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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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Should the CDC Oversee Vaccine Safety When They Purchase Over $5 Billion of Vaccines from Big Pharma?

The U.S. Centers for Disease Control and Prevention (CDC) is tasked by the U.S. Government with overseeing vaccine safety. They claim on their website: "The United States’ long-standing vaccine safety program closely and constantly monitors the safety of vaccines. A critical part of the program, CDC’s Immunization Safety Office identifies possible vaccine side effects and conducts studies to determine whether health problems are caused by vaccines. Data show that the current U.S. vaccine supply is the safest in history." However, the CDC is the largest purchaser of vaccines in the world, and their budget to purchase vaccines from pharmaceutical companies was over $5.1 BILLION in 2018, and is set to increase to over $5.4 BILLION in 2019. Can we trust the CDC to oversee vaccine safety with such a blatant conflict of interest?

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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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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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Japan has the Lowest Infant Mortality Rate Following Ban on Mandatory Vaccinations

Fact: Japan has the lowest infant mortality rate following ban on mandatory vaccinations, and they urge other countries to follow this firm stance. The citizens of Japan are statistically proven to be the healthiest and longest-living people in the world. The country also has the lowest infant mortality rate on the planet. It may come as no surprise to many that the Japanese Government banned a number of vaccines that are currently mandatory in the United States and has strict regulations in place for other Big Pharma drugs and vaccines in general. Japan’s anti-vax policies have long been criticised by vaccine pushers in the US who claim that vaccinating the public “promotes health.” However, Japanese people live longer, healthier lives than Americans, with babies born in the US twice as likely to die in infancy than those born in Japan. It’s clear to see that Western nations have a lot to learn from the Japanese when it comes to their approach to vaccinations and issues facing public health. The Japanese are vaccine sceptics, to put it simply, and due to adverse reactions suffered by Japanese children, have banned many vaccines. The Japanese are well educated on the dangers of over-vaccinating their children and oppose the use of multi-shot vaccinations such as the MMR vaccine. Following a record number of children developing adverse reactions, including meningitis, loss of limbs, and even sudden death, the Japanese government banned the measles, mumps, and rubella (MMR) vaccine from its vaccination program, despite facing serious opposition from Big Pharma.

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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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Lawsuits Mount Against Shingles Vaccine

Drugwatch.com is reporting that Merck's shingles vaccine, Zostavax, is facing several lawsuits for causing shingles, the very thing the vaccine is supposed to protect against. Eighteen people from across the country filed one of the first Zostavax lawsuits in New Jersey. The lawsuit alleges the vaccine caused people to develop shingles. The outbreak led to hospitalization and chronic nerve pain called post-herpetic neuralgia. “Merck knew or should have known that its product caused viral infection and was therefore not safe,” the suit said. Jane Boda filed one of the early lawsuits in Wisconsin in May 2018. The lawsuit claims Zostavax gave Boda shingles. She says she suffered chronic nerve damage as a result.

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Whistleblower Accuses CDC of Manipulating Shingles Data with Chickenpox Vaccine

The controversy over varicella vaccine safety and mandates has raged since its introduction in the U.S. nearly 25 years ago. When it was licensed in 1995, the National Vaccine Information Center (NVIC) questioned the strength of the scientific evidence for safety and effectiveness used by CDC and the American Academy of Pediatrics (AAP) to make a universal use recommendation and argued the vaccine should not be mandated because, in part, universal use of the vaccine could drive chickenpox into older children and adults and raise the risks for shingles later in life. Gary S. Goldman, PhD served for eight years as Research Analyst for the Varicella Active Surveillance Project (VASP) in a cooperative project with the CDC. In March 2018, Dr. Gary S. Goldman published an article in Annals of Clinical Pathology, “The US Universal Varicella Vaccination Program: CDC Censorship of Adverse Public Health Consequences.” In that article he provided evidence to support his allegation that CDC officials manipulated varicella data to affirm the CDC’s support for chickenpox vaccine mandates that that will require a lifetime of expensive vaccine boosters. In what Goldman described as a deliberate “attempt to quash the unwanted outcomes in the years following 2000,” he said it became apparent that the methods for interpretation of data were flawed, skewing CDC and VASP conclusions in favor of the varicella mass vaccination program.

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Pro-Vaccine Maryland Parent Outraged over Corruption in Mass Gardasil Vaccination Policies

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.

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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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Are Front-line Emergency Room Doctors the Key to Identifying Vaccine Injuries and Reporting Them?

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.

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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.

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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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HPV Vaccine Scandal Affects Cochrane Biased Review as Critics Speak Out in BMJ

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.”

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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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Lawfirm Announces $101 Million Measles Vaccine Settlement for Infant that Suffered Brain Injury

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."

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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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