CENSORED: National Vaccine Information Center

A highly-rated nonprofit vaccine safety charity has been censored by Facebook on behalf of pharmaceutical industry interests in a purge of vaccine safety information.

The National Vaccine Information Center (NVIC) had maintained a Facebook page since 2008.

The organization was started 39-years ago. Co-founder and president is Barbara Loe Fisher. Fisher became a vaccine safety advocate after her two-and-a-half-year-old son suffered a severe neurological reaction to DPT vaccine in 1980. He was left with multiple learning disabilities that required him to remain in a special education classroom throughout his public school education.

Far from a fringe group, as propagandists try to convince the public, Fisher has provided consumers with crucial vaccine safety information for decades and served as an appointed member of the U.S. Department of Health and Human Services on the National Vaccine Advisory Committee as part of the Vaccine Safety Writing Group, on the agency’s Vaccine Policy Analysis Collaborative, on the Blue Ribbon Panel on Vaccine Safety, and Chair of the Subcommittee on Vaccine Adverse Events.

Additionally, Fisher has served as a member of the FDA’s Vaccine and Related Biological Products Advisory Committee. And she has been a member of the National Academy of Sciences Institute of Medicine Vaccine Safety Forum.

We are not surprised that Mark Zuckerberg views the truthful information that NVIC publishes about vaccine science, policy and law as a threat to perpetuating false narratives about vaccine safety created by the pharmaceutical industry and its business partners. The U.S Congress has encouraged the creation of public-private business partnerships between vaccine manufacturers and federal agencies for the past three decades. In order to be part of those lucrative partnerships, Silicon Valley companies like Facebook are clearly happy to engage in censorship. If NVIC had not done such a good job educating the public about vaccination and health for four decades, our Facebook page would still be up.

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COVID-19: Israel finds possible link between vaccine, myocarditis cases

About one in 100,000 people who received the Pfizer coronavirus vaccine suffered from myocarditis – an inflammation of the heart muscle – a preliminary report redacted by the committee of experts tasked by the Health Ministry to monitor the inoculation’s side effect has found, Channel 12 reported on Friday.The researchers also stressed that more research is needed to confirm the connection between the vaccine and the phenomena.The leaked document showed that most cases were reported among young men aged 18-30. A total of 62 cases of myocarditis have occurred so far in Israel around the time of the vaccination, 56 of them after the second dose. Some 55 cases occurred among men.

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OSHA Abruptly Reverses Course, Says Employers Will Not Be Liable for COVID Vaccine Injuries After All

The federal Occupational Safety and Health Administration (OSHA) Friday reversed its position on requiring companies that mandate COVID vaccines to treat adverse reactions as “recordable injuries,” announcing that it will no longer enforce its previous ruling.

OSHA said it made the change in order to avoid “the appearance of discouraging workers” from getting the COVID vaccine and also because it did not wish to “disincentivize employers’ vaccination efforts.”

According to the agency’s website:

“DOL [U.S. Department of Labor] and OSHA, as well as other federal agencies, are working diligently to encourage COVID-19 vaccinations. OSHA does not wish to have any appearance of discouraging workers from receiving COVID-19 vaccination, and also does not wish to disincentivize employers’ vaccination efforts. As a result, OSHA will not enforce 29 CFR 1904’s recording requirements to require any employers to record worker side effects from COVID-19 vaccination through May 2022. We will reevaluate the agency’s position at that time to determine the best course of action moving forward.”

As The Defender reported May 20, OSHA’s website previously stated:

“If you require your employees to be vaccinated as a condition of employment (i.e., for work-related reasons), then any adverse reaction to the COVID-19 vaccine is work-related. The adverse reaction is recordable if it is a new case under 29 CFR 1904.6 and meets one or more of the general recording criteria in 29 CFR 1904.7.”

In general, an adverse reaction to the COVID vaccine is recordable if the reaction is: (1) work-related, (2) a new case and (3) meets one or more of the general recording criteria in 29 CFR 1904.7 (e.g., days away from work, restricted work or transfer to another job, medical treatment beyond first aid).”

According to OSHA, the requirement that employers must record serious work-related injuries and illness can leave employers with worker’s compensation claims, which can have a negative impact on the employer’s safety record.

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According To ALARMING New Report: Pfizer And Moderna COVID Vaccines Could Easily Trigger Alzheimer’s, ALS, And Other Neurological Degenerative Diseases

As we already reported a few days ago, over 60% of the new COVID cases involve people who have already been vaccinated.

And now, an alarming new report in Microbiology and Infectious Disease reveals the mRNA vaccines could easily trigger Alzheimer’s disease, ALS, and other neurological and cognitive degenerative diseases.

From the report of J. Bart Classen, MD:

Development of new vaccine technology has been plagued with problems in the past. The current RNA based SARS- CoV-2 vaccines were approved in the US using an emergency order without extensive long term safety testing.

Dr. Classen and his colleagues discovered that the vaccine increases the likelihood of these hideous diseases by opening a pathway into human DNA, which is exactly what this gene-therapy drug is intended to do:

The results indicate that the vaccine RNA has specific sequences that may induce TDP-43 and FUS to fold into their pathologic prion confirmations. In the current analysis a total of sixteen UG tandem repeats (ΨGΨG) were identified and additional UG (ΨG) rich sequences were identified.

Two GGΨA sequences were found. Potential G Quadruplex sequences are possibly present but a more sophisticated computer program is needed to verify these. Furthermore, the spike protein, created by the translation of the vaccine RNA, binds angiotensin converting enzyme 2 (ACE2), a zinc containing enzyme.

More about that issue with zinc:

This interaction has the potential to increase intracellular zinc. Zinc ions have been shown to cause the transformation of TDP-43 to its pathologic prion configuration. The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases.

Dr. Classen’s ALARMING conclusion:

The enclosed finding as well as additional potential risks leads the author to believe that regulatory approval of the RNA based vaccines for SARS-CoV-2 was premature and that the vaccine may cause much more harm than benefit.

Click HERE if you want to read the full report of J. Bart Classen, MD.

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Connecticut form requires health care professionals to sign away their lives saying “I voluntarily assume full responsibility for any reactions” caused by covid vaccines

Medical workers in the state of Connecticut are having to sign a special liability form upon getting injected with the Wuhan coronavirus (Covid-19) that makes them solely responsible for their own negative health outcomes, whether that be injury or death.

The form contains a questionnaire asking “vaccine” recipients to indicate if they feel sick, have received a previous injection for the Chinese Virus, are allergic to polyethylene glycol (PEG), and if they have ever tested positive for the Wuhan Flu.

“Do you have a weakened immune system caused by something such as HIV infection or cancer or do you take immunosuppressive drugs or therapies?” another of the questions asks.

The list reads like something one might fill out at a doctor’s office before going in for an appointment. However, upon closer examination, its purpose is to basically have the signer sign away his or her life in the event that the jab causes life-threatening illness or death.

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CDC: Death Toll Following Experimental COVID Injections Now at 4,434 – More than 21 Years of Recorded Vaccine Deaths from VAERS

The CDC released the latest death figures following the experimental COVID injections this week, and that death toll now stands at 4,434 people, adults and children, that have been recorded as dying after receiving one of the experimental COVID injections.

To put this number in perspective, since the CDC continues to claim that these deaths do “not establish a causal link to COVID-19 vaccines,” these deaths now exceed the total number of deaths reported to VAERS following vaccination for the past 21 years!

From 1/1/2000 through 11/30/2020 (the last month before COVID shots were given emergency use) there were 4,394 deaths recorded for a span of 21 years.

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Employers may be liable for ‘any adverse reaction’ from mandated coronavirus shots: OSHA

The federal Occupational Safety and Health Administration (OSHA) has put employers on notice that should they attempt to require employees to receive injections of experimental COVID-19 gene-therapy vaccines a resulting adverse reaction will be considered “work-related” for which the employer may be held liable.

OSHA released its new guidance on April 20 under a “Frequently Asked Questions” section of its website having to do with COVID-19 safety compliance.

The question asks whether an employer who mandates employees receive these experimental COVID-19 shots is required to record any adverse events as a result of these injections. Such recording requirements of serious work-related injuries and illness may not only leave an employer vulnerable to worker’s compensation claims, but such incidents could also impact the employer’s safety record.

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NEW STUDY: COVID Vaccines Linked to Prion Brain Degeneration Similar to Mad Cow Disease

A new scientific report suggest that there may be potentially fatal risks involved with the experimental mRNA gene therapy vaccines being rushed into the public sphere without any real regulation or long-term safety testing.

The name of the report authored by Dr Greg Nigh is Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19, which explicitly warns that “the exceptionally rapid movement of these vaccines through controlled trials and into mass deployment raises multiple safety concerns.”

This is what many critics, like former chair of the Council of Europe Health Committee, Dr Wolfgang Wodarg and former Pfizer executive Dr Micheal Yeadon have been warning for months, but instead of engaging with this potentially catastrophic situation, instead governments, corporate media and censorship engineers at YouTube, Facebook, Twitter have all sought to silence any criticism of the current range of experimental vaccines from well-connected pharmaceutical firms.

In the past, an “Emergency Use Authorization” (EUA) would only be for a limited period and only for use in section of the population who is most vulnerable to a disease. But the current EUA regime is being allowed to run indefinitely and for any “top-up vaccines” and is being used to try and vaccination the entire population – regardless of who is health or sick, or at risk or not.

Already, both in the US and also in the UK, vaccine injuries and deaths have far eclipsed anything seen before without a full government recall of the products in question.

Will government regulators admit they were wrong to wave the normal drug regulatory process, and instead capitulating to extreme political and corporate pressure?

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