
Side effects…


A publicly available FDA “fact sheet” document reveals that 86% of children who participated in a Pfizer covid vaccine trial reported adverse reactions ranging from “mild” to “serious.”
As part of the vaccine experiments, children aged 12 to 15 are being injected with mRNA sequences that take control of their cells, causing them to churn our spike proteins in their blood. Spike proteins cause vascular disease and blood clots. Even the Jonas Salk Institute conclusively identifies spike proteins as the culprit behind vascular disease and blood clots.
This is all openly admitted by the FDA, which has published extremely disturbing reports of adverse reactions experienced by children in a Pfizer covid vaccine “fact sheet” labeled 144413. See the original FDA document here (PDF).
In case the FDA removes this sheet, we have archived it at Natural News servers here (PDF).

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.
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.
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.
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.

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.

You must be logged in to post a comment.