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The Great PCR Scandal, Tricked Into Lockdown?
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STORY AT-AGLANCE
- The German Corona Extra-Parliamentary Inquiry Committee, founded July 10, 2020, is leading an international effort to hold accountable those responsible for using fraudulent testing to engineer the appearance of a dangerous pandemic to implement economically devastating lockdowns
- Pandemic measures have caused tremendous harm, killing more people than the virus itself by restricting routine medical care to people with acute and chronic health conditions that have nothing to do with COVID-19
- While the governments of many nations have the same separation of power as the U.S., where you have separate legislative, judiciary and executive branches, we are now finding that this separation has been breached and nearly destroyed in most places
- We now have plenty of data showing the lethality of SARS-CoV-2 is on par with the common flu and that the absolute risk of death is equivalent to the risk of dying in a car accident
- The flaws of PCR testing have been capitalized upon to incite fear in order to benefit an agenda developed by private corporations, which include not only Big Tech companies, the Bill & Melinda Gates Foundation and the Wellcome Trust, but also the World Health Organization, the United Nations and the World Economic Forum
Landmark Study Finds Masks Are Ineffective
STORY AT-A-GLANCE
- The first randomized controlled trial of more than 6,000 individuals to assess the effectiveness of surgical face masks against SARS-CoV-2 infection found masks did not statistically significantly reduce the incidence of infection
- Among mask wearers, 1.8% ended up testing positive for SARS-CoV-2, compared to 2.1% among controls. When they removed the people who did not adhere to proper mask use, the results remained the same — 1.8%, which suggests adherence makes no significant difference
- Among those who reported wearing their face mask “exactly as instructed,” 2% tested positive for SARS-CoV-2 compared to 2.1% of the controls
- 1.4% tested positive for antibodies at the end of the month-long study compared to 1.8% of controls
- 0.5% in the mask group and 0.6% tested positive for one or more respiratory viruses other than SARS-CoV-2
The Eugenicist Mindset Propelling Operation Warp Speed W/ Whitney Webb
DR. FAUCI’S COVID-19 SHOT: WILL YOU GET ONE?
COVID Vaccine Hesitancy Widespread, Even Among Medical Professionals And More!!

From: globalpeace999@aol.com
To: globalpeace999@aol.com
Sent: 12/3/2020 12:17:20 PM Pacific Standard Time
Subject: Fwd: COVID Vaccine Hesitancy Widespread, Even Among Medical Professionals And More!!
Definitive Up To Date Dynamite Material Regarding the Current Covid-19 “PanFeardemic”…KNOWLEDGE IS POWER!
TO LEARN MORE :
The COVID-19 RT-PCR Test: How to Mislead All HumanityHead of Pfizer Research: Covid Vaccine is Female Sterilization
Health & Money NewsDecember 2, 2020News
Post navigation
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.
Dr. Wodarg and Dr. Yeadon request a stop of all corona vaccination studies and call for co-signing the petition
2020NEWS
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.
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.
COVID Vaccine Hesitancy Widespread, Even Among Medical Professionals And More!!
Head of Pfizer Research: Covid Vaccine is Female Sterilization
Health & Money NewsDecember 2, 2020News
Post navigation
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.
Dr. Wodarg and Dr. Yeadon request a stop of all corona vaccination studies and call for co-signing the petition
2020NEWS
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.
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.
Latest messages from Matthew Seasonal thoughts, feelings; covid-19: statistics, masks, tests, vaccine; rebelling citizenries; US election; imminent changes; unconditional love
PCR: Using a “Test” to Lock Down Society + Chemtrails, Transhumanism + Synthetic Biiology
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