we {tried} to warn you

We can all just check our brains at the door and allow them to do all of the thinking for us, or we can recall who is pushing these experimental vaccines on EVERYONE (Biden is on a mission) and remember they are NOT LIABLE FOR ANYTHING that happens to you.
And instead of proving safety, the CDC would rather make a slide presentation to boost confidence, touting safety and effectiveness. Lord, help us. –>> Vaccinate with Confidence Tips for the Healthcare Team
And the government would rather invest $1 BILLION to strengthen confidence in the vaccine program, again… instead of proving safety and effectiveness.
Pfizer
AstraZeneca
There’s a reason they do NOT want people sharing their injuries online:
If we can convince others that big government does not care, and pHARMa is in the business of wealth, not health (not to be confused with urgent, lifesaving care), and the “church” doesn’t hold our best interest… all other dominoes of cognitive dissonance fall more readily.

“I’m telling people to treat their vaccinated and vaccine-injured friends and family as though they are in hospice. Yes, miracles can happen in hospice, and maybe they’ll be lucky, but the covid shot is a ticking timebomb.” -Dr. Sherri Tenpenny


If we can convince others that big government does not care, and pHARMa is in the business of wealth, not health (not to be confused with urgent, lifesaving care), and the “church” doesn’t hold our best interest… all other dominoes of cognitive dissonance fall more readily.

Contrary to popular belief, there are no “FDA-approved” COVID-19 vaccines. The FDA allowed the distribution and use of Moderna’s “experimental” mRNA-1273 vaccine and Pfizer/BioNTech’s “experimental” BNT162b2 vaccine under Emergency Use Authorization (EUA). This means that, if you decide to get one of these two vaccines, you are agreeing to be part of a human medical experiment.

When the professions of Public Health and Medicine collude to do away with TRUE informed consent, they become a threat to every individual.
And just how will we know for sure that when someone develops autoimmune disorders, cancers, infertility, or other health problems down the road they are, or are not, associated with these novel gene therapy biologics? They are ERASING ALL EVIDENCE of the ability to compare vaxxed vs unvaxxed. No immediate reactions does NOT mean no long-term consequences. How convenient.  –>> Moderna And Pfizer Vaccine Studies Hampered As Placebo Recipients Get Real Shot

Rona vax injury reports –>> Search Results from the VAERS Database

Schools close due to reactions:

The shots will just keep coming. When it comes to Bill Gates, how do we vote out someone we didn’t vote in? Population control is real.
This isn’t a prideful “We told you so” moment, but rather… a heartbreaking,  “We tried to warn you.
@woketxmama

Covid Vaccine is Female Sterilization –> Head of Pfizer


The vaccine contains a  spike protein (see image) called  syncytin-1, vital for the formation of human placenta in women. If the vaccine works so that we form an immune response AGAINST the spike protein, we are also training the female body to attack syncytin-1, which could lead to infertility in women of an unspecified duration.

On December 1, 2020, the ex-Pfizer head of respiratory research Dr. Michael Yeadon and the lung specialist and former head of the public health department Dr. Wolfgang Wodarg filed an application with the EMA, the European Medicine Agency responsible for EU-wide drug approval, for the immediate suspension of all SARS CoV 2 vaccine studies, in particular the BioNtech/Pfizer study on BNT162b (EudraCT number 2020-002641-42).

Dr. Wodarg and Dr. Yeadon demand that the studies – for the protection of the life and health of the volunteers – should not be continued until a study design is available that is suitable to address the significant safety concerns expressed by an increasing number of renowned scientists against the vaccine and the study design.StarGate TV Series Warned Us In 2001 About the Vaccination Disaster Facing Us Today

On the one hand, the petitioners demand that, due to the known lack of accuracy of the PCR test in a serious study, a so-called Sanger sequencing must be used. This is the only way to make reliable statements on the effectiveness of a vaccine against Covid-19. On the basis of the many different PCR tests of highly varying quality, neither the risk of disease nor a possible vaccine benefit can be determined with the necessary certainty, which is why testing the vaccine on humans is unethical per se.

Furthermore, they demand that it must be excluded, e.g. by means of animal experiments, that risks already known from previous studies, which partly originate from the nature of the corona viruses, can be realized. The concerns are directed in particular to the following points:

  • –The formation of so-called “non-neutralizing antibodies” can lead to an exaggerated immune reaction, especially when the test person is confronted with the real, “wild” virus after vaccination. This so-called antibody-dependent amplification, ADE, has long been known from experiments with corona vaccines in cats, for example. In the course of these studies all cats that initially tolerated the vaccination well died after catching the wild virus.

    –The vaccinations are expected to produce antibodies against spike proteins of SARS-CoV-2. However, spike proteins also contain syncytin-homologous proteins, which are essential for the formation of the placenta in mammals such as humans. It must be absolutely ruled out that a vaccine against SARS-CoV-2 could trigger an immune reaction against syncytin-1, as otherwise infertility of indefinite duration could result in vaccinated women.

    –The mRNA vaccines from BioNTech/Pfizer contain polyethylene glycol (PEG). 70% of people develop antibodies against this substance – this means that many people can develop allergic, potentially fatal reactions to the vaccination.

    –The much too short duration of the study does not allow a realistic estimation of the late effects. As in the narcolepsy cases after the swine flu vaccination, millions of healthy people would be exposed to an unacceptable risk if an emergency approval were to be granted and the possibility of observing the late effects of the vaccination were to follow. Nevertheless, BioNTech/Pfizer apparently submitted an application for emergency approval on December 1, 2020.

CALL FOR HELP: Dr. Wodarg and Dr. Yeadon ask as many EU citizens as possible to co-sign their petition by sending the e-mail prepared here to the EMA.

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Covid Vaccine is Female Sterilization – Head of Pfizer Research: