Surely, what needs to be shouted from the Inquiry ‘rooftops’ is the fact that batches of the vaccines had, it would appear, systematically varying toxicity – from likely to cause ‘sudden death’, spontaneous abortion, still birth, myocarditis, to no reaction (placebo) - and everything else in-between, AND that both Pfizer and t…
Surely, what needs to be shouted from the Inquiry ‘rooftops’ is the fact that batches of the vaccines had, it would appear, systematically varying toxicity – from likely to cause ‘sudden death’, spontaneous abortion, still birth, myocarditis, to no reaction (placebo) - and everything else in-between, AND that both Pfizer and the FDA were very well aware of this when the EUA was granted.
By way of example, see the following 3-minute video clip featuring long-time investigative journalist and author, Naomi Wolf.
By way of background, following the approval for general deployment of the Pfizer Covid “vaccine” in August 2021, using the provisions of the very powerful US Freedom of Information Act (FOIA), In September 2021, the US-based professional group ‘Public Health and Medical Professionals for Transparency’ (PHMPT) sought FOIA release of all Pfizer's internal clinical trial reports that had been provided to the US Food and Drug Administration (FDA) in pursuit of the their EUA and general approval. This was prompted because so many researchers and clinicians, world-wide, had queried the feasibility/veracity of the “Safe and Effective” mantra attached to the injections when they were so quickly approved for Emergency Use, and then approved for general deployment a mere few months later.
Release of the documents (a total of some 450,000 pages) occurred in late 2022 after much prevarication by the FDA and the ruling of a Federal Appeal Court (responding to a legal action filed on behalf of PHMPT by managing partner, Aaron Siri, of the law firm Siri & Glimstad. The action was funded by Del Bigtree's publicly supported Informed Consent Action Network, icandecide.org .)
Through her organisation, The Daily Clout, Naomi Wolf led a call for appropriately qualified volunteer professionals to participate in analysing and categorising Pfizer's own findings. Thousands came forward and some 3,200 were selected.
This resulted in the book ‘THE PFIZER PAPERS: Pfizer’s Crimes Against Humanity’ published in the US mid-October this year.
The book provides a devastating insight into what Pfizer and the FDA knew about the harmful effects of the COVID “vaccines” at the time the EUA was granted and the “vaccines” then deployed as “Safe and Effective”. Presumably our own MHRA and the EMA were also aware?
Note that Moderna's internal trials reports have also now been FOIA released. Scheduled for the middle of next year is the book ‘THE MODERNA PAPERS: Moderna’s Crimes Against Humanity’.........
Hi Isabel –
Surely, what needs to be shouted from the Inquiry ‘rooftops’ is the fact that batches of the vaccines had, it would appear, systematically varying toxicity – from likely to cause ‘sudden death’, spontaneous abortion, still birth, myocarditis, to no reaction (placebo) - and everything else in-between, AND that both Pfizer and the FDA were very well aware of this when the EUA was granted.
By way of example, see the following 3-minute video clip featuring long-time investigative journalist and author, Naomi Wolf.
https://rumble.com/v5l91uc-naomi-wolf-the-centerpiece-of-the-pfizerpapers-is-human-reproduction..html?playlist_id=watch-history
Then see the much broader scope discussion with Del Bigtree of the Highwire.com (and icandecide.org) which can be viewed at https://thehighwire.com/ark-videos/dr-naomi-wolf-reveals-shocking-details-in-the-pfizer-papers-2/
By way of background, following the approval for general deployment of the Pfizer Covid “vaccine” in August 2021, using the provisions of the very powerful US Freedom of Information Act (FOIA), In September 2021, the US-based professional group ‘Public Health and Medical Professionals for Transparency’ (PHMPT) sought FOIA release of all Pfizer's internal clinical trial reports that had been provided to the US Food and Drug Administration (FDA) in pursuit of the their EUA and general approval. This was prompted because so many researchers and clinicians, world-wide, had queried the feasibility/veracity of the “Safe and Effective” mantra attached to the injections when they were so quickly approved for Emergency Use, and then approved for general deployment a mere few months later.
Release of the documents (a total of some 450,000 pages) occurred in late 2022 after much prevarication by the FDA and the ruling of a Federal Appeal Court (responding to a legal action filed on behalf of PHMPT by managing partner, Aaron Siri, of the law firm Siri & Glimstad. The action was funded by Del Bigtree's publicly supported Informed Consent Action Network, icandecide.org .)
Through her organisation, The Daily Clout, Naomi Wolf led a call for appropriately qualified volunteer professionals to participate in analysing and categorising Pfizer's own findings. Thousands came forward and some 3,200 were selected.
This resulted in the book ‘THE PFIZER PAPERS: Pfizer’s Crimes Against Humanity’ published in the US mid-October this year.
The book provides a devastating insight into what Pfizer and the FDA knew about the harmful effects of the COVID “vaccines” at the time the EUA was granted and the “vaccines” then deployed as “Safe and Effective”. Presumably our own MHRA and the EMA were also aware?
Note that Moderna's internal trials reports have also now been FOIA released. Scheduled for the middle of next year is the book ‘THE MODERNA PAPERS: Moderna’s Crimes Against Humanity’.........