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Children’s Health Defense (CHD) filed a lawsuit on Monday, August 17, 2020 in San Francisco Federal Court charging Facebook, Mark Zuckerberg, and three fact-checking companies with censoring truthful public health posts and for fraudulently misrepresenting and defaming CHD. On Wednesday, Attorneys Robert F. Kennedy, Jr., Roger Teich, Mary Holland, Dafna Tachover and Dr. Liz Mumper, a pediatrician directly affected by Facebook's censorship, took questions from the media and concerned citizens at a virtual press conference. |
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By Robert F. Kennedy, Jr., Chairman, Children’s Health Defense On July 29, YouTube terminated Del Bigtree’s “The Highwire” account after he posted a video of the two of us discussing my debate with Alan Dershowitz on vaccine mandates. YouTube also purged hundreds of other truthful videos on vaccines. YouTube’s owner, Google, is effectively a vaccine company. Two subsidiaries of Google’s parent company, Alphabet, market and manufacture vaccines: Calico and Verily. Arthur Levinson, Genentech’s former CEO, runs Calico, an anti-aging drug company while Verily teams with Pharma to conduct drug and vaccine clinical trials. |
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On Wednesday, August 19th, the Digital Freedom Platform hosted the world premier of Plandemic: Indoctornation, a new feature length piece that promises to be the most revelatory film on what is driving the vaccine agenda—the various roles and backgrounds of the WHO, Bill Gates, Tedros Adhanom, Anthony Fauci and more. The film was created by the team behind the game-changing Plandemic video that went viral and was banned on every major social media platform for exposing the truth about Covid-19—information that health officials and Pharma don’t want you to know. Plandemic: Indoctornation delves deeper into what’s really happening with mainstream media, Silicon Valley tech giants, big pharma and our government agencies, patent laws, and more. Register and watch this mind-blowing film and connect the truth-dots like never before! And don't miss London Real’s Brian Rose’s interview with Mikki Willis, the director. |
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By Conan Milner, Epoch Times The case challenges the FCC to reconsider its wireless health and safety guidelines that have been in place since 1996. "We know now, from thousands and thousands of peer-reviewed published studies, that microwave radiation injures the human body and human cells at a tiny fraction of what it takes to raise the temperature of your body," Kennedy said. "It shows a grim inventory of injuries connected to Wi-Fi, including oxidative stress, sperm and testicular damage, cell damage, DNA damage, and neuropsychiatric damage. The neuropsychiatric damage can be so powerful that it can be read almost immediately on EEGs in children, and those effects do not disappear after you withdraw the radiation." But you’re not likely to hear these details of this unsettled science in the mainstream media. Kennedy said one of the most frustrating issues in getting the public to understand the harms related to RF radiation is the powerful influence the wireless industry has in silencing the story. In a world where media companies are often intimately tied to big telecom companies that have a stake in the 5G rollout, such stories are bad for business. Facebook, in particular, admits to censoring criticism of 5G. |
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On August 19th, the national law firm of Baum Hedlund Aristei & Goldman and co-counsel Robert F. Kennedy, Jr. filed a Gardasil lawsuit against Merck on behalf of a 19-year-old woman, alleging the company misled the FDA, legislators, doctors and moms about the safety and efficacy of its Gardasil vaccine. The lawsuit asserts Merck purposely downplayed the risk of Gardasil’s ingredients, including a proprietary aluminum compound (a potent neurotoxin) and secret and potentially hazardous DNA particles. Plaintiff Julia Balasco alleges she suffered and continues to suffer severe and permanent physical injuries such as an autoimmune disease known as postural orthostatic tachycardia syndrome (POTS) after receiving multiple injections of the human papillomavirus (HPV) Gardasil vaccine. |
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By Anne Dachel, CHD Contributing Writer, Age of Autism Editor, LossofBrainTrust.com We’ve watched the numbers explode with no end in sight. Over the last 20 years the Centers for Disease Control and Prevention have routinely updated the autism rate, from one in 250 in 2001 to one in 54 in 2020. The increases are real. Children with autism will continue to flood our schools in ever-increasing numbers at the same time young adults aging out of school will need massive amounts of adult services. Why aren’t legislators asking about these constant increases? |
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Guest Commentary by John Stone, UK Editor, Age of Autism In a complementary article to JB Handley’s ‘Vaccines and Autism—Is the Science Really Settled?’ John Stone writes of his parallel British experience, and notes that sadly, while Autism Spectrum Disorders are heading for 5% in schools, and going up by 20-25% a year, the world’s health officials are still hiding behind poor data such as Taylor’s ‘Vaccines are not associated with autism: an evidence-based meta-analysis of case-control and cohort studies'. |
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Iain Morris, News Editor, Light Reading This race analogy is not original. First, there was the arms race. Then came the space race. Most recently, the world has been hosting a race to develop a coronavirus vaccine . . . How has a network technology been elevated into this elite group? In a world dominated by internet companies, the simple answer is that politicians are more cognizant of telecom's importance than ever before. Plenty of telecom experts are unconvinced 5G deserves this billing, though. |
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Guest Editorial by Kristina Kristen Government officials’ interventions for COVID-19 have been strategically one-sided and myopic. Many leaders, in response to the perceived virus threat, completely abandoned rational considerations to lower overall suffering and death. In a blind focus intended to “stop the virus,” officials recklessly locked down billions of people globally with little to no debate, while ignoring the cost factor, an indispensable half of a “cost-benefit” analysis in calculating any solution. If a so-called solution “works” but in doing so creates massive, disproportionate collateral damage and increases overall harm, then clearly it cannot be called a solution, and certainly should never be mandated onto a population. |
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Excerpt: "In their recent review on aluminum and vaccines, JP Goullé & L Grangeot-Keros described general knowledge on aluminum (Al) exposure, kinetics and toxicity but made very little effort to delineate the scientific questions specifically related to Al adjuvants in vaccines. Instead of representing the bulk of their review, the subject of Al adjuvants covered no more than one third of the 3 page-text. Numerous important papers on the topic were omitted, i.e. 20 years of scientific publications in clinical, post-mortem, in vitro and in vivo experimental studies published by independent research teams, worldwide experts in this topic, were simply omitted." |
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By Ben Adams, FiercePharma As the FDA was prepping to allow emergency use of blood plasma donation from recovered COVID-19 patients, government officials have put pay to that. The authorization is on hold for now as more data are reviewed, and H. Clifford Lane, M.D., clinical director at the National Institute of Allergy and Infectious Diseases, said an emergency approval could still be issued in the near future, as quoted by The New York Times. This comes after National Institutes of Health leader Francis Collins, M.D., and COVID-19 response leader Anthony Fauci, M.D., recently questioned how efficacious treatments from it could be. |
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By Tom Hals, Reuters A U.S. government program that compensates people who say they have been harmed by an emergency vaccine has paid out on fewer than 10% of claims, raising questions whether the process should be used to address any potential side effects from a coronavirus shot, according to some lawyers who have filed such claims. The Countermeasures Injury Compensation Program (CICP), run by an agency under the U.S. Department of Health and Human Services (HHS), has been designated to handle any issues with a COVID-19 vaccine. |
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Singulair (montelukast) is a drug prescribed to patients suffering from asthma or severe allergies that can provide symptom relief and help them manage their condition. It is a very successful drug for its manufacturer, Merck & Co. Singulair received the U.S. Food & Drug Administration’s (FDA) marketing approval in 1998; by 2004, Singulair was doing $2.62 billion in sales. But by 2009, there were concerns that Singulair may have an adverse effect on its users’ mental health. That year, the FDA updated its potential side effect warning about Singulair to include the potential for “neuropsychiatric events.” Merck & Co. is now facing lawsuits from Singulair users who allege that the medication caused them to experience adverse mental health symptoms, including suicidal ideation. |
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