The HPV vaccine controversy has been raging since the FDA approved Gardasil in 2006 in virtually every country utilizing this new medical intervention. Dr. Stig Gerdes wrote this open letter to Danish Health authorities, the medical community, and local journalists hoping to shed some light on the very real consequences many Danish families were forced to deal with post-HPV vaccine use. Dr. Gerdes wrote: "The vaccine should be stopped immediately! There are so many unanswered questions that should be answered before we continue to vaccinate. With each injection, there is a risk of incapacitating a previously young strong human." Unfortunately, HPV vaccine stakeholders are still trying to deny the facts Dr. Gerdes was courageous enough to put in writing.
Parents, Scientists and Doctors from Around the World Gather to Discuss How to Handle Increasing HPV Vaccine Injuries
Earlier this year (2018) parents, scientists and doctors from all over the world gathered in Ireland at an IFICA conference to discuss the future of the HPV vaccine injured. The theme was "Working Together." The Ireland Government HSE (Health Service Executive) was invited to send representatives to attend, but they refused the opportunity to speak or listen to the world-renowned experts who attended. Instead, the HSE claims that the HPV vaccine is "100% safe" and labeled parents of HPV vaccine injured children as "Emotional Terrorists." As a result, victims suffering from Gardasil vaccine injuries in Ireland cannot get treatment, and must travel outside of the country to find medical help for their injuries.
Following a June, 2018 “Priority Review” by the FDA to approve Merck's Gardasil 9 vaccine to be expanded to women and men, ages 27 to 45, after 10 years of the FDA denying Merck's request to expand the Gardasil market to adults, the FDA approved Gardasil 9 to be expanded to adults, aged 27 to 45, on October 8, 2018. Granting approval to a vaccine after a "Priority Review" by the FDA in only 3 months is a "fast nod" according to FiercePharma, the market trade publication of the pharmaceutical industry. Merck did not even have to supply any new trials or data to get the vaccine approved for adults, in spite of the fact that the FDA denied their request for 10 years on the older Gardasil vaccine. According to FiercePharma: "Because Gardasil 9 and sister shot Gardasil are manufactured similarly, the FDA based the Gardasil 9 decision on results from a study of its predecessor." The study the FDA relied upon to approve Gardasil 9 for adults, was considered insufficient for 10 years as the FDA denied Merck approval to market the vaccine to adults: "Back in 2008, after agreeing to a faster review in the age group, the FDA decided against Merck’s case for an additional Gardasil approval in females 27 to 45. The agency in 2009 issued a second complete response letter for that application, demanding Merck to provide longer-term efficacy data in the age group. That set of data apparently didn’t turn things around for Merck. In both Gardasil’s and Gardasil 9’s current labels, information about a study on 3,253 women, 27 through 45 years of age, states that there was “no statistically significant efficacy” demonstrated by the vaccine in preventing high-grade cervical lesions or cervical cancer." Yet somehow, that same study is now deemed to be sufficient to approve Gardasil 9 for adults.
Christopher Bunch, 14 years old, died on Aug. 14, 2018 of complications from a rare neurological disease called Acute Disseminated Encephalomyelitis (ADEM). The teenager began experiencing symptoms, including headaches, nausea and vomiting, on Aug. 6. He spent much of the next two days sleeping. Christopher had apparently received the HPV (human papillomavirus) vaccine Gardasil three weeks prior to his death. ADEM is a reported side effect of Gardasil. It is listed in the Gardasil package insert.
Was Texas Mom’s Baby who was Accidentally Vaccinated with Gardasil Medically Kidnapped for Medical Research?
When Anita Vasquez sought medical care for the reactions her baby girl was having after mistakenly being given the Gardasil vaccine at only 4 months old, she had no way of knowing that she was walking into a hospital that was working on vaccine development in collaboration with one of the largest pharmaceutical companies in the world. She found herself tangled in what appeared to her to be a deep web of interests that were in direct conflict with her only goal, which was simply trying to get help for her baby. Instead of finding help, she was met with accusations that she had somehow caused harm. Doctors and social workers testified that Anita had Munchausen Syndrome by Proxy (also known as "factitious disorder"), which means she was accused of making up her daughter's medical conditions when there were none. Anita is a licensed nurse by profession. The state of Texas recently terminated her parental rights to her daughter Aniya Blu. It was apparent to Anita from the very beginning that there was more going on than meets the eye. Evidence was hidden. Medical records were kept from her and her attorneys. Medical diagnoses of real problems were covered up. The deception continued throughout the ordeal with Child Protective Services, and it followed Anita into the courtroom. There were many facts of the case that Anita didn't learn about until just before the termination hearing. Even then, the evidence was ignored. Anita Vasquez has appealed the termination of her parental rights for her daughter, who was mistakenly injected at 4 months old with the Gardasil 9 vaccine intended for her older brother. Anita received a letter on August 31, 2018, from the Thirteenth District of Texas Court of Appeals noting that her appeal was accepted.
Maryland parent Josh Mazer is a pro-vaccine parent. He has stated: "A properly administered, robust vaccine policy is instrumental in promoting the public welfare." (We disagree on this point.) However, there is one vaccine he does not promote, and after the local health department started promoting this vaccine to 12 and 13-year-old children without parental consent or knowledge, he decided to do some investigating behind this large public campaign of mass vaccination. The vaccine in question is Merck's HPV vaccine Gardasil, which is well-known to the readers of Health Impact News, but less so among the general public. Mazer was notified of the policy earlier this year (2018) by a "a career public school nurse" who told him that she was "being forced" to market Gardasil to 11 and 12-year-old kids at her school. Mazer decided to investigate why this was being presented as a "public health crisis," but none of the local health department officials gave him any useful facts or information to justify the mass HPV vaccine campaign. So he filed a Public Information Act request with the local government Prevention and Health Promotion Administration. He learned the state health department received $91.6 million just since 2012 from pharma funded non-profits to promote the HPV vaccine in Maryland. Bingo. Welcome to our world, Mr. Mazer.
French Oncologist Analysis of Gardasil Vaccine Finds Higher Rates of Cervical Cancer Associated with High Vaccination Rates
A medical doctor in France, Dr. Gérard Delépine, an oncologist, has published an analysis of the HPV vaccine Gardasil on the independent news site, Agora Vox, showing how increased rates of Gardasil vaccinations are actually correlated with a higher rate of cervical cancer. The analysis was published as an Open letter to parliamentarians, and to all citizens, in response to a recent meeting between French President Emmanuel Macron and "thirty leaders of the world's largest pharmaceutical groups," and to the call among some politicians to make the HPV vaccine Gardasil mandatory in France. Using statistics from several countries, Dr. Delépine shows that cervical cancer was decreasing in all these countries due to the implementation of regular pap smears. However, in some countries where mass Gardasil vaccination took place, the incidence of cervical cancer actually increased.
15 Year Old French Girl’s “Descent into Hell” After Gardasil Vaccine – Wheelchair Bound and Paralyzed
Jean-Jacques and Yveline say that their daughter Océane was a girl full of joy, health, and laughter before her 15th birthday. They affectionately called her their ‘little pearl.’ She never had to visit the doctor for an illness. That is until her life was turned upside-down because of trust. Océane was 15 years old when she went to her family doctor to get a medical certificate for dancing with a friend. The doctor suggested Gardasil for cervical cancer prevention. Her parents trusted their family doctor and consented to the vaccination. They did not realize this decision would set off a chain of events that would make Dante’s Inferno look like a picnic. The year 2011 was a descent into hell for Océane’s parents. One stroke had left their daughter in a wheelchair without vision or hearing due to the acute encephalomyelitis. For two years, Océane could not attend school. Wheelchairs, facial paralysis, dizziness and great fatigue kept her home. Today, they seek justice in court, not only for their daughter, but for the more than 700 other French families who have suffered injuries due to the Gardasil vaccine.
Texas Mom Who is a Nurse Fights to Regain Custody of Daughter Taken Away After Gardasil Vaccine Injury
Social workers told a Texas mother that Monday was her last visit with her daughter. Aniya Blu Vasquez was medically kidnapped from her family after she became ill following a medical error in which her pediatrician injected her with the Gardasil 9 vaccine intended for her older brother. Aniya was just 4 months old at the time. A Texas court decided last month that the parental rights of her mother, Anita Vasquez, should be terminated, devastating the family and supporters alike. However, their story is not over. In a quirk of legalities, Anita Vasquez filed a Declaration of Recision of Signature/Contracts before the court was able to file the entry of judgement on the termination of parental rights. As a result, there will be another hearing on Monday, July 23, 2018, at the Victoria County Courthouse at 9 a.m. She says that there is substantial new evidence in her case that was not considered by the court. Anita asserts that the very basis upon which CPS seized custody of Aniya was fraudulent, and CPS knew it all along. Concerned citizens are rallying around the family that they believe is suffering a grave injustice.
Gardasil Vaccine Legal Victory: Canada Federal Court Rules to Release Clinical Trial Data to American Researcher
CBC News and the British Medical Journal (BMJ) are reporting that Professor Peter Doshi has won a major legal victory against pharmaceutical companies trying to hide clinical trial data from the public due to "confidential agreements" for 5 pharmaceutical products. Doshi sued Health Canada to release clinical trial data submitted to Health Canada by the manufacturers of the HPV vaccines Gardasil, Gardasil 9 and Cervarix, and the anti-viral flu medications, Tamiflu and Relenza. A Canadian Federal Court judge ordered Health Canada to release the pharmaceutical clinical trial data, undercutting the Canadian government's attempts to keep the information confidential. As far as I can determine, this landmark court ruling out of Canada has been completely censored in the U.S. corporate-sponsored "mainstream" media. This appears to be a brilliant legal strategy by Doshi and his attorneys, since they had little to no chance of obtaining this clinical trial data from any court in the U.S., where pharmaceutical companies enjoy legal immunity from most lawsuits. The importance of receiving this data, particularly on Merck's Gardasil vaccine, cannot be overstated. As we have reported many times here at Health Impact News, the entire medical approval process to bring the HPV vaccine into the U.S. market is full of scandals and cover-ups, which has resulted in the injuries and deaths of many young people, particularly young women aged 12 to 26, many of whom can no longer bear children due to the vaccine making them infertile. "I hope my case sets a precedent and allows researchers, clinicians, and the public easy access to clinical trial data," Doshi reportedly stated in an email to CBC News. "Regulators shouldn't have a monopoly on judging the risks and benefits of medicines or hinder others from doing the same via confidentiality agreements."