There are new concerns about Gardasil, the vaccine that prevents a virus that may cause cervical cancer.
What makes this new information even more compelling is that Spain actually withdrew 75, 000 doses of the vaccine from their market just last week.
The National Vaccine Information Center (NVIC) has compared Gardasil adverse events to the meningitis vaccine; Gardasil injections resulted in three times the number of Emergency Room visits -- more than 5,000. Reports of side effects were up to 30 times higher with Gardasil.
Barbara Loe Fisher, co-founder of the NVIC, said,
"Now we know from this report that there are more reactions and deaths associated with Gardasil than with another vaccine given in the same age group. It's irresponsible not to take action."
We are also proud to announce a joint collaboration with NVIC, and after many months of intensive effort they have a new site up that will allow them to serve as the premier source of vaccine safety information.
Over 10,000 adverse reactions, including 27 deaths, have been reported to the Vaccine Adverse Event Reporting System (VAERS) in relation to Gardasil. Yet, the CDC and FDA are alleging that the vast majority, or even ALL, of these cases are unrelated to the vaccine. Therefore, they claim, Gardasil is safe.
Says Barbara Loe Fisher, President and co-founder of the National Vaccine Information Center (NVIC):
“The tragic story of Gardasil vaccine is one that is playing out real time in the homes of trusting parents, who thought they were doing the right thing to try to make their daughters "one less," and in the 21st century cyberspace forum of public opinion as well as on television.”
The Gardasil vaccine is one of the most blatant deceptions going on in modern medicine. Well-meaning mothers are being deceived into thinking this shot will protect their daughters from cervical cancer, and some of them are now wondering HOW and WHY their young child died or became suddenly paralyzed.
NVIC Petitions White House and Congress to Investigate Gardasil
On February 9, the NVIC launched a petition and issued a national press release calling on President Barack Obama, his Administration and Congress, to investigate the fast track licensure and universal use recommendation of Gardasil in 2006, and the dismissal of more than 10,000 reports of Gardasil-related reactions, injuries and deaths to the Vaccine Adverse Events Reporting System as a "coincidence" by federal health officials.
NVIC's latest Gardasil risk report, which compares the number and severity of adverse events reported to VAERS through November 30, 2008, reveals that death and serious health problems such as stroke, blood clots, cardiac arrest, seizures, fainting, lupus and rechallenge cases are reported three to 30 times more frequently after Gardasil vaccination than after meningococcal (Menactra) vaccination.
Barbara Loe Fisher explains the significance of this fact:
“If the deaths and serious injuries reported after Gardasil were only a "coincidence," there would be little or no difference between the frequency and severity of vaccine-related adverse events between two vaccines, if the vaccines were equally reactive, and the number of doses were roughly the same.
Gardasil and Menactra vaccines were licensed within a year of each other and recommended by the CDC for universal use in 11-12 year olds.
Although Menactra is given to boys and girls and has already been mandated in many states for high school and college entry, Gardasil is only given to girls and is not yet mandated.
Menatra is given as a one-dose series and, by February 25, 2008, the CDC reported that about 15.5 million doses of Menactra had been distributed in the U.S.. Gardasil is given in a three dose series and the CDC reported that, by July 2008, about 16 million doses had been distributed in the U.S.
This means that about 15 million doses of Menactra were given to about 15 million boys and/or girls and about 16 million doses of Gardasil - if every girl got three doses - were given to about five million girls.
It is individuals - not doses of vaccine - who collapse, convulse, become paralyzed, have heart attacks, develop lupus and other chronic health problems after being vaccinated. The fact that death and serious health problems are reported 3 to 30 times more frequently after Gardasil than after Menactra is highly significant and it is irresponsible for federal health officials and Merck to blow it off as unimportant.”
What Does Merck Have to Say About it?
It’s incomprehensible that the CDC, FDA, and Merck -- the makers of Gardasil – cannot see the facts presented in this VAERS analysis, and choose instead to cling to worn-out propaganda slogans and pre-written advertising messages that fly in the face of reason.
In the hours before the CBS News report shown above was broadcast, Merck addressed the differences between adverse events associated with Gardasil and Menactra as follows:
"It's important to remember that the proven benefit of GARDASIL is that it helps prevent cervical cancer caused by the two virus types responsible for most cases of cervical cancer.
Nothing is more important to Merck than the safety of our products and we carefully monitor the safety of GARDASIL on a routine basis. Experts at the FDA and CDC also continue to review data and, as recently as four months ago, said "GARDASIL continues to be safe and effective, and its benefits continue to outweigh its risks."
NVIC is not a medical organization and has a long history of raising concerns about vaccines that are in direct conflict with the opinion of leading medical experts. We encourage consumers to get reliable information about the safety of vaccines from www.cdc.gov."
Spain Already Removed the Vaccine
Spain has, as recently as last week, withdrawn 75, 000 doses of the HPV vaccine from their market, after two teenagers who received the shots were hospitalized.
Seems they weren’t as influenced by the drug company’s rhetoric as U.S. authorities, and are more concerned about the safety of their citizens.
Get Involved and Help Save the Daughters of This Nation
“In the past 27 years, the stories of death and brain damage that have been reported to the NVIC have never changed. Whether the vaccine victims are 15 months old or 15 years old, the stories are the same: a trusting parent took a bright, healthy child to a doctor for a routine vaccination and the child was never the same again.
The Gardasil vaccine was inappropriately fast tracked and licensed by the FDA and recommended by the CDC with too little attention paid to the reports of brain and immune system dysfunction that developed after vaccination in pre-licensure clinical trials.
That same cavalier attitude toward Gardasil-related deaths and serious health problems, which have been experienced by many girls and young women after licensure, is inexcusable.”
Most Americans have blindly placed their trust in the vaccine makers and in federal health agencies, whose responsibility is to ensure that drugs and vaccines licensed for public use are safe, effective and necessary.
However, over the years it has become very clear that those responsible for protecting your health are not looking out for your best interest and that of your children.
And if they won’t do it, then it is up to you and me to do it.
I urge you to sign the Investigate Gardasil Vaccine Risks Now! petition available on the http://www.NVIC.org web site that my team helped create for them.
If you believe strongly in NVIC's effort to inform the public about these types of issues, you can support their cause by making a donation of $25 or more to NVIC and receive a gift of Barbara's 2008 book Vaccines, Autism & Chronic Inflammation: The New Epidemic. Click HERE to make a donation.
You may also print out this NVIC flyer detailing how to recognize a vaccine reaction.
“In 2009, I have a sense of déjà vu as the story of Gardasil vaccine plays out real time. There are striking parallels between how those operating the mass vaccination system reacted in the 1980's to persistent reports that the DPT vaccine was harming more children than originally assumed, and the way they are reacting now to persistent reports that Gardasil is more reactive than it was originally assumed.
Assumption of safety is no substitute for proof of safety.
And turning away from human suffering in order to protect the status quo is not the way to run a government that needs the trust and support of the people.
In the 18th century, Queen Marie Antoinette looked down at a starving people pleading for bread to stay alive and said "Let them eat cake." It is time for everyone in government, industry and medicine to take a different approach to persistent reports of vaccine injuries and deaths or risk metaphorically suffering the same fate that ended the monarchy in France.
In the 21st century, today's peasants don't have pitchforks - they have laptops, desktops, smartphones and the internet.”
I strongly urge you to join in petitioning our new U.S. administration and Congress to take a close, hard look at the HPV vaccine, to end the needless suffering of tens of thousands of young, bright, innocent girls.
And, please, forward this important message to everyone you know by using the ‘Email this article to a friend’ button, located in the top left corner of this page.