Bee Venom Kills HIV, experiments find

Discovery could lead to topical gel to prevent HIV transmission

By JASON KOEBLER | USNEWS | MARCH 13, 2013

Bees could hold the key to preventing HIV transmission. Researchers have discovered that bee venom kills the virus while leaving body cells unharmed, which could lead to an anti-HIV vaginal gel and other treatments.

Scientists at the Washington University School of Medicine in St. Louis found that melittin, a toxin found in bee venom, physically destroys the HIV virus, a breakthrough that could potentially lead to drugs that are immune to HIV resistance. The study was published Thursday in the journal Antiviral Therapy.

“Our hope is that in places where HIV is running rampant, people could use this as a preventative measure to stop the initial infection,” Joshua Hood, one of the authors of the study, said in a statement.

The researchers attached melittin to nanoparticles that are physically smaller than HIV, which is smaller than body cells. The toxin rips holes in the virus’ outer layer, destroying it, but the particles aren’t large enough to damage body cells.

“Based on this finding, we propose that melittin-loaded nanoparticles are well-suited for use as topical vaginal HIV virucidal agents,” they write.

Theoretically, the particles could also be injected into an HIV-positive person to eliminate the virus in the bloodstream.

Because the toxin attacks the virus’ outer layer, the virus is likely unable to develop a resistance to the substance, which could make it more effective than other HIV drugs.

“Theoretically, melittin nanoparticles are not susceptible to HIV mutational resistance seen with standard HIV therapies,” they write. “By disintegrating the [virus’] lipid envelope [it’s] less likely to develop resistance to the melittin nanoparticles.”

The group plans to soon test the gel in clinical trials.

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.

Anticorpos Induzidos por Vacinas são Desnecessários para Combater Doença

POR LUIS R. MIRANDA | THE REAL AGENDA | 15 ABRIL 2012

Historicamente, o estabelecimento médico-farmacêutico promoveram vacinas como a solução milagrosa para todos os problemas de saúde que os seres humanos enfrentam. Casas farmacêuticas concluiram que as vacinas eram necessárias porque o corpo necessita delas para construir anticorpos para combater doenças e que as vacinas eram a melhor ferramenta para garantir que o sistema imunológico humano tivesse a capacidade de produzir estes anticorpos. No entanto, as vacinas são coqueteis ineficazes e tóxicos de metais pesados e vírus vivos, que não só nao previnem doenças mas que as causam.

Inúmeros estudos — por favor, faça sua própria investigação — têm mostrado a ligação entre ingredientes das vacinas, como o mercúrio, o esqualeno, adjuvantes e condições médicas, como o autismo, câncer, condições do sistema nervoso, danos ao cérebro, e assim por diante. Os profissionais médicos como Russell Blaylock e Andrew Wakefield tem falado interminavelmente sobre os perigos das vacinas — devido a forma em que são produzidas — para a saúde humana. Mas apesar dos inúmeros estudos e avisos de profissionais médicos, autoridades de saúde e empresas farmacêuticas sempre trabalharam em conjunto para impor regras — não leis — que todos devem ser vacinados para seu próprio bem.

Enquanto a maioria das políticas oficiais do governo indicam que as vacinas são devidamente testadas e continuamente monitoradas pelos seus possíveis efeitos colaterais e reações, a maioria das vacinas são testadas e monitoradas apenas pelos produtores destas vacinas, que enviam seus resultados para as autoridades “vigilantes”. Estas autoridades permitem aos fabricantes a liberdade de produzir vacinas em massa, que mais tarde são recomendadas e acrescentadas à lista cada vez maior de vacinas, especialmente crianças, que são injetadas desde o nascimento.

Só que agora há um problema, um problema novo para o cartel médico-farmacêutico: O corpo humano não necessita de anticorpos induzidos pelas vacinas para combater doenças, vírus, bactérias ou outros agentes patogénicos. O nosso sistema imunológico na verdade, tem a capacidade de produzir anticorpos naturais que por sua vez, funcionam como defesas contra as doenças. O sistema imunológico humano é composto de características originais e outros que são fabricados pelo organismo — criado depois que uma pessoa nasce e cresce — que trabalham juntos para manter o corpo a salvo de doenças sem a necessidade de produtos artificiais criados em laboratórios. Isto pode vir como uma surpresa para muitos, mas não para outros indivíduos que estão bem informados sobre como evitar e curar doenças.

A pseudociencia usada para implementar as políticas de vacinação diz que quando uma pessoa é injectada com uma vacina, o sistema imunológico responde aos ingredientes da vacina como se fosse um ataque real a partir de um vírus ou outro agente patogénico. O corpo responde a este suposto ataque, criando anticorpos para tratá-lo. No futuro, se o vírus ou o organismo ataca a pessoa novamente, o sistema imunológico sabe como reagir e se defender do ataque. Isso é explicado como se o sistema imunológico “aprendesse” como agir em caso de uma infecção. O problema é que o suposto “aprender” para combater a doença é algo que o corpo já sabe como fazê-lo; é uma habilidade natural, como é sua capacidade de produzir anticorpos. O que a reação induzida pela vacina realmente faz é alterar a resposta natural do sistema imunitário humano que por sua vez prejudica o sistema imunológico, porque ao longo do tempo, o corpo não pode responder a outros vírus ou organismos que podem causar doenças mais do que aquelas injectadas através de uma vacina. Este é o caso com a gripe comum.

O vírus da influenza é um organismo que está sempre mudando, nunca é o mesmo. Quando as pessoas injetadas com a vacina contra a gripe comum que contem a cepa do ano passado, elas acham que estarão protegidos, mas a nova cepa não tem nenhum problema para entrar num sistema imunológico degradado  que não é apenas indefeso contra ela, mas também incapaz de lidar com a nova versão do vírus em si.

Este é o momento onde o estudo publicado na revista Immunity confirma nossas suspeitas. O estudo mostra que anticorpos induzidos pela vacina são incapazes de combater doenças por si sós, uma característica que só ocorre naturalmente em anticorpos produzidos pelo nosso sistema imunológico. Este é o fato que absolutamente quebra o mito de que as vacinas são necessárias para manter as pessoas livres de vírus ou bactérias que podem causar doenças. Como em muitos outros casos, a teoria científica alegada é apenas isso, uma teoria. Como mencionado no estudo, as vacinas não ajudam a prevenir ou combater infecçoes. “Nossos resultados contradizem a visão atual de que os anticorpos criados em resposta às vacinas são absolutamente necessários para sobreviver a infecções com vírus como o VSV (vírus da estomatite vesicular), e estabelecer uma função inesperada para as células B como guardiões de macrófagos na imunidade antiviral “, diz Dr. H. von Andrian Uldrich Harvard University Medical School.

Dr. von Andrian acrescentou que “é importante dissecar o papel dos anticorpos e interferon na imunidade contra vírus similares, que atacam o sistema nervoso, tais como raiva, vírus do Nilo Ocidental e Encefalite.”

Então, se as vacinas não funcionam como anunciadas pelas grandes empresas farmacêuticas, e se são prejudiciais para o sistema imunológico natural, porque as agências governamentais sempre recomendam que todos usemos tais vacinas? De acordo com o neurocirurgião Russell Blaylock, as vacinas suprimem o sistema imunológico sendo que este não pode produzir citocinas de tipo Th2 e também suprimem a imunidade celular. O resultado é um enfraquecimento do sistema imunológico que resulta em um corpo fraco que é mais vulnerável às doenças, e que também faz com que o corpo leve mais tempo para se recuperar. O que os resultados deste estudo representam é o prego final no caixão da pseudociência das vacinas. As vacinas foram — segundo os cientistas — a melhor invenção desde o advento da roda, para tornaran-se um mal perigoso, mas necessário, e agora são um método ineficaz para combater doenças.

“Incrivelmente, nunca houveram estudos controlados comparando uma população de pacientes vacinados contra outro grupo de pacientes não vacinados,” diz o Dr. Phillip Incao. A crítica do Dr. Incao é suportada por muitos médicos independentes como o Harold Buttram. “Não houve nenhum estudo desta natureza, e, aparentemente, nunca foi tentado”, diz Dr. Buttram.

Além das informações acima, é importante dizer que a vacinação obrigatória atual — não há lei que obrigue ninguém a usar uma vacina — em quase todos os países violam o Código de Nuremberg, o conjunto de regras que todos os profissionais da medicina devem seguir, quando se trata da utilização de vacinas. De acordo com o Sistema de Informação de Efeitos Adversos Causados por Vacinas (VAERS), existem pelo menos 2.142 mortes confirmadas e 3.177 pessoas portadoras de deficiências permanentes entre 1991 e 2001, que foram causadas por vacinas. Veja a pagina Vigilância após a Imunização. Mas, na realidade, as estatísticas globais mostram que as conseqüências são muito piores. As mortes são entre 21,420 a 142.800 mortes, se considerarmos que apenas 1,5 a 10% de eventos adversos são relatados.

Segundo o Instituto Mundial das Vacinas, estas são responsáveis por causar doenças como a AIDS, Câncer, Diabetes, Audição e perda de visão, hepatite B, MMR, caxumba, poliomielite, rubéola e autismo, sem que ninguém jamais demonstrasse que uma vacina curou ou ajudou a tratar nenhuma doença.

Se você está curioso para saber quais são alguns dos ingredientes utilizados na produção de vacinas — muitos dos que se acumulam em seu corpo — por favor, seja corajoso e veja a lista fornecida pela CDC.

As vacinas nunca ajudaram a reduzir a incidência de nenhuma doença, muito menos a cura-las. Veja os gráficos abaixo que demonstram como as vacinas sempre foram usadas DEPOIS que as doenças começaram a desaparecer o qual foi usado para justificar o seu uso.

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Vaccine-Induced Antibodies not Necessary to Fight Viruses

By LUIS MIRANDA | THE REAL AGENDA | MARCH 28, 2012

Historically, the medical-pharmaceutical establishment have pushed vaccines as the miraculous solution for every single health problem that humans face. The pharmaceutical power houses came to the conclusion that vaccines were necessary because the body needed to build antibodies in order to fight disease and that vaccines were the best tool to ensure that the human immune system would have the capacity to produce such antibodies. As we already know, vaccines are at the very least ineffective, toxic cocktails of heavy metals and live viruses that not only don’t prevent disease, but that actually cause it.

Countless studies — please do your own research — have shown the relationship between vaccine ingredients such as mercury, squalene, adjuvants and medical conditions such as autism, cancer, conditions of the nervous system, brain injury, and so on. Medical professionals like Rossell Blaylock and Andrew Wakefield have spoken endlessly about the dangers that vaccines pose — as they are now produced and administered — to human health. But despite the numerous studies and warnings from uncompromised medical professionals, health authorities and pharmaceutical companies have always worked in unison to impose a criminal standard that everyone must be vaccinated for their own good.

Although most official government policies indicate that vaccines are properly tested and continuously monitored for side effects and reactions, most of those vaccines are tested and monitored by the vaccine producer, who then sends its findings to the “vigilant authorities”. These authorities then give the makers thumbs up to mass produce it and later recommend it and add it to the ever growing number of inoculations that people, especially children, must take from birth.

There is only one problem; a new problem, for the medical-pharmaceutical cartel: The Human body does not need vaccine produced antibodies to fight disease such as viruses, bacteria or other pathogens. Our human immune system actually has the capacity to produce natural antibodies which then work as defenses against disease. The human immune system is composed by original and constructed elements — created after a person is born and grows up — that work together to keep the body safe from illnesses without the need for artificially, lab-made products. This may come as a surprise to many, but it is not new for others who freely and independently educate themselves about ways to prevent and cure disease.

Current official vaccine science establishes that when a person is injected with a vaccine, the ingredients in it cause the body to respond to the vaccine as if it were a real attack from a virus or any other pathogen. The body then responds to this supposed attack by creating antibodies to deal with it. In the future, if the virus or organism attacks the person again, the immune system will know how to react and defend from the attack. This is explained as the immune system “learning” how to act in case of an infection. The problem is that “learning” how to fight disease is something the body already knows how to do, it is a natural ability, as so is its capacity to produce antibodies. What vaccine-induced antibody creation does is actually alter the natural response the human immune system has which in fact impairs the body to react to a disease that is not exactly the same as the one injected in our body through a vaccine. This is the case if the seasonal flu.

The flu virus is, due to the use of vaccines — an ever morphing organism that is NEVER the same. When people inject themselves with the seasonal flu vaccine that contains last year’s strain of the virus, the new strain does not have any problem penetrating a degrade immune system that is not only defenseless against it, but also incapable of dealing with the new version of the virus by itself.

This is where the study published in the Journal Immunity comes in handy. The study shows that vaccine induced antibodies are not able to fight disease by themselves, a feature that is only present in naturally occurring antibodies generated by our immune system. This is the fact that absolutely debunks the myth that vaccines are necessary to remain free of pesky viruses and bacteria that may cause disease. As in many other cases, the supposed scientific theory is just that; theory. As cited by the study, vaccines do not help prevent or combat infections. “Our findings contradict the current view that antibodies are absolutely required to survive infection with viruses like VSV (vesicular stomatitis virus), and establish an unexpected function for B cells as custodians of macrophages in antiviral immunity,” says Dr. Uldrich H. von Andrian from Harvard Medical School.

Dr. von Andrian added that “It will be important to further dissect the role of antibodies and interferons in immunity against similar viruses that attack the nervous system, such as rabies, West Nile virus, and Encephalitis.”

So if vaccines do not work as the pharmaceutical power houses advertise and if they impair the natural immune system from actually fighting disease, why are government agencies always recommending that we all use them? According to brain surgeon Russell Blaylock, vaccines inhibit the immune system from producing TH2-type cytokines on top of suppressing cellular immunity. The result of a weakened, useless immune system is a weaker human body that will not only be more vulnerable to get sick, but that will also take longer to recover, if it does. What the results of this study represent is the last nail in the coffin of vaccine pseudoscience. Vaccines have gone from being the best invention since the appearance of the wheel, to becoming a dangerous but necessary evil, to an ineffective method to fight disease.

“Incredible as it sounds, such a common-sense controlled study comparing vaccinated to unvaccinated children has never been done in America for any vaccination,” says Dr. Phillip Incao MD. Dr. Incao is backed by many independent medical professionals, such as doctor Harold Buttram. “There have never been any studies of this nature, and apparently none have been attempted,” says Dr. Buttram MD.

In addition to the information above, it is important to say that the current mandatory vaccination systems — there is no law that legally obligates anyone to take a vaccine — in almost all countries violate the  Nuremberg Code, the set of rules that all medical professional must follow, but that few implement when dealing with the use of vaccines.According to the Vaccine Adverse Reporting Systems (VAERS), there were  at least 2,142, confirmed deaths and 3,177 people permanently disabled from 1991-2001 from vaccinations. See Surveillance for Safety After Immunization. But in actuality, complete statistics show that the consequences are significantly worse. Deaths amount to between 21,420 – 142,800 deaths if one takes into account that only 1.5-10% of adverse events are reported.

According to the Global Vaccine Institute, vaccinations are responsible for causing disease such as AIDS, Cancer, Diabetes, Hearing/Vision Loss, Hepatitis B, MMR, Mumps, Polio, Rubella and Autism, without anyone ever demonstrating that a single vaccine cured any existing disease.

If you are curious to learn what are some of the ingredients used in the production of vaccines — many of which make their way into your body — please be courageous and see the list provided by the CDC here.

Vaccines NEVER helped decrease the incidence of any disease, much less to cure anyone.

 

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Alimentos Modificados Genéticamente – ¿Envenenando Nuestra Gente?

Traducción Luis R. Miranda
allAfrica.com
Junio 9, 2011

Opinión

Uno de los más extensos experimentos no regulados en seres humanos se está llevando a cabo aquí en África del Sur. Los sudafricanos fueron los primeros en el mundo en consumir alimentos genéticamente modificados (OGM)como parte de su dieta. Según fuentes de la industria más del 75% de nuestro maíz blanco es ahora GM. Esto significa que la papilla consumida a diario en la mayoría de los hogares de Sudáfrica está compuesto de maíz genéticamente modificado.

La afirmación de la industria que nadie se ha enfermado después de ingerir alimentos modificados genéticamente es científicamente deshonesta. Se basa en el principio de “si no miras, no encuentras”. Debido a que los alimentos modificados genéticamente no están claramente identificados a través de un etiquetado claro, es muy imposible saber qué enfermedades están relacionadas con el consumo del producto.

Se dice que estos alimentos han sido probados y son seguros. Al mismo tiempo, los productores de transgénicos afirman que sus productos son “sustancialmente equivalentes” – idénticos a sus contra partes naturales. Como tales, no requieren pruebas. Cuando las pruebas se ha hecho han sido presas de las mismas trampas que han afectado las pruebas de toxicología hechas a productos químicos durante décadas. No es sorprendente que las empresas que producen OGM, sin excepción han evolucionado a partir de las empresas químicas agrícolas, infames en su abuso de los protocolos estadísticos y experimentales.

La mayoría de las pruebas se han realizado en los alimentos y presentado por las mismas compañías que buscan su aprobación. El diseño de estas pruebas ha sido opaco y engañoso. Las investigaciones han demostrado que los resultados han sido sistemáticamente manipulados y sesgados. Dice la epidemióloga Judy Carman: “Su enfoque conjunto para el análisis no sería útil para una clase de estadística básica.”

Los primeros análisis de todos los estudios de alimentación encuentran exactamente tres experimentos. Aún estas pruebas muestran tendencias preocupantes. Más reciente meta-análisis han reforzado estas preocupaciones. Un hallazgo consistente ha sido el daño al hígado y los riñones. Cabe destacar que el hígado y la enfermedad renal han aumentado desde que los cultivos transgénicos se introdujeron en los EE.UU..

Lo notable es que cuando los investigadores empleados o conectados a los desarrolladores de los alimentos GM hicieron estudios, no se reportaron problemas. Por otra parte, estudios realizados por científicos independientes siempre motivan su preocupación. Un análisis publicado recientemente puso de relieve esta tendencia. Esta relación es común en los análisis de otros productos químicos y alimentos.

Más preocupante aún es el hecho de que los estudios de alimentación fueron hechos a muy corto plazo, con no más de tres meses. Fundamentalmente, ninguno de ellos utiliza más de un tercio de los productos transgénicos en la dieta. En el sur de África, comemos maíz transgénico no identificado como un alimento básico en niveles que en muchos casos puede alcanzar el 100% de la dieta. La pregunta es: Si el daño es preocupante y está estadísticamente demostrado que los riñones, el hígado y otros órganos son destruídos cuando los animales son alimentados con un tercio de su dieta con productos modificados genéticamente, en estudios de una duración de tres meses, entonces ¿qué diablos va a pasar con aquellos de nosotros que comemos una dieta que es predominantemente a base de maíz GM, todos los días durante años?

Esto no es nada menos que un experimento masivo no regulado. Para empeorar las cosas este experimento no se lleva a cabo en una población sana, sino en una cuya salud está doblemente comprometida: en primer lugar, las personas no comen una dieta lo suficientemente variada. En segundo lugar, tenemos el mayor número de habitantes con VIH, SIDA e infecciones de tuberculosis en el mundo.

Hay muchos otros estudios que han señalado los problemas del consumo de los cultivos transgénicos, incluso a niveles reducidos de una tercera parte de la dieta total. Los estudios han demostrado menor recuento de espermatozoides y esterilidad. Los investigadores han pedido constantemente para que se siga investigando. Todo lo que la industria de los transgénicos hace es lo de siempre; intentar salirse con la suya.

Esta situación escandalosa cuenta con la asistencia de nuestra mala regulación de los alimentos modificados genéticamente que sólo se identificarán a finales de este año. En otras palabras, las personas han estado comiendo alimentos GM en la ignorancia total de los hechos. Hasta el momento, no hay una prueba independiente, llevada a cabo durante generaciones sobre como la dieta de varias de las personas se ve afectada al consumir alimentos GM. Esto equivale a poco menos que negligencia criminal por parte de nuestro gobierno, que siempre ha hecho caso omiso de estas preocupaciones, y en lugar ha tomado el lado de una industria con una trayectoria muy defectuosa.

Por supuesto esta industria insiste en que la Unión Europea y otros han producido informes que demuestran que los cultivos transgénicos no tienen ningún riesgo para la salud. El hecho es que los reguladores de la UE se han basado en exactamente las mismas pruebas producidas por la propia industria. En segundo lugar, la influencia de la industria en el régimen normativo es significativo. Esta industria tiene no sólo los reguladores habitualmente mal informados, a través de pruebas con el suministro de datos estadísticos sesgados, pero siempre ha interferido en el régimen de reglamentación.
Por ejemplo, la normativa que regula los cultivos transgénicos en los EE.UU. fue redactada por el ex jefe de asuntos reguladores de Monsanto, Michael Taylor, quien dejó la empresa Monsanto para trabajar en el gobierno con el fin de elaborar una legislación favorable a la industria. Luego regresó a Monsanto. Desde entonces, ha vuelto al gobierno, en lo que se conoce como “la puerta giratoria”. Esto no es en absoluto un caso aislado y una situación similar existe en el sur de África.

Esta es sólo la punta del iceberg. Hay casos documentados de como la industria restringe y prohíbe las pruebas independientes de sus productos. Esto es posible debido a que estos productos están patentados se necesita permiso de las empresas para accesar diversos aspectos cruciales de e información en las pruebas científicas, el cual es siempre negado.

No se trata sólo de los peligros inherentes de los cultivos transgénicos. El producto GM más cultivado en el mundo, la soja resistente a los herbicidas, se ha relacionado con niveles altos del herbicida Roundup, fabricado por Monsanto, que también es propietaria de las patentes en más del 90% de todos los cultivos transgénicos a nivel mundial. Monsanto también introdujo el maíz resistentes a los herbicidas, que se cultivan en el sur de África. Pese a las afirmaciones de que los cultivos transgénicos reducen el uso de productos químicos, hemos visto exactamente que lo contrario ocurre en todo el mundo.

Por ejemplo, en Argentina, el uso de herbicidas ha aumentado 180 veces en 13 años. En los EE.UU., 174 000 toneladas más se usan cada año. En Brasil es de hasta un 95%. La responsabilidad del impacto ambiental y en la salud de las personas no es la preocupación de los agricultores, sino que simplemente es pasada a los consumidores, que no son los más sabios. Y los riesgos que estos productos químicos crean son cada vez más y más preocupantes que los cultivos transgénicos en sí.

Cuando los primeros cultivos transgénicos se introdujeron la cantidad permitida legalmente de residuos de herbicidas en los alimentos se aumento en 200 veces en el caso de la Unión Europea, con incrementos similares en otros lugares, todo para acomodar las peticiones de las corporaciones. Roundup está vinculado a graves impactos en la salud humana, incluidos los daños al crecimiento del embrión y el feto (impactos tetragénicos), así como el daño celular, entre muchos otros impactos sobre los mamíferos. Hay literalmente docenas de estudios publicados que indican las preocupaciones acerca de este producto químico. También afecta a los anfibios, insectos, lombrices y bacterias del suelo que liberan nutrientes para las plantas.

Además de estas preocupaciones, hay una inconsistencia evidente en el argumento de que los cultivos transgénicos son necesarios para alimentar al mundo: El hecho de que el producto GM más cultivado en el mundo, la soja, siempre ha sido demostrado que rinden menos que la soja convencional y natural. A pesar de años de promesas de que los cultivos GM son más resistentes a la sequía estas promesas siguen sin cumplirse.

Oxfam Internacional publicó recientemente un informe que indica que los precios de los alimentos se duplicaran, desde sus ya altos niveles en las próximas dos décadas. ¿Cómo podemos solucionar este problema? Somos constantemente informados por los partidarios de los cultivos transgénicos que debemos adoptar la tecnología para alimentar al mundo. La realidad es que los programas de mejoramiento convencional de plantas han logrado mucho más, a un costo mucho más bajo, mejorando el rendimiento, la resistencia viral, la mejora nutricional y resistencia a la sequía.

Quince años de cultivos genéticamente modificados en África del Sur han demostrado que la rápida adopción de cultivos transgénicos no ha tenido impacto alguno sobre la cantidad de alimentos que llegan a la boca de los más necesitados. La única conclusión que puede ser obtenida es que los cultivos transgénicos no son la solución. Más importante es que estamos jugando un peligroso juego de la ruleta rusa genética con la salud de nuestro pueblo.

La Evaluación Internacional del Papel del Conocimiento, Ciencia y Tecnología para el Desarrollo (IAASTD), en su informe titulado “Agricultura en la encrucijada”, señaló que los cultivos transgénicos en el mejor de los casos desempeñará un papel limitado en la lucha contra el hambre mundial. El enfoque en la agricultura de altos insumos industriales y los OGM han marginado las prácticas agrícolas más eficaces. El estudio de la IAASTD fue financiado por el Banco Mundial y varios organismos de la ONU, e involucró a más de 400 expertos en agricultura de todo el mundo.

El enfoque perjudicial en los cultivos transgénicos en las últimas dos décadas ha contribuido a retrasar el desarrollo de la investigación que se necesita con urgencia. En lugar de centrarse en el clima y los aspectos relacionados en los sistemas de producción de las comunidades que necesitamos para fomentar la seguridad alimentaria y la verdadera independencia, el enfoque político-institucional sobre los cultivos transgénicos nos ha dirigido hacia la confianza en el modelo de dependencia personificado por la agricultura industrial, en cuanto erosiona nuestra salud y la ya precaria situación.
Se mire como se mire, los cultivos transgénicos personifican el problema, no la solución.