The 21st Century Cures Act legislation was originally passed in the house last year on July 10, 2015 as HR 6

The 21st Century Cures Act legislation was originally passed in the house last year on July 10, 2015 as HR 6.
– FDA Fast Tracking of ALL New Vaccines (3091 and 3092)
– Unconscionable Pharma and Vaccine Administrator Liability Shield for Fetal Vaccine Injury or Death Caused by Vaccines Given in Pregnancy (3093)
NVIC issued a press release on July 22, 2015 and Barbara Loe Fisher, NVIC Co-founder and President, released a referenced commentary in opposition to this proposed legislation in which she said,
“The 21st Century Cures Act is a drug company stockholder’s dream and a consumer’s worst nightmare,” said Barbara Loe Fisher, NVIC Co-founder and President. “Making experimental drugs quickly available for the sick and dying, who voluntarily choose to use them, is one thing but Congress should not be greasing the skids to license experimental vaccines that government will recommend and legally require healthy children and adults to use. It is a prescription for disaster.”
After passing the house in 2015, the legislation stalled. Many of the provisions of HR 6 were broken up into several smaller bills, but over the Thanksgiving holiday, the legislation was quickly reassembled into a new version including some sections from HR 6 and adding some new sections, amending them all onto bill HR 34. HR 34 was originally a bill that only addressed “Tsunami Warning, Education, and Research”, but was passed by the US House of Representatives on November 30th as an 824 page monstrosity!

National Vaccine Information Center Says Proposed 21st Century Cures Act Will Endanger the Public Health by Lowering FDA Licensing Standards
WASHINGTON–(EON: Enhanced Online News)–The non-profit National Vaccine Information Center (NVIC) says the proposed 21st Century Cures Act (H.R. 6) will endanger the public health by lowering scientific and informed consent standards used by the Food and Drug Administration (FDA) to license experimental biological products (vaccines), drugs and medical devices in order to expedite delivery to the U.S. market. Under the proposed law, drug companies could avoid conducting large randomized clinical trials and researchers would be able to test new products on humans without obtaining informed consent.
“if the proposed clinical testing poses no more than minimal risk”
The bill passed the U.S. House of Representatives on July 10, 2015. It mandates that an additional $9 billion be given to National Institutes of Health (NIH) to develop new vaccines and drugs and $550 million be given to the FDA to fast track licensure.
“The 21st Century Cures Act is a drug company stockholder’s dream and a consumer’s worst nightmare,” said Barbara Loe Fisher, NVIC Co-founder and President. “Making experimental drugs quickly available for the sick and dying, who voluntarily choose to use them, is one thing but Congress should not be greasing the skids to license experimental vaccines that government will recommend and legally require healthy children and adults to use. It is a prescription for disaster.”
The proposed law would allow drug companies to use surrogate endpoints to evaluate the effectiveness of experimental vaccines and drugs, and would permit the FDA to accept novel statistical analyses and clinical experience evidence instead of requiring drug companies to produce evidence from large randomized clinical trials. The legislation states that “if the proposed clinical testing poses no more than minimal risk,” informed consent would not be required from test subjects, but it is not clear who decides what constitutes “minimal risk.”
“Informed consent is the gold standard in human experimentation and the practice of ethical medicine, and there is no substitute for the requirement that drug companies conduct large, well designed randomized clinical trials before the FDA licenses a new vaccine,” said Fisher. “Moving numbers around in a computer is a poor substitute for actually proving a new vaccine works and does not kill and injure real human beings before it is recommended and used by millions of people.”

Here Comes the 21st Century Cures Act: Say Goodbye to Vaccine Safety Science

Here comes the 21st Century Cures Act (H.R. 6),7 which is a Pharma-driven bill8 blessed by the FDA9 that seriously compromises the integrity of the FDA drug and vaccine licensing process. 10 The 362-page bill sailed through the U.S. House of Representatives on July 10, 201511 and mandates that about $9 billion dollars be given to NIH to develop more drugs and vaccines and $550 million be given to the FDA to fast track products to market.12
Bill Lowers FDA Licensing Standards
The bill allows the FDA to lower licensing standards for testing of experimental drugs, medical devices and “biological products” – a category that includes vaccines -13 14 15 so companies will no longer be required to conduct large, case controlled clinical trials16 17 18 to evaluate safety and effectiveness. Instead, FDA can accept novel statistical analyses 19 and “clinical experience,”20 such as anecdotal evidence from patients.21
It is interesting that clinical experience and anecdotal evidence will constitute “good science” for the purpose of demonstrating a vaccine is safe before it is licensed, while clinical experience and anecdotal evidence has never been good enough to demonstrate that a vaccine is unsafe after it is licensed.22 23 24 25
Greasing Skids to License Drugs and Vaccines
Sick in bedThe 21st Century Cures Act is being sold as a way for the FDA to quickly license experimental pharmaceutical products for people suffering with rare or life threatening diseases, whether or not those products have been adequately tested.26 However, greasing the FDA licensure skids to make experimental drugs available for the sick and dying, who voluntarily choose to use them, is one thing, while greasing the skids to bum rush experimental vaccines to licensure that government will legally require healthy children and adults to buy and use, is something quite different.27 28 29 30 31
Nearly every single vaccine that the pharmaceutical industry creates and the FDA licenses for child use is eventually recommended for all children and mandated by state governments for daycare and school entry.32 33 34 35 36 And, now, many adults are being brought into the vaccine mandate net as well.37 38 39
Ensuring Drugs & Vaccines Dominate U.S. Health Care
Coming on the heels of the Affordable Health Care Act,40 which guaranteed that the pharmaceutical industry and their products will continue to dominate the most expensive health care system in the world,41 42 43 44 45 46 there are so many breathtaking ways the 21st Century Cures Act will endanger the public health that it is hard to know where to begin. The word “vaccines” is not being publicly uttered by anyone sponsoring the bill. However, the Biotechnology Industry Organization (BIO), which represents more than 1,500 pharmaceutical and other health product corporations, is already crowing about how they managed to influence Capitol Hill politicians to incorporate the “Vaccine Access, Certainty and Innovation Act of 2015” into the 21st Century Cures Act.47 48

TEXT OF H.R. 6, 21 ST CENTURY CURES ACT

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MORE THAN 50 PEER REVIEWED SCIENTIFIC Studies from the US National Library of Medicine National Institutes of Health that link Autism to Vaccines

MORE THAN 50 PEER REVIEWED SCIENTIFIC Studies from the US National Library of Medicine National Institutes of Health that link Autism to Vaccines

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878266/
http://www.ncbi.nlm.nih.gov/pubmed/21623535
http://www.ncbi.nlm.nih.gov/pubmed/25377033
http://www.ncbi.nlm.nih.gov/pubmed/24995277
http://www.ncbi.nlm.nih.gov/pubmed/12145534
http://www.ncbi.nlm.nih.gov/pubmed/21058170
http://www.ncbi.nlm.nih.gov/pubmed/22099159
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/
http://www.ncbi.nlm.nih.gov/pubmed/17454560
http://www.ncbi.nlm.nih.gov/pubmed/19106436
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3774468/
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697751/
http://www.ncbi.nlm.nih.gov/pubmed/21299355
http://www.ncbi.nlm.nih.gov/pubmed/21907498
http://www.ncbi.nlm.nih.gov/pubmed/11339848
http://www.ncbi.nlm.nih.gov/pubmed/17674242
http://www.ncbi.nlm.nih.gov/pubmed/21993250
http://www.ncbi.nlm.nih.gov/pubmed/15780490
http://www.ncbi.nlm.nih.gov/pubmed/12933322
http://www.ncbi.nlm.nih.gov/pubmed/16870260
http://www.ncbi.nlm.nih.gov/pubmed/19043938
http://www.ncbi.nlm.nih.gov/pubmed/12142947
http://www.ncbi.nlm.nih.gov/pubmed/24675092
http://www.ncbi.nlm.nih.gov/pubmed/25198681
http://www.ncbi.nlm.nih.gov/pubmed/21623535
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878266/
http://www.ncbi.nlm.nih.gov/pubmed/21623535
http://www.ncbi.nlm.nih.gov/pubmed/25377033
http://www.ncbi.nlm.nih.gov/pubmed/24995277
http://www.ncbi.nlm.nih.gov/pubmed/12145534
http://www.ncbi.nlm.nih.gov/pubmed/21058170
http://www.ncbi.nlm.nih.gov/pubmed/22099159
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/
http://www.ncbi.nlm.nih.gov/pubmed/17454560
http://www.ncbi.nlm.nih.gov/pubmed/19106436
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3774468/
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697751/
http://www.ncbi.nlm.nih.gov/pubmed/21299355
http://www.ncbi.nlm.nih.gov/pubmed/21907498
http://www.ncbi.nlm.nih.gov/pubmed/11339848
http://www.ncbi.nlm.nih.gov/pubmed/17674242
http://www.ncbi.nlm.nih.gov/pubmed/21993250
http://www.ncbi.nlm.nih.gov/pubmed/15780490
http://www.ncbi.nlm.nih.gov/pubmed/12933322
http://www.ncbi.nlm.nih.gov/pubmed/16870260
http://www.ncbi.nlm.nih.gov/pubmed/19043938
http://www.ncbi.nlm.nih.gov/pubmed/12142947
http://www.ncbi.nlm.nih.gov/pubmed/24675092

Study – A two-phase study evaluating the relationship between Thimerosal-containing vaccine administration and the risk for an autism spectrum disorder diagnosis in the United States
Results
In phase I, it was observed that there was a significantly increased risk ratio for the incidence of ASD reported following the Thimerosal-containing DTaP vaccine in comparison to the Thimerosal-free DTaP vaccine. In phase II, it was observed that cases diagnosed with an ASD were significantly more likely than controls to receive increased organic-Hg from Thimerosal-containing hepatitis B vaccine administered within the first, second, and sixth month of life.
Conclusions
Routine childhood vaccination is an important public health tool to reduce the morbidity and mortality associated with infectious diseases, but the present study provides new epidemiological evidence supporting an association between increasing organic-Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of an ASD diagnosis.

Study – What is regressive autism and why does it occur? Is it the consequence of multi-systemic dysfunction affecting the elimination of heavy metals and the ability to regulate neural temperature?
Abstract
There is a compelling argument that the occurrence of regressive autism is attributable to genetic and chromosomal abnormalities, arising from the overuse of vaccines, which subsequently affects the stability and function of the autonomic nervous system and physiological systems. That sense perception is linked to the autonomic nervous system and the function of the physiological systems enables us to examine the significance of autistic symptoms from a systemic perspective. Failure of the excretory system influences elimination of heavy metals and facilitates their accumulation and subsequent manifestation as neurotoxins: the long-term consequences of which would lead to neurodegeneration, cognitive and developmental problems. It may also influence regulation of neural hyperthermia. This article explores the issues and concludes that sensory dysfunction and systemic failure, manifested as autism, is the inevitable consequence arising from subtle DNA alteration and consequently from the overuse of vaccines.

The National Vaccine Injury Compensation Program has paid out over $25 million in damages

The National Vaccine Injury Compensation Program has paid out over $25 million in damages to victims of serious shoulder injuries related to vaccine administration in the United States so far this year, according to WSOC-TV.
Over 220 people have been compensated so far in 2016 for SIRVA — shoulder injury related to vaccine administration — a painful and debilitating side effect that sometimes comes after vaccination.
Dr. Tom Shimabukuro of the CDC says that the condition is rare. These injuries occur when vaccines are not given in the proper part of the shoulder. Vaccines should be given in the thick portion of the deltoid muscle, he says, not higher up near the shoulder.

CDC Requests Your Comments Regarding the MMR and the MMRV Vaccines; Let’s Give Our All to Them Now!

CDC Requests Your Comments Regarding the MMR and the MMRV Vaccines; Let’s Give Our All to Them Now!
Informed Consent
According to the Federal Register publication notice, October 18, 2016, (Pp. 71735-71736):
The National Childhood Vaccine Injury Act of 1986 (Pub. L. 99-660), as amended by section 708 of Public Law 103-183, added section 2126 to the Public Health Service Act, Section 2126, codified at 42 U.S.C. 300aa-26, requires the Secretary of Health and Human Services to develop and disseminate vaccine information materials for distribution by all health care providers in the United States to any patient (or to the parent or legal representative in the case of a child) receiving vaccines covered under the National Vaccine Injury Compensation Program (VICP).
That is something most, if not all, health professionals who administer vaccines/vaccinations DO NOT comply with nor abide by since most information disseminated states that vaccines are ‘safe’ when we find contradictory information on all vaccine package inserts, including the MMR-II and MMRV.

National Vaccine Information Center (NVIC) Renews Call for End to Product Liability Shield for Vaccine Manufacturers During 2016 Vaccine Awareness Week

National Vaccine Information Center (NVIC) Renews Call for End to Product Liability Shield for Vaccine Manufacturers During 2016 Vaccine Awareness Week
WASHINGTON–(BUSINESS WIRE)–On the 30th Anniversary of the enactment of the National Childhood Injury Act and during the Seventh Annual Vaccine Awareness Week Nov. 13-20, 2016, the non-profit National Vaccine Information Center (NVIC) is renewing its call for an end to the 1986 product liability shield Congress gave vaccine manufacturers for injuries and deaths caused by government licensed and mandated vaccines.
In the 1986 tort reform legislation that created a federal vaccine injury compensation program alternative to product liability and malpractice lawsuits, NVIC co-founders secured vaccine safety informing, recording and reporting provisions that have not been enforced. In 2011, the US Supreme Court banned design defect lawsuits when there was evidence a drug company could have made a vaccine less reactive. Between 2011 and 2016, medical trade associations and special interest groups funded by pharmaceutical companies and government have lobbied state legislatures to remove non-medical and severely restrict medical vaccine exemptions.
“Drug companies should be liable in civil court for vaccine injuries and deaths and so should anyone giving vaccines to people being denied the human right to informed consent to medical risk taking,” said NVIC co-founder and president Barbara Loe Fisher. “There is an urgent need to hold vaccine manufacturers and doctors accountable in civil court for the safety of vaccines and how they are being given.”
The federal vaccine injury compensation program (VICP) has paid $3.5 billion to victims of vaccine injury and death, but two out of three claims are denied. Today, most of the VICP awards go to adults injured by flu vaccine and not to children injured by vaccines required to attend school.

The National Childhood Vaccine Injury Act of 1986
The law preserved the right for vaccine injured persons to bring a lawsuit in the court system if federal compensation is denied or is not sufficient. By 2012, the U.S. Court of Claims had awarded over $3 billion dollars to vaccine victims for their catastrophic vaccine injuries, although two out of three applicants have been denied compensation. Below are links to the National Vaccine Injury Act of 1986 broken down into specific sections, as listed by the US Government Publishing Office. The law may also be viewed in its entirety on the US House of Representatives Office of the Law and Revision Council here.

Japan has one of the lowest infant mortality rates in the world

Hiroko Mori, a vaccine researcher, is one of those experts. He was the former head of the infectious disease division at Japan’s National Institute of Public Health.
He has noted that Japan has one of the lowest infant mortality rates in the world and has advocated for fewer vaccines, stating that the country’s excellent sanitation and nutrition has boosted children’s health.
He observed,
“Medicine is supposed to be about healing, but babies who cannot speak are being given unnecessary shots because parents are scared. Children are losing their ability to heal naturally.
There are so many people who have suffered side effects. All we are asking is to establish the right to say ‘no.’ The right to choose should be recognized as a fundamental human right.”

TV2 Denmark Documentary on HPV Vaccine Shows Lives of Young Women Ruined

Merck holds parents accountable in new Gardasil ad campaign
On the heels of a recently renewed push by researchers and doctors to encourage HPV vaccinations, Merck–maker of market-leader Gardasil–is out with a new HPV awareness campaign that puts the onus of vaccination on parents.
In the TV ad, a young adult man with cancer caused by HPV is shown in a series of pictures that go back in time. He wonders whether his parents just didn’t know about the vaccine that could have protected him when he was 11 or 12. The ad ends with a female voiceover asking, “What will you say?”

TV2 Denmark Documentary on HPV Vaccine Shows Lives of Young Women Ruined

TV2 Denmark has done something no mainstream media network in the United States will dare to do: look into the controversial HPV vaccine that many have claimed has ruined the lives of so many young women, and publish an investigative report.
In December of 2013 Katie Couric did a show on the HPV Gardasil Vaccine where she dared to interview the mother of a young woman who died shortly after receiving the vaccine. Couric’s program was hardly pro-vaccine, as she gave both sides of the controversy, with a huge emphasis on the pharmaceutical side claiming the vaccine was safe, but she was viciously attacked by the mainstream media anyway and forced to apologize for even asking questions about the possible risks of the HPV vaccine.

March 26, 2015, TV2 one of Denmark’s national television stations aired a documentary on HPV vaccines entitled, The Vaccinated Girls – Sick and Betrayed. It focused on the condition of 3 girls suffering from serious new medical conditions after being vaccinated against HPV with Gardasil. The one thing they have in common with thousands of other girls around the world is they were healthy before they got the vaccine – now, they are seriously ill.
All three girls have been examined from head to toe with no conclusive diagnosis and no help with their symptoms, much like the girls in other countries where HPV vaccines are being used.
During the documentary, two Danish doctors from Frederiksberg Hospital said they have never seen anything similar to this during their entire careers. Both doctors said they had sent correspondence to the Danish Health and Medicines Authority a total of four times during the last year to warn them of possible adverse events after HPV injections.
Dr. Louise Brinth of Frederiksberg Hospital has personally examined around 80 girls whom she suspects may be suffering adverse effects of HPV vaccinations.