Open Letter & Evidentiary Document sent to the UK Prime Minister and Cabinet Ministers (COVID-19 vaccine harm, SARS-CoV-2's gain-of-function origin)

Download a copy of the: (1) Evidentiary Document referred to in this Open Letter (PDF: EvidentiaryDocument_COVID19NationalLevelHarm_01122022, MS Word (clickable citations): EvidentiaryDocument_COVID19NationalLevelHarm_01122022), (2) Slide Deck of Evidentiary Document including annotated graphics EvidentiaryDocument_COVID19NationalLevelHarm_Slidedeck_01012023, and (3) associated study results and graphics (ADE_VAED_Vaccine-failure), (Toxic COVID-19 vaccine Lots (VEARS, USA))

Investigation into UKHSA COVID-19 rate fabrication requested. FW: Evidentiary Document sent to the New Zealand Prime Minister, Ministers & MPs: COVID-19 negative vaccine effectiveness and harm evidence (05/12/22)
To: “rishi.sunak.mp@parliament.uk” <rishi.sunak.mp@parliament.uk>, “kemi.badenoch.mp@parliament.uk” <kemi.badenoch.mp@parliament.uk>, “stephen.barclay.mp@parliament.uk” <stephen.barclay.mp@parliament.uk>, “suella.braverman.mp@parliament.uk” <suella.braverman.mp@parliament.uk>, “james.cleverly.mp@parliament.uk” <james.cleverly.mp@parliament.uk>, “therese.coffey.mp@parliament.uk” <therese.coffey.mp@parliament.uk>, “david.davies.mp@parliament.uk” <david.davies.mp@parliament.uk>, “michelle.donelan.mp@parliament.uk” <michelle.donelan.mp@parliament.uk>, “oliver.dowden.mp@parliament.uk” <oliver.dowden.mp@parliament.uk>, “john.glen.mp@parliament.uk” <john.glen.mp@parliament.uk>, “michael.gove.mp@parliament.uk” <michael.gove.mp@parliament.uk>, “mark.harper.mp@parliament.uk” <mark.harper.mp@parliament.uk>, “simon.hart.mp@parliament.uk” <simon.hart.mp@parliament.uk>, “chris.heatonharris.mp@parliament.uk” <chris.heatonharris.mp@parliament.uk>, “huntj@parliament.uk” <huntj@parliament.uk>, “alister.jack.mp@parliament.uk” <alister.jack.mp@parliament.uk>, “robert.jenrick.mp@parliament.uk” <robert.jenrick.mp@parliament.uk>, “gillian.keegan.mp@parliament.uk” <gillian.keegan.mp@parliament.uk>, “johnny.mercer.mp@parliament.uk” <johnny.mercer.mp@parliament.uk>, “andrew.mitchell.mp@parliament.uk” <andrew.mitchell.mp@parliament.uk>, “penny.mordaunt.mp@parliament.uk” <penny.mordaunt.mp@parliament.uk>, “victoria.prentis.mp@parliament.uk” <victoria.prentis.mp@parliament.uk>, “jeremy.quin.mp@parliament.uk” <jeremy.quin.mp@parliament.uk>, “dominic.raab.mp@parliament.uk” <dominic.raab.mp@parliament.uk>, “shappsg@parliament.uk” <shappsg@parliament.uk>, “mel.stride.mp@parliament.uk” <mel.stride.mp@parliament.uk>, “tom.tugendhat.mp@parliament.uk” <tom.tugendhat.mp@parliament.uk>, “wallaceb@parliament.uk” <wallaceb@parliament.uk>
Cc: “j.ardern@ministers.govt.nz” <j.ardern@ministers.govt.nz>, “a.little@ministers.govt.nz” <a.little@ministers.govt.nz>, “p.henare@ministers.govt.nz” <p.henare@ministers.govt.nz>, “a.verrall@ministers.govt.nz” <a.verrall@ministers.govt.nz>, “a.sio@ministers.govt.nz” <a.sio@ministers.govt.nz>, “c.sepuloni@ministers.govt.nz” <c.sepuloni@ministers.govt.nz>, “c.hipkins@ministers.govt.nz” <c.hipkins@ministers.govt.nz>, “d.oconnor@ministers.govt.nz” <d.oconnor@ministers.govt.nz>, “d.parker@ministers.govt.nz” <d.parker@ministers.govt.nz>, “d.clark@ministers.govt.nz” <d.clark@ministers.govt.nz>, “m.woods@ministers.govt.nz” <m.woods@ministers.govt.nz>, “g.robertson@ministers.govt.nz” <g.robertson@ministers.govt.nz>, “j.shaw@ministers.govt.nz” <j.shaw@ministers.govt.nz>, “j.tinetti@ministers.govt.nz” <j.tinetti@ministers.govt.nz>, “k.davis@ministers.govt.nz” <k.davis@ministers.govt.nz>, “k.mcanulty@ministers.govt.nz” <k.mcanulty@ministers.govt.nz>, “k.allan@ministers.govt.nz” <k.allan@ministers.govt.nz>, “m.davidson@ministers.govt.nz” <m.davidson@ministers.govt.nz>, “m.whaitiri@ministers.govt.nz” <m.whaitiri@ministers.govt.nz>, “m.wood@ministers.govt.nz” <m.wood@ministers.govt.nz>, “n.mahuta@ministers.govt.nz” <n.mahuta@ministers.govt.nz>, “p.twyford@ministers.govt.nz” <p.twyford@ministers.govt.nz>, “p.williams@ministers.govt.nz” <p.williams@ministers.govt.nz>, “p.radhakrishnan@ministers.govt.nz” <p.radhakrishnan@ministers.govt.nz>, “s.nash@ministers.govt.nz” <s.nash@ministers.govt.nz>, “w.jackson@ministers.govt.nz” <w.jackson@ministers.govt.nz>, “cabinetoffice@dpmc.govt.nz” <cabinetoffice@dpmc.govt.nz>

Subsequently sent to the Cabinet Office (I suspect its delivery was intercepted): ——- Original Message ——- On Saturday, January 7th, 2023 at 4:43 PM, Cabinet Office Contact Webform <cabinet.office.contact.webform@notifications.service.gov.uk> wrote (the Cabinet email confirmation of my submission is on file):

Dear Rt Hon Prime Minister Rishi Sunak and Cabinet Ministers and Attendees

Please find attached or via a link below an Open Letter and Evidentiary Document sent to the New Zealand Prime Minister and Ministers (05/12/22, cc-ed), which is highly pertinent to the UK Government. This email is being responded to by Hon Dr. Ayesha Verrall (NZ COVID-19 Response Minister).

This Evidentiary Document shares my research results for England, Scotland, New Zealand, Canada, and Globally (77 nations), indicating Irreparable COVID-19 vaccine-induced harm. I also share unequivocal evidence that SARS-CoV-2 originated from gain-of-function/bioweapon research, likely originating beyond China, and remind you that zero evidence exists for its animal-to-human origin. Statistical bias is highly evident in the UKHSA (i.e., demographically-biased rate fabrication), which consequentially eliminated or diminished the negative vaccine effectiveness harm signal from ready public view. Because mass COVID-19 vaccination compliance was obtained using this bias-infused data and harmful vaccine mandates were enforced I pose you the hypothetical question: did elements within the UK Government or its Agencies operating beyond Cabinet control intentionally immunologically program the UK population for a rolling Genocide to be realized in the years-decades ahead? (i.e., by predictable mechanisms, including antibody-dependent enhancement of virus infection (ADE), vaccine-associated enhanced disease (VAED), and antigenic imprinting (AI), all realizable with the future emergence of antigenically distinct SARS-CoV-2 strains).

You are requested to (1) investigate this COVID-19 harm data and the biases evident in the UKHSA COVID-19 case rates, and its cessation of providing this data once the negative vaccine effectiveness became all too obvious, (2) update the UK population on their recently acquired life-long health risks and their putatively shortened life-expectancy, and urgently amend informed consent guidelines associated with COVID-19 vaccination, (3) Investigate the US Department of Defense-funded BTRP-biolabs/bioweapons labs and Metabiota (i.e., formerly par-owned by Hunter Biden) in a potential Ukraine-Cameroon-Other Biolab origin for SARS-CoV-2, (4) investigate the conduct of the WHO during COVID-19 linked to seven critical points detailed in section 2.7 and any potential conflict-of-interest associated with its partnership with Ukraine-BTRP-biolabs and its broader SARS-CoV-2 origin sham-investigation, and (5) Belatedly conduct clinical research in the UK population for predictable COVID-19 vaccine-associated ADE, VAED, and AI.

Please see below for the Open Letter and attached Evidentiary Document (with a link to a slide deck version https://grandsolarminimum.com/2022/12/01/covid-19-vaccine-harm-evidence/ or https://independent.academia.edu/grandsolarminimum).

Thank you.

Dr. Carlton Brown BVSc (Massey University, NZ) MBA (London Business School, UK)

Former CEO and co-innovator at Immune Targeting Systems Ltd (UK), “Vaccines for Mutating Viruses.” (London Development Agency co-funded)

Raising awareness for antibody-dependent enhancement of virus infection, vaccine-associated enhanced disease, and antigenic imprinting by COVID-19 vaccination, and SARS-CoV-2’s gain-of-function origin and a potential globally coordinated vaccine-genocide.

https://www.linkedin.com/in/carlton-brown-13b66232/, https://orcid.org/0000-0003-4871-7521, https://independent.academia.edu/grandsolarminimum, https://twitter.com/ADE_Bioweapon

Download the Evidentiary Document: https://grandsolarminimum.com/2022/12/01/covid-19-vaccine-harm-evidence/

Author: Revolution: Ice Age Re-Entry Amazon https://amzn.to/2PyQsxV, Google Play http://bit.ly/2JFHz08 (free)

Sent with Proton Mail secure email.

Dear Rt Hon Jacinda Ardern, Prime Minister, Hon Andrew Little, Minister of Health, Hon Dr. Ayesha Verrall, Minister of COVID-19 Response, and Hon Peeni Henare and Hon Aupito William Sio, Associate Ministers of Health

In this Open Letter and evidentiary document, I share my research results on overseas government and Ministry of Health (MoH) COVID-19 vaccine surveillance and pharmacovigilance data indicating irreparable vaccine-induced harm. Furthermore, I share important evidence that SARS-CoV-2 originated from gain-of-function research, remind you that no evidence exists for an animal-to-human origin, and highlight that its potential source lay beyond Wuhan, China. A series of requests for investigations are made below linked to this evidence, including the statisticalbiases evident in the Ministry of Health and other healthcare agencies’ calculable unvaccinated COVID-19 case rates. These biases essentially eliminated the negative vaccine effectiveness harm signal from ready public view. This evidentiary document is provided by a former European corporate venture capital-funded CEO/vaccine innovator (“Vaccines for Mutating Viruses”), veterinarian with 36 years of vaccine use experience, and a private researcher. It is supported by 525 unique data, scientific, and other citations.

According to New Zealand, England, Scotland, and Canada healthcare agencies and Global surveillance data (77 nations), these vaccines failed to prevent SARS-CoV-2 infection as initially touted. Significant negative vaccine effectiveness and vaccine failure were evident with the emergence of antigenically distinct strains (i.e., Delta, Omicron). The vaccine industry experienced antibody-dependent enhancement of virus infection (ADE) and vaccine-associated enhanced disease (VAED) with three other different coronaviruses and their spike protein vaccine prototypes in the last 30 years, giving my study results a predictable context. Furthermore, one year of US lot-numbered COVID-19 vaccine-associated deaths and hospitalizations equaled 32x (Comirnaty 15.4x) and 20x (Comirnaty 10.5x) of all US vaccine-associated deaths and hospitalizations, respectively. These adverse outcomes were highly skewed and peaked across vaccine lots and were associated with a minority of lots sent to a larger number of US States. This data highlights that there was an urgent need for investigation by the US and other regulatory and healthcare agencies before expanded population use.

A vast chasm exists between the vaccine safety and efficacy experienced in 2021-2022 and the falsifiable 95% vaccine efficacy and safety proclaimed by governments with Comirnaty’s first Emergency Use Authorization in 2020 (USA). This document reviews critical pharmacotoxicology and clinical safety package deficiencies evident in overseas regulatory reviews. This helps explain why Pfizer then struggled to cope with the sheer volume of Comirnaty adverse event reports in the first 90 days post-launch. This was uncharacteristic of a safe vaccine. Numerous vaccine-associated enhanced disease mechanisms are evident by which vaccine spike proteins can cause disease or exacerbate comorbidities common to severe COVID-19 outcomes.These mechanisms place upregulated furin and angiotensin-converting enzyme-2 receptors (ACE2) and prevalent comorbidities in tissues and organs common to all three center-stage. At the same time, SARS-CoV-2’s spike protein provides itsuniquely encoded furin cleavage site for the furin to cleave its S1 and S2 sub-units and activate its ACE2-receptor-mediated infectivity and pathogenicity.

Of grave concern for global public health is a gain-of-function origin to SARS-CoV-2 is indicated by its spike protein incorporating human infectivity and pathogenicity enhancing features unprecedented in nature while synthetic biology left its fingerprints. Furthermore, there is no evidence supporting a Wuhan Huanan market zoonosis because no virus progenitor or animal host was ever identified. There are two reasons for detailing a coronavirus gain-of-function origin to SARS-CoV-2. Firstly, the negative vaccine effectiveness evident in governments’ COVID-19 surveillance data could have been enhanced by a genetically modified SARS-CoV-2. Secondly, the world will be left vulnerable to future pandemics if there was no accidental release from the Wuhan Institute of Virology. At least two other potential SARS-CoV-2 origins exist beyond Wuhan, with one of these potentially involving a WHO, Five Eyes, and NATO-spearhead member nation connected with Ukraine.

The US Department of Defense (DoD) and National Institutes of Health (NIH) funding of EcoHealth Alliance (EHA, $69 million) and its connections one-degree-removed were scrutinized because EHA’s leader led a failed attempt to cover up SARS-CoV-2’s gain-of-function origin. EHA directed research that genetically modified bat SARSr-CoVs that could not infect humans so that they could. EHA’s $14.2 million funding application to the DoD in 2018 showed its intent to insert a codon-optimized furin cleavage site (FCS) into bat SARSr-CoVs. A uniquely encoded Arginine-doublet containing FCS now sits between SARS-CoV-2’s spike protein S1 and S2 sub-units, which has no precedent in known viruses and may have infringed patents. Besides EHA’s long-standing collaborations with two coronavirus gain-of-function research epicenters in the USA and China, it had another with Metabiota. Metabiota’s Series-A lead investor was a Hunter Biden part-owned investment firm. The DoD-funded Metabiota operated in Pentagon Biolabs in Ukraine and US-funded Biolabs in Cameroon and researched corona-, monkeypox-, influenza-, and Ebola viruses. Metabiota has implemented major DoD and Homeland Security contracts across Central Africa while its surveillance role in Sierra Leone’s Ebola outbreak in 2014 created significant controversies.

You are requested to investigate: (1) this New Zealand and overseas evidence for negative vaccine effectiveness, vaccine failure, and toxic vaccine lots, (2) the statistical biases evident in the MoH and other healthcare agencies’ calculable unvaccinated COVID-19 case rates, which essentially eliminated the negative vaccine effectiveness signal, (3) the role of COVID-19 vaccination in exacerbatingcomorbidities most frequently associated with serious-severe COVID-19 outcomes, (4) SARS-CoV-2’s gain-of-function origin while internationally championing a punitive global ban on gain-of-function R&D, and (5) the conduct of the WHO during COVID-19 linked to seven critical points detailed in section 2.7. Would you please ensure New Zealanders are updated on their recently acquired life-long health risks and that informed consent guidelines associated with COVID-19 vaccination be urgently amended? Would government please prioritize clinical research into COVID-19 antibody-dependent enhancement of virus infection, vaccine-associated enhanced disease, and antigenic imprinting in the New Zealand population? Thank you.

Yours sincerely

Dr. Carlton Brown BVSc (1986, Massey University), MBA (1997, London Business School).

Former CEO and co-innovator at Immune Targeting Systems Ltd (UK), “Vaccines for Mutating Viruses.”

Raising awareness for antibody-dependent enhancement of virus infection (ADE), vaccine-associated enhanced disease (VAED), and antigenic imprinting.

https://www.linkedin.com/in/carlton-brown-13b66232/, https://orcid.org/0000-0003-4871-7521, https://gettr.com/user/covid19_ade_vaed.

Download the Open Letter and Evidentiary Document: https://grandsolarminimum.com/2022/12/01/covid-19-vaccine-harm-evidence/.

Open Letter & Evidentiary Document sent to the UK Prime Minister and Cabinet Ministers (COVID-19 vaccine harm, SARS-CoV-2’s gain-of-function origin)

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