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.

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.

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.

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.

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.”

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.

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."

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.

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?

Unable to Sue Big Pharma, Vaccine Injury Victims Now Being Denied Legal Counsel in Vaccine Court

How does the National Vaccine Injury Compensation Program (NVICP) and the Federal Court of Claims deprive petitioners, who are seeking compensation for their injuries, the opportunity to seek and retain legal counsel? Very cleverly. But it takes some understanding of how legal representation in the program has evolved and more importantly, how fees are paid. Today, our government is shutting the door on those who have been injured or have died as a result of a vaccine.