On December 23, 2009, the U.S. Food and Drug Administration (FDA) approved use of Fluzone High-Dose flu vaccine for the elderly. This new product is four times more powerful, that is, contains four times the amount of flu virus antigen per dose as the product used previously (Fluzone). The vaccine is given as a single injection. FDA approval was given even though its Advisory Committee on Immunization Practices made no indication it was better than the previously-used Fluzone after reviewing studies of safety and effectiveness. The Centers for Disease Control and Prevention stated, “Data demonstrating greater protection against influenza illness after vaccination with Fluzone High-Dose are needed to evaluate whether Fluzone High-Dose is a more effective vaccine for patients age 65 years.” The largest study reviewed by the FDA committee showed that the new high-dose vaccine had a 50% higher rate of side effects within the first week after the injection, and four times the chance that patients would develop fever after the shot. The approval was given even though a large three-year study of effectiveness and safety had just begun (U.S. Centers for Disease Control and Prevention, 2010). Prior to 2013, fewer than 1,000 elderly Americans died from the flu in all but one year. But in the most recent five years available, the average jumped to over 3,000 per year, exceeding 5,000 in the most recent year (2017). The 2013-2017 flu death rate among Americans over 65 jumped 328.6%, or more than four times than it was in the period 2006-2012. The influenza death rate did not change among Americans age under 35, while it rose 132.4% (more than doubled) among those age 35-64. The recent mortality rise in elderly flu deaths should be taken seriously, and future trends should be monitored by health officials.
The Medical Journals’ Sell-Out: Big Pharma Buys Advertising and Decides What Gets Published – Anything Negative About Vaccines Not Allowed
The vaccine industry and its government and scientific partners routinely block meaningful science and fabricate misleading studies about vaccines. They could not do so, however, without having enticed medical journals into a mutually beneficial bargain. Pharmaceutical companies supply journals with needed income, and in return, journals play a key role in suppressing studies that raise critical questions about vaccine risks—which would endanger profits. This concerted campaign to prevent dissemination of vaccine content that does not toe the party line will make it harder than ever for American families to do their due diligence with regard to vaccine risks and benefits.
Kerri Rivera made the following remarks about the Chlorine Dioxide Protocol during her 2019 presentation at AutismOne. She stated: "Autism is avoidable, treatable, and curable. I have seen the faces of the children. I have met them. I have spoken with them and with the mothers, the parents, and the families who got their lives back. They are back – they are totally back from autism – and I want to share that with you. The CD protocol is tried and true. This is the tenth year for this protocol. I appreciate you keeping an open mind for recovering yourself and your children from illness, especially autism. For those of you who want the information about the CD protocol and are ready for it, here it is. I am happy to help you and I wish you all the best in your journey." The protocol brings about healing by killing pathogens, resolving systemic inflammation, and revitalizing damaged immune system functioning. It addresses candida, bacteria, parasites, viruses, and heavy metals. The CD protocol is not just for autism. It also addresses conditions such as Asperger's, PANDAS, PANS, PITAND, ADD and ADHD, and PDD-NOS (Pervasive Developmental Disorder-not otherwise specified) which is often another label for autism. These related conditions can exist side by side with autism, overlap with it, or be separate from it. If 557 people have already lost their autistic diagnosis through the use of the CD protocol, then how many more must be set free from this modern illness before the scientific and medical communities will wake up and recognize the truth that autism can be treated and cured?
Bill and Melinda Gates Foundation and World Health Organization Work Together to Conceal Vaccine Death Statistics in Poor Countries
The promotion for the utilization of vaccines and the inadequate surveillance systems in poor, Third World countries is largely controlled by the Bill and Melinda Gates Foundation through the mantle of the World Health Organization (WHO) which administers public health programs in poor and middle income countries. Vaccine safety is the domain of the WHO Global Advisory Committee on Vaccine Safety (GACVS), established in 1999. The WHO-GACVS developed a two-tiered classification system for assessing and reporting adverse events following immunization (AEFI). The AEFI classification system used in Third World countries disqualifies Deaths following vaccination, as having any causal association with vaccines. The dubious rationale given by the WHO: if there was no statistically significant increase in deaths recorded during Phase 3 vaccine trials, death is not associated with vaccination. Those phase 3 trials are too small and too short to detect rare lethal adverse effects. After a vaccine is licensed, all deaths and serious adverse reactions that had not been detected in Phase 3 trials are labelled as ‘coincidental deaths /events’ or ‘unclassifiable’. The association of death with vaccination is discounted. An Exploratory Analysis (2018) by Dr. Jacob Puliyel, head of pediatrics at St. Stephens Hospital Delhi, India, and member of the National Technical Advisory Group on Immunization (NTAGI) of the Government of India, documented that following the shift from the DPT – diphtheria, pertussis, tetanus – vaccine in 2011, to the pentavalent vaccine, the number of deaths rose precipitously. Dr. Puliyel calculated that data from states with good reporting of adverse events, suggest that there are likely to be 7,020–8,190 additional deaths each year in India, because of the shift from DPT to Pentavalent vaccine. The shocking conclusion one cannot help but draw is that the WHO classification system for adverse events following vaccination was crafted for use in devalued populations in the Third Word, where its use is imposed. This harks back to the days of institutionalized Apartheid. Understandably, Dr. Puliyel concluded that: “deaths and other serious adverse events following vaccination in the third world, that use WHO-AEFI classification are not recorded in any database for pharmacovigilance. It is as if the deaths of children in low (and middle) income countries are of no consequence.”
Fighting Academic Censorship on Gardasil Vaccine Research, Dr. Sin Hang Lee Challenges Medical and Scientific Community to Debate in Open Forum
In an unprecedented move, pathologist/clinical microbiologist, Dr. Sin Hang Lee has decided to invite the international community of scientists and medical professionals to peer-review and/or discuss his latest research “Toll-like receptor 9 agonist in HPV vaccine Gardasil 9” in an open public forum. According to Dr. Lee, during 2011/12, when he tried to publish papers describing HPV DNA fragments he had discovered in Gardasil 4, his first paper was rejected by three medical journal editors despite the fact that the manufacturer had assured health authorities worldwide no such fragments were in the final product. The first of his papers regarding this subject was favorably peer-reviewed by three scientists who recommended publication. However, upon subsequent review by a journal editor publication was inexplicably denied. Both papers were subsequently published in non-medical journals which deal with ‘pure science’ thereby limiting access to most medical professionals. Dr. Lee also states that after submission of his latest research to “Vaccines” the editor-in-chief sent his paper out requesting a peer review. However, the editor’s subordinates refused to process the manuscript even though the journal claims to be “an international, peer-reviewed open access journal focused on laboratory and clinical vaccine research, utilization and immunization.” Dr. Lee believes this unusual response illustrates a top-level concerted effort by vaccine stakeholders to suppress any information which could potentially impact the published safety profile of HPV vaccines.
Former FDA Commissioner Gottlieb Joins Pfizer: World’s Largest Pharmaceutical Company and Second Largest Manufacturer of Vaccines
Former Food and Drug Administration (FDA) Commissioner Scott Gottlieb, MD has joined the board of directors of Pfizer, Inc.—the world’s largest pharmaceutical company and second largest manufacturer of vaccines. Pfizer, which posted total revenues of $53.7 billion in 2018, announced Dr. Gottlieb’s election to the board on June 27, 2019. Dr. Gottlieb, who led the FDA from May 11, 2017 to Apr. 5, 2019, has also been appointed to the Regulatory and Compliance Committee and the Science and Technology Committee of Pfizer’s board. As FDA Commissioner, Dr. Gottlieb often expressed strong opinions about the safety and mandatory use of vaccines. He has said he does not believe there is a need for further scientific research into reported vaccine side effects, such as the development of regressive autism in previously healthy children after vaccination. He was also outspoken this year about his belief that children attending school with vaccine exemptions are to blame for measles outbreaks and the federal government should intervene if states do not restrict or eliminate vaccine exemptions.
Attorneys Sussman and Kennedy filed a lawsuit in New York State (NYS) Supreme Court challenging the constitutionality of the NYS legislature’s June 13, 2019 repeal of the religious exemption to vaccination, Public Health Law Section 2164(9). The plaintiffs, 55 NYS families who held lawful religious exemptions, request that the court enjoin the enactment of the repeal temporarily, preliminarily and permanently. The plaintiffs are of diverse religious faiths, including Christianity, Judaism and Islam. As a result of the repeal, these families can no longer educate their children in any schools or camps in New York without violating their religious faith. The parents who bring the suit seek to represent thousands of other families likewise affected by the repeal. Kennedy, Chief Legal Counsel for Children’s Health Defense, stated, “Religious rights are fundamental. It is unconstitutional for the state to deprive people of such important rights when religious animus has played a key role. To enact such harsh legislation without any legislative fact-finding, and with the legislators’ open display of prejudice towards religious beliefs different than their own, is simply un-American; it is essential that we fight this.”
Mother, Therapist, Educator, Paralegal, Advocate and Vaccine Court Victim Speaks Out on How Vaccine-Autism Denial Destroys Families
In 2002, I was a young, ambitious 24-year-old finishing graduate school as a credentialed teacher, marriage and family therapist, and behavior analyst. Like all good moms, I took my healthy, talking, responsive, playful son Dominic into the doctors for his routine vaccine shots at 15 months old. That night I watched in heart-wrenching fear as my son developed a 105 fever, uncontrollable screaming, dizziness, diarrhea, and seizures. The following days as Dominic became lethargic, unable to eat, ridden with a rash, and struggled with his breathing, my panic grew uncontrollable. I took Dominic back to the doctors demanding to know what the vaccines had done to him, but more importantly, how we could help him. They said there was no correlation between the vaccines he received that day and his newly developed symptoms. I was told I was paranoid, and we were referred to psychiatry.
SB 276 was heard in the Assembly Appropriations Committee today, July 10, 2019. Due to the exorbitant costs, it was sent to the Suspense File. Typically this is where a bill goes to die. However, SB 276 could be removed from the Suspense File on August 31st and continue to move during this session. It would have to pass the Assembly Floor before going back to the Senate for a Concurrence vote on the Assembly amendments and pass the Senate once more before hitting Newsom's desk for his signature or veto.
“Fear-Based Medical Misinformation” Causes Vaccine and Statin “Hesitancy” or is Public Waking Up to the Truth? Dr. Brownstein Reponds to AMA
An article in the June, 2019 edition of JAMA Cardiology was titled, “Fear-Based Medical Misinformation and Disease Prevention: From Vaccines to Statins." In this article, the author states “fake medical news” as the reason that patients are exhibiting hesitancy about utilizing statins and vaccines. The author blames vaccine refusers for fueling outbreaks of measles. However, mandating that every child receive the MMR does not guarantee a measles-free population. China continues to have measles outbreaks even though Chinese children are the most vaccinated in the world—over 99% of Chinese children are fully vaccinated for measles. Furthermore, there has been a rash of mumps outbreaks across the US since 2006–all in fully vaccinated populations. In fact, from 2016-2017, there have been over 9,200 cases of mumps in the US, mostly from fully vaccinated people. The author blames fake news because patients are concerned about statin safety. A large percentage of patients stop statin drugs due to side effects. I find it doubtful that fake news is responsible for a large percentage of patients to suffer adverse effects from statin therapy. I have been a clinician for over 25 years and regularly heard patients complaining about statin adverse effects.