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.
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.
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.
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.
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."
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."
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.
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?
I just got a video of the child I mentioned in my last post. He has severe autism. He is the son of a respected board certified physician who has declared with 100% certainty that his beloved son was vaccine injured. He, like any parent, would move heaven and earth for his child. He has given permission to share. Two days ago the child had his fourth ozone treatment in our office. As usual, we had to restrain him. But strange, the high pitched cries were absent. We had already been told that a few days before, in his sleep, he was actually talking sentences, though the parents could not make out the words. This was new. He has also been taking supplements to reduce his high levels of aluminum documented by lab in his system. The video you see here is also showing quite new behavior. In the doctor’s words, “He was actually processing how to ride the scooter. It was the first time I’ve ever seen that in him. In the past he’d get frustrated. This time he moved the scooter backwards and time he accomplished riding it. He was smiling and was happy, also a first. He was playful. He was smiling. This has never happened before. A few days ago he was talking in his sleep, he was engaging in a conversation while sleeping. This was also a first. I am just to impressed and thankful to God, and to you and Dr. Su and your staff. You care.” I told the doctor that a case like this means more to us that most any other case. This child still has a life to live.
Over the past several decades, American children’s physical and mental well-being has steadily deteriorated. Over half (54%) of all U.S. children (as of 2007) had a chronic health condition—with developmental and behavioral problems, obesity, allergies, asthma and mental health conditions leading the pack—and the prevalence of many of these conditions doubled from 1988 to the mid-2000s. Federal reporting on pediatric health indicators in 2017 showed that one in five children (kindergarteners through adolescents) were obese, one in ten had activity limitations resulting from chronic health problems, and one in seventeen (more males than females) had, according to a parent, “serious difficulties with emotions, concentration, behavior or getting along with other people.” In addition, 12% of adolescents suffered a major depressive episode in the previous year, with the prevalence of teenage depression rising continuously since 2004 and suicide representing the second leading cause of death for both teens and young adults. Vaccines are one of the most widespread and ongoing sources of prenatal and childhood exposure to metals that negatively affect the brain. Prenatal exposure—as occurs with the mercury-containing flu shots and aluminum-containing pertussis vaccines now routinely administered to pregnant women—is particularly dangerous as early exposure can impair subsequent growth and development of neurons. The U.S. requires the largest number of vaccines for school entry of any developed nation, although compulsory vaccination has been trending upward in Europe as well.