The Knesset Reviews 

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TrustScore 3.5 out of 5

3.4

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3.4

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TrustScore 3.5 out of 5

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3.4

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Rated 3 out of 5 stars

Rating and help

The Knesset is responsible for the defense of Jewish rights.

This is not only an internet rating, but also a cry for help. My wife and child are of Jewish descent. We want to have future children - healthy children as well. Unfortunately there is a danger for all people of Jewish descent.

The German government will circulate a corona vaccine that is in danger of making women infertile. My wife is a civil servant and there will be mandatory vaccinations for public servants and officials. Please fight this hidden genocide against the Jewish people, packed in an emergency vaccination license. I would like to quote Dr. Yeadon, ex-vice-president and ex-research chief for respiratory diseases at PFIZER Pharma. This is about "Phase III clinical trial(s) of BNT162b (EudraCT Number 2020-002641-42)".

Yeadon Ph.D says:

- 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.

YHWH is with us
Shalom

2 December 2020
Unprompted review

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