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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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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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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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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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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.

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Do You Know How to Recognize a Vaccine Reaction?

Do you know how to recognize a vaccine reaction? Like with prescription drugs and other pharmaceutical products, reactions to vaccines can be mild or severe. There can be complete recovery or long lasting health problems after vaccine reactions. Rarely, vaccine reactions can be fatal. If you are making a decision about vaccination for yourself or your child, it is important to first become fully informed about each vaccine’s reported side effects, precautions and contraindications, which means reasons for why a person may be at risk for having a serious reaction. It is especially important for parents to become informed about vaccine complications and how to recognize the symptoms of a vaccine reaction.

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4 Years After CDC Whistleblower Reveals Vaccine Fraud Still Nothing Happens

It was four years ago, August 2014, that a senior CDC scientist—Dr. William Thompson–claimed whistleblower protection by claiming that the CDC had committed fraud by hiding and manipulating data that showed the MMR vaccine was associated with a higher risk of autism. According to the CDC, we are currently suffering through an exponential increase in autism since the 1970s. In 1970, the autism rate was 1 in 10,000. In 2018, the rate of autism epidemically increased to 1 in 59 children. That is a 169-fold increase in autism in U.S. children over nearly 50 years! You would think a senior CDC scientist who claims malfeasance at the CDC is responsible for the rapid rise in autism would immediately trigger Congressional investigations to find out the truth. However, our dysfunctional Congress would prove you wrong.

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U.S. Children Have Highest Rates of Diabetes and the Most Vaccines in the World

Type 1 diabetes—also called insulin-dependent diabetes mellitus (IDDM) or juvenile diabetes— is one of the most common and rapidly increasing autoimmune diseases in children. The U.S. has more children with type 1 diabetes than any other country in the world, with a prevalence in children and adolescents that grew by 21% from 2001 to 2009. The U.S. also has the highest number of new cases annually, well ahead of India (with a population four times bigger). Puzzling over the dramatic rise of type 1 diabetes in young children over the past several decades, scientists are reaching consensus that environmental factors play a significant role. Two of the most widely discussed environmental candidates are dietary factors and viral infections. In light of the hypothesis that viruses can be precipitating factors, it has appeared logical to at least some researchers to consider whether live virus vaccines also could be contributors, particularly given the temporal association between expansion of the childhood vaccine schedule and the escalating type 1 diabetes rates.

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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.

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FDA Approves Experimental Hepatitis B Vaccine for Adults Despite Higher Incidence of Heart Attacks

In February 2018, the FDA and CDC approved the recommendation for a new hepatitis B vaccine, Heplisav-B targeting adults over the age of 18. The U.S. Food and Drug Administration (FDA) had twice rejected the application for licensure for Heplisav-B in the past four years because of safety signals. Heplisav-B differs from other licensed hepatitis B vaccines in that it contains a new synthetic adjuvant known as cytosine phosphoguanine 1018 (CpG 1018) composed of short synthetic DNA molecules. In 2016, the FDA rejected an application for licensure for the Heplisav-B vaccine, because the agency was concerned about an increased rate of heart attacks and deaths in people who had been given the vaccine. During the trial, approximately 14 subjects had heart attacks. In July 2017, the FDA committee convened to re-evaluate the scientific evidence and make a decision on whether Heplisav B should or should not be approved for use in the U.S. This committee had only one cardiologist on the team, Milton Packer, MD, who is a distinguished scholar in cardiovascular science at the Baylor University Medical Center in Dallas, Texas. According to Dr. Packer, it was possible that the Heplisav B vaccine’s novel adjuvant was related to the higher number of heart attacks in study participants who received the experimental vaccine. He stated: "To know if the 7 -1 heart attack imbalance represented a real risk, we’d need comparative data in 50,000 people." However, the only way to conduct such a large trial would be to approve the vaccine and see what happens in the public. With Dr. Packer abstaining in his vote to recommend the vaccine, the FDA committee approved it anyway. Dr. Packer stated: "Why did I abstain? Based on the available data, it was impossible for anyone to know if the increase in heart attack risk was real. There is a simple rule in life: if you don’t know, you should say you don’t know." The vaccine is now available to the public, and all those who receive it are basically guinea pigs to find out if heart attacks will result from the experimental vaccine, and if it will continue to have FDA approval.

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UK Government to Begin Giving HPV Vaccine to Boys Amid Public Outcry

The UK government has recently announced that, by September 2019, boys aged 12 to 13 years will be given the human papillomavirus (HPV) vaccine, a vaccine that has been available to girls in the UK for the past ten years. There has been documented evidence that the HPV vaccine has caused more injuries than any other vaccination in history. Despite this evidence, however, the HPV vaccination has continued to be hailed a success by the pharmaceutical industry and governments alike. According to the MHRA, the adverse event reporting system in the UK, there have been a total of 9,119 reports of adverse reactions reported in the UK since the vaccine was launched in 2008. These reports equate to 23,882 different ailments and include a total of 8 deaths. The UK’s decision to include boys into the equation has alarmed many parents whose daughters have already been injured by the vaccine.

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Are Vaccines Linked to Increase in Mast Cell Disease and Allergies?

Do you or does someone you know have severe symptoms of itching, rashes, flushing, stomach or other body pain, frequent diarrhea, nausea, fatigue, brain fog, headache and severe allergies to certain foods, medications or insect stings that may include fainting episodes or anaphylaxis? Although it has been classified as a rare immune system disorder, there are indications that Mast Cell Activation Syndrome (MCAS) may be more prevalent than previously thought and people can suffer for years without being correctly diagnosed. With severe allergies and chronic inflammatory diseases increasing in populations around the world, scientists are investigating the association between mast cell dysregulation and various brain and immune system disorders ranging from asthma, inflammatory bowel disease and chronic fatigue syndrome to ADHD, depression, autism and cancer. Mast cells play an important part in keeping the body healthy, but when they malfunction, can cause system wide chronic inflammation in the body that interferes with quality of life or can even cause death. Although for the past several decades, most pediatricians and public health officials have rejected the possibility of a relationship between vaccination and the development of allergic and autoimmune disorders, the apparent increase in mast cell dysregulation in highly vaccinated populations deserves more in-depth investigation.

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Soaring Infertility Rates Linked to Vaccines

A plague is spreading silently across the globe. The young generation in America, the United Kingdom, France, Italy, Japan, Australia – in virtually every western country -- is afflicted by rapidly increasing rates of infertility. This spring, the United States reported its lowest birth rate in 30 years, despite an economic boom. Finland’s birth rate plummeted to a low not seen in 150 years. Russian President Vladimir Putin recently introduced a string of reforms aimed at stemming the country’s “deep demographic declines.” The government of Denmark introduced an ad campaign to encourage couples to “Do it for Denmark” and conceive on vacations, and Poland produced a campaign urging its citizens to “breed like rabbits.” The “population bomb” we were all endlessly warned about by environmentalists failed to blow, and instead, demographers have been trying to raise the alarm about the population implosion crisis unfolding across the West -- the graying of societies facing an unprecedented aging demographic in which there will be too few young to support the old. Most often, they blame social factors: young women embracing careers instead of motherhood, men shunning marriage and fatherhood, rising consumerism or couples choosing to delay raising a family until the economy settles. But there is another phenomenon that is rarely mentioned – the growing numbers of young people who are not childless by choice but who are incapable of bearing children. So, earlier this month, when an unprecedented study was released that looked at a database of more than eight million American women and singled out a whopping 25 percent increase in childlessness associated with one particular vaccine that young women have been taking for only a decade -- in tandem with a marked decline in fecundity -- you would have thought there would be significant interest from public health, the medical profession and the media, wouldn’t you?

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