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Is the Current Epidemic of “Mystery Illnesses,” Similar to Polio, the Result of Vaccine Side Effects?

The CDC and other medical "authorities" refer to them as "mystery illnesses," but they have been around and identified for the past 5 years now, and actually are not all that "mysterious." Young children are affected the most. They are the result of "enteroviruses," the same as the polio virus, but they are not called "polio." There is currently another outbreak of enteroviruses being reported in the corporate media, usually referred to as acute flaccid myelitis (AFM). The symptoms are similar to polio, including paralysis. Health Impact News first reported on these outbreaks back in 2014, providing information you are not likely to read in the corporate media. See our 2014 coverage: As Enterovirus D68 Deaths Increase, Are Vaccine Contaminants to Blame? Lyn Redwood, the president of Children's Health Defense, addresses the current outbreaks and also provides information you are not likely to read in the corporate-sponsored "mainstream" media, which generally ignores all environmental factors, including vaccines, as a possible cause: The Non-Polio Illness That “Looks Just Like Polio.”

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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.

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FDA Approves Dangerous Gardasil Vaccine for Adults in the U.S.

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.

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Did 80,000 People Really Die from the Flu Last Year? Inflating Flu Death Estimates to Sell Flu Shots

The Centers for Disease Control and Prevention estimated that the 2017-2018 flu season killed 80,000 and hospitalized 900,000 Americans. Of course, the mainstream media reported this as fact. Deaths from flu are always estimates because if the Powers-That-Be reported the true numbers of deaths from actual influenza infections, the numbers would be much lower and people would not be so inclined to receive a flu shot. How does the CDC overestimate the number of flu deaths? The CDC accomplishes this by reporting a combined pneumonia and influenza death rate. For example, in 2001 the CDC reported that 62,034 died from influenza and pneumonia. After a painful hour of searching the CDCs database, I found the true 2001 numbers: 257 died from influenza and 61,777 died from pneumonia. 80,000 deaths would lead one to conclude that 13,333 died per month (80,000/6 months) from the flu. Since the internet provides 24-hour news cycles, I think we all would have heard that about 9 people (267/30 days per month) in every state dying daily from the flu. I have five practitioners in my office. We have over 100 years of experience in treating patients. None of us has can recall a single patient dying from the flu. In fact, I can guarantee you that if 9 people were dying in my state daily from the flu, my partners and I would hear about it. In fact, there are always headlines on the internet when one person dies from the flu. Studying the past CDC data shows that each year a few hundred to a few thousand die from the flu.

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The War Against Vitamin D – A Threat to Big Pharma

Natural substances with tremendous healing capabilities that cannot be patented are a huge threat to the pharmaceutical industry and their FDA-approved drugs, and certainly vitamin D is at the top of this list. For example, published scientific literature shows that vitamin D is more effective in preventing annual influenza than the dangerous flu shot. Since the best and primary source of vitamin D is from the sun, most people in North America are vitamin D deficient, even during the summer months when we are told to block the sun's rays due to the fear of skin cancer. When a natural substance like vitamin D can cure and prevent so many diseases, usually in ways far superior to FDA-approved drugs and vaccines, it should come as no surprise that Big Pharma will pull out all the stops to discredit the science behind these natural substances, as they affect their profits from pharmaceutical products. This is routinely done by funding their own biased studies, and then attacking medical doctors and scientists who promote natural cures. One of the areas of vitamin D deficiency that affects many of the families we work with here at Health Impact News, is in the area of Medical Kidnapping and the widely debunked theory of Shaken Baby Syndrome (SBS) that is used to medically kidnap children. Vitamin D deficiency can lead to brittle bones in infants and children, where multiple hairline fractures occur giving the appearance of "abuse" according to proponents of the Shaken Baby Syndrome medical theory. One doctor who is a world-renown authority on vitamin D and has testified in court on behalf of parents falsely accused of SBS, is Dr. Michael Holick. He has recently come under fire and was attacked in the corporate-sponsored "mainstream" media that derives much of its advertising revenue from Big Pharma. William B. Grant, PhD, the director for the Sunlight, Nutrition, and Health Research Center, and former senior research scientist at SRI International, the Jet Propulsion Laboratory, and the NASA Langley Research Center, has recently published a commentary with the Orthomolecular Medicine News Service exposing Big Pharma's "disinformation playbook" and how they attack natural cures, and vitamin D health benefits specifically. Dr. Grant has authored or coauthored over 60 articles in peer-reviewed journals.

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Fraud Uncovered in U.S. Government’s Claim that Vaccines do not Cause Autism – Will Congress and DOJ Act?

Robert F. Kennedy Jr., Chairman of Children’s Health Defense (CHD) and Rolf Hazlehurst, the father of a vaccine-injured child have petitioned Michael Horowitz, the Inspector General of the Department of Justice (DOJ) to investigate the conduct of two DOJ attorneys, Vincent Matanoski and Lynn Ricciardella. The two attorneys represented the Secretary of Health and Human Services in the National Vaccine Injury Compensation Program (NVICP), otherwise known as the “Vaccine Court”, in the Omnibus Autism Proceedings (OAP), which ruled that vaccines do not cause autism. The alleged actions of the two attorneys in the OAP were fraudulent and obstructed justice. Kennedy and Hazlehurst allege that Matanoski and Ricciardella acted together to intentionally misrepresent the opinion of one of their own witnesses, Dr. Andrew Zimmerman, to conceal evidence of his true opinion from the Special Masters who presided in the “Vaccine Court” and the petitioners who were seeking justice and compensation. The evidence that Matanoski and Ricciardella concealed was a report authored by Dr. Zimmerman showing how vaccines may cause autism in a subset of children with underlying mitochondrial issues. After Dr. Zimmerman submitted his report, the DOJ attorney informed Dr. Zimmerman that he would no longer be needed as a witness. Zimmerman’s full opinion was devastating to the government’s case. Simply stated, it was now entirely possible that the government would lose thousands of the OAP cases. The cost could be into the billions and the fund that compensated the vaccine injured would be bankrupted. Even worse, the government’s claim that vaccines are “safe and effective” would evaporate and the claim that “vaccines don’t cause autism” would be debunked.

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Why was the Dangerous and Contagious FluMist Vaccine Approved by the CDC?

In February 2018, the U.S. Centers for Disease Control and Prevention’s (CDC) Advisory Committee on Immunization Practices (ACIP) voted to re-recommend the live virus nasal spray influenza vaccine, FluMist, for the 2018-19 “flu season” after a two-year hiatus. The live attenuated influenza vaccine (LAIV) is popular, particularly with children, since it is sprayed up the nose and does not require a needle for administration. The ACIP voted against recommending the quadrivalent FluMist for the 2016-17 and 2017-18 influenza seasons due to the vaccine’s ineffectiveness in protecting against the H1N1 strain (Influenza A). It is important to note that there are cases reported in the medical literature that FluMist has resulted in shedding and transmission of vaccine strain influenza virus. Despite the fact that the efficacy and effectiveness of this vaccine is unknown, Cynthia Pellegrini, senior vice president of public policy and government affairs for March of Dimes stated, “This vaccine is better than not being vaccinated and there are kids who will not be vaccinated without this option…” The assumption that using FluMist is better than not being vaccinated given the lack of data on the efficacy is not rational because it is not based on scientific evidence.

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Financial Incentives for Doctors to Vaccinate as Many Children as Possible – Keep Patients on Statins

There are monetary awards for doctors and other mainstream medical practitioners who maintain high levels of compliance for prescription drugs (including vaccines), and doctors’ visits. These incentives to get more patients into their offices and to receive as many vaccines and prescription drugs as possible come from the insurance industry. The busier a doctor, pediatrician, or clinic is to maintain quotas for vaccinations and drugs, the more insurance awards them with kickbacks. Despite the ostensible stated reason of ensuring a high level of healthcare, this practice can lead to more health problems due to known side effects of these pharmaceutical products. Educating patients on prevention, such as learning how to eat healthy and avoiding environmental toxins, provides no financial benefits to medical professionals.

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Legislative Update on Battle to Oppose Mandatory Vaccines in Each State

The corporate-sponsored "mainstream" media, along with Big Pharma and the U.S. Government, would like the public to believe that the "science is settled" when it comes to vaccines, and that all vaccines are safe and effective. They spend a great deal of effort to try to convince the public that this is the only view held by medical doctors and scientists. This message to the public, however, is not true, and can be properly called "propaganda." As we have previously written, there are a variety of opinions and viewpoints regarding the science of vaccines among medical doctors and researchers. The extremist view regarding vaccines, and not the one necessarily held by most doctors and scientists, is the view that ALL vaccines are safe and effective for ALL people, ALL the time, by force if necessary. Propaganda is used to try and achieve their agenda, which is a form of medical tyranny by taking away people's choice to refuse vaccines for themselves or their children. Fortunately, the National Vaccine Information Center has volunteers in all 50 states opposing legislative efforts to impose mandatory vaccines and take away informed consent and the freedom to refuse medical treatments like vaccines. They have successfully mobilized the American public through grassroots efforts to oppose most of these bills that have been proposed in recent years. The following is their 2018 annual report. To keep up to date on what is going on in your state regarding vaccine laws, be sure to sign up for their portal on their website.

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The Pertussis Vaccine and Children Brain Damage: America’s Dark Vaccine History

It is a primitive bacterial vaccine licensed in 1914. It has not been given to babies in America for 20 years. It is the vaccine that had brain damaged so many children and caused so many vaccine injury lawsuits that Big Pharma used it to blackmail Congress into giving vaccine manufacturers a partial product liability shield in 1986, which the U.S. Supreme Court made even bigger in 2011. I’m talking about whole cell pertussis vaccine in DPT, a crude brew of whole B. pertussis bacteria heated and washed with formaldehyde but still full of neurotoxic aluminum and mercury along with shock-inducing endotoxin, as well as brain damaging bioactive pertussis toxin, a toxin so lethal that researchers use it to deliberately induce acute experimental autoimmune encephalomyelitis (EAE) in lab animals. Whole cell pertussis vaccine: the most reactive vaccine still given to infants and children in developing countries because it costs drug companies just pennies to make a dose of it.

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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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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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Get Your Flu Shot? DOJ Report From Vaccine Court Reveals Flu Shot is Most Dangerous Vaccine in U.S.

The 2018 push for the flu shot is now in full swing. Pharmacies are advertising enticing offers, including free flu shots with discounts on other products (CVS), and the opportunity to give a free flu shot to children in Africa (Walgreens). These retail outlets offer no-wait shots, making it appear to be as easy as purchasing candy or tissue paper in your visit to your local drug store. What these retail outlets will most likely fail to mention, however, is that according to the Department of Justice's quarterly reports listing compensations for injuries and deaths due to vaccines from the Vaccine Court, the flu shot is the most dangerous vaccine in the U.S. with crippling and fatal side effects. How many people taking advantage of "free" flu shots will know that there is a long list of debilitating side effects from the flu shot, as compensated by the U.S. Government in the federal Vaccine Court? These side effects include (among others): GBS - Guillain–Barré syndrome is a rapid-onset muscle weakness caused by the immune system damaging the peripheral nervous system. TM - Transverse myelitis is an inflammation of both sides of one section of the spinal cord. This neurological disorder often damages the insulating material covering nerve cell fibers (myelin). ADEM - Acute disseminated encephalomyelitis, or acute demyelinating encephalomyelitis, is a rare autoimmune disease marked by a sudden, widespread attack of inflammation in the brain and spinal cord. CIDP - Chronic inflammatory demyelinating polyneuropathy is a neurological disorder -- a condition that targets your body's nerves. MS - Multiple sclerosis is a demyelinating disease in which the insulating covers of nerve cells in the brain and spinal cord are damaged. SIRVA - SIRVA stands for “Shoulder Injury Related to Vaccine Administration.” SIRVA can lead to intense, prolonged pain, limited range of motion, and shoulder-related injuries such as Adhesive Capsulitis or Frozen Shoulder Syndrome. Myasthenia gravis is a long-term neuromuscular disease that leads to varying degrees of skeletal muscle weakness. Peripheral Neuropathy is damage to or disease affecting nerves, which may impair sensation, movement, gland or organ function, or other aspects of health, depending on the type of nerve affected. DEATH by the flu vaccine. All of these debilitating side effects were reported as being compensated in recent DOJ reports.

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