Tag Archives: Swine Flu Vaccine

Gardasil HPV -Sudden Death

Gardasil HPV-Sudden Death  Updated August 30, 2011 2:00 p.m. EST

Originally Posted: February 4, 2010  

Gardasil HPV -Sudden Death takes Toll on Teenagers

You can go anywhere in the world where the vaccine Gardasil is sold to a government which starts vaccinating in schools without testing and without safety against the side effects and see the results. Many teens die within hours, some after a few days and some are damaged for life.

Fatal Doses of Gardasil HPV and Sudden Death

In New Zealand it is the same story as in Denver -schools are being used and paid to administer Gardasil but in Denver they are giving kids 5 vaccines at once. 

The parents of these kids are barely aware of what they are allowing school officials to administer 5 vaccines that were never tested for causing cancer to be given to their children without questions. The vaccines cause irreparable harm to young teens and their immune system with deadly viruses and heavy metal chemicals.

In Denver elementary schools kids are being given high doses of piled on vaccines which include the H1N1 Swine Vaccine which is still untested.   No long term studies have ruled out permanently damage to the human body.

In the Vaccine Totalitarians from 2004 Larry Solomon discusses the CDC’s Phony Crisis of that year which is five years before the Swine Flu Hoax of last year.  Back then as Larry states there was a faked “shortage of vaccines” from the pharmas in the UK., which used a misleading and untrue shortage as a marketing campaign.

Gardasil HPV -Sudden Death

What the FDA is hiding about Gardasil HPV-Sudden Death

The same tactic was used in 2009 with the CDC doing a poor job at fudging the numbers and cooking the books on swine flu deaths by falsely overstating deaths that occurred due to other factors.

If you sneezed and died you had Swine Flu, if you had a cough before you died you died of Swine Flu and the numbers were highly suspiciously inflated to ensure people were frightened.

Here is Jasmine’s Story

 

In 2008  THE FDA APPROVED GARDASIL FOR BOYS AND GIRLS

NO TESTING
NO TESTING FOR CANCER CAUSING AGENTS
NO SAFETY OR PROOF OF CANCER PREVENTION

Updated Feb 5, 2010

Editors Note:

If you are a Parent and are Concerned that YOU are not being GIVEN ENOUGH INFORMATION on what long term effects Gardasil will have on your children this site will give you more details.
For further Reading on Gardasil from an unbiased and unpaid source contact :

OFF THE RADAR

This site has documented information on Gardasil for parents and for young daughters and sons who are not given truthful research and information on ingredients.

It breaks down all the chemical names that the pharmaceuticals hide from the general public by changing the names of chemicals and the average person would need an physicians drug reference book to look this information up.  Well it is all here for you to read.  From the aluminum to the MSG in this vaccine and what it does – you need to read this before you vaccinate your kids.

Read more here

Capitalism Magazine:

Vaccine Totalitarianism The CDC’s Phony Crisis Over the Flu Vaccine

Dr. Oz -Vaccine Pusher Owns Pharma Stock

You had to go back to where Dr Oz was interviewed by Campbell Brown on CNN where he stated that his own family would not get the H1N1 Swine Flu Vaccine, but he would take the shot. That really doesn’t make sense Dr. Oz because if you cared about yourself as much as your family there would have been no phony stunt.

On a show backed by Oprah’s big bucks Dr. Mehmet Oz supposedly got the swine flu vaccine which was his biggest mistake.  He failed to ensure the vaccine was safe and he failed to back his opinion on sound medical science.

Here on one hand Dr. Oz states his family will not receive the swine flu vaccine quite clearly.

In fact Dr. Oz promotes the swine flu vaccine on his Oprah Show.

In this article Walgreens distributes its swine flu vaccine on the Dr Oz show for free.  It is doubtful Dr. Oz received an actually flu shot and this was just another stunt to promote vaccines.  The vial could and would have contain only a salt solution or saline solution which is harmless.

The scenario that Dr. Oz’s family would not receive the vaccine and yet he did a stunt on national television doesn’t hold water and is highly suspicious of a media hoax.   Annual flu shots are more harmful than have any benefit to the public, and Tamiflu does so much damage that recipients will be defenseless against the H1N1 strain. There is no scientific or medical proof that these vaccines are effective at all and mostly likely represent the greatest fraud on the public.

Dr. Oz’s Phony Stunt Ruins His Reputation on Oprah’s Shows

You would have to be really uninformed to think these ingredients would ever do you any good:

Egg or chicken embryo-or viruses grown on diseased monkey genes.

Aluminum (neurotoxin linked to Alzheimer’s disease)

Triton X-100 (a detergent)

Phenol (carbolic acid)

Ethylene glycol (antifreeze)

Betapropiolactone (a disinfectant)

Thimerosal [mercury] (a harmful preservative)

Octoxinol 9 (a vaginal spermicide)

Formaldehyde (embalming fluid)

Sodium phosphate (irritant and toxin)

These ingredients harm the human body and you would be better off drinking a cup of Drano than to take these flu shots at your own risk.  Formaldehyde is for dead body part preservation not for living human beings.  Read more on Disease Prevention.

The vaccine remains untested for disease beyond 21 days which is not a viable study and should not be accepted as proof that it even works.  This vaccine has carcinogens that damage the human body and that is proof enough for millions who are refusing even Oprah’s medical expert.  The fact is that Dr. Oz is no expert he is just another doctor working for the drug pushing system.

Why Doctor Oz is a Phony Pharma Pusher

It turns out that Dr. Oz holds approximately 1 million dollars worth of stock in a pharma company called SIGA which makes vaccines involved in biological warfare including small pox and other pathogens. See Doctor Oz’s Stock Holdings in SIGA Pharmaceuticals.
This company also has strong ties to the National Institute of health and the Department of Defense as well as other government agencies.  The drug cartels have used their influence to buy a spokesperson right under Oprah’s nose. In fact SIGA Pharmaceuticals has since 1998 owned a patent on the strep throat vaccine and other vaccines.

Dr. Oz Mehmet C MD Number 0001139299 registered with the FTC has 150,000 shares inn SIGA and stands to profit from the same of said vaccines which he bought on September 30, 2009.  Perhaps that was a down payment on his integrity and for his services of pushing vaccines on the air on his Oprah Show.
Transaction dates are May 13, 2009, May 14, 2009, May 30, 2009 and date back to December 12, 2006.

Dr Oz – 150,000 shares?  Really did you think no one would find out?
If Dr. Oz was at all truthful he would have disclosed this information before he did his stunt on a national TV network stating he had a “financial interest” in the sale and promotion of Vaccines.  After all is this not the truthful way to conduct an endorsement for the swine flu vaccine?  There are FTC rules that Dr. Oz has broke on this show promoting a product in which he has a definite “conflict of interest” and he is being dishonest, untruthful and deceiving the public.  Oprah should pull him off the air if she had the same integrity and maybe that explains why Oprah wants her own network.  Actually Oprah should have her own network and in this manner she would not be “owned” by the drug company influences on her shows.

TAGS: Dr. Oz a Phony Pharma Shill, Dr. Oz Vaccine stunt, Dr. Oz-150,000 shares of SIGA big pharma, Oprah Shows, Dr. Oz family will not take swine flu vaccine, swine flu vaccine, flu shots.

Robert Kennedy Jr-On Mercury in Vaccines and Autism

Update: November 1, 2009 9:09 p.m

From a Post At: The Rolling Stone dated June 20, 2005-  this was over 4 years ago

Entitled:   Deadly Immunity

Four years ago Kennedy spoke out about mercury in vaccines and still mercury is in all vaccines but now squalene, aluminum, 3 viruses and the drug company’s beloved use of mercury where they could use saline (salt) solutions for safety and health -they prefer to make money on the mercury.  Thermisol which is patented with the US government for use in vaccines.  Your government agencies the National Institute of Health, the Food and Drug Administration and the Center for Disease Control are all allowing this to happen to you.

Read what Robert F. Kennedy Jr has to say about Immunity:

Quote:

In June 2000, a group of top government scientists and health officials gathered for a meeting at the isolated Simpsonwood conference center in Norcross, Georgia. Convened by the Centers for Disease Control and Prevention, the meeting was held at this Methodist retreat center, nestled in wooded farmland next to the Chattahoochee River, to ensure complete secrecy. The agency had issued no public announcement of the session — only private invitations to fifty-two attendees. There were high-level officials from the CDC and the Food and Drug Administration, the top vaccine specialist from the World Health Organization in Geneva and representatives of every major vaccine manufacturer, including GlaxoSmithKline, Merck, Wyeth and Aventis Pasteur. All of the scientific data under discussion, CDC officials repeatedly reminded the participants, was strictly “embargoed.” There would be no making photocopies of documents, no taking papers with them when they left.

The federal officials and industry representatives had assembled to discuss a disturbing new study that raised alarming questions about the safety of a host of common childhood vaccines administered to infants and young children. According to a CDC epidemiologist named Tom Verstraeten, who had analyzed the agency’s massive database containing the medical records of 100,000 children, a mercury-based preservative in the vaccines — thimerosal — appeared to be responsible for a dramatic increase in autism and a host of other neurological disorders among children. “I was actually stunned by what I saw,” Verstraeten told those assembled at Simpsonwood, citing the staggering number of earlier studies that indicate a link between thimerosal and speech delays, attention-deficit disorder, hyperactivity and autism.

Since 1991, when the CDC and the FDA had recommended that three additional vaccines laced with the preservative be given to extremely young infants — in one case, within hours of birth — the estimated number of cases of autism had increased fifteenfold, from one in every 2,500 children to one in 166 children.

Even for scientists and doctors accustomed to confronting issues of life and death, the findings were frightening. “You can play with this all you want,” Dr. Bill Weil, a consultant for the American Academy of Pediatrics, told the group. The results “are statistically significant.” Dr. Richard Johnston, an immunologist and pediatrician from the University of Colorado whose grandson had been born early on the morning of the meeting’s first day, was even more alarmed. “My gut feeling?” he said. “Forgive this personal comment — I do not want my grandson to get a thimerosal-containing vaccine until we know better what is going on.”

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But instead of taking immediate steps to alert the public and rid the vaccine supply of thimerosal, the officials and executives at Simpsonwood spent most of the next two days discussing how to cover up the damaging data. According to transcripts obtained under the Freedom of Information Act, many at the meeting were concerned about how the damaging revelations about thimerosal would affect the vaccine industry’s bottom line. “We are in a bad position from the standpoint of defending any lawsuits,” said Dr. Robert Brent, a pediatrician at the Alfred I. DuPont Hospital for Children in Delaware. “This will be a resource to our very busy plaintiff attorneys in this country.” Dr. Bob Chen, head of vaccine safety for the CDC, expressed relief that “given the sensitivity of the information, we have been able to keep it out of the hands of, let’s say, less responsible hands.”

Dr. John Clements, vaccines advisor at the World Health Organization, declared that “perhaps this study should not have been done at all.” He added that “the research results have to be handled,” warning that the study “will be taken by others and will be used in other ways beyond the control of this group.”

In fact, the government has proved to be far more adept at handling the damage than at protecting children’s health. The CDC paid the Institute of Medicine to conduct a new study to whitewash the risks of thimerosal, ordering researchers to “rule out” the chemical’s link to autism. It withheld Verstraeten’s findings, even though they had been slated for immediate publication, and told other scientists that his original data had been “lost” and could not be replicated. And to thwart the Freedom of Information Act, it handed its giant database of vaccine records over to a private company, declaring it off-limits to researchers. By the time Verstraeten finally published his study in 2003, he had gone to work for GlaxoSmithKline and reworked his data to bury the link between thimerosal and autism.

Vaccine manufacturers had already begun to phase thimerosal out of injections given to American infants — but they continued to sell off their mercury-based supplies of vaccines until last year. The CDC and FDA gave them a hand, buying up the tainted vaccines for export to developing countries and allowing drug companies to continue using the preservative in some American vaccines — including several pediatric flu shots as well as tetanus boosters routinely given to eleven-year-olds.

ACTIVE? Try Dr. Weil's Vitamin Advisor

The drug companies are also getting help from powerful lawmakers in Washington. Senate Majority Leader Bill Frist, who has received $873,000 in contributions from the pharmaceutical industry, has been working to immunize vaccine makers from liability in 4,200 lawsuits that have been filed by the parents of injured children. On five separate occasions, Frist has tried to seal all of the government’s vaccine-related documents — including the Simpsonwood transcripts — and shield Eli Lilly, the developer of thimerosal, from subpoenas. In 2002, the day after Frist quietly slipped a rider known as the “Eli Lilly Protection Act” into a homeland security bill, the company contributed $10,000 to his campaign and bought 5,000 copies of his book on bioterrorism. The measure was repealed by Congress in 2003 — but earlier this year, Frist slipped another provision into an anti-terrorism bill that would deny compensation to children suffering from vaccine-related brain disorders. “The lawsuits are of such magnitude that they could put vaccine producers out of business and limit our capacity to deal with a biological attack by terrorists,” says Dean Rosen, health policy adviser to Frist.

Even many conservatives are shocked by the government’s effort to cover up the dangers of thimerosal. Rep. Dan Burton, a Republican from Indiana, oversaw a three-year investigation of thimerosal after his grandson was diagnosed with autism. “Thimerosal used as a preservative in vaccines is directly related to the autism epidemic,” his House Government Reform Committee concluded in its final report. “This epidemic in all probability may have been prevented or curtailed had the FDA not been asleep at the switch regarding a lack of safety data regarding injected thimerosal, a known neurotoxin.” The FDA and other public-health agencies failed to act, the committee added, out of “institutional malfeasance for self protection” and “misplaced protectionism of the pharmaceutical industry.”

The story of how government health agencies colluded with Big Pharma to hide the risks of thimerosal from the public is a chilling case study of institutional arrogance, power and greed. I was drawn into the controversy only reluctantly. As an attorney and environmentalist who has spent years working on issues of mercury toxicity, I frequently met mothers of autistic children who were absolutely convinced that their kids had been injured by vaccines. Privately, I was skeptical.

I doubted that autism could be blamed on a single source, and I certainly understood the government’s need to reassure parents that vaccinations are safe; the eradication of deadly childhood diseases depends on it. I tended to agree with skeptics like Rep. Henry Waxman, a Democrat from California, who criticized his colleagues on the House Government Reform Committee for leaping to conclusions about autism and vaccinations. “Why should we scare people about immunization,” Waxman pointed out at one hearing, “until we know the facts?”

It was only after reading the Simpsonwood transcripts, studying the leading scientific research and talking with many of the nation’s pre-eminent authorities on mercury that I became convinced that the link between thimerosal and the epidemic of childhood neurological disorders is real. Five of my own children are members of the Thimerosal Generation — those born between 1989 and 2003 — who received heavy doses of mercury from vaccines. “The elementary grades are overwhelmed with children who have symptoms of neurological or immune-system damage,” Patti White, a school nurse, told the House Government Reform Committee in 1999. “Vaccines are supposed to be making us healthier; however, in twenty-five years of nursing I have never seen so many damaged, sick kids. Something very, very wrong is happening to our children.”

More than 500,000 kids currently suffer from autism, and pediatricians diagnose more than 40,000 new cases every year. The disease was unknown until 1943, when it was identified and diagnosed among eleven children born in the months after thimerosal was first added to baby vaccines in 1931.

Some skeptics dispute that the rise in autism is caused by thimerosal-tainted vaccinations. They argue that the increase is a result of better diagnosis — a theory that seems questionable at best, given that most of the new cases of autism are clustered within a single generation of children. “If the epidemic is truly an artifact of poor diagnosis,” scoffs Dr. Boyd Haley, one of the world’s authorities on mercury toxicity, “then where are all the twenty-year-old autistics?” Other researchers point out that Americans are exposed to a greater cumulative “load” of mercury than ever before, from contaminated fish to dental fillings, and suggest that thimerosal in vaccines may be only part of a much larger problem. It’s a concern that certainly deserves far more attention than it has received — but it overlooks the fact that the mercury concentrations in vaccines dwarf other sources of exposure to our children.

What is most striking is the lengths to which many of the leading detectives have gone to ignore — and cover up — the evidence against thimerosal. From the very beginning, the scientific case against the mercury additive has been overwhelming. The preservative, which is used to stem fungi and bacterial growth in vaccines, contains ethylmercury, a potent neurotoxin. Truckloads of studies have shown that mercury tends to accumulate in the brains of primates and other animals after they are injected with vaccines — and that the developing brains of infants are particularly susceptible. In 1977, a Russian study found that adults exposed to much lower concentrations of ethylmercury than those given to American children still suffered brain damage years later. Russia banned thimerosal from children’s vaccines twenty years ago, and Denmark, Austria, Japan, Great Britain and all the Scandinavian countries have since followed suit.

“You couldn’t even construct a study that shows thimerosal is safe,” says Haley, who heads the chemistry department at the University of Kentucky. “It’s just too darn toxic. If you inject thimerosal into an animal, its brain will sicken. If you apply it to living tissue, the cells die. If you put it in a petri dish, the culture dies. Knowing these things, it would be shocking if one could inject it into an infant without causing damage.”

Internal documents reveal that Eli Lilly, which first developed thimerosal, knew from the start that its product could cause damage — and even death — in both animals and humans. In 1930, the company tested thimerosal by administering it to twenty-two patients with terminal meningitis, all of whom died within weeks of being injected — a fact Lilly didn’t bother to report in its study declaring thimerosal safe. In 1935, researchers at another vaccine manufacturer, Pittman-Moore, warned Lilly that its claims about thimerosal’s safety “did not check with ours.” Half the dogs Pittman injected with thimerosal-based vaccines became sick, leading researchers there to declare the preservative “unsatisfactory as a serum intended for use on dogs.”

In the decades that followed, the evidence against thimerosal continued to mount. During the Second World War, when the Department of Defense used the preservative in vaccines on soldiers, it required Lilly to label it “poison.” In 1967, a study in Applied Microbiology found that thimerosal killed mice when added to injected vaccines. Four years later, Lilly’s own studies discerned that thimerosal was “toxic to tissue cells” in concentrations as low as one part per million — 100 times weaker than the concentration in a typical vaccine. Even so, the company continued to promote thimerosal as “nontoxic” and also incorporated it into topical disinfectants. In 1977, ten babies at a Toronto hospital died when an antiseptic preserved with thimerosal was dabbed onto their umbilical cords.

In 1982, the FDA proposed a ban on over-the-counter products that contained thimerosal, and in 1991 the agency considered banning it from animal vaccines. But tragically, that same year, the CDC recommended that infants be injected with a series of mercury-laced vaccines. Newborns would be vaccinated for hepatitis B within twenty-four hours of birth, and two-month-old infants would be immunized for haemophilus influenzae B and diphtheria-tetanus-pertussis.

The drug industry knew the additional vaccines posed a danger. The same year that the CDC approved the new vaccines, Dr. Maurice Hilleman, one of the fathers of Merck’s vaccine programs, warned the company that six-month-olds who were administered the shots would suffer dangerous exposure to mercury. He recommended that thimerosal be discontinued, “especially when used on infants and children,” noting that the industry knew of nontoxic alternatives. “The best way to go,” he added, “is to switch to dispensing the actual vaccines without adding preservatives.”

For Merck and other drug companies, however, the obstacle was money. Thimerosal enables the pharmaceutical industry to package vaccines in vials that contain multiple doses, which require additional protection because they are more easily contaminated by multiple needle entries. The larger vials cost half as much to produce as smaller, single-dose vials, making it cheaper for international agencies to distribute them to impoverished regions at risk of epidemics. Faced with this “cost consideration,” Merck ignored Hilleman’s warnings, and government officials continued to push more and more thimerosal-based vaccines for children. Before 1989, American preschoolers received eleven vaccinations — for polio, diphtheria-tetanus-pertussis and measles-mumps-rubella. A decade later, thanks to federal recommendations, children were receiving a total of twenty-two immunizations by the time they reached first grade.

As the number of vaccines increased, the rate of autism among children exploded. During the 1990s, 40 million children were injected with thimerosal-based vaccines, receiving unprecedented levels of mercury during a period critical for brain development. Despite the well-documented dangers of thimerosal, it appears that no one bothered to add up the cumulative dose of mercury that children would receive from the mandated vaccines. “What took the FDA so long to do the calculations?” Peter Patriarca, director of viral products for the agency, asked in an e-mail to the CDC in 1999. “Why didn’t CDC and the advisory bodies do these calculations when they rapidly expanded the childhood immunization schedule?”

But by that time, the damage was done. At two months, when the infant brain is still at a critical stage of development, infants routinely received three inoculations that contained a total of 62.5 micrograms of ethylmercury — a level 99 times greater than the EPA’s limit for daily exposure to methylmercury, a related neurotoxin. Although the vaccine industry insists that ethylmercury poses little danger because it breaks down rapidly and is removed by the body, several studies — including one published in April by the National Institutes of Health — suggest that ethylmercury is actually more toxic to developing brains and stays in the brain longer than methylmercury.

Officials responsible for childhood immunizations insist that the additional vaccines were necessary to protect infants from disease and that thimerosal is still essential in developing nations, which, they often claim, cannot afford the single-dose vials that don’t require a preservative. Dr. Paul Offit, one of CDC’s top vaccine advisers, told me, “I think if we really have an influenza pandemic — and certainly we will in the next twenty years, because we always do — there’s no way on God’s earth that we immunize 280 million people with single-dose vials. There has to be multidose vials.”

But while public-health officials may have been well-intentioned, many of those on the CDC advisory committee who backed the additional vaccines had close ties to the industry. Dr. Sam Katz, the committee’s chair, was a paid consultant for most of the major vaccine makers and was part of a team that developed the measles vaccine and brought it to licensure in 1963. Dr. Neal Halsey, another committee member, worked as a researcher for the vaccine companies and received honoraria from Abbott Labs for his research on the hepatitis B vaccine.

Indeed, in the tight circle of scientists who work on vaccines, such conflicts of interest are common. Rep. Burton says that the CDC “routinely allows scientists with blatant conflicts of interest to serve on intellectual advisory committees that make recommendations on new vaccines,” even though they have “interests in the products and companies for which they are supposed to be providing unbiased oversight.” The House Government Reform Committee discovered that four of the eight CDC advisers who approved guidelines for a rotavirus vaccine “had financial ties to the pharmaceutical companies that were developing different versions of the vaccine.”

Offit, who shares a patent on one of the vaccines, acknowledged to me that he “would make money” if his vote eventually leads to a marketable product. But he dismissed my suggestion that a scientist’s direct financial stake in CDC approval might bias his judgment. “It provides no conflict for me,” he insists. “I have simply been informed by the process, not corrupted by it. When I sat around that table, my sole intent was trying to make recommendations that best benefited the children in this country. It’s offensive to say that physicians and public-health people are in the pocket of industry and thus are making decisions that they know are unsafe for children. It’s just not the way it works.”

Other vaccine scientists and regulators gave me similar assurances. Like Offit, they view themselves as enlightened guardians of children’s health, proud of their “partnerships” with pharmaceutical companies, immune to the seductions of personal profit, besieged by irrational activists whose anti-vaccine campaigns are endangering children’s health. They are often resentful of questioning. “Science,” says Offit, “is best left to scientists.”

Still, some government officials were alarmed by the apparent conflicts of interest. In his e-mail to CDC administrators in 1999, Paul Patriarca of the FDA blasted federal regulators for failing to adequately scrutinize the danger posed by the added baby vaccines. “I’m not sure there will be an easy way out of the potential perception that the FDA, CDC and immunization-policy bodies may have been asleep at the switch re: thimerosal until now,” Patriarca wrote. The close ties between regulatory officials and the pharmaceutical industry, he added, “will also raise questions about various advisory bodies regarding aggressive recommendations for use” of thimerosal in child vaccines.

If federal regulators and government scientists failed to grasp the potential risks of thimerosal over the years, no one could claim ignorance after the secret meeting at Simpsonwood. But rather than conduct more studies to test the link to autism and other forms of brain damage, the CDC placed politics over science. The agency turned its database on childhood vaccines — which had been developed largely at taxpayer expense — over to a private agency, America’s Health Insurance Plans, ensuring that it could not be used for additional research. It also instructed the Institute of Medicine, an advisory organization that is part of the National Academy of Sciences, to produce a study debunking the link between thimerosal and brain disorders. The CDC “wants us to declare, well, that these things are pretty safe,” Dr. Marie McCormick, who chaired the IOM’s Immunization Safety Review Committee, told her fellow researchers when they first met in January 2001. “We are not ever going to come down that [autism] is a true side effect” of thimerosal exposure. According to transcripts of the meeting, the committee’s chief staffer, Kathleen Stratton, predicted that the IOM would conclude that the evidence was “inadequate to accept or reject a causal relation” between thimerosal and autism. That, she added, was the result “Walt wants” — a reference to Dr. Walter Orenstein, director of the National Immunization Program for the CDC.

For those who had devoted their lives to promoting vaccination, the revelations about thimerosal threatened to undermine everything they had worked for. “We’ve got a dragon by the tail here,” said Dr. Michael Kaback, another committee member. “The more negative that [our] presentation is, the less likely people are to use vaccination, immunization — and we know what the results of that will be. We are kind of caught in a trap. How we work our way out of the trap, I think is the charge.”

Even in public, federal officials made it clear that their primary goal in studying thimerosal was to dispel doubts about vaccines. “Four current studies are taking place to rule out the proposed link between autism and thimerosal,” Dr. Gordon Douglas, then-director of strategic planning for vaccine research at the National Institutes of Health, assured a Princeton University gathering in May 2001. “In order to undo the harmful effects of research claiming to link the [measles] vaccine to an elevated risk of autism, we need to conduct and publicize additional studies to assure parents of safety.” Douglas formerly served as president of vaccinations for Merck, where he ignored warnings about thimerosal’s risks.

In May of last year, the Institute of Medicine issued its final report. Its conclusion: There is no proven link between autism and thimerosal in vaccines. Rather than reviewing the large body of literature describing the toxicity of thimerosal, the report relied on four disastrously flawed epidemiological studies examining European countries, where children received much smaller doses of thimerosal than American kids. It also cited a new version of the Verstraeten study, published in the journal Pediatrics, that had been reworked to reduce the link between thimerosal and autism. The new study included children too young to have been diagnosed with autism and overlooked others who showed signs of the disease. The IOM declared the case closed and — in a startling position for a scientific body — recommended that no further research be conducted.

The report may have satisfied the CDC, but it convinced no one. Rep. David Weldon, a Republican physician from Florida who serves on the House Government Reform Committee, attacked the Institute of Medicine, saying it relied on a handful of studies that were “fatally flawed” by “poor design” and failed to represent “all the available scientific and medical research.” CDC officials are not interested in an honest search for the truth, Weldon told me, because “an association between vaccines and autism would force them to admit that their policies irreparably damaged thousands of children. Who would want to make that conclusion about themselves?”

Under pressure from Congress and parents, the Institute of Medicine convened another panel to address continuing concerns about the Vaccine Safety Datalink Data Sharing program. In February, the new panel, composed of different scientists, criticized the way the VSD had been used in the Verstraeten study, and urged the CDC to make its vaccine database available to the public.

So far, though, only two scientists have managed to gain access. Dr. Mark Geier, president of the Genetics Center of America, and his son, David, spent a year battling to obtain the medical records from the CDC. Since August 2002, when members of Congress pressured the agency to turn over the data, the Geiers have completed six studies that demonstrate a powerful correlation between thimerosal and neurological damage in children. One study, which compares the cumulative dose of mercury received by children born between 1981 and 1985 with those born between 1990 and 1996, found a “very significant relationship” between autism and vaccines. Another study of educational performance found that kids who received higher doses of thimerosal in vaccines were nearly three times as likely to be diagnosed with autism and more than three times as likely to suffer from speech disorders and mental retardation. Another soon-to-be published study shows that autism rates are in decline following the recent elimination of thimerosal from most vaccines.

As the federal government worked to prevent scientists from studying vaccines, others have stepped in to study the link to autism. In April, reporter Dan Olmsted of UPI undertook one of the more interesting studies himself. Searching for children who had not been exposed to mercury in vaccines — the kind of population that scientists typically use as a “control” in experiments — Olmsted scoured the Amish of Lancaster County, Pennsylvania, who refuse to immunize their infants. Given the national rate of autism, Olmsted calculated that there should be 130 autistics among the Amish. He found only four. One had been exposed to high levels of mercury from a power plant. The other three — including one child adopted from outside the Amish community — had received their vaccines.

At the state level, many officials have also conducted in-depth reviews of thimerosal. While the Institute of Medicine was busy whitewashing the risks, the Iowa legislature was carefully combing through all of the available scientific and biological data. “After three years of review, I became convinced there was sufficient credible research to show a link between mercury and the increased incidences in autism,” says state Sen. Ken Veenstra, a Republican who oversaw the investigation. “The fact that Iowa’s 700 percent increase in autism began in the 1990s, right after more and more vaccines were added to the children’s vaccine schedules, is solid evidence alone.” Last year, Iowa became the first state to ban mercury in vaccines, followed by California. Similar bans are now under consideration in thirty-two other states.

But instead of following suit, the FDA continues to allow manufacturers to include thimerosal in scores of over-the-counter medications as well as steroids and injected collagen. Even more alarming, the government continues to ship vaccines preserved with thimerosal to developing countries — some of which are now experiencing a sudden explosion in autism rates. In China, where the disease was virtually unknown prior to the introduction of thimerosal by U.S. drug manufacturers in 1999, news reports indicate that there are now more than 1.8 million autistics. Although reliable numbers are hard to come by, autistic disorders also appear to be soaring in India, Argentina, Nicaragua and other developing countries that are now using thimerosal-laced vaccines. The World Health Organization continues to insist thimerosal is safe, but it promises to keep the possibility that it is linked to neurological disorders “under review.”

I devoted time to study this issue because I believe that this is a moral crisis that must be addressed. If, as the evidence suggests, our public-health authorities knowingly allowed the pharmaceutical industry to poison an entire generation of American children, their actions arguably constitute one of the biggest scandals in the annals of American medicine. “The CDC is guilty of incompetence and gross negligence,” says Mark Blaxill, vice president of Safe Minds, a nonprofit organization concerned about the role of mercury in medicines. “The damage caused by vaccine exposure is massive. It’s bigger than asbestos, bigger than tobacco, bigger than anything you’ve ever seen.”

It’s hard to calculate the damage to our country — and to the international efforts to eradicate epidemic diseases — if Third World nations come to believe that America’s most heralded foreign-aid initiative is poisoning their children. It’s not difficult to predict how this scenario will be interpreted by America’s enemies abroad. The scientists and researchers — many of them sincere, even idealistic — who are participating in efforts to hide the science on thimerosal claim that they are trying to advance the lofty goal of protecting children in developing nations from disease pandemics. They are badly misguided. Their failure to come clean on thimerosal will come back horribly to haunt our country and the world’s poorest populations.

NOTE: This story has been updated to correct several inaccuracies in the original, published version. As originally reported, American preschoolers received only three vaccinations before 1989, but the article failed to note that they were innoculated a total of eleven times with those vaccines, including boosters. The article also misstated the level of ethylmercury received by infants injected with all their shots by the age of six months. It was 187 micrograms – an amount forty percent, not 187 times, greater than the EPA’s limit for daily exposure to methylmercury. Finally, because of an editing error, the article misstated the contents of the rotavirus vaccine approved by the CDC. It did not contain thimerosal. Salon and Rolling Stone regret the errors.

An earlier version of this story stated that the Institute of Medicine convened a second panel to review the work of the Immunization Safety Review Committee that had found no evidence of a link between thimerosal and autism. In fact, the IOM convened the second panel to address continuing concerns about the Vaccine Safety Datalink Data Sharing program, including those raised by critics of the IOM’s earlier work. But the panel was not charged with reviewing the committee’s findings. The story also inadvertently omitted a word and transposed two sentences in a quote by Dr. John Clements, and incorrectly stated that Dr. Sam Katz held a patent with Merck on the measles vaccine. In fact, Dr. Katz was part of a team that developed the vaccine and brought it to licensure, but he never held the patent. Salon and Rolling Stone regret the errors.

CLARIFICATION: After publication of this story, Salon and Rolling Stone corrected an error that misstated the level of ethylmercury received by infants injected with all their shots by the age of six months. It was 187 micrograms ? an amount forty percent, not 187 times, greater than the EPA’s limit for daily exposure to methylmercury. At the time of the correction, we were aware that the comparison itself was flawed, but as journalists we considered it more appropriate to state the correct figure rather than replace it with another number entirely.

Since that earlier correction, however, it has become clear from responses to the article that the forty-percent number, while accurate, is misleading. It measures the total mercury load an infant received from vaccines during the first six months, calculates the daily average received based on average body weight, and then compares that number to the EPA daily limit. But infants did not receive the vaccines as a ?daily average? ? they received massive doses on a single day, through multiple shots. As the story states, these single-day doses exceeded the EPA limit by as much as 99 times. Based on the misunderstanding, and to avoid further confusion, we have amended the story to eliminate the forty-percent figure.

Correction: The story misattributed a quote to Andy Olson, former legislative counsel to Senator Bill Frist. The comment was made by Dean Rosen, health policy adviser to the senator. Rolling Stone and Salon.com regret the error.

End Quote.

Tags:  Robert F. Kennedy Jr-Rolling Stones Article 2005, Thermisol in vaccines, deadly vaccines, swine flu vaccine, vaccine hoax, politics of profits, news media, vaccine ingredients, autism and vaccines.

Obama’s Swine Emergency is Fraud against Americans

On a slow news day which is Friday afternoon is when the Whitehouse likes to release statements it doesn’t want the media to catch but this was a clear bombshell from President Obama and constitutes fraud.

Piggy Obama Fraudulent Emergency Statement
Piggy Obama Fraudulent Emergency Statement

On Friday October 23 Obama released a statement that the world has come crashing to an end with a flu bug hoax.  The drug company backed Obama administration is following the footsteps of George Bush and is becoming less credible as a President.  Change has not happened and we can’t believe him anymore.

What President Obama has done with this declaration is put us one step closer to mandating vaccines by the Emergency Preparedness Act which can be used to force people to be vaccinated. Obama’s declaration of an emergency allows vaccinations outside of doctors’ offices, hospitals and medical clinics and has created panic again. As doctor Mercola points out we have entered the “Twight Zone” of a government control medical system and Obama has just boosted health care costs from the damage this vaccine will cause to Americans.

Swine Flu Vaccine-Damages Children's Immune System Permanently - Is it worth the Risk?
Swine Flu Vaccine-Damages Children's Immune System Permanently - Is it worth the Risk?

One has to know that the Obama girls and Michelle Obama will not take this vaccine for a reason firstly Michelle Obama does follow a vegetarian healthy diet and anyone who follows this regiment will not jeopardize their children or families health.  We doubt Michelle Obama will vaccinate her mother or allow that to happen anytime in the future.  If the Obama family does do a “photo op” to take this vaccine -they use a trick where the vaccine is really really in the needle its usually a safe saline or salt water solution.  The bag of tricks to prove this vaccine is safe just boggles the mind and to what lengths corporations will go to for profits.

The media is still continuing on its paid commercial distortions of the swine flu during air time to promote this hyperactive, false and misleading information which is actually a program paid for by the drug company revenues they receive for ads on their networks. These are the major networks such as NBC, CNN, CBS and ABC that get millions of dollars in revenue and they remain loyal to their advertisers. We also know that the “news on swine flu” is distorted to instill fear and the networks are being manipulated for and by the drug corporations.

The Swine Flu Hoax is Upon the American Public-Fake  Emergency
The Swine Flu Hoax is Upon the American Public-Fake Emergency

It is evident that President Obama is following the likes of George Bush in bending over for the drug company’s campaign contributions but his policies are a disaster for Americans. President Obama is in the pocket of the major drug corporations-curses foiled Americans have been fooled again.

TAGS: Obama Swine Emergency is Fraud, Obama Fraud Swine Flu Pandemic, Obama bends over for drug company profits, drug company profits, swine flu vaccine, H1N1 vaccine fraud pandemic, H1N1 ingredients, politics, news media, CNN news, network news for corporate profits, change you can’t believe in Obama, President Obama emergency.

AP Survey-75 % Fear Swine Flu Vaccine Side Effects

The Associated Press recently conducted a survey amongst persons they questioned about the H1N1 Vaccine and the results are not surprising as many fear the side effects of the vaccine.  The vaccine is only monitored for side effects for 21 days after that -you are on your own for any damages from taking the Swine Flu vaccine.

The side effects of this Swine Flu Vaccine are unknown and since they are left up to chance they present a very risky and dangerous substance in to the human body.  Never in history has any drug company conducted tests on whether their vaccines cause cancer. All the while they maintain secrets about the carcinogens that are contained in the products and will not advertise the ingredients in their literature unless they were made to by law.

Only once in history has such a massive campaign to experiment  with  pregnant mothers which proved to be disastrous and caused birth defects. This was in 1960’s  and the experimental drug known as Thalidomide caused birth defects in babies that were  born with no arms, hands or feet.  Now it is happening again with the government allowing the  targeting of pregnant mothers -with no proof that it will not harm the fetus.  Of those surveyed a greater percentage of mothers reject the swine flu vaccine and will not give it to their children or themselves.

The Facts about  Drug Company Products

Tamiflu is brand name of a drug in pill form that will compromise the body, so the person is more susceptible to the  H1Ni  virus and it will actually weaken your immune system.  Recent researched scientific studies dispute its value and indicate it is not effective in preventing flu viruses.  In fact with the over 300 types of flu viruses in the world today Tamiflu does not work on any of the bugs so it is totally worthless.

The N1H1 Swine Virus Vaccine- is made by the Baxter Drug Company who applied for the patents one year before the Swine Flu outbreak of 2009. Baxter applied for the patents in 2008 and at some point documents are dated 2007 even earlier.

Any and all regular flu seasonal flu shots contain mercury and/ or  aluminum as a preservative to increase shelf life. One of the problems Baxter did not count on in its haste to throw this vaccine onto the unsuspecting market is storage temperatures of the H1N1 vaccine.  If the vaccine vials are not stored properly at the right temperature they are rendered worthless which happened in a school storage facility in Pennsylvania.  Also batches of over 270,000 where returned from Canada because of high incidents of allergic reaction, which must have been a real bad batch.

Baxter was also chosen under the orders of the Whole Health Organization that prematurely declared this swine Flu a pandemic, before it was widespread earlier this year in March from its origin in Mexico on a pig farm.  The pig farm is still in business happily making more pork products for Americans and was not investigated further. T he pig farm was never closed down for inspection and never investigated again.  The pork was not inspected, tested for contamination or the swine virus while in Russia they destroyed most of their pigs in case of swine contamination with the virus.

You have to ask yourself why a World Health Organization has the right to order a drug maker to make a vaccine, and allow it to be sold untested? You have to ask yourself why the WHO organization is so involved with drug making at all. Never in the past would the WHO presume to be the authority on drugs and what works but they relied on faulty information from the Baxter Drug Company.

Incidentally since the Baxter Drug Company applied for the Patent on all N1H1 Vaccines in 2008,  this is recorded in the U.S. Patent Office and is a matter of public record makes this company highly suspicious of  conspiring to initiate a planned pandemic.

Any vaccine created in the last 10 years or more contains mercury or thermisol which causes brain damage and autism. If you care about your child you do not want mercury anywhere near your children especially in the bloodstream.

 

The survey by the Associated Press indicates 50 percent of the population does not want the swine flu vaccine and or will not take it for themselves  or their unborn babies. Doctors and health care workers are among those that are refusing this vaccine on the same grounds.

The numbers are quite higher than 50 percent it is more like 75 percent are against this swine flu vaccine since the N1H1 Vaccine ingredients are just not safe or proven to work. How can they work when they destroy your immune system and cause permanent harm to humans. Those that have the most to risk are pregnant mothers  and the life of their unborn baby that is in grave danger of damage.

Pregnant mothers will be give their baby a large dose of mercury before it takes a breathe. This fetus will also be given 3 live viruses, Squalene, A59 (chemical adjuvant), aluminum and this comprises the baby’s natural immune system that it will need all throughout its lifetime.  Squalene has never been approved before 2009 in the United States or Europe because it has dangerous side effects.

A MAJOR DOSE OF TOXINS IN THE N1H1 SWINE FLU VACCINE

In the AP Poll more than 72 percent of those polled say they are very concerned with the Side Effects of the Swine Flu vaccine which has not been tested for the long term. They are concerned because they are taking a gamble with their lives, and the potential for damage is greater than the benefits of the vaccine. Again since the ingredients are so harmful it is not a surprise that many parents will not allow their children or parents to receive this swine flu vaccine.

Toxins in Swine Flu Vaccines are Untested and UnHealthy
Toxins in Swine Flu Vaccines are Untested and UnHealthy

All these facts present a tidy little picture of drug company influence over government and health authorities and they have succeeded in conning both with lies and medically unsafe vaccines. This is the second time a drug company has released a virus in a foreign country only to come to the rescue with an unproven vaccine that will kill off the old, the pregnant and the unborn.

SQUALENE- THE SWINE FLU VACCINE DIRTY LITTLE SECRET

The fetus will not be protected as these chemicals will be in the mothers’ blood stream. The fetus will be damaged permanently in brain, blood and its tissues with the toxins spreading throughout its body. The mother’s body will offer no protection from the toxins as the mother won’t be able to detoxify these chemicals before it hits her baby.  What on earth are we doing to our bodies which making massive profits for the pharmaceuticals.  This vaccine is not for safety or health it damages the brains of  our babies and children and is not proven to even work against the swine virus.

The more that the government agency NIH, FDA or CDC  and medical so called experts working for pharmaceuticals push and advertise this dangerous vaccine the more suspicious people are becoming and more aware of its impending damage to their health.

Source is  Associated Press: October 8, 2009

TAGS: AP Poll, AP Survey on Swine Vaccine, Ingredients of Swine Flu Vaccine, Swine Flu vaccine, N1H1 Vaccine, H1N1 vaccine, CDC and Swine Flu Vaccine, Squalene in Swine Flu vaccine,  A major dose of toxins Swine Flu Vaccine, Swine Flu Dangers, Pharmaceuticals and swine Flu vaccine, Baxter Drugs applies for patent 1 year before Swine Flu outbreak, Swine Flu Outbreak a sham, CDC corruption.

Babies Condemned to Vaccine Damage which is Irreversible
Babies Condemned to Vaccine Damage which is Irreversible

Mercury is in vaccines although drug company’s deny it,  is an ingredient inspite of the fact that they have long term patents and make millions in profits for using the poisonous chemical injected into humans and babies.  Drug company’s make money from mercury or thermisol as it is called and  not from a safer salt solution. The drug makers  could use saline solution or salt but they would not make as much money.  You can look up patents on Thermisol all day long at the US Patent Office which is open to the public -mercury is big business in the drug trade.  Also you will note that the US FDA warns about mercury in fish like canned tuna, but allow mercury into your bloodstream in numerous vaccines.

Pharmaceutical company’s like to keep their costs down and make more money per vaccine,   so they use mercury which is unsafe and untested for cancer.  The drug company’s cannot make a profit from a salt solution which would work but they are putting profits before your safety and health.

You will have to determine that taking this vaccine is of any value to you after doing your own research.   People will also have to  consider the fact that they are putting drug company profits -before their own health.

Permanent Damage from Swine N1H1 Vaccine

The Truth about Swine Flu Vaccine Ingredients: watch the video and have a laugh. If you really want to take this shot after watching this-good luck.

The Drug Company Baxter -applied for the H1N1 Vaccine Patents- 1 year before the outbreak of swine flu.   This vaccine is full of bacteria, and two ingredients which hyper activate and trick your immune system in an unnatural way.  You do not need to hyper activate the human immune system and this damage could be permanent.  This means your immune system will not work properly due to the squalene in the vaccine.

For further Information : Get the Truth on Vaccines from Researchers who are not Paid for By Drug Companies.

Remember your giving up your body’s only defense mechanism and permanently damaging it -for a free swine flu shot that also contains : aborted fetus cell lines.  Think about it.

TAGS:  Truth about Swine Flu Vaccine Ingredients, Swine Flu vaccine, vaccine ingredients, N1H1 Swine Vaccine, permanent damage from swine flu vaccine, vaccine damage, vaccine damages human immune system.

FDA Injects US Soldiers with Untested Swine Vaccine

FDA NEWS RELEASE ***

For Immediate Release: Aug. 25, 2009

Media Inquiries: Peper Long, 301-796-4671, [email protected]
Consumer Inquiries:
888-INFO-FDA

FDA Authorizes Emergency Use of H1N1 Test for U.S. Troops Serving Overseas

The U.S. Food and Drug Administration today announced it has issued an Emergency Use Authorization (EUA) that allows a 2009 H1N1 influenza virus test to be used to detect the virus in troops serving overseas.

The EUA allows the U.S. Department of Defense to distribute the H1N1 test to its qualified laboratories that have the required equipment and trained personnel to perform the test and interpret its results. An EUA authorizes the use of unapproved medical products or unapproved uses of approved medical products during a declared public health emergency.

“The FDA worked quickly with the Defense Department to authorize the use of this test to better protect our troops. The test will aid in more rapid diagnosis of 2009 H1N1 influenza infections so that deployed troops can quickly begin appropriate medical treatment,” said Commissioner of Food and Drugs Margaret A. Hamburg, M.D.

The U.S. Centers for Disease Control and Prevention (CDC) developed the test, which is called the CDC swH1N1 (swine) Influenza Real-Time RT-PCR.

Under this new EUA, the Defense Department’s Joint Biological Agent Identification and Diagnostic System (JBAIDS) can be used to run the CDC’s test. The FDA previously cleared other assays for use on the JBAIDS beginning in 2005.

For more information:

Department of Defense Aug. 24, 2009, News Release on EUA

FDA Authorizes Emergency use of Influenza Medicines, Diagnostic Test in Response to Swine Flu Outbreak in Humans, April 27, 2009

FDA’s Web site on 2009 H1N1 Influenza Virus

What the FDA is not taking into consideration is the massive damage done to the immune systems of our soldiers and the 21 day tests are not sufficient to approve this big pharma vaccine. The only benefit to this vaccine is to the profits of the drug companies who manufactured it with aborted fetus tissues, 3 strains of bacteria, mercury, aluminum and 2 unapproved ingredients.  The damage done to the soldiers and people taking this vaccine is enormously dangerous and this is an unprecedented example of the FDA’s corrupt alliances with drug companies.

TAGS: FDA uses U.S. soldiers as guinea pigs, FDA speeds up Swine Flu Mistake, Swine Flu untested vaccine,  Swine Flu Hype, Swine Flu media hype, FDA hysterical vaccine tests on soldiers, U.S. Soldiers Guinea Pigs-swine flu vaccine, Swine Flu Vaccine, FDA disregards long term effects of swine flu vaccine, H1N1 Untested vaccine.

Swine Flu Cartoon-Politicol-News-Humor

This goes out to Georgie C- who sent us this cartoon on Swine Flu and Fema.
Thanks Georgie!!

FEMA Swine Flu Shots-- to Kill Off the Rest of the Population
FEMA Swine Flu Shots-- to Kill Off the Rest of the Population

Politicol News- Swine Cartoon

It maybe a funny cartoon but the swine flu came from 3 different viruses which have mingled together to create this virus in a pig in Mexico who got it from a boy from Texas, who got it from thin air. No one cares to investigate the release of this hoax virus on the people of America using Mexico as a method of releasing deadly viruses.

The investigation on where the swine flu originated and how on earth -in the natural world could these viruses have “been mixed together”? This puzzle is not going away- the boy has disappeared, the pig farm goes unregulated and they did not followup investigating nor have they changed the way they farm these huge industrialized farms to put profit above animal and human health.

The US government is more concentrated through the hype the WHO and drug companies have managed to garner in the media, on the untested and bacteria filled vaccines -they are planning to pump us – up with in the Fall. This H1N1 vaccine will be doled out to everyone including new born babies- and older people like it was candy. The WHO organization raised the bells of alarms with all the drama this spring of 2009 -while they increased the Pandemic Numbers – we all knew where they were headed.

Its a farce. More people die of the common cold than this pork-filled artificially created flu bug, and it is nothing more than that. Unfortunately the Obama administration and the FDA robots -bought it all – hook, line and sinker because the FDA is run by drug company directives.
One Billion Dollars worth of the N1 H1 vaccine- will be coming soon -to your arm….filled with all the carcinogens they could throw in the mix in the syringe. It is not tested, it will be hastily approved and it will make people sick and some will die from the vaccine.
Buyer be ware -of your next Flu Vaccine -then again -the University of Iowa geniuses have thought of another way to trick you and lie to the public -by putting the vaccine in your very food. Yes -the scientific researchers figured you may not take the flu vaccine voluntarily so they are putting it in their GMO corn out there in Iowa. Well GMO corn is not identified as GMO corn either, so you really will not even know what you are getting but -watch out for : H1N1-GMO Corn-From-Iowa. Doesn’t really sound like food anymore does it, thanks to Monsanto who have teamed up the the University of Iowa and the profit hungry drug companies.

Oink ….Oink…..

TAGS : Swine Flu Hullabaloo, Swine Flu, H1N1 Flu hype, Monsanto, GMO, Pig Flu, Pig Swine flu, GMO corn, University of Iowa, Fall N1 H1 Flu Vaccine,  Swine Flu Vaccine, FDA, FDA robots, drug companies, pig farms.

Swine Flu Vaccine Dangerous Mix of Bacteria from Diseased Monkeys

Flu Infected Pigs-But Where Did the Get It?
Flu Infected Pigs-But Where Did the Get It?

“WASHINGTON (Reuters) – The seasonal flu vaccine provides virtually no protection against the new H1N1 influenza strain, federal health researchers confirmed on Thursday.

Their study using stored blood samples supports an intriguing theory that people over the age of 60 have some immunity to the new H1N1 strain, perhaps because it resembles an older version of seasonal flu.

The findings are important as U.S. and global health officials grapple with the question of whether to offer a vaccine against the new swine flu virus, which has infected more than 11,000 people globally and killed at least 85. “

Read more at Reuters

Meanwhile the WHO head Mrs. Chan will not be undermined by naysayers and will issues a Pandemic Alert if needed and will not stop with the Swine Flu media fear of a flu bug that has not been investigated.

Studies of the swine flu confirmed that the flu itself is a mixture of several biologically strange mixes of the : Avian Flu, the SARS virus, and the Spanish Flu of 1918. How this mixture came about or was initiated is no one’s guess and the World Health Organizations are not too busy trying to find the answers fast.  This makes life all so much more profitable for drug manufacturers who are making a killing – so to speak on flu vaccines now and in the future.  Vaccines are big money simply because they are mandated vaccines in some states, have infiltrated third world countries and are given to each person or child, and that makes vaccines a very profitable venture.

Untested Swine Flu Vaccine with 3 Strong Virus Ingredients

There are plans to put the new swine flu vaccine in the genetically modified corn in studies underway at the University of Iowa.  See More at: Swine Flu in GMO Corn

TAGS: Swine Flu Vaccine, Swine Flu in GMO Corn, Vaccines, drug companies, WHO, World Health Organization, mandated vaccines, genetically modified corn, H1N1 Swine Flu, H1N1 Pig Flu, pigs infected with flu.

Taking the swine flu shot is similar to taking Drano to get rid of a cold.  These ingredients do not prevent diseases-they cause them to flourish.  When has the FDA ever approve a tested drug or vaccine? Certainly not in the past 30 years so why would this vaccine be safe. If you follow the history of the FDA and who works at the top executive level the trail all leads back to the drug manufacturers and why would you trust their own reports?