(NaturalNews) The FDA has now suddenly granted approval to four different H1N1 vaccines, all on the same day! With virtually no testing, these fast-tracked vaccines are now approved for use on everyone: Infants, children, adults, senior citizens and even expectant mothers. But does everyone really need these vaccines?

According to the CDC, by June of 2009, one million Americans had already been exposed to H1N1 swine flu. Although the CDC hasn't released official infection statistics in recent months, with the rapid spread of the mild virus, it's not unreasonable to suspect that by now, three months later, the number of Americans who have been exposed to H1N1 swine flu has at least doubled to two million.

Yet here's the interesting part: You don't see two million Americans dying from swine flu.

That's because many of those who were infected by swine flu never had any idea they were infected at all. They were so-called "symptomless carriers," because they never experienced a sniffle or other flu-like symptoms. Their immune systems conquered swine flu automatically and effectively, creating antibodies and overcoming the infection by relying on fundamental human physiology.

Even for those who got sick, virtually everyone survived the sickness. After a few days of extra rest in bed (and hopefully some nutritional supplementation), they were able to kick the virus and return to normal life. This is all a normal part of beating any flu.

All these millions of people who were infected by H1N1 anddidn't die have naturally made their own swine flu antibodies. They are now immune to the swine flu, and they now have zero risk of being infected or killed by this H1N1 swine flu in the future.

At the same time, the CDC has no idea how many Americans already have H1N1 antibodies from surviving a swine flu infection. The WHO has no idea of this worldwide figure, either. It is likely in the tens of millions of peoplearound the world.

So here's the relevant question: What happens when you give an H1N1 vaccine to a person who already has H1N1 antibodies?

All of the risk, none of the benefit

The answer is that injecting such a person with an H1N1 vaccine exposes them to all the risks of a vaccine with none of the purported benefits. In other words, such a vaccine cannot help them in any way because they're already immune to H1N1!

The vaccine can only harm them or have no effect.

Given that there is zero reward but some measurable risk for these people taking the vaccine, it only makes sense thatpeople who have existing H1N1 antibodies should never be given an H1N1 vaccine shot.

To determine this, however, each person about to receive a vaccine shot would have to be tested to see if they already have H1N1 influenza antibodies. But to conduct that test for the entire U.S. population would take years to complete. (The CDC testing labs are already overrun and can't handle millions of tests in a timely manner...)

Thus, there is currently no effort to test anyone for H1N1 antibodies before injecting them with the H1N1 vaccine... a vaccine that may have been rendered utterly useless to that person even before the shot!

No medical justification, just FEAR marketing

Millions of people around the world, you see, have already survived H1N1 swine flu. For those individuals, there is absolutely no medical justification for being vaccinated. The only justification for a vaccine is economic -- to sell another vaccine to someone who doesn't need it.

FDA OKs 4 Swine Flu Vax - Virtually Unproven, Untested

FDA NEWS RELEASE

For Immediate Release: Sept. 15, 2009

Media Inquiries: Pat El-Hinnawy, 301-796-4763, patricia.el-hinnawy@fda.hhs.gov; Peper Long, 301-796-4671, mary.long@fda.hhs.gov
Consumer Inquiries: 1-888-INFO-FDA

FDA Approves Vaccines for 2009 H1N1 Influenza Virus
Approval Provides Important Tool to Fight Pandemic

The U.S. Food and Drug Administration announced today that it has approved four vaccines against the 2009 H1N1 influenza virus. The vaccines will be distributed nationally after the initial lots become available, which is expected within the next four weeks.

“Today's approval is good news for our nation's response to the 2009 H1N1 influenza virus,” said Commissioner of Food and Drugs Margaret A. Hamburg, M.D. “This vaccine will help protect individuals from serious illness and death from influenza.”

The vaccines are made by CSL Limited, MedImmune LLC, Novartis Vaccines and Diagnostics Limited, and sanofi pasteur Inc. All four firms manufacture the H1N1 vaccines using the same processes, which have a long record of producing safe seasonal influenza vaccines.

”The H1N1 vaccines approved today undergo the same rigorous FDA manufacturing oversight, product quality testing and lot release procedures that apply to seasonal influenza vaccines,” said Jesse Goodman, M.D., FDA acting chief scientist.

Based on preliminary data from adults participating in multiple clinical studies, the 2009 H1N1 vaccines induce a robust immune response in most healthy adults eight to 10 days after a single dose, as occurs with the seasonal influenza vaccine.

Clinical studies under way will provide additional information about the optimal dose in children. The recommendations for dosing will be updated if indicated by findings from those studies. The findings are expected in the near future.

As with the seasonal influenza vaccines, the 2009 H1N1 vaccines are being produced in formulations that contain thimerosal, a mercury-containing preservative, and in formulations that do not contain thimerosal.

People with severe or life-threatening allergies to chicken eggs, or to any other substance in the vaccine, should not be vaccinated.

In the ongoing clinical studies, the vaccines have been well tolerated. Potential side effects of the H1N1 vaccines are expected to be similar to those of seasonal flu vaccines.

For the injected vaccine, the most common side effect is soreness at the injection site. Other side effects may include mild fever, body aches, and fatigue for a few days after the inoculation. For the nasal spray vaccine, the most common side effects include runny nose or nasal congestion for all ages, sore throats in adults, and -- in children 2 to 6 years old -- fever.

As with any medical product, unexpected or rare serious adverse events may occur. The FDA is working closely with governmental and nongovernmental organizations to enhance the capacity for adverse event monitoring, information sharing and analysis during and after the 2009 H1N1 vaccination program. In the U.S. Department of Health and Human Services, these agencies include the Centers for Disease Control and Prevention.

Vaccines against three seasonal virus strains are already available and should be used (see information on the seasonal flu). However, they do not protect against the 2009 H1N1 virus (see information on H1N1 flu).

Patrick Swayze dead at 57 after chemotherapy for pancreatic cancer by Mike Adams the Health Ranger

Patrick Swayze dead at 57 after chemotherapy for pancreatic cancer by Mike Adams the Health Ranger

German Man Injured By Swine Flu Vax Trial Talks

A participant in the german H1N1 vaccine trials reports serious adverse reactions, including coughing up blood, but the lead researcher blows it off. Yet another story of problems in vaccine safety studies that are ignored.

Why test a vaccine exactly, if you already have decided what the outcomes can or cannot be? Apparently Heir Doctor will only accept 'redness and swelling at the injection site' as a side effect.

A swine flu vaccine test subject from Munich complains about horror side-effects – researchers deny allegations

The article does not say which version of the vaccine he got. Wish there was more information on this case.

21.08.09|Munich iFacebook

Translation into English by Erwin Alber

Munich – A harmless prick – and thereby possibly save thousands of people. This is what several hundreds of volunteers thought, who each collected a payment of 250 Euro for their participation in the study of the swine flu vaccine trial at the Ludwig-Maximilians-University.

One of them has now quit the trial: The Diploma-businessman Axel Sch. (40). He claims : "The vaccination has made me ill! – the test is irresponsible.” He says that within a few hours after the vaccination, on August 10, he had sweat on his forehead. "I felt totally beat. On the third day, my kidneys and head were aching and I got a fever. I then had a coughing fit - and the wash basin was suddenly red - it was blood!“

LMU-medical researcher Frank von Sonnenburg, who is in charge of the country-wide study, doesn’t consider these accounts credible. He says that such side-effects cannot be related to the vaccine. He does not deny that, as with other flu-vaccinations, flu-like symptoms may occur as a reaction to the vaccination. "Additionally, there may be light pain, redness or swelling at the injection site."

"Obviously many of the test subjects would have side-effects. We do such a study precisely because we want to find out any possible side-effects. If flu cases were to become more severe and we had not done any tests, – there would be a big outcry by everyone."

Was the vaccine admitted too quickly to the study? The fact is that in this composition, the vaccine has not yet been applied to humans. The Federal Health Minister Ulla Schmidt explained on Wednesday that she had felt put under pressure by the pharmaceutical industry from the beginning. Criticism is being voiced with increasing frequency. The Paul-Ehrlich-Institute points out that side-effects to this vaccine are to be more expected than in connection with a normal flu-vaccine. The Paediatric Association points to a possibly increased number of unknown side-effects.

British researchers even warn about a neurological disorder known as the Guillain-Barré-Syndrome. They point to a vaccination campaign with a similar swine flu vaccine carried out in the USA in 1976, which resulted in the deaths of 25 people.

Probably because of this, the USA only test vaccines without so-called adjuvants. These lead to greater side-effects, explains study leader Frank von Sonnenburg. "The adjuvants produce more anti-bodies, which is why the body’s defensive reaction is also greater." Kidney pains and bloody cough of the kind Axel Sch. Experienced were however not to be expected, even with this adjuvant. "We conduct a clean study."

Axel Sch. however insists that his complaints were a result of the vaccination. "Surely it is no coincidence that they occurred directly after the vaccination." He criticizes the university, saying that he was not properly informed prior to the study. He said that for three days he was flat on his back during this heat. "When I phoned the LMU, they simply asked me the question needed to fill in their form and told me to see my doctor." He now wants the medical costs and loss of earnings compensated by the medical insurance covering the trial.

Axel Sch. has participated in medical trials even when he was a student. He had also had good experiences with an LMU flu-vaccine study. "This is the reason why I immediately consented when they asked me if I would test the new vaccine."

Now his trust in research is gone, he is quitting the vaccine trial. In October he will fly to Latin America for professional reasons. He had looked forward to traveling unconcerned – by then he would have received the second of three vaccinations. "I’m not fearful just the same – I don’t belong to an at risk group. Also, the swine flu can’t possibly be as bad as the side-effects of the vaccine."

A man in India is turning heads - and stomachs - snacking on spider - Paul Chapman reports

Adjuvants designed to make the vaccine "work."

The WHO and US Government CDC are escalating a public psychological conditioning to create hysteria and panic among an uninformed public about an alleged "virus" H1N1 Influenza A, aka Swine Flu, whose alleged effects to date appear comparable with a common cold. Before people line up in the streets demanding their vaccinations for their children and themselves, it would be wise to remember, to paraphrase a 1992 campaign statement of Bill Clinton to George H.W. Bush: "It's the vaccination, Stupid!"

By countless scientific accounts, far more dangerous to human health than any reported incidences of Swine Flu are the dangers of severe health issues including paralysis, brain damage and even death arising from what is added to vaccines by virtually every major vaccine maker. Almost without exception, all commercial vaccines today contain various substances known as adjuvants designed to make the vaccine "work." These adjuvants are the source of horrendous and sometimes deadly damage.

It has been speculated for some time that there might be a link in the alarming rise in cases of autism among tiny infants and children and massive multiple vaccinations today given routinely to infants and children from the first hours of birth. There is clear and shocking evidence of the link between the two. If you do not have a strong constitution, you are advised not to read further.

A new study shows a direct link between standard childhood vaccination series, MMR, and autism-like symptoms in monkeys. The principal scientist involved in the study, Dr. Laura Hewitson of the University of Pittsburgh, presented the alarming conclusions as an abstract pending publication at the International Meeting for Autism Research. It has been presented at scientific conferences in both London and Seattle, USA.

The study compared vaccinated macaque monkeys with non-vaccinated macaques. No major flaws in the study have been revealed by any attending scientist. The vaccines included the popular MMR series. The study found a marked increase in "gastrointestinal tissue gene expression" and "inflammation issues" with those monkeys which received vaccinations. They are a common symptom of children with regressive autism.

The study also found marked behavior changes and development differences in those monkeys given the vaccines versus those who were not. "Compared with unexposed animals, significant neuro-developmental deficits were evident for exposed animals in survival reflexes, tests of color discrimination and reversal, and learning sets," the study`s authors reported. "Differences in behaviors were observed between exposed and unexposed animals and within the exposed group before and after MMR vaccination."

US Government-mandated research approved by Congress was to begin this year, but the funds were rescinded in early January. Claiming "conflict of interest" because of ongoing court cases, the Centers for Disease Control and Prevention (CDC), a long-time supporter of infant vaccinations, withdrew the research plans.

The most shocking of all is the recent and now common medical practice, reinforced by an aggressive pharmaceutical industry, of giving multiple vaccines, often virtually within hours of birth, to infants despite the fact that no study including all of the vaccine series commonly given to children in the US and UK, about 30 in all, has been conducted until now. The practice of newborn multiple vaccinations has become widespread in Germany and other EU countries over the past decade. Significantly there have surfaced reports of dramatically increased instances of autism in newborn and infants in various German hospitals over the past decade, precisely the period multiple vaccinations of newborn and infants has become routine.

US Government coverup

Tragically, the US Government agency theoretically entrusted with guarding public health, the Food and Drug Administration (FDA), as with the case of health dangers of GMO foods, as well with the dramatic evidence of the link between autism and adjuvants used in typical vaccines, is accepting the argument of big and politically powerful Pharmaceutical companies.

The Food and Drug Administration considers vaccines safe but, just as with GMO, they have done no studies into the effects of multiple vaccinations as given in the common childhood series which started in the 1990s in the USA and spread to the UK and now across the EU.

According to Robert F. Kennedy, Jr., son of the late Attorney General and an attorney active in campaigning to expose mercury (Thimerosal) and other toxicity dangers in vaccines, recently stated, "as autism is a behavioral affliction rather than a precisely defined biological injury -- epidemiological studies are critical to establishing its causation. But the greatest source of epidemiological data is the Vaccine Safety Datalink (VSD) -- the government maintained medical records of hundreds of thousands of vaccinated children -- which Health and Human Services Department has gone to great lengths to keep out of the hands of plaintiffs' attorneys and independent scientists. The raw data collected in the VSD would undoubtedly provide the epidemiological evidence needed to understand the relationship between vaccines and autism. The absence of such studies makes it easy for judges to say to plaintiffs they have not met their burden of proving causation."

Autism was virtually unknown in the United States until 1943 when it was diagnosed and identified eleven months after Thimerosal, a mercury-based vaccine "adjuvant" was first added to baby vaccines along with various aluminium compounds in the United States. Thimerosal is often used to stem fungi and bacterial growth in vaccines despite massive evidence of its severe effects as a potent neurotoxin. Following independent studies, Russia, Japan, Austria, Denmark, Sweden and Britain have banned Thimersol from childrens' vaccines. Germany to date has no such ban.

The toxin was developed in 1930 by Eli Lilly. Tragically in 1991, despite overwhelming evidence to the contrary the US Government's Center for Disease Control (CDC), the same agency fuelling the current hysteria over the non-proven H1N1 Swine Flu virus danger, recommended that infants be injected with a series of mercury-containing vaccines in some cases within 24 hours of birth for Hepatitis B and two months for diphtheria-tetanus-pertussis.

Before 1989 US pre-school children received eleven vaccinations-polio, diphtheria-tetanus-pertussis, measles-mumps-rubella (MMR).

By 1999, because of the various CDC recommendations, the number of vaccinations was twenty two before first grade of school. Parallel with this explosive rise in vaccinations of the very young in the United States, according to Kennedy, the rate of autism among children. The state of Iowa reported a 700% increase in autism in children beginning in the 1990's and along with California has banned mercury in vaccines. Despite evidence, however the US FDA continues to allow drug makers to include Thimerosal in numerous over-the-counter non-prescription medications as well as steroids and injected collagen. The US Government ships vaccines preserved with Thimerosal to numerous developing countries as well, where some are reporting sudden explosion of autism rates as well. In China, where autism was unknown before introduction of Thimerosal by US drug makers in 1999, press reports indicate there are almost two million autistic children.

Instances of autism in the US exploded as some 40 million children were injected during the 1990's with Thimersol-based vaccines, giving them unprecedented accumulations of mercury poison. The level of ethylmercury in a vaccine routinely given then to children of two months age was 99 times greater than the US Government's daily limit for exposure. As with the current WHO pandemic declaration around H1N1 Swine Flu, the CDC Vaccine Advisory Committee is filled with scientists with close ties to the pharmaceutical industry. Dr. Sam Katz, chairman of the committee was a paid consultant to most companies producing the vaccines he "recommended."

The aluminium danger remains

While vaccines available in the US today exist with no Thimerosal (50% mercury), virtually all vaccines still contain aluminum, which has been linked to impaired neurological development in children. Aluminum has not replaced thimerosal as a vaccine preservative; it has always been used in vaccines.

In the recent past, most US children got exposed to both thimerosal and aluminum simultaneously with the hepatitis B, Hib, DTaP (diphtheria, tetanus and pertussis) and pneumococcal vaccines. Combining mercury with aluminum increases the likelihood that the mercury will damage human tissue.

According to a recent report by Michael Wagnitz, an American chemist, "Currently eight childhood vaccines that contain aluminum ranging from 125 to 850 micrograms (mcg). These vaccines are administered 17 times in the first 18 months of life, an almost six-fold increase compared to the vaccine schedule of the 1980s."

Wagnitz adds, "According to the American Society for Parenteral and Enteral Nutrition, based on IV feeding solutions, a child should not exceed a maximum daily dose of 5 mcg of aluminum per kilogram of weight per day. That means if a child weighs 11 pounds, the child should not exceed 25 mcg in a day. This level was determined to be the maximum safety limit based on a study published in the New England Journal of Medicine titled "Aluminum Neurotoxicity in Preterm Infants Receiving Intravenous Feeding Solutions."

The hepatitis B vaccine, administered at birth, contains 250 mcg.

In a 1996 policy statement, "Aluminum Toxicity in Infants and Children," the American Academy of Pediatrics states, "Aluminum can cause neurological harm. People with kidney disease who build up bloodstream levels of aluminum greater than 100 mcg per liter are at risk of toxicity. The toxic threshold of aluminum in the bloodstream may be lower than 100 mcg per liter." What level of aluminium toxicity is contained in vaccines routinely given German, French and other children n the EU is not known. It might be time for a public demand for such information to be disclosed, and before governments launch mass vaccination campaigns for untested vaccines against a non-proven H1N1 Swine Flu threat.

Sep 2009

F. William Engdahl

F. William Engdahl is the author of Seeds of Destruction: The Hidden Agenda of Genetic Manipulation.

He also authored 'A Century of War: Anglo-American Oil Politics,'

Pluto Press Ltd.

Vaccine May Be More Dangerous Than Swine Flu

Vaccine May Be More Dangerous
Than Swine Flu
By Dr. Russell Blaylock MD
9-10-9

What the good doctor say is true. Don't be taken for a ride. So what if you catch this mild 3-4 days flu. It is even weaker than seasonal flu. We need to counter all the MSM propaganda BS that we should look to vaccines to save us! Dr Blaylock writes : An outbreak of swine flu occurred in Mexico this spring that eventually affected 4,910 Mexican citizens and resulted in 85 deaths. By the time it spread to the United States, the virus caused only mild cases of flu-like illness. Thanks to air travel and the failure of public health officials to control travel from Mexico, the virus spread worldwide. Despite predictions of massive numbers of deaths and the arrival of doomsday, the virus has remained a relatively mild disease, something we know happens each year with flu epidemics. Worldwide, there have only been 311 deaths out of 70,893 cases of swine flu. In the United States, 27,717 cases have resulted in 127 deaths. Every death is a tragedy, but such a low death rate should not be the basis of a draconian government policy. It is helpful to recall that the Centers for Disease Control with the collusion of the media, constantly tell us that 36,000 people die from the flu each year, a figure that has been shown to be a lie. In this case, we are talking about 300 plus deaths for the entire world. This virus continues to be an enigma for virologists. In the April 30, 2009 issue of Nature, a virologist was quoted as saying,"Where the hell it got all these genes from we don't know." Extensive analysis of the virus found that it contained the original 1918 H1N1 flu virus, the avian flu virus (bird flu), and two new H3N2 virus genes from Eurasia. Debate continues over the possibility that swine flu is a genetically engineered virus. Naturally, vaccine manufacturers have been in a competitive battle to produce the first vaccine. The main contenders have been Baxter Pharmaceuticals and Novartis Pharmaceuticals, the latter of which recently acquired the scandal-ridden Chiron vaccine company. Both of these companies have had agreements with the World Health Organization to produce a pandemic vaccine. The Baxter vaccine, called Celvapan, has had fast track approval. It uses a new vero cell technology, which utilizes cultured cells from the African green monkey. This same animal tissue transmits a number of vaccine-contaminating viruses, including the HIV virus. The Baxter company has been associated with two deadly scandals. The first event occurred in 2006 when hemophiliac components were contaminated with HIV virus and injected in tens of thousands of people, including thousands of children. Baxter continued to release the HIV contaminated vaccine even after the contamination was known. The second event occurred recently when it was discovered that Baxter had released a seasonal flu vaccine containing the bird flu virus, which would have produced a real world pandemic, to 18 countries. Fortunately, astute lab workers in the Czech Republic discovered the deadly combination and blew the whistle before a worldwide disaster was unleashed. Despite these two deadly events, WHO maintains an agreement with Baxter Pharmaceuticals to produce the world's pandemic vaccine. Novartis, the second contender, also has an agreement with WHO for a pandemic vaccine. Novartis appears to have won the contract, since their vaccine is near completion. What is terrifying is that these pandemic vaccines contain ingredients, called immune adjuvants that a number of studies have shown to cause devastating autoimmune disorders, including rheumatoid arthritis, multiple sclerosis and lupus. Animal studies using this adjuvant have found them to be deadly. A study using 14 guinea pigs found that when they were injected with the special adjuvant, only one animal survived. A repeat of the study found the same deadly outcome. So, what is this deadly ingredient? It is called squalene, a type of oil. The Chiron company, maker of the deadly anthrax vaccine, makes an adjuvant called MF-59 which contains two main ingredients of concern-squalene and gp120. A number of studies have shown that squalene can trigger all of the above-mentioned autoimmune diseases when injected. The MF-59 adjuvant has been used in several vaccines. These vaccines, including tetanus and diphtheria, are the same vaccines frequently associated with adverse reactions. I reviewed a number of studies on this adjuvant and found something quite interesting. Several studies done on human test subjects found MF-59 to be a very safe immune adjuvant. But when I checked to see who did these studies, I found-to no surprise-that they were done by the Novartis Pharmaceutical Company and Chiron Pharmaceutical Company, which have merged. They were all published in "prestigious" medical journals. Also, to no surprise, a great number of studies done by independent laboratories and research institutions all found a strong link between MF-59 and autoimmune diseases. Squalene in vaccines has been strongly linked to the Gulf War Syndrome. On August 1991, Anthony Principi, Secretary of Veterans Affairs admitted that soldiers vaccinated with the anthrax vaccine from 1990 to 1991 had an increased risk of 200 percent in developing the deadly disease amyotrophic lateral sclerosis (ALS), also called Lou Gehrig's disease. The soldiers also suffered from a number of debilitating and life-shortening diseases, such as polyarteritis nodosa, multiple sclerosis (MS), lupus, transverse myelitis (a neurological disorder caused by inflammation of the spinal cord), endocarditis (inflammation of the heart's inner lining), optic neuritis with blindness and glomerulonephritis (a type of kidney disease). Because squalene, the main ingredient in MF-59, can induce hyperimmune responses and induce autoimmunity, a real danger exists for prolonged activation of the brain's immune cells, the microglia. This type of prolonged activation has been strongly associated with such diseases as multiple sclerosis, Alzheimer's disease, Parkinson's disease, ALS and possibly vaccine-related encephalitis. It has been shown that activation of the systemic immune system, as occurs with vaccination, rapidly activates the brain's microglia at the same time, and this brain inflammation can persist for long periods. So, how would the gp120 get into the brain? Studies of other immune adjuvants using careful tracer techniques have shown that they routinely enter the brain following vaccination. What most people do not know, even the doctors who recommend the vaccines, is that most such studies by pharmaceutical companies observe the patients for only one to two weeks following vaccination-these types of reactions may take months or even years to manifest. It is obvious that the vaccine manufacturers stand to make billions of dollars in profits from this WHO/government-promoted pandemic. Novartis, the maker of the new pandemic vaccine, recently announced that they would not give free vaccines to impoverished nations-everybody pays. One must keep in mind that once the vaccine is injected, there is little you can do to protect yourself -at least by conventional medicine. It will mean a lifetime of crippling illness and early death. There are much safer ways to protect oneself from this flu virus, such as higher doses of vitamin D3, selective immune enhancement using supplements, and a good diet. _______ Dr. Russell Blaylock, is a board certified neurosurgeon, author and lecturer. An expert on nutrition and vaccines, he is also editor of the widely distributed Blaylock Wellness Report. http://www.russellblaylockmd.com/