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U.S. Zika Vaccine Trial: A Vaccine Looking for a Disease to Cure – Natural Immunity has Already Eliminated the Zika Virus

The experimental Zika vaccine is a controversial DNA vaccine, never before used in humans. An earlier NIH attempt to develop a West Nile DNA vaccine was aborted. But the unexpected happened; the virus has disappeared. The adults who had been infected recovered without treatment—and they have gained the advantage of lifetime immunity. Zika no longer poses a health problem for humans. In 2017, when “new cases have dropped to a trickle throughout the Americas” Sanofi pulled the plug on its Zika vaccine. Dr. Fauci acknowledges that: “Right now, there are no infections, and certainly not enough to even think about an efficacy signal at this point”. Science Magazine, notes: “Further complicating the trial, many people throughout Latin America and the Caribbean have already been infected with Zika and recovered, which has left them immune to the virus and hence ineligible for vaccine trials.” To overcome “the problem” that Mother Nature resolved – NIAID officials and the researchers are intent on facilitating the continuation of the vaccine trial. They propose to intentionally infect people who may then spread the virus and create an epidemic that has receded. The motivating factors for completing the trial by resorting to unethical exposure of human subjects to potentially serious harm, is that a Zika vaccine will be brought to market – whether or not Zika poses a threat. The trial is about protecting the financial investment, career advancement for the researchers, and launching yet another profit generating vaccine.

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Vaccine Awareness Week: National Vaccine Information Center Calls on Health Officials to Protect Babies in U.S. from Toxic DPT Vaccine

During the Ninth Annual Vaccine Awareness Week co-sponsored by the non-profit charity National Vaccine Information Center (NVIC) and Dr. Joseph Mercola, NVIC is calling on the U.S. Department of Health and Human Services (DHHS) to protect newborns from being subjected to the risks of an old and crude whole cell pertussis vaccine in DPT that has not been given to babies in America for 20 years. During this year’s Vaccine Awareness Week, NVIC is also releasing a 2018 Annual Report on U.S. State Vaccine Legislation: Breakdown, Trends and Predictions. The report is an analysis of which state legislatures passed bills that affected vaccine exemptions or added new vaccine mandates, enrolled citizens in electronic vaccine tracking registries, approved vaccine promotion programs in daycares and schools or enacted other vaccine-related legislation. NVIC reports that for the third year in a row, exemptions in vaccine laws remained stable with no losses in any state. Vaccine Awareness Week Sept. 23-30, 2018 was launched with an article and video reviewing the risks and failures of influenza vaccines and will include an article on fast tracking and marketing of vaccines, such as Gardasil (HPV) vaccine, by federal health agencies. Saturday will feature online viewing of excerpts from the international award winning HPV vaccine documentary, Sacrificial Virgins.

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After 20 Month Old Son Dies from Vaccines Professional Fighter with Nurse Wife Put Up Billboards as Warning

Nick Catone is a professional MMA martial arts fighter, and his wife, Marjorie Catone, is a registered nurse who works in an intensive care unit at a local hospital where they live. 17 days after their 20 month old healthy and active son, Nicholas, was vaccinated with the DTaP (Diphtheria, Tetanus, Pertussis) vaccine, his parents found him dead in his bed one morning. In an interview with Del Bigtree, Marjorie comments about how her nursing education never trained her in the possible adverse reactions to vaccines, and she never bothered to check the ingredients of the vaccine, even though as a wife of a professional MMA fighter and mother she was meticulous to check ingredient lists of foods to make sure her family was eating healthy. The autopsy report of their son listed the cause of death as "sudden unexplained" (SIDS) and "natural," as medical authorities apparently refused to consider their son's vaccines as a contributing factor to his death, and they allegedly did not conduct a thorough exam during the autopsy. Nick and Marjorie now want to warn others about the dangers of vaccines, so that parents can be informed before making a decision to vaccinate their children, before it is too late and they find themselves in the same situation as they are, grieving over the death of their formerly healthy child. They are putting up billboards in several states in an effort to educate the public on the risks of vaccines.

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Vaccine Safety Untested on Pregnant Women, But Big Pharma Not Liable for Vaccine Injuries to Unborn Children and Pregnant Mothers

We are here today because in 2016, Congress amended the 1986 National Childhood Vaccine Injury Act to add vaccines recommended by the CDC for routine administration to pregnant women to the Vaccine Injury Table. Congressional action was required to do it because the 1986 Act was not about vaccines recommended for adults or unborn babies developing in the womb. As stated in multiple congressional hearings between 1982 and 1986, the National Childhood Vaccine Injury Act was created by Congress for one purpose: to protect the availability and lower the costs of federally recommended vaccines for children that are state mandated for school attendance. Although this NPRM requests public comment on how the addition of this new maternal vaccination category should be formatted on the Vaccine Injury Table, the public is hampered from making informed comments because of knowledge gaps about the safety and effectiveness of administering vaccines to pregnant women and potential negative health outcomes for the unborn child developing in the womb. Various package inserts for these vaccines contain warnings such as “it is not known whether the vaccine can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity;” and “there are no adequate and well controlled studies in pregnant women;” and “available data on the vaccine administered to pregnant women are insufficient to inform vaccine associated risks in pregnant women;” and “the vaccine should be given to pregnant women only if clearly needed.” There is no single vaccine-related issue of more concern to Americans than protection of this internationally recognized human right for pregnant women, parents of minor children and adults of all ages, who are too often being threatened and sanctioned if they do not agree to receive all government recommended and mandated vaccines for which the pharmaceutical industry has had no product liability since 2011.

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Robert F. Kennedy, Jr. Demands the Office of the Inspector General and Congress Investigate Fraud in Vaccine Court by Denying Autism Vaccine Injuries

Robert F. Kennedy Jr., Chairman of Children’s Health Defense (CHD), and Rolf Hazlehurst, parent of a vaccine-injured child, petitioned the Department of Justice (DOJ) Office of Inspector General (OIG), and the Senate and House Judiciary Committees today to investigate actions taken by federal personnel during the “Vaccine Court” Omnibus Autism Proceedings (OAP). Recently discovered evidence provided by Kennedy and Hazlehurst details obstruction of justice and appallingly consequential fraud by two DOJ lawyers who represented the Department of Health and Human Services (HHS) in 2007. These actions led to a denial of justice and compensation for over 5,000 families who filed claims of vaccine injury leading to autism in their children. The fraud by the two DOJ attorneys directly influenced the 2011 Bruesewitz v. Wyeth Supreme Court decision which all but shut the door forever for families seeking redress for vaccine injury in the civil court system. Since this miscarriage of justice, roughly one million children have been diagnosed with autism. An unknown percentage of these cases are the result of vaccine injury.

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Are Vaccine Manufacturers Concealing Deaths Caused by Vaccines by Manipulating Post-marketing Data?

National and international health agencies such as the Centers for Disease Control and Prevention (CDC), the European Medicines Agency (EMA) and the World Health Organization (WHO) routinely and emphatically claim that serious adverse events following vaccination are rare. Nowhere is officialdom’s minimization of vaccine risks more apparent than in these agencies’ position on vaccine-related deaths. The WHO, for example, states that “so few deaths can plausibly be attributed to vaccines that it is hard to assess the risk statistically.” Nevertheless, once regulators have deemed that a given vaccine is safe enough to be licensed and widely marketed, vaccine manufacturers are supposed to do just that—that is, continue to statistically assess a vaccine’s risks, including the risk of death—and regulators are supposed to carefully review the postlicensure data that pharmaceutical companies submit. A 2017 commentary by India-based physicians Jacob Puliyel and C. Sathyamala in the Indian Journal of Medical Ethics describes a shocking dereliction of duty on the part of regulators who were presented with vaccine data carefully tailored to obscure serious risks. Tackling concerns about infant deaths that have occurred following hexavalent vaccination in several European countries, the authors of the commentary show that GlaxoSmithKline (GSK) neglected to report to regulatory authorities that there was a statistically significant increased risk of sudden infant death in the four days after administration of its hexavalent vaccine—and the regulatory agency in question (the EMA) ignored the omission and accepted GSK’s apparently whitewashed data at face value.

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The End of Scientific Integrity? Cochrane Collaboration Expels Critic of Big Pharma – 4 Other Board Members Resign

Dr. Peter Gøtzsche recently sent out an email to the public explaining that he is the first person in 25 years to be expelled from the Cochrane Collaboration. He writes: "No clear reasoned justification has been given for my expulsion aside from accusing me of causing 'disrepute' for the organization. This is the first time in 25 years that a member has been excluded from membership of Cochrane." Four other board members have resigned from the Cochrane Collaboration as a result of this action. Health Impact News has covered the work of Dr. Gøtzsche frequently over the years, as he is an outspoken critic of Big Pharma, referring to them as "organized crime." He is author of the book, "Deadly Medicines and Organized Crime: How big pharma has corrupted healthcare." The Cochrane Collaboration is considered to be the "gold standard" in scientific integrity, but they have come under fire recently for what appears to be biased reviews influenced by the pharmaceutical industry. They received a $1.15 million "gift" from the Bill & Melinda Gates Foundation to fund "project work" from 2016 to 2017. Earlier this year (2018), researchers from the Nordic Cochrane Centre published a critique in the British Medical Journal stating that the Cochrane’s review of the HPV vaccine "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."

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Illinois Teen Dies Three Weeks After Being Injected with HPV Gardasil Vaccine

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.

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Michigan Department of Health Tracking Student Vaccination Status in Violation of Federal Law

The group Michigan for Vaccine Choice has sent a letter to parents in Michigan informing them that the Michigan Department of Health and Human Services (MDHHS) and the Michigan Department of Education (MDE) are violating federal law (FERPA) by transferring private medical records about minor children, without the consent of their parents, regarding each student's vaccination status into a vaccine tracking database.

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American Academy of Pediatrics Concerned About Unregulated Food Additives, but Not Vaccine Additives

In July, 2018, The American Academy of Pediatrics (AAP) released a policy statement titled, Food Additives and Child Health. The report begins by stating, “Our purposes with this policy statement and its accompanying technical report are to review and highlight emerging child health concerns related to the use of colorings, flavorings, and chemicals deliberately added to food during processing (direct food additives) as well as substances in food contact materials, including adhesives, dyes, coatings, paper, paperboard, plastic, and other polymers, which may contaminate food as part of packaging or manufacturing equipment (indirect food additives); to make reasonable recommendations that the pediatrician might be able to adopt into the guidance provided during pediatric visits; and to propose urgently needed reforms to the current regulatory process at the US Food and Drug Administration (FDA) for food additives." However, one important subject that the AAP doesn’t address is the toxins in pediatric vaccines. Mercury, the second most dangerous substance known to mankind is still in childhood vaccinations–influenza, meningitis, HIB, Tdap, and Td; aluminum, a neurotoxin, is in a plethora of vaccines including hepatitis A and B, DTaP, Td, HIB, HPV; formaldehyde a known carcinogen is found in DTaP, Td, Hepatis A, Hib, influenza, and Tdap. There are other toxic substances in many different vaccines. Our children are the most vaccinated young people on the planet. Unfortunately, our children are the sickest when compared to any major Western country. It is long overdue for the AAP to address the elephant in the room; toxic additives in childhood vaccines.

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