World Health Organization sees ‘weak evidence’ of human poisoning by endocrine disruptors in chemicals

While admitting humans are experiencing the highest incidence of disease and that thousands of dangerous chemicals are used in products people consume, a World Health Organization report says there is only weak evidence that human health has been adversely affected by the abundance of those chemicals in food and other products.

By LUIS MIRANDA | THE REAL AGENDA | FEBRUARY 25, 2013

There are two facts that are undeniable when it comes to human health. First, despite great advances in science and technology, humans are sicker beings today –both mentally and physically–, when compared to half a century ago, for example. Even worse, the incidence of previously unknown or inexistant diseases has grown exponentially due to ‘inexplicable’ reasons. Second, those who were charged with verifying the safety of the production processes and the goods that are mass-produced for human consumption, failed to point out the dangers, and the side effects of thousands of substances used in the manufacture of industrial products.

The reason for the failure to properly guard human health and the environment from toxic chemicals varies, and it needs to be investigated on a case to case basis, but generally it occurred either due to lack of knowledge or because those watching out for our safety overlooked clear evidence that certain chemicals posed a direct threat to humanity and the environment. Three cases in point: DDT, fluoride in the water, mercury in vaccines, pesticides and herbicides.

In 2013, 41 years after its creation, the World Health Organization finally decided to publish a document where it expresses its concern about the adverse effects that toxic chemicals may have in humans; specifically on the human endocrine system. The document issued by the WHO titled Global Assessment of the State‐of‐the‐Science of Endocrine Disruptors, addresses what millions of people around the world, and thousands of health care practitioners have warned about for many years: chemicals put in the foods we eat, the water we drink and others used in industrial processes harm human health and gravely contaminate the environment.

Unfortunately, the report starts by playing down the role of industrial chemicals in the exponential appearance of disease among humans. The WHO cites as its final conclusion that “although it is clear that certain environmental chemicals can interfere with normal hormonal processes, there is weak evidence that human health has been adversely affected by exposure to endocrine-active chemicals.” As many other unaccountable global organizations, the WHO refused to look at independently gathered evidence that raised concerns about the poisoning of humans and the environment by the industrial process and how chemicals used in the production of food, for example, was the origin of previously unknown diseases.

It took 16 years for the WHO to accept and implement the advice provided by various health groups about the serious problem with the way food is produced as well as the way toxic chemicals are used in the production of the food we ingest. Back in 1997, the Intergovernmental Forum on Chemical Safety and the Environment Leaders of the Eight regarding the issue of EDCs, the International Programme on Chemical Safety (IPCS), a joint programme of WHO, UNEP and the International Labour Organization, began preparing the report issued in 2013.

Along with its general conclusion that its panel of scientists did not find enough evidence –despite all the evidence that exists– that human health is indeed adversely affected by exposure to endocrine disruptors found in toxic chemicals, the WHO report highlights just over a dozen other warning signs that humans, animals and the environment as a whole MAY be experiencing the consequences of systematic poisoning.

After explaining that life on Earth depends on its ability to reproduce and developed normally, the WHO report explains that there is a high incidence and a growing trend of endocrine-related disorders in humans; that there are observations of endocrine-related effects in wildlife populations; and that there is enough evidence that chemicals to which everyone is exposed to have endocrine disrupting properties linked to disease outcomes in laboratory studies. Amazingly, the WHO admits that there is more evidence to suggest that toxic chemicals DO cause endocrine disruptions on animals than on humans.

Endocrine Disruption

Figure 2. Overview of the endocrine system. Obtained from WHO report “State of the Science of Endocrine Disrupting Chemicals”. 2013.

The report found that endocrine-related diseases and disorders are on the rise, especially on young men. It related that in some countries, up to 40% of young men show low semen quality, which translates in their inability to have children. In addition to infertility, the report calls attention to the incidence of genital malformations, adverse pregnancy outcomes, neurobehavioural disorders associated with thyroid disruption, an unexplained rise in endocrine-related cancers that include breast, endometrial, ovarian, prostate, testicular and thyroid, earlier development of the breasts in young girls and the prevalence of obesity and type 2 diabetes, which increased exponentially all over the world for the past 40 years.

The World Health Organization reports that some 800 chemicals are confirmed or suspected to interfere with hormone receptors, hormonal synthesis or conversion and that only a small amount of those chemicals have been properly studied to determine their negative effects on the organisms. That is to say, health watchdogs –both at the national and international levels– traditionally failed to test for the potential or demonstrated threats that toxic chemicals used in the manufacture of food products presented to humans and other forms of life. “The vast majority of chemicals in current commercial use have not been tested at all,” the study admits.

As many independent observations have previously warned, humans and all life on this planet are continuously exposed to Endocrine Disruptive Chemicals (EDC), which traditionally occurs in low but permanent levels. The WHO report confirms this fact by saying that evidence shows that humans and wildlife are exposed to more EDCs than just those found in persistent organic pollutants. The report also confirms that food and drinking water are two major contributors of human and animal poisoning, but that the list of those elements that poison us all is long.

“Children can have higher exposures to chemicals compared with adults—for example, through their hand-to-mouth activity and higher metabolic rate. The speed with which the increases in disease incidence have occurred in recent decades rules out genetic factors as the sole plausible explanation.”

Endocrine Disruption in Babies

Figure 3. Sensitive windows of development. Each tissue has a specific window during development when it is forming. Obtained from WHO report “State of the Science of Endocrine Disrupting Chemicals”. 2013.

The statement above is damning evidence that most, if not all supposedly genetically transmitted diseases, are not really passed on to humans by their progenitors, but by their exposure to chemicals created or used during the production of food and other products. The report goes on detailing that chemicals such as DDT, PCB’s, diethylstilbestrol (DES) and polybrominated diphenyl ethers (PBDEs), often used in pesticides and herbicides, or for controlling insect reproduction, are to blame for breast cancer, prostate cancer, non-descended testes.

How can they then say that the evidence is weak when it comes to the relation between toxic chemicals and mass spread disease?

The assessment on endocrine disruptors clarified that much of the damage caused by toxic chemicals happens during pregnancy or early in human life. “Numerous laboratory studies support the idea that chemical exposures contribute to endocrine disorders in humans and wildlife.”

Again, where is the weak link then?

“Developmental exposures can cause changes that, while not evident as birth defects, can induce permanent changes that lead to increased incidence of diseases throughout life.

These insights from endocrine disruptor research in animals have an impact on current practice in toxicological testing and screening. Instead of solely studying effects of exposures in adulthood, the effects of exposures during sensitive windows in fetal development, perinatal life, childhood and puberty require careful scrutiny.”

The WHO report openly admits that organizations that are supposed to be vigilant about the adverse effects of poisons used in the industrial manufacture process have failed time after time to do that very task. “There has been a failure to adequately address the underlying environmental causes of trends in endocrine diseases and disorders.”

Is there room here for liability?

According to the WHO, disease risk induced by endocrine disrupting chemicals may have been significantly underestimated. That is to say, doctors and other health care practitioners who up until today follow the teachings of modern medicine as their base to diagnose disease while ignoring –sometimes purposely– the evidence presented by many studies on the adverse effects of EDC’s, are also to blame for current wave of ‘unknown’ or ‘untreatable disorders.

“We know that humans and wildlife are simultaneously exposed to many EDCs; thus, the measurement of the linkage between exposure to  mixtures of EDCs and disease or dysfunction is more physiologically relevant. In addition, it is likely that exposure to a single EDC may cause disease syndromes or multiple diseases, an area that has not been adequately studied.” Why not? Certainly nor because of lack of funding. Perhaps disinterest from the part of large pharmaceutical conglomerates who conduct their own studies with the ONLY intention to show whether a product is effective, but not to determine its safety or the long-term adverse effects on humans. The same is true for companies like Monsanto, DuPont, Syngenta and others which brag about their technological discoveries even though many independent tests prove, beyond reasonable doubt that their GMO’s, herbicides and pesticides are killing people all over the world.

Despite the mounting evidence presented in its own study, the skyrocketing incidence of disease in the last 50 years and the growing trends that show how EDC’s are more and more involved in causing adverse effects on human populations, the WHO again limits the relation between EDC’s and disease as a matter of association, instead of going beyond and calling it a matter of cause and effect. The report says that human studies can show associations only. But what happens when those associations continue to appear, study after study? Doesn’t that build a clear relationship of cause and effect?

Since most main stream corporate or government financed studies do not properly test for the effects of EDC’s on humans, because they are conducted with a very low number of subjects and for a very short time, the WHO has determined that this ‘association’ does not go beyond casual results that do not offer enough evidence to pose a cause and effect relationship. This is so, because although the mounting evidence, most tests are not designed to show that cause-effect relationship, which immediately invalidates them as reliable proof or evidence that toxic chemicals have –for a long time– caused disease in people and polluted the environment.

The report correctly points out that the shift already taking place from determining associations to testing for links –cause and effect– is the way to go to show what it deems as solid evidence that toxic chemicals indeed cause disease. But the WHO still fails to recognize what many studies have determined: that the adverse effects of early and continuous exposure to toxic chemicals are only detected late in life. Those effects, as explained before, are usually misdiagnosed by most doctors, who usually tell their patients that the origin of their illness is still unknown and that there is no way to treat the causes; only the symptoms. At this point, patients are condemned to taking pharmaceutical drugs for the rest of their lives, which eventually end up killing them due to their own adverse effects.

So, the state of human health today is equally bad from two different fronts. People are either killed by long-term exposure to toxic chemicals used in the production process of food or in the food itself, or they die while trying to ‘cure’ their diseases with industrialized pharmaceuticals whose own side effects are as deadly as those from the chemicals people are trying to get rid of. Either way, people die long, painful deaths.

So what is next? What needs to be done to end this vicious circle of disease? Can long-term studies be the solution? I think it is too little too late for that. Waiting another 10 or 20 years to see the result of long-term tests is not something a lot of people can afford now. That does not mean that those studies should not be done. It means that people need to find solutions by themselves. Now that the World Health Organization has finally confessed they have not done their job to protect people from dangerous substances –quite the opposite is true–  people need to understand that their nutrition is their responsibility. It always has been so. From the part of the organizations that are supposed to keep us safe from the dangers of toxic chemicals, it is time to stop talking and start walking.

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Mycoplasma: The Linking Pathogen in Neurosystemic Diseases

Several strains of mycoplasma have been “engineered” to become more dangerous. They are now being blamed for AIDS, cancer, CFS, MS, CJD and other neurosystemic diseases.

By DONALD W. SCOTT MA, MSc | THE REAL AGENDA | FEBRUARY 13, 2013

There are 200 species of Mycoplasma. Most are innocuous and do no harm; only four or five are pathogenic. Mycoplasma fermentans (incognitus strain) probably comes from the nucleus of the Brucella bacterium. This disease agent is not a bacterium and not a virus; it is a mutated form of the Brucella bacterium, combined with a visna virus, from which the mycoplasma is extracted.

The pathogenic Mycoplasma used to be very innocuous, but biological warfare research conducted between 1942 and the present time has resulted in the creation of more deadly and infectious forms of Mycoplasma. Researchers extracted this mycoplasma from the Brucella bacterium and actually reduced the disease to a crystalline form. They “weaponised” it and tested it on an unsuspecting public in North America.

Dr Maurice Hilleman, chief virologist for the pharmaceutical company Merck Sharp & Dohme, stated that this disease agent is now carried by everybody in North America and possibly most people throughout the world.

Despite reporting flaws, there has clearly been an increased incidence of all the neuro/systemic degenerative diseases since World War II and especially since the 1970s with the arrival of previously unheard-of diseases like chronic fatigue syndrome and AIDS.

According to Dr Shyh-Ching Lo, senior researcher at The Armed Forces Institute of Pathology and one of America’s top mycoplasma researchers, this disease agent causes many illnesses including AIDS, cancer, chronic fatigue syndrome, Crohn’s colitis, Type I diabetes, multiple sclerosis, Parkinson’s disease, Wegener’s disease and collagen-vascular diseases such as rheumatoid arthritis and Alzheimer’s.

Dr Charles Engel, who is with the US National Institutes of Health, Bethesda, Maryland, stated the following at an NIH meeting on February 7, 2000: “I am now of the view that the probable cause of chronic fatigue syndrome and fibromyalgia is the mycoplasma…”

I have all the official documents to prove that mycoplasma is the disease agent in chronic fatigue syndrome/fibromyalgia as well as in AIDS, multiple sclerosis and many other illnesses. Of these, 80% are US or Canadian official government documents, and 20% are articles from peer-reviewed journals such as the Journal of the American Medical Association, New England Journal of Medicine and the Canadian Medical Association Journal. The journal articles and government documents complement each other.

How the Mycoplasma Works

The mycoplasma acts by entering into the individual cells of the body, depending upon your genetic predisposition.

You may develop neurological diseases if the pathogen destroys certain cells in your brain, or you may develop Crohn’s colitis if 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 or disease pathogens, they primarily focused on the Brucella bacterium and began to weaponise it.

From its inception, the biowarfare program was characterised by continuing in-depth review and participation by the most eminent scientists, medical consultants, industrial experts and government officials, and it was classified Top Secret.

The US Public Health Service also closely followed the progress of biological warfare research and development from the very start of the program, and the Centers for Disease Control (CDC) and the National Institutes of Health (NIH) in the United States were working with the military in weaponising these diseases. These are diseases that have existed for thousands of years, but they have been weaponised—which means they’ve been made more contagious and more effective. And they are spreading.

The Special Virus Cancer Program, created by the CIA and NIH to develop a deadly pathogen for which humanity had no natural immunity (AIDS), was disguised as a war on cancer but was actually part of MKNAOMI.2 Many members of the Senate and House of Representatives do not know what has been going on.  For example, the US Senate Committee on Government Reform had searched the archives in Washington and other places for the document titled “The Special Virus Cancer Program: Progress Report No. 8”, and couldn’t find it. Somehow they heard I had it, called me and asked me to mail it to them. Imagine: a retired schoolteacher being called by the United States Senate and asked for one of their secret documents! The US Senate, through the Government Reform Committee, is trying to stop this type of government research.

Crystalline Brucella

The title page of a genuine US Senate Study, declassified on February 24, 1977, shows that George Merck, of the pharmaceutical company, Merck Sharp & Dohme (which now makes cures for diseases that at one time it created), reported in 1946 to the US Secretary of War that his researchers had managed “for the first time” to “isolate the disease agent in crystalline form”.3

They had produced a crystalline bacterial toxin extracted from the Brucella bacterium. The bacterial toxin could be removed in crystalline form and stored, transported and deployed without deteriorating. It could be delivered by other vectors such as insects, aerosol or the food chain (in nature it is delivered within the bacterium). But the factor that is working in the Brucella is the mycoplasma.

Brucella is a disease agent that doesn’t kill people; it disables them. But, according to Dr Donald MacArthur of the Pentagon, appearing before a congressional committee in 1969,(4) researchers found that if they had mycoplasma at a certain strength—actually, 10 to the 10th power—it would develop into AIDS, and the person would die from it within a reasonable period of time because it could bypass the natural human defences.  If the strength was 10 to 8, the person would manifest with chronic fatigue syndrome or fibromyalgia. If it was l0 to 7, they would present as wasting; they wouldn’t die and they wouldn’t be disabled, but they would not be very interested in life; they would waste away.

Most of us have never heard of the disease brucellosis because it largely disappeared when they began pasteurising milk, which was the carrier. One salt shaker of the pure disease agent in a crystalline form could sicken the entire population of Canada. It is absolutely deadly, not so much in terms of killing the body but disabling it.

Because the crystalline disease agent goes into solution in the blood, ordinary blood and tissue tests will not reveal its presence. The mycoplasma will only crystallise at 8.1 pH, and the blood has a pH of 7.4 pH. So the doctor thinks your complaint is “all in your head”.

Crystalline Brucella and Multiple Sclerosis

In 1998 in Rochester, New York, I met a former military man, PFC Donald Bentley, who gave me a document and told me: “I was in the US Army, and I was trained in bacteriological warfare. We were handling a bomb filled with brucellosis, only it wasn’t brucellosis; it was a Brucella toxin in crystalline form. We were spraying it on the Chinese and North Koreans.”

He showed me his certificate listing his training in chemical, biological and radiological warfare. Then he showed me 16 pages of documents given to him by the US military when he was discharged from the service. They linked brucellosis with multiple sclerosis, and stated in one section: “Veterans with multiple sclerosis, a kind of creeping paralysis developing to a degree of 10% or more disability within two years after separation from active service, may be presumed to be service-connected for disability compensation. Compensation is payable to eligible veterans whose disabilities are due to service.” In other words: “If you become ill with multiple sclerosis, it is because you were handling this Brucella, and we will give you a pension. Don’t go raising any fuss about it.” In these documents, the government of the United States revealed evidence of the cause of multiple sclerosis, but they didn’t make it known to the public—or to your doctor.

In a 1949 report, Drs Kyger and Haden suggested “the possibility that multiple sclerosis might be a central nervous system manifestation of chronic brucellosis”. Testing approximately 113 MS patients, they found that almost 95% also tested positive for Brucella.(5)We have a document from a medical journal, which concludes that one out of 500 people who had brucellosis would develop what they call neurobrucellosis; in other words, brucellosis in the brain, where the Brucella settles in the lateral ventrides—where the disease multiple sclerosis is basically located.6

Contamination of Camp Detrick Lab Workers

A 1948 New England Journal of Medicine report titled “Acute Brucellosis Among Laboratory Workers” shows us how actively dangerous this agent is.7   The laboratory workers were from Camp Detrick, Frederick, Maryland, where they were developing biological weapons. Even though these workers had been vaccinated, wore rubberised suits and masks and worked through holes in the compartment, many of them came down with this awful disease because it is so absolutely and terrifyingly infectious.

The article was written by Lt Calderone Howell, Marine Corps Captain Edward Miller, Marine Corps, Lt Emily Kelly, United States Naval Reserve; and Captain Henry Bookman. They were all military personnel engaged in making the disease agent Brucella into a more effective biological weapon

III — COVERT TESTING OF MYCOPLASMA

Testing the Dispersal Methods

Documented evidence proves that the biological weapons they were developing were tested on the public in various communities without their knowledge or consent.

The government knew that crystalline Brucella would cause disease in humans. Now they needed to determine how it would spread and the best way to disperse it. They tested dispersal methods for Brucella suis and Brucella melitensis at Dugway Proving Ground, Utah, in June and September 1952. Probably, 100% of us now are infected with Brucella suis and Brucella melitensis.(8)

Another government document recommended the genesis of open-air vulnerability tests and covert research and development programs to be conducted by the Army and supported by the Central Intelligence Agency.

At that time, the Government of Canada was asked by the US Government to cooperate in testing weaponised Brucella, and Canada cooperated fully with the United States. The US Government wanted to determine whether mosquitoes would carry the disease and also if the air would carry it. A government report stated that “open-air testing of infectious biological agents is considered essential to an ultimate understanding of biological warfare potentialities because of the many unknown factors affecting the degradation of micro-organisms in the atmosphere”.9

Testing via Mosquito Vector in Punta Gorda, Florida

A report from The New England Journal of Medicine reveals that one of the first outbreaks of chronic fatigue syndrome was in Punta Gorda, Florida, back in 1957.(10)   It was a strange coincidence that a week before these people came down with chronic fatigue syndrome, there was a huge influx of mosquitoes.

The National Institutes of Health claimed that the mosquitoes came from a forest fire 30 miles away. The truth is that those mosquitoes were infected in Canada by Dr Guilford B. Reed at Queen’s University. They were bred in Belleville, Ontario, and taken down to Punta Gorda and released there.

Within a week, the first five cases ever of chronic fatigue syndrome were reported to the local clinic in Punta Gorda. The cases kept coming until finally 450 people were ill with the disease.

Testing via Mosquito Vector in Ontario

The Government of Canada had established the Dominion Parasite Laboratory in Belleville, Ontario, where it raised 100 million mosquitoes a month. These were shipped to Queen’s University and certain other facilities to be infected with this crystalline disease agent The mosquitoes were then let loose in certain communities in the middle of the night, so that the researchers could determine how many people would become ill with chronic fatigue syndrome or fibromyalgia, which was the first disease to show.

One of the communities they tested it on was the St Lawrence Seaway valley, all the way from Kingston to Cornwall, in 1984. They let out hundreds of millions of infected mosquitoes. Over 700 people in the next four or five weeks developed myalgic encephalomyelitis, or chronic fatigue syndrome.

Mad Cow Disease/Kuru/CJD in the Fore Tribe

Before and during World War II, at the infamous Camp 731 in Manchuria, the Japanese military contaminated prisoners of war with certain disease agents.

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

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

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

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

Testing Carcinogens over Winnipeg, Manitoba

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

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

Shortly after, the Pentagon held a press conference on May 14, 1997, where they admitted what they had done. Robert Russo, writing for the Toronto Star11 from Washington, DC, reported the Pentagon’s admission that in 1953 it had obtained permission from the Canadian Government to fly over the city of Winnipeg and spray out this chemical—which sifted down on kids going to school, housewives hanging out their laundry and people going to work. US Army planes and trucks released the chemical 36 times between July and August 1953. The Pentagon got its statistics, which indicated that if the chemical released had been full strength, approximately a third of the population of Winnipeg would have developed cancers over the next five years.

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

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

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

V – BRUCELLA MYCOPLASMA AND DISEASE AIDS

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

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

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

In laboratories throughout the United States and in a certain number in Canada including at the University of Alberta. the US Government provided the leadership for the development of AIDS for the purpose of population control. After the scientists had perfected it, the government sent medical teams from the Centers for Disease Control-under the direction of Dr Donald A. Henderson, their investigator into the 1957 chronic fatigue epidemic in Punta Gorda—during 1969 to 1971 to Africa and some countries such as India, Nepal and Pakistan where they thought the population was becoming too large.13 They gave them all a free vaccination against smallpox; but five years after receiving this vaccination, 60% of those inoculated were suffering from AIDS. They tried to blame it on a monkey, which is nonsense.

A professor at the University of Arkansas made the claim that while studying the tissues of a dead chimpanzee she found traces of HIV. The chimpanzee that she had tested was born in the United States 23 years earlier. It had lived its entire life in a US military laboratory where it was used as an experimental animal in the development of these diseases. When it died, its body was shipped to a storage place where it was deep-frozen and stored in case they wanted to analyse it later. Then they decided that they didn’t have enough space for it, so they said, “Anybody want this dead chimpanzee?” and this researcher from Arkansas said: “Yes. Send it down to the University of Arkansas. We are happy to get anything we can get.” They shipped it down and she found HIV in it. That virus was acquired by that chimpanzee in the laboratories where it was tested.14

Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis

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

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

Many people with chronic fatigue syndrome, myalgic encephalo-myelitis and fibromyalgia who apply to the Canada Pensions Plan Review Tribunal will be turned down because they cannot prove that they are ill. During 1999 I conducted several appeals to Canada Pensions and the Workers Compensation Board (WCB, now the Workplace Safety and Insurance Board) on behalf of people who have been turned down. I provided documented evidence of these illnesses, and these people were all granted their pensions on the basis of the evidence that I provided.

In March 1999, for example, I appealed to the WCB on behalf of a lady with flbromya1gia who had been, denied her pension back in 1993. The vice-chairman of the board came to Sudbury to hear the appeal, and I showed him a number of documents which proved that this lady was physically ill with fibromyalgia. It was a disease that caused physical damage, and the disease agent was a mycoplasma. The guy listened for three hours, and then he said to me: “Mr Scott, how is it I have never heard of any of this before? I said: “We brought a top authority in this area into Sudbury to speak on this subject and not a single solitary doctor came to that presentation.”

VI-TESTING FOR MYCOPLASMA IN YOUR BODY

Polymerase Chain Reaction Test

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

Your doctor may diagnose you with Alzheimer’s disease, and he will say:

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

This mycoplasma couldn’t be detected until about 30 years ago when the polymerase chain reaction (PCR) test was developed, in which a sample of your blood is examined and damaged particles are removed and subjected to a polymerase chain reaction. This causes the DNA in the particles to break down. The particles are then placed in a nutrient, which causes the DNA to grow back into its original form. If enough of the substance is produced, the form can be recognised, so it can be determined whether Brucella or another kind of agent is behind that particular mycoplasma.

Blood Test

If you or anybody in your family has myalgic encephalomyelitis, fibromyalgia, multiple sclerosis or Alzheimer’s, you can send a blood sample to Dr Les Simpson in New Zealand for testing.

If you are ill with these diseases, your red blood cells will not be normal doughnut-shaped blood cells capable of being compressed and squeezed through the capillaries, but will swell up like cherry-filled doughnuts which cannot be compressed. The blood cells become enlarged and distended because the only way the mycoplasma can exist is by uptaking pre-formed sterols from the host cell. One of the best sources of pre-formed sterols is cholesterol, and cholesterol is what gives your blood cells flexibility. If the cholesterol is taken out by the mycoplasma, the red blood cell swells up and doesn’t go through, and the person begins to feel all the aches and pains and all the damage it causes to the brain, the heart, the stomach, the feet and the whole body because blood and oxygen are cut off.

And that is why people with fibromyalgia and chronic fatigue syndrome have such a terrible time. When the blood is cut off from the brain, punctate lesions appear because those parts of the brain die. The mycoplasma will get into portions of the heart muscle, especially the left ventricle, and those cells will die. Certain people have cells in the lateral ventricles of the brain that have a genetic predisposition to admit the mycoplasma, and this causes the lateral ventricles to deteriorate and die. This leads to multiple sclerosis, which will progress until these people are totally disabled; frequently, they die prematurely. The mycoplasma will get into the lower bowel, parts of which will die, thus causing colitis. All of these diseases are caused by the degenerating properties of the mycoplasma.

In early 2000, a gentleman in Sudbury phoned me and told me he had fibromyalgia. He applied for a pension and was turned down because his doctor said it was all in his head and there was no external evidence. I gave him the proper form and a vial, and he sent his blood to Dr Simpson to be tested. He did this with his family doctor’s approval, and the results from Dr Simpson showed that only 4% of his red blood cells were functioning normally and carrying the appropriate amount of oxygen to his poor body, whereas 83% were distended, enlarged and hardened, and wouldn’t go through the capillaries without an awful lot of pressure and trouble. This is the physical evidence of the damage that is done.

ECG Test

You can also ask your doctor to give you a 24-hour Holter ECG. You know, of course, that an electrocardiogram is a measure of your heartbeat and shows what is going on in the right ventricle, the left ventricle and so on. Tests show that 100% of patients with chronic fatigue syndrome and fibromyalgia have an irregular heartbeat. At various periods during the 24 hours, the heart, instead of working happily away going “bump-BUMP, bump-BUMP”, every now and again goes “buhbuhbuhbuhbubbuhbuhbuhbuh”. The T-wave (the waves are called P, Q, R, S and T) is normally a peak, and then the wave levels off and starts with the P-wave again. In chronic fatigue and fibromyalgia patients, the T-wave flattens off, or actually inverts. That means the blood in the left ventricle is not being squeezed up through the aorta and around through the body.

My client from Sudbury had this test done and, lo and behold, the results stated: “The shape of T and S-T suggests left ventricle strain pattern, although voltage and so on is normal.” The doctor had no clue as to why the T-wave was not working properly. I analysed the report of this patient who had been turned down by Canada Pensions and sent it back to them. They wrote back, saying: “It looks like we may have made a mistake. We are going to give you a hearing and you can explain this to us in more detail.”

So it is not all in your imagination. There is actual physical damage to the heart. The left ventricle muscles do show scarring.

That is way many people are diagnosed with a heart condition when they first develop fibromyalgia, but it’s only one of several problems because the mycoplasma can do all kinds of damage.

Blood Volume Test

You can also ask your doctor for a blood volume test. Every human being requires a certain amount of blood per pound of body weight, and it has been observed that people with fibromyalgia, chronic fatigue syndrome, multiple sclerosis and other illnesses do not have the normal blood volume their body needs to function properly. Doctors aren’t normally aware of this.

This test measures the amount of blood in the human body by taking out 5 cc, putting a tracer in it and then putting it back into the body. One hour later, take out 5 cc again and look for the tracer. The thicker the blood and the lower the blood volume, the more tracer you will find.

The analysis of one of my clients stated: “This patient was referred for red cell mass study. The red cell volume is 16.9 ml per kg of body weight. The normal range is 25 to 35 ml per kg. This guy has 36% less blood in his body than the body needs to function.” And the doctor hadn’t even known the test existed.

If you lost 36% of your blood in an accident, do you think your doctor would tell you that you are allright and should just take up line dancing and get over it? They would rush you to the nearest hospital and start transfusing you with blood. These tragic people with these awful diseases are functioning with anywhere from 7% to 50% less blood than their body needs to function.

VII- UNDOING THE DAMAGE

The body undoes the damage itself. The scarring in the brain of people with chronic fatigue and fibromyalgia will be repaired. There is cellular repair going on all the time. But the mycoplasma has moved on to the next cell.

In the early stages of a disease, doxycydine may reverse that disease process. It is one of the tetracycline antibiotics, but it is not bactericidal; it is bacteriostatic—it stops the growth of the mycoplasma. And if the mycoplasma growth can be stopped for long enough, then the immune system takes over.

Doxycycline treatment is discussed in a paper by mycoplasma expert Professor Garth Nicholson, PhD, of the Institute for Molecular Medicine.” Dr Nicholson is involved in a US$8 million mycoplasma research program funded by the US military and headed by Dr Charles Engel of the NIH. The program is studying Gulf War veterans, 450 of them, because there is evidence to suggest that Gulf War syndrome is another illness (or set of illnesses) caused by mycoplasma.

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.

You may contact Donald Scott at: 190 Mountain St., Ste. 405, Sudbury, Ontario, Canada P3B 4G2. 705-670-0180.

Endnotes

1. “Pathogenic Mycoplasma”, US Patent No. 5,242,820, issued September 7, 1993. Dr Lo is listed as the Inventor” and the American Registry of Pathology, Washington, DC, is listed as the “Assignee”.
2. “Special Virus Cancer Program: Progress Report No. 8”, prepared by the National Cancer Institute, Viral Oncology, Etiology Area, July 1971, submitted to NIH Annual Report in May 1971 and updated July 1971.
3. US Senate, Ninety-fifth Congress, Hearings before the Subcommittee on Health and Scientific Research of the Committee on Human Resources, Biological Testing Involving Human Subjects by the Department of Defense, 1977; released as US Army Activities in the US Biological Warfare Programs, Volumes One and Two, 24 February 1977.
4. Dr Donald MacArthur, Pentagon, Department of Defense Appropriations for 1970, Hearings before Subcommittee of the Committee on Appropriations, House of Representatives, Ninety-First Congress, First Session, Monday June 9, 1969, pp 105—144, esp. pp. 114, 129.
5. Kyger, E. R. and Russell L. Haden, “Brucellosis and Multiple Sclerosis”, The American journal of Medical Sciences 1949:689-693.
6. Colmonero et al., “Complications Associated with Brucella melitensis Infection: A Study of 530 Cases”, Medicine 1996;75(4).
7. Howell, Miller, Kelly and Bookman, “Acute Brucellosis Among Laboratory Workers”, New England Journal of Medicine 1948;236:741.
8. “Special Virus Cancer Program: Progress Report No. 8”, ibid., table 4, p. 135.
9. US Senate, Hearings before the Subcommittee on Health and Scientific Research of the Committee on Human Resources, March 8 and May 23, 1977, ibid.
10. New England journal of Medicine, August 22, 1957, p. 362.
11. Toronto Star, May 15, 1997.
12. Dr Donald MacArthur, Pentagon, Department of Defense Appropriations for 1970, Hearings, Monday June 9, 1969, ibid., p.129.
13. Henderson, Donald A., “Smallpox: Epitaph for a Killer”, National Geographic, December 1978, p. 804.
14. Blum, Deborah, The Monkey Wars, Oxford University Press, New York, 1994.
15. Nicholson, G. 1., “Doxycycline treatment and Desert Storm”, JAMA 1995;273:61 8-619.

This article first appeared on The Vaccination Racket.

Consumo de frituras aumenta incidência de substâncias cancerígenas

POR LUIS MIRANDA | THE REAL AGENDA | FEVEREIRO 12, 2013

Consumir alimentos fritos frequentemente, como batatas ou frango, está associado a um risco aumentado de câncer de próstata, segundo um estudo realizado por pesquisadores do Fred Hutchinson Cancer Research Center, em Seattle, EUA.

Estudos anteriores sugeriram que o consumo de alimentos preparados com métodos de cozimento que utilizam temperaturas elevadas podem aumentar o risco de câncer de próstata, no entanto, este é o primeiro a examinar a adição de fritura.

Especificamente, o autor Janet L. Stanford e sua equipe analisaram dados de 1.549 homens diagnosticados com câncer de próstata. Os participantes foram convidados a preencher um questionário sobre a dieta e ingestão regular de alimentos, incluindo alimentos fritos.

Eles descobriram que os homens que comeram batatas, frango frito, peixe e donuts, entre outros alimentos, pelo menos uma vez por semana, tiveram um risco aumentado de câncer de próstata em comparação com aqueles que comiam apenas uma vez por mês. Portanto, aqueles que comeram uma ou mais vezes na semana tinham um risco maior de câncer de próstata – entre 30 e 37%.

O consumo semanal destes alimentos também foi associado com um risco levemente maior de câncer de próstata mais agressivo. “A relação entre o câncer de próstata e os alimentos fritos pareceu limitado ao nível mais elevado de consumo – no estudo é definido como mais do que uma vez por semana, o que sugere que o consumo regular de alimentos fritos cria um risco particular de câncer de próstata “, disse Stanford.

Sua hipótese é a de que, quando o óleo é aquecido, criam-se compostos potencialmente carcinogénicos, tais como aminas heterocíclicas, acrilamida, hidrocarbonetos policíclicos, aldeídos e acroleína. A presença destes compostos tóxicos aumenta com a reutilização de óleo, que é algo que é feito em praticamente todos os restaurantes de fast food do mundo.

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Fried oil enhances appearance of carcinogens, concludes study

By LUIS MIRANDA | THE REAL AGENDA | JANUARY 29, 2013

Frequently consuming fried foods such as potatoes or chicken is associated with an increased risk of prostate cancer, according to a study by researchers at Fred Hutchinson Cancer Research Center in Seattle, USA.

Previous studies have suggested that eating foods prepared with cooking methods that use high temperatures could increase the risk of prostate cancer, however, this is the first to examine the addition of frying.

Specifically, lead author Janet L. Stanford and his team analyzed data from 1,549 men diagnosed with prostate cancer. Participants were asked to complete a questionnaire about diet and regular intake of foods including fried foods.

They found that men who ate potatoes, fried chicken, fish and donuts, among other foods, at least once a week had a higher risk of prostate cancer compared to those who only ate at least once a month. So, those who ate one or more of the items above per week had a higher risk of prostate cancer — 30 to 37 %.

Weekly consumption of these foods was also associated with a slightly increased risk of developing prostate cancer of the more aggressive type. “The relationship between prostate cancer and fried foods seemed limited to the highest level of consumption — defined in the study, as more than once a week, which suggests that regular consumption of fried foods creates a particular risk to develop prostate cancer, “said Stanford.

His hypothesis is that when the oil is heated, potentially carcinogenic compounds, such as acrylamide, heterocyclic amines, polycyclic aromatic hydrocarbons, aldehyde and acrolein are created. The presence of these toxic compounds increases with oil reuse, which is something done at virtually every single fast-food restaurant in the world.

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Will the ‘Revolution’ continue in Venezuela?

By LUIS MIRANDA | THE REAL AGENDA | DECEMBER 10, 2012

The long time Venezuelan dictator, Hugo Chavez feels that his time as chief of the government is coming to an end, so he has officially named Vice-president and Foreign Minister, Nicolas Maduro, as the man who should occupy his post.

Hugo Chavez seems to have assumed that the cancer he suffers from will not allow him to complete or even the fourth six-year term to which he was elected on 7 October. Given this situation, Chavez addressed Venezuelans on Saturday to anoint Vice President Maduro as his successor. Minutes earlier, Chavez had announced that he would be subjected to a fourth surgery to treat a cancer that was diagnosed back in June 2011.

Chavez explained the situation of his illness: “Due to the presence of some symptoms my medical team decided to run new tests. Unfortunately, the tests revealed the presence of cancer cells in the same area affected before. So, it is absolutely necessary to submit a new surgery. ”

If the president does not survive the operation, the Venezuelan Constitution states that the vice president should take over the presidency until new elections are due. Under this assumption, Chavez said: “Nicolas Maduro not only should end the period, as mandated by the Constitution, but it is my firm opinion that he has the skills to be re-elected in the following presidential elections”.

It is the first time that Chavez openly discussed the possibility of his death and ordered his followers what to do in case he dies during or after the surgery. “I ask all the support of the people and of all streams, civil, military, under these circumstances. All support, first for the revolutionary government at this juncture and the support and unity to the decisions that have to be taken. Today we have a country, make no mistake. ”

Since being diagnosed with cancer last year, Chavez had refused to reveal the severity of their disease and the organs of the body that have been affected by it. So far, Chavez has undergone three operations, two of them to remove two separate malignancies, and received radiotherapy and chemotherapy sessions. This Friday he returned to Venezuela after spending nine days in Cuba, where he received an alternative therapy called “hyperbaric oxygenation”.

After the fourth re-election of Chavez, Nicolas Maduro has become the strong man of the Revolution. In Venezuela, he has been Foreign Minister since 2006 and has been in charge of the presidency during Chavez’s most recent trip. Maduro was a bus driver and union leader and is recognized as loyal and friendly.

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