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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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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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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.

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Texas Mom Who is a Nurse Fights to Regain Custody of Daughter Taken Away After Gardasil Vaccine Injury

Social workers told a Texas mother that Monday was her last visit with her daughter. Aniya Blu Vasquez was medically kidnapped from her family after she became ill following a medical error in which her pediatrician injected her with the Gardasil 9 vaccine intended for her older brother. Aniya was just 4 months old at the time. A Texas court decided last month that the parental rights of her mother, Anita Vasquez, should be terminated, devastating the family and supporters alike. However, their story is not over. In a quirk of legalities, Anita Vasquez filed a Declaration of Recision of Signature/Contracts before the court was able to file the entry of judgement on the termination of parental rights. As a result, there will be another hearing on Monday, July 23, 2018, at the Victoria County Courthouse at 9 a.m. She says that there is substantial new evidence in her case that was not considered by the court. Anita asserts that the very basis upon which CPS seized custody of Aniya was fraudulent, and CPS knew it all along. Concerned citizens are rallying around the family that they believe is suffering a grave injustice.

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Gardasil Vaccine Legal Victory: Canada Federal Court Rules to Release Clinical Trial Data to American Researcher

CBC News and the British Medical Journal (BMJ) are reporting that Professor Peter Doshi has won a major legal victory against pharmaceutical companies trying to hide clinical trial data from the public due to "confidential agreements" for 5 pharmaceutical products. Doshi sued Health Canada to release clinical trial data submitted to Health Canada by the manufacturers of the HPV vaccines Gardasil, Gardasil 9 and Cervarix, and the anti-viral flu medications, Tamiflu and Relenza. A Canadian Federal Court judge ordered Health Canada to release the pharmaceutical clinical trial data, undercutting the Canadian government's attempts to keep the information confidential. As far as I can determine, this landmark court ruling out of Canada has been completely censored in the U.S. corporate-sponsored "mainstream" media. This appears to be a brilliant legal strategy by Doshi and his attorneys, since they had little to no chance of obtaining this clinical trial data from any court in the U.S., where pharmaceutical companies enjoy legal immunity from most lawsuits. The importance of receiving this data, particularly on Merck's Gardasil vaccine, cannot be overstated. As we have reported many times here at Health Impact News, the entire medical approval process to bring the HPV vaccine into the U.S. market is full of scandals and cover-ups, which has resulted in the injuries and deaths of many young people, particularly young women aged 12 to 26, many of whom can no longer bear children due to the vaccine making them infertile. "I hope my case sets a precedent and allows researchers, clinicians, and the public easy access to clinical trial data," Doshi reportedly stated in an email to CBC News. "Regulators shouldn't have a monopoly on judging the risks and benefits of medicines or hinder others from doing the same via confidentiality agreements."

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HHS Sued for Not Upholding Vaccine Safety Testing Mandated by Law

In 2017, Health Impact News reported that the Informed Consent Action Network (ICAN), supported by 55 organizations, representing over 5 million people, had taken the unprecedented step of serving a notice to Mr. Don Wright, M.D., M.P.H., who was the acting secretary of the Health and Human Services (HHS) department at the time, stating that HHS had failed in their duty to conduct the proper scientific research required to demonstrate vaccine safety as was required by law, and that they should take immediate action to remedy this negligence. Last week (July, 2018), Del Bigtree interviewed Robert F. Kennedy Jr. on his program HighWire, announcing that they had filed a lawsuit against HHS for violating U.S. law on vaccine safety, and won.

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Hundreds of HPV Vaccine Victims Take to the Streets in Dublin to Protest – 2 Girls Suffer Seizures During Protest

Hundreds of HPV vaccine-injured people took to the streets to protest at Leinster House, Dublin, on July 9th, 2018, while Professor Ian Frazier, one of the co-inventors of the vaccine, gave a speech next door at the Royal College of Physicians. During the protest, 3 Gardasil vaccine victims took ill, with 2 of them having seizures. Both of the girls suffering seizures had to be taken to the hospital. The following video was taken of the protest, and towards the end of the video you can see one of the girls having a seizure. This protest has been mostly censored in the "mainstream" corporate-sponsored media.

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Samoa Seizes All MMR Vaccines After Two Infants Die Minutes After Receiving the Vaccine

TV1 in Samoa is reporting that two infants have died within minutes of receiving the measles, mumps, and rubella (MMR) vaccine. "Tala Fou brings you breaking news on the death of two young children both aged 1-year-old from the villages of Safotu and Sasina in Savaii. Both children died within minutes of being vaccinated with the MMR vacine at Safotu Hospital on Friday morning the 6th of July. Our News Reporter Alisa Faamaoni met with both families in Savaii today. The parents of the first child Marietta and Samuelu Tuisuesue of Sasina explained in detail to Tala Fou that within three minutes of their 1-year-old daughter Lannacallystah Samuelu being injected with the MMR vacine by a nurse she was dead." What is so tragic, and has this island nation in such an uproar, is that the parents of the second child who died had reportedly already learned about the first infant's death a couple hours earlier and declined to have their child receive the same MMR vaccine. The mother reports that the nurse administered the vaccine against her consent, leading to the child's immediate death upon receiving the vaccine.

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Should Women be Given the Tdap Vaccine During Pregnancy?

A great debate is raging about whether we should have mandatory vaccination to prevent childhood illnesses. Mandatory vaccination would do away with a religious, ethical, or scientific disapproval of a vaccine. A study from the University of North Carolina School of Medicine reported that the Tdap vaccination during pregnancy reduced the occurrence of infantile pertussis. This study is a perfect example of why we need informed consent on the safety and efficacy of vaccines and why we should not have government mandates about vaccines. The researchers looked at infants admitted to the hospital with pertussis and compared two groups of pregnant women: one group who received the Tdap and the other group that did not. This study showed that the Tdap vaccine is 0.02% effective at preventing hospitalization from pertussis. In other words, the vaccine will not benefit 99.98% who take it. The Tdap vaccine contains a known neurotoxin (aluminum) and carcinogen (formadehyde). There are ZERO safety studies shown that it is safe to inject either substance into a human much less a pregnant human. When I was trained, I was taught to be very careful when prescribing any therapy for a pregnant woman. I was always taught to err on the side of caution. I think that was sage advice. Tdap for pregnant women? Give women the appropriate information and let them decide.

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World Health Organization’s New Lax Vaccine Safety Policy Leads to More Child Deaths by Vaccines

Two leading pediatricians in India have published a critique of the World Health Organization's (WHO) newly revised manual on the classification of Adverse Events Following Immunization (AEFI). The doctors claim that the new guidelines are too lax, resulting in more children dying from adverse reactions to vaccines, with no accountability for the vaccine manufacturers to produce safer vaccines. In the U.S., pharmaceutical companies manufacturing vaccines cannot be sued due to faulty vaccines, which allows them to put as many vaccines into the market as they want, with no repercussions if the vaccine proves to be faulty or have a high injury and death rate. Victims must sue the U.S. government and top DOJ attorneys who protect the drug companies. This move by the WHO may very well be an attempt to protect drug companies manufacturing vaccines by preventing lawsuits in the rest of the world for faulty vaccines. According to the report of these two doctors, the consequence of India adopting WHO's new classification can be seen from the causality assessment of 132 serious AEFI cases uploaded on the website of the Ministry of Health and Family Welfare. Of the total AEFI cases, 54 babies died and 78 survived, "but not even one death was classified as vaccine-related. Nearly all the deaths were simply classified as unclassifiable or coincidental."

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Japanese Attorneys Representing HPV Vaccine Victims Urge Government to Ban HPV Vaccines

In a recent press release commemorating the 5-year anniversary of the Japanese Government suspending its recommendation of the HPV vaccine, the National Attorneys Association for the HPV Vaccines Lawsuits called upon the Japanese Government to ban the HPV vaccine completely. This is the type of news that is routinely censored in the corporate-sponsored "mainstream" media in the United States. The fact that there is a national organization of attorneys litigating against one specific vaccine and the injuries it is causing, is itself newsworthy. The vaccine manufacturers who are being sued in Japan, GlaxoSmithKline PLC and Merck Sharp & Dohme Corp., enjoy 100% legal immunity in the United States, due to the 1986 National Childhood Vaccine Injury Compensation Act. We must look outside of the U.S., therefore, to learn about just how devastating Gardasil and the HPV vaccine is, as the National Association for the HPV Vaccines Lawsuits reports: "Compared to other routine vaccinations, an average of over seven times the number of serious adverse effects per one million HPV vaccinations have been reported, and the number of disability certifications by the Adverse Drug Reaction Relief System is almost ten times higher."

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Who Will Take a Stand Against Forced Vaccination and Fight for Medical Freedom in the U.S.?

Every July Americans celebrate the day in 1776 when we declared our independence from a monarchy and began to create a Constitutional Democratic Republic to secure liberty and justice for all. Today, we are witnessing the erosion of core values that our constitutional democracy was founded upon. One example is a public campaign led by the medical establishment to demonize and discriminate against anyone opposing zero tolerance vaccine laws that violate human rights in the name of public health. There are only two laws that require American citizens to risk their lives. The first is a federal law, the military draft, which requires all healthy male adults to risk their lives in a war declared by the government to protect national security. Adults objecting to a war for religious beliefs or conscience can obtain a conscientious objection exemption without being punished. The second is a state law requiring all healthy children to risk their lives in a war that doctors declared on microbes two centuries ago. However, unlike adults who are not punished for following their conscience and refusing to fight in a war to protect national security, parents can be punished for following their conscience and refusing to risk their children’s lives in a war to theoretically protect the public health. State sanctions include segregation and loss of the unvaccinated child’s right to a school education or permitting pediatricians to deny medical care to children if their parents refuse one or more government recommended vaccinations. The forced vaccination lobby backed by industry and medical trade is already making plans to double down and target multiple states in 2019 for removal of religious and conscientious belief exemptions, while also placing further restrictions on medical exemptions to vaccination. Will you stand up and defend vaccine freedom in America?

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California Pediatrician Bob Sears Breaks Silence on Medical Board Opposition to Vaccine Exemptions

Two years ago we covered the story about Dr. Bob Sears in California who faced discipline by the California state Medical Board after he wrote a medical exemption for vaccines on behalf of a 2-year-old patient who experienced adverse reactions from earlier vaccines. This action taken against Dr. Sears happened after the new law in California, SB277, went into effect removing religious and philosophical exemptions for vaccines. After the passage of SB277 in 2015, only a doctor can issue an exemption for vaccines for medical reasons. Dr. Bob Sears is internationally renown for his stance on parental rights and informed consent, and although he is not anti-vaccine, he does believe that a one-size-fits-all approach to vaccines is misguided, and that the medical needs of his patients need to be taken into consideration regarding vaccines and the spacing of vaccines. Therefore, the attack on Dr. Sears was generally seen as a political move in California to try and intimidate him and other doctors who write medical exemptions for vaccines for their patients, which is perfectly legal, even after the passage of SB277. California lawmakers are heavily lobbied and influenced by Big Pharma, which would like to see all vaccines mandated for everyone, regardless of medical conditions. Dr. Sears has broken his silence after 2 years, and he has revealed that there are several other cases the California Medical Board is looking into regarding his medical practice.

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Merck Receives FDA Priority Review to Expand Dangerous Gardasil Vaccine to Women and Men Ages 27 to 45

Gardasil vaccine manufacturer, Merck, announced earlier this month (June, 2018) that the U.S. Food and Drug Administration (FDA) has granted them a "Priority Review" to approve the dangerous and controversial Gardasil 9 vaccine to women and men, ages 27 to 45. The Gardasil vaccine is currently approved for girls and boys, ages 9 through 26. The request by Merck to expand its market to women and men, ages 27 to 45, and the FDA's approval to grant it a Priority Review by October 6, 2018, follows 10 years after the FDA struck down a similar request to expand the older version of Gardasil to the same age group. Besides the hundreds of stories of young women being injured or even killed by the Gardasil vaccine, as well as the lawsuits mounting in countries outside the U.S., the published data regarding Gardasil just keeps getting worse. Will the FDA consider these studies in determining if Gardasil should be expanded to a larger population? Shouldn't the FDA instead be determining if Gardasil should even stay in the market, as other countries are beginning to ask?

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Texas Mom Blamed for 4-Month-Old Daughter’s Accidental Gardasil Vaccine Injury – Loses Parental Rights

A Texas jury decided Thursday afternoon, June 21, to terminate the parental rights of a mother whose 4-month-old baby was injected with the Gardasil-9 vaccine in error. Anita Vasquez is devastated. She and her friends and supporters are shocked that this could happen. Instead of doctors and social workers considering the possibility that the symptoms her daughter, Aniya Blu Vasquez, experienced could be related to the vaccine that is not approved for children under 9-years-of-age, Anita was blamed, and her daughter was taken from her by Child Protective Services (CPS). Anita tells us that there was important information that the jury did not hear before making their decision. There were things that she believes her attorney should have presented but did not. For example, only doctors who believed that there were no side effects from the Gardasil vaccine were allowed to testify.

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