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.
Are front-line emergency room doctors the key to identifying vaccine injuries and reporting them? At least one ER doctor thinks so. David Denton Davis MD, a former Emergency Physician, claims neither our Centers for Disease Control (CDC) nor our Department of Health and Human Services (HHS) has requested help from the American College of Emergency Physicians (ACEP) in identifying illnesses and deaths occurring hours, days and weeks following childhood vaccinations. In his soon-to-be-published book “Who Can Parents Trust? Vaccines: Avoidable and Unsafe," he claims the vast majority of serious vaccine related illnesses coming into Emergency rooms will continue to go unrecognized, unless nurses and physicians ask the last vaccination date (LVD). He believes during the past thirty years several million serious Adverse Events (AE's), including deaths presenting nationwide to more than 5,000 Emergency rooms have never been recognized, documented or submitted for investigation, in accordance with our National Childhood Vaccine Injury Act (NCVIA). All suspicions of a vaccine related adverse event are required by law to be submitted using our Vaccine Adverse Event Reporting System (VAERS). Sadly, he goes on, very few Emergency Physicians or Nurses have received any NCVIA or VAERS education. As a charter member of ACEP, Dr. Davis served on the Board of Directors during the creation of Emergency Medicine (EM) as a specialty. He admits his own reporting failures were due to a lack of vaccine education. Dr. Davis states he is concerned many pediatricians know, but are not reporting illnesses following vaccinations, for financial reasons. Although neither makers nor physicians are liable for vaccine damage, the ultimate truth for safety was made contingent on investigating physician, parent or third party VAERS submissions. With only a very small percentage being reported, no one can honestly say vaccines are safe.
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.
In May 2018, Cochrane, the research organization that bills itself as the “international gold standard for high quality, trusted information,” released a flattering review of human papillomavirus (HPV) vaccines. The Cochrane review methodology involves pulling together data from clinical trials and reviewing the assembled evidence in what is supposed to be a standardized, systematic and neutral manner. In June, we reported that Cochrane’s sources of funding—agencies and foundations that are unwilling to brook any questions about vaccine safety—raise reasonable doubts about Cochrane’s conflicts of interest and ability to remain independent from its funders’ agendas. Now, researchers affiliated with one of Cochrane’s regional member centers (the Nordic Cochrane Centre) and with the Oxford-based Centre for Evidence Based Medicine (OCEBM) have come out with an exhaustive critique of Cochrane’s HPV review, published in BMJ Evidence-Based Medicine. Not mincing their words, the authors state: "We believe that the Cochrane [HPV vaccine] review does not meet the standards for Cochrane reviews or the needs of the citizens or healthcare providers that consult Cochrane reviews to make ‘Informed decisions,’ which…is part of Cochrane’s motto." The Nordic and OCEBM authors make many solid arguments about the Cochrane reviewers’ omissions and errors, including the reviewers’ inexplicable characterization of the higher death rate in the HPV group as “a chance occurrence.”
The lawfirm of Maglio Christopher & Toale, P.A. announced earlier this month (July, 2018) that they had negotiated a $101 million dollar settlement for an infant who suffered a severe reaction to the Measles Mumps Rubella (MMR) vaccine. A one-year-old healthy baby girl, who was already walking and climbing, received vaccinations for Measles Mumps Rubella (MMR), Hepatitis A, Haemophilus Influenzae type B (Hib), Prevnar (pneumonia), and Varicella (chickenpox) on February 13, 2013. That evening, the mother noticed the baby was irritable and feverish. After a call to the pediatrician, the doctor advised Mom to give her Tylenol and Benadryl. The fever continued for several days, and on the evening before the baby’s scheduled pediatrician visit, the baby began having severe seizures. She was rushed to the emergency room. She went into cardiac and respiratory arrest, and doctors placed her on a ventilator. The seizures and cardiac arrest left the baby with a severe brain injury, encephalopathy, cortical vision impairment, truncal hypotonia (low muscle tone), and kidney failure. After months of treatment at the hospital, the baby finally went home, but her disabilities required specialized medical care and supervision around the clock for the rest of her life. The $101 million dollar settlement will pay for the child’s constant high-level medical care for the rest of her life. The family received a lump sum of $1 million dollars to cover the immediate costs of medical bills and expenses. The rest will be paid out through an annuity over the child’s lifetime. Don't expect to read this story in the Big Pharma-sponsored corporate "mainstream" media, where the official doctrine is that vaccines are "safe and effective."
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."
In 2017, Health Impact News reported that the Informed Consent Action Network (ICAN), supported by 55 organizations, representing over 5 million people, had taken the unprecedented step of serving a notice to Mr. Don Wright, M.D., M.P.H., who was the acting secretary of the Health and Human Services (HHS) department at the time, stating that HHS had failed in their duty to conduct the proper scientific research required to demonstrate vaccine safety as was required by law, and that they should take immediate action to remedy this negligence. Last week (July, 2018), Del Bigtree interviewed Robert F. Kennedy Jr. on his program HighWire, announcing that they had filed a lawsuit against HHS for violating U.S. law on vaccine safety, and won.
Hundreds of HPV Vaccine Victims Take to the Streets in Dublin to Protest – 2 Girls Suffer Seizures During Protest
Hundreds of HPV vaccine-injured people took to the streets to protest at Leinster House, Dublin, on July 9th, 2018, while Professor Ian Frazier, one of the co-inventors of the vaccine, gave a speech next door at the Royal College of Physicians. During the protest, 3 Gardasil vaccine victims took ill, with 2 of them having seizures. Both of the girls suffering seizures had to be taken to the hospital. The following video was taken of the protest, and towards the end of the video you can see one of the girls having a seizure. This protest has been mostly censored in the "mainstream" corporate-sponsored media.
TV1 in Samoa is reporting that two infants have died within minutes of receiving the measles, mumps, and rubella (MMR) vaccine. "Tala Fou brings you breaking news on the death of two young children both aged 1-year-old from the villages of Safotu and Sasina in Savaii. Both children died within minutes of being vaccinated with the MMR vacine at Safotu Hospital on Friday morning the 6th of July. Our News Reporter Alisa Faamaoni met with both families in Savaii today. The parents of the first child Marietta and Samuelu Tuisuesue of Sasina explained in detail to Tala Fou that within three minutes of their 1-year-old daughter Lannacallystah Samuelu being injected with the MMR vacine by a nurse she was dead." What is so tragic, and has this island nation in such an uproar, is that the parents of the second child who died had reportedly already learned about the first infant's death a couple hours earlier and declined to have their child receive the same MMR vaccine. The mother reports that the nurse administered the vaccine against her consent, leading to the child's immediate death upon receiving the vaccine.
Two leading pediatricians in India have published a critique of the World Health Organization's (WHO) newly revised manual on the classification of Adverse Events Following Immunization (AEFI). The doctors claim that the new guidelines are too lax, resulting in more children dying from adverse reactions to vaccines, with no accountability for the vaccine manufacturers to produce safer vaccines. In the U.S., pharmaceutical companies manufacturing vaccines cannot be sued due to faulty vaccines, which allows them to put as many vaccines into the market as they want, with no repercussions if the vaccine proves to be faulty or have a high injury and death rate. Victims must sue the U.S. government and top DOJ attorneys who protect the drug companies. This move by the WHO may very well be an attempt to protect drug companies manufacturing vaccines by preventing lawsuits in the rest of the world for faulty vaccines. According to the report of these two doctors, the consequence of India adopting WHO's new classification can be seen from the causality assessment of 132 serious AEFI cases uploaded on the website of the Ministry of Health and Family Welfare. Of the total AEFI cases, 54 babies died and 78 survived, "but not even one death was classified as vaccine-related. Nearly all the deaths were simply classified as unclassifiable or coincidental."