)

Click here to listen: http://www.1shoppingcart.com/app/?Clk=1870270


I trust you'll enjoy this...

Not part of our healing alkaline community?
Visit our website at:

www.phmiracleliving.com


To learn more about the science of Dr. Robert and Shelley Young go to:

www.articlesofhealth.blogspot.com

'Miracles happen not in opposition to nature, but in opposition to what we know of nature.' St. Augustine

'Any sufficiently advanced technology is indistinguishable from magic' ....Arthur C. Clarke

'There are only two ways to live your life. One, is as though there are no miracles. The other is as though everything is a miracle.' Albert Einstein

Copyright 2007 Dr. Robert and Shelley Young*

pH Miracle Living Center
16390 Dia Del Sol
Valley Center, California 92082 US

*Posted for you with the personal written permission of Dr. Robert O. Young
==============================================================================
 
 
 

 

 

 
Printer-friendly version of this page Email this message to a friend
Alert Moderators
Report Spam or bad message  Alert Moderators on This GOOD Message

This Forum message belongs to a larger discussion thread. See the complete thread below. You can reply to this message!


 

Donate to CureZone


CureZone Newsletter is distributed in partnership with https://www.netatlantic.com


Contact Us - Advertise - Stats

Copyright 1999 - 2021  curezone.com

0.875 sec, (15)