by Carlton Brown | Jan 8, 2023 |
Dear LinkedIn Customer Support team and Executive Leadership team
Thanks for your email. As you will appreciate from my profile use I have not used LinkedIn to post in years until recently and was not aware that LinkedIn was censoring the devastating impact of COVID-19 vaccination around the world. Shame on your company.
Firstly, what does restricted access mean? How long will this be in place? You leave me no option at this stage but to comply with your policies. I confirm that I will no longer post the truth about vaccine-induced harm by covid-19 vaccination and will seek other channels to communicate this evidence of global-scale vaccine-induced harm. Would you please cancel my premium paid membership and stop direct debiting my bank account for this monthly sum?
In consequence:
Secondly, I request that you please submit this email and the attached Open Letter and Evidentiary Document to your executive management team who determines company policies. This document is provided as evidence that LinkedIn’s COVID-19 policy is in fact akin to censorship of this devastating global scale COVID-19 vaccine-induced harm. This harm is also being censored by the WHO, WHO member state governments, and their media and big tech affiliates, while the evidence is there in their own vaccine surveillance and pharmacovigilance data and regulatory documents. LinkedIn’s policies do not ensure member safety but actually censor them from this WHO member state government-implemented vaccine-induced harm.
This document provides significant government/national-level data-derived evidence of negative vaccine effectiveness and vaccine failure in NZ, England, Scotland, and Canada (Study-1: 75 million vaxed, 108 million population), globally (Study-2: 77 nations, 2.6 billion vaxed, 3.9 billion people), and vaccine-induced harm in the USA (Study-3: vaccine adverse event reporting system, one year of lot numbered deaths/hospitalizations). Studies 1 and 2 points to the antibody-dependent enhancement of virus infection (ADE), antigenic imprinting (AI), and vaccine-associated enhanced disease (VAED) by multiple mechanisms of pathogenicity, all of which were predictable-preventable pathologies (i.e., inherent to coronaviruses and those inserted by gain-of-function research).
This document also details the unequivocal molecular, scientific, and other evidence for SARS-CoV-2’s
gain-of-function origin, which
implicates a potential non-China origin. This document scrutinizes those parties one degree separated from EcoHealth Alliance whose leader was caught covering up SARS-CoV-2’s gain-of-function origin (2020). Those parties one degree separated included Hunter Biden’s ex-Metabiota zoonosis surveillance specialist (Ukraine-Cameroon), the Department of Defense, the National Institutes of Health, and WHO. Presumably, you know the US Senate investigated Hunter Biden before the 2020 US election theft (
https://www.hsgac.senate.gov/imo/media/doc/HSGAC_Finance_Report_FINAL.pdf), while both of these issues were censored.
This evidentiary document is provided by a former European corporate venture capital-funded CEO/vaccine innovator (“Vaccines for Mutating Viruses”, 2003-2012), a veterinarian with 36 years of vaccine use experience, and a private researcher and author (theme: UN global strategies that portend 21st-century genocide). It is supported by 525 unique data, scientific, and other citations and took me one year of full-time research to complete. It is effectively a Gap analysis of the falsifiable vaccine efficacy and safety claims in 2020 versus the 2023 reality of vaccine-induced harm evident in government data, plus a review of how gain-of-function inserted these pathogenicity mechanisms (and who merits investigation).
Implications: The implications of the evidentiary document and its prolifically cited science on vaccine-induced harm and the SARS-CoV-2 bioweapon is that LinkedIn’s censorship policies are akin to facilitating this WHO member state government caused vaccine-induced harm. One day, maybe this might also be judged as a globally coordinated genocide.
Please reconsider amending your company policies to lift the lid on censorship so LinkedIn members and business leaders can know the truth and make informed decisions based on balanced – not censored – information.
Thank you.
Kind regards
Dr. Carlton Brown BVSc MBA
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 by COVID-19 vaccination, and for a globally coordinated Genocide.
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Carlton Brown |
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Status: Waiting For Information
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You may reply to this case for up to 14 days
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Response (01/06/2023 00:21 CST)
Hi Carlton,
Your account was restricted due to multiple violations of LinkedIn’s User Agreement and Professional Community Policies against sharing content that contains misleading or inaccurate information:
Shared post: “Read the evidence of how gain-of-function research created the 21stC human culling machine (by antibody-dependent enhancement of virus infection, antigenic imprinting, and vaccine-associated enhanced disease.) Download the Open Letter and Evidentiary Document sent to Prime Minister Ardern (plus the slide deck version). https://lnkd.in/gDExai-k“
Content Creation Time: Wed, 04 Jan 2023 18:19:48 GMT
Shared post:”COVID-19 vaccination increased the risk of SARS-CoV-2 infection over the unvaccinated. REASON: Antibody-dependent enhancement of virus infection (ADE) + antigenic imprinting (AI) = realizable upon (re)infection with an antigenically distinct strain (Omicron, Delta). Coronavirus spike protein-based vaccines had a 30yr legacy of ADE in the vaccine industry pre-2019 (SARS, MERS, FIP). CONCLUSION: the gate-keeper FDA approved a predictably unsafe SARS-CoV-2 spike protein vaccine strategy,”
Content Creation Time: Sun, 01 Jan 2023 23:11:22 GMT
Any additional violation of our terms can result in the permanent restriction of your account. We have these policies in place to help keep LinkedIn a safe, trusted and professional network for everyone.
You may appeal the restriction by responding to this email with your agreement and intent to comply with our User Agreement and our Professional Community Policies.
If you have any questions regarding your appeal you can reply to this email. Thank you for being part of the LinkedIn community.
Regards,
Chandler
Member Safety and Recovery Consultant
Response (01/05/2023 18:54 CST)
Hi Carlton,
I’m sorry for not having a quick answer about your issue. I’ve forwarded your message to another group for additional review and advice. We’ll be in contact with you as quickly as possible. Your issue may require additional research, which may extend your wait time.
Please note that if you can’t log in to your account, you won’t be able to check the status of your case. We ask that you don’t create additional cases in the meantime. We’re working as quickly as possible to resolve your inquiry.
Thanks for your patience.
Auto-Response (01/05/2023 12:07 CST)
We are experiencing higher than normal support volumes. Please allow 3-5 days for a reply. Note: • If you can’t log in to your account, you won’t be able to check the status of your case. We ask that you don’t create additional cases in the meantime. • If you can log into your account, you can check the status of your case on the LinkedIn Help Center Your cases page: https://www.linkedin.com/help/linkedin/casesWe are sorry for the inconvenience and will reply as soon as we are able.
Member (01/05/2023 12:07 CST)
SubmissionId: Pwd-Reset:1826ce3c-45d4-4105-b302-d7fb317d1e0d
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FOLLOW UP EMAIL
Re: LinkedIn Account Recovery Appeal [Case: 230105-012596]
To: LinkedIn Customer Support <linkedin_support@cs.linkedin.com>
Cc: COVID19VaccineSafetyNZ <covid19vaccinesafetynz@proton.me>, Carlton Brown <carlton@grandsolarminimum.com>
Dear LinkedIn Team
There was no misunderstanding.
I appealed the restriction by providing my agreement and intent to comply with your User Agreement and our Professional Community Policies. Sorry, if that was not clear or specifically stated in those words.
I repeat this in your exact words, “I would like to appeal the restriction by providing my agreement and intent to comply with our User Agreement and our Professional Community Policies.” Thank you.
I then followed this with a request for you to forward that information to your executive management team, because they are censoring WHO member state government caused vaccine-induced harm, and potentially Genocide. In this scenario LinkedIn’s censorship policies could be interpreted as aiding and abetting that putative global genocide.
Senior management should review that Evidentiary Document (re-attached again) because this issue could be financially material to LinkedIn in the future (i.e., bankrupting). That is to say, when Nuremberg-like trials commence for the perpetrators of crimes against humanity (i.e., SARS-CoV-2 bioweapon release, vaccination with predictably harmful COVID-19 vaccines, and WHO IHR2005 Article breaches and critical actions during the pandemic) then those who aided and abetted that alleged WHO/member state government crime will come under scrutiny for their complicity in that crime (i.e., social media and big tech).
I am trying to give LinkedIn a heads-up on what is actually happening in the pandemic, versus the fake narrative and sham-science your company sets its policies to. As a former CEO of a corporate venture capital funded vaccine biotech whose USP was “vaccines for mutating viruses” (developed a synthetic universal pandemic flu vaccine), a veterinarian with 36 years vaccine use experience, and a private researcher, there are few people on the face of the planet with my unique insight, knowledge, experience, and expertise.
I am not an anti-vaxer – I am anti-Genocide and I work on behalf of 8 billion human citizens to raise awareness, and must work around this censorship madness the best way I can. I am trying to use these instances of censorship reprimand to inform and educate senior management teams with evidence-based information.
The last email has now been posted online, where it will remain for now. Depending on the outcome with removing these restrictions I will press the Web Archive button and ensure this is saved as permanent evidence for future court use (i.e., that LinkedIn had been informed).
Thank you.
<EvidentiaryDocument_COVID19NationalLevelHarm_01122022.pdf>
<EvidentiaryDocument_COVID19NationalLevelHarm_Slidedeck_01012023.pdf>
Kind regards
Dr. Carlton Brown BVSc MBA
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 by COVID-19 vaccination.
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Carlton Brown |
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Status: Waiting For Information
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You may reply to this case for up to 14 days
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Response (01/07/2023 21:27 CST)
Regards,
Chandler
Member Safety and Recovery Consultant
Member (01/07/2023 17:57 CST)
Kind regards Dr. Carlton Brown BVSc MBA 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 by COVID-19 vaccination, and for a globally coordinated 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). days Response (01/06/2023 00:21 CST) Hi Carlton, Your account was restricted due to multiple violations of LinkedIn’s User Agreement and Professional Community Policies against sharing content that contains misleading or inaccurate information: Shared post: “Read the evidence of how gain-of-function research created the 21stC human culling machine (by antibody-dependent enhancement of virus infection, antigenic imprinting, and vaccine-associated enhanced disease.) Download the Open Letter and Evidentiary Document sent to Prime Minister Ardern (plus the slide deck version). https://lnkd.in/gDExai-k ” Content Creation Time: Wed, 04 Jan 2023 18:19:48 GMT Shared post:”COVID-19 vaccination increased the risk of SARS-CoV-2 infection over the unvaccinated. REASON: Antibody-dependent enhancement of virus infection (ADE) + antigenic imprinting (AI) = realizable upon (re)infection with an antigenically distinct strain (Omicron, Delta). Coronavirus spike protein-based vaccines had a 30yr legacy of ADE in the vaccine industry pre-2019 (SARS, MERS, FIP). CONCLUSION: the gate-keeper FDA approved a predictably unsafe SARS-CoV-2 spike protein vaccine strategy,” Content Creation Time: Sun, 01 Jan 2023 23:11:22 GMT Any additional violation of our terms can result in the permanent restriction of your account. We have these policies in place to help keep LinkedIn a safe, trusted and professional network for everyone. You may appeal the restriction by responding to this email with your agreement and intent to comply with our User Agreement and our Professional Community Policies. • User Agreement: https://www.linkedin.com/legal/user-agreement • Professional Community Policies: https://www.linkedin.com/legal/professional-community-policies If you have any questions regarding your appeal you can reply to this email. Thank you for being part of the LinkedIn community. Regards, Chandler Member Safety and Recovery Consultant Response (01/05/2023 18:54 CST) Hi Carlton, I’m sorry for not having a quick answer about your issue. I’ve forwarded your message to another group for additional review and advice. We’ll be in contact with you as quickly as possible. Your issue may require additional research, which may extend your wait time. If you can log into your account, you can update and check the status of your case on the LinkedIn Help Center Your cases page: https://www.linkedin.com/help/linkedin/cases Please note that if you can’t log in to your account, you won’t be able to check the status of your case. We ask that you don’t create additional cases in the meantime. We’re working as quickly as possible to resolve your inquiry. Thanks for your patience. Auto-Response (01/05/2023 12:07 CST) We are experiencing higher than normal support volumes. Please allow 3-5 days for a reply. Note: • If you can’t log in to your account, you won’t be able to check the status of your case. We ask that you don’t create additional cases in the meantime. • If you can log into your account, you can check the status of your case on the LinkedIn Help Center Your cases page: https://www.linkedin.com/help/linkedin/cases We are sorry for the inconvenience and will reply as soon as we are able. Member (01/05/2023 12:07 CST) SubmissionId: Pwd-Reset:1826ce3c-45d4-4105-b302-d7fb317d1e0d Privacy Policy | User Agreement | Copyright Policy This is a support email in response to your request submitted on LinkedIn. This email was intended for Carlton Brown. Learn why we include this. © 2023 LinkedIn Corporation, 1000 West Maude Avenue, Sunnyvale, CA 94085. LinkedIn and the LinkedIn logo are registered trademarks of LinkedIn. ==================== application File Attachment ==================== EvidentiaryDocument_COVID19NationalLevelHarm_Slidedeck_01012023.pdf, 6693915 bytes, added to ticket ==================== text File Attachment ==================== Attachment 2.html, 230 bytes, added to ticket ==================== application File Attachment ==================== EvidentiaryDocument_COVID19NationalLevelHarm_01122022.pdf, 1163971 bytes, added to ticket ==================== text File Attachment ==================== Attachment 4.html, 6767 bytes, added to ticket Response (01/06/2023 00:21 CST)
Hi Carlton,
Your account was restricted due to multiple violations of LinkedIn’s User Agreement and Professional Community Policies against sharing content that contains misleading or inaccurate information:
Shared post: “Read the evidence of how gain-of-function research created the 21stC human culling machine (by antibody-dependent enhancement of virus infection, antigenic imprinting, and vaccine-associated enhanced disease.) Download the Open Letter and Evidentiary Document sent to Prime Minister Ardern (plus the slide deck version). https://lnkd.in/gDExai-k“
Content Creation Time: Wed, 04 Jan 2023 18:19:48 GMT
Shared post:”COVID-19 vaccination increased the risk of SARS-CoV-2 infection over the unvaccinated. REASON: Antibody-dependent enhancement of virus infection (ADE) + antigenic imprinting (AI) = realizable upon (re)infection with an antigenically distinct strain (Omicron, Delta). Coronavirus spike protein-based vaccines had a 30yr legacy of ADE in the vaccine industry pre-2019 (SARS, MERS, FIP). CONCLUSION: the gate-keeper FDA approved a predictably unsafe SARS-CoV-2 spike protein vaccine strategy,”
Content Creation Time: Sun, 01 Jan 2023 23:11:22 GMT
Any additional violation of our terms can result in the permanent restriction of your account. We have these policies in place to help keep LinkedIn a safe, trusted and professional network for everyone.
You may appeal the restriction by responding to this email with your agreement and intent to comply with our User Agreement and our Professional Community Policies.
If you have any questions regarding your appeal you can reply to this email. Thank you for being part of the LinkedIn community.
Regards,
Chandler
Member Safety and Recovery Consultant
Response (01/05/2023 18:54 CST)
Hi Carlton,
I’m sorry for not having a quick answer about your issue. I’ve forwarded your message to another group for additional review and advice. We’ll be in contact with you as quickly as possible. Your issue may require additional research, which may extend your wait time.
Please note that if you can’t log in to your account, you won’t be able to check the status of your case. We ask that you don’t create additional cases in the meantime. We’re working as quickly as possible to resolve your inquiry.
Thanks for your patience.
Auto-Response (01/05/2023 12:07 CST)
We are experiencing higher than normal support volumes. Please allow 3-5 days for a reply. Note: • If you can’t log in to your account, you won’t be able to check the status of your case. We ask that you don’t create additional cases in the meantime. • If you can log into your account, you can check the status of your case on the LinkedIn Help Center Your cases page: https://www.linkedin.com/help/linkedin/casesWe are sorry for the inconvenience and will reply as soon as we are able.
Member (01/05/2023 12:07 CST)
SubmissionId: Pwd-Reset:1826ce3c-45d4-4105-b302-d7fb317d1e0d
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by Carlton Brown | Jan 8, 2023 |
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)
——- Forwarded Message ——-
From: COVID19VaccineSafetyNZ <
covid19vaccinesafetynz@proton.me>
Date: On Monday, December 5th, 2022 at 4:35 PM
Subject: Open Letter & Evidentiary Document for the Prime Minister and all Ministers: COVID-19 negative vaccine effectiveness and harm evidence in New Zealand and overseas (Results, Call to Action)
To:
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>
CC:
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>,
covid19vaccinesafetynz@protonmail.com <
covid19vaccinesafetynz@protonmail.com>
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/.
by Carlton Brown | Dec 1, 2022 |
PREPRINT: Carlton B. Brown (2021), Influenza pandemic risk factors associated with solar cycle extremes, low solar and geomagnetic activity, cold-glacial climate change, and geographic origination (1500-2018).
Author: Carlton B. Brown (https://orcid.org/0000-0003-4871-7521, https://www.linkedin.com/in/carlton-brown-13b66232/).
Download: Research Article (Pandemic_Influenza_Risk_Factors), Supplementary Materials (Supplementary_Materials_Pandemic_Influenza_Risk_Factors)
Abstract: There is no means of predicting when influenza pandemics could occur because risk factors are poorly understood. Risk factor assessment utilized numerous statistical methods, 10 multi-century solar activity, climate change datasets, and expert-confirmed influenza outbreaks. The mid-study coldest temperature was compared with glacial cycle peak temperatures (n=16 ice cores). There was a grand mean of 0.92 pandemics per 11-year sunspot number cycle (SE=0.15, n=25, 1700-) and a higher pandemic probability at cycle peaks and troughs +/-1-year (logistic regression, Peaks: P=0.01, OR=4.2. Troughs: P=0.03, OR=3.4). Multiple logistic regression confirmed peak+trough+/-1-year stages and positive cosmic ray intensity anomalies relative to its 1961-1990 mean as pandemic and epidemic predictors-triggers, respectively (Pr>|z|<0.05, 1700-). Simple logistic1 and linear2 regression identified colder Greenland and Northern Hemisphere temperatures, increased cosmic ray intensity, Arctic sea ice cover, and Greenland ice accumulation rate relative to their 1961-1990 means as outbreak1 and annual outbreak rate2 predictors (P<0.05, 1-11yr moving average1 and cycle mean2 anomalies, 1500-1, 1700-1,2). Greenland was at its coldest mid-study, 8 kiloyears after the glacial cycle peak temperature (mean -4.8°C, n=10 ice cores), or -21% of its prior Holocene interglacial increase. Four categories of risk factors were identified, including solar cycle extremes, low solar and geomagnetic activity, Arctic cold-glaciation linked to the glacial cycle stage, and geographic risk.
Keywords: influenza pandemic; zoonosis; risk factor; circadian system; cold stress; immunosuppression; low solar activity; geomagnetism; cosmic rays; cold climate change.
Preprint: this research article was peer-reviewed by a global public health journal and is “held up” with professional editors before resubmission.
Note: 2019 was perfect timing for a pandemic, if only you knew. There were predictable times and locations more frequently associated with influenza pandemics, which appear relevant to COVID-19. Since 1700 a statistically significant 76% of influenza pandemics and major regional epidemics occurred within a year of the peak or trough of the 11-year sunspot number cycle, including all 20th and 21st-century pandemics and the first avian H5N1 (1997) and H7N9 (2013) zoonoses. Human-to-human COVID-19 transmission was confirmed in 2019 during the 11-year sunspot number minimum and, more generally, during this current grand solar minimum period. An earlier version of these results was provided by email to WHO (Switzerland, 2018) and WHO center contacts in the UK, USA, and China (2018) in my attempt to raise a pandemic alarm. However, no reply was forthcoming on numerous occasions.
Risk factors thematically-putatively associated with immunological susceptibility and regional-scale induced immunosuppression were identified linked to solar-/geo-magnetic cycles, natural climate change, and geographical risks (i.e., China, Europe, North America). Zoonoses and regional-scale viral transmission putatively implicated the circadian system-, cosmic ray-induced ionization-, and cold stress-induced- immunosuppression, and climate-weather-optimized infectious aerosols. The circadian system (CS) controls the immuno-inflammatory systems, and respiratory viruses jack their replication cycles into the CS. Circadian system core clock cryptochrome repressors are magnetoreceptive, giving solar magnetic polarity changes and flux a putative bio-lever on viral disease. Geographical risk putatively implicated single nucleotide polymorphisms (i.e., genetic immune susceptibility) in patient-zero and associated family clusters (i.e., Han Chinese, Caucasian). China’s COVID-19 patient-zero location (i.e., tropical warm-humid) going into the Northern Hemisphere winter (i.e., high latitude regional-scale immunosuppression) putatively facilitated human susceptibility and aerosol transmission of the virus.
by Carlton Brown | Dec 1, 2022 |
Title: COVID-19 vaccination was associated with higher rates of COVID-19 infection, hospitalization, and death. Carlton B. Brown, 2022.
Keywords: Antibody-dependent enhancement of viral infection (ADE), vaccine-associated enhanced disease (VAED), negative vaccine effectiveness, antigenic-imprinting, vaccine failure.
Summary: At the national level, during the Omicron wave, COVID-19 vaccination did not prevent SARS-CoV-2 infection. On the contrary, in general, the COVID-19 infection rates were significantly higher in the 1-, 2-, and 3-dose COVID-19 vaccinated than in the unvaccinated (New Zealand, England, Scotland, and Canada). There was a significant COVID-19 death and hospitalization prevention disbenefit or no benefit at all to COVID-19 vaccination across the various dose and demographic categories. Government claims (in general) that COVID-19 vaccination prevented COVID-19 death and hospitalization despite enhanced infection rates are unsupported by the majority of its data, especially in the elderly, who accounted for most of the COVID-19 death and hospitalization burden. At the global scale, high rates of COVID-19 vaccination were associated with significantly higher infection and death rates than low vaccination rates (77 nations). This study’s results and annotated graphic summaries can be downloaded (ADE_VAED_Vaccine-failure).
Evidentiary Document: This study supported an evidentiary document and Open Letter sent to New Zealand’s Prime Minister, Minister of Health, other Ministers, and many senior healthcare-related executives, specialists, and researchers. This evidentiary document provided the results of my private research into (1) negative COVID-19 vaccine effectiveness and vaccine failure in New Zealand, England, Scotland, and Canada across the Omicron wave and Globally (2021), (2) the evidence for toxic vaccine lots in the US Vaccine Adverse Event Reporting System database and its global implications, and (3) the significant evidence for SARS-CoV-2’s gain-of-function origin and the mechanisms used to enhance infectivity and pathogenicity (https://grandsolarminimum.com/2022/12/01/covid-19-vaccine-harm-evidence/).
by Carlton Brown | Dec 1, 2022 |
Title: Evidence for toxic COVID-19 vaccine lots identified in the Vaccine Adverse Event Reporting System (VAERS, USA). Carlton B. Brown, 2022.
Evidentiary Document: This VAERS study supported an evidentiary document, and Open Letter sent to New Zealand’s Prime Minister, Minister of Health, other Ministers, and many senior healthcare-related executives, specialists, and researchers. This evidentiary document provided the results of my private research into (1) negative COVID-19 vaccine effectiveness and vaccine failure in New Zealand, England, Scotland, and Canada across the Omicron wave and Globally (2021), (2) the evidence for toxic vaccine lots in the US Vaccine Adverse Event Reporting System database and its global implications, and (3) the significant evidence for SARS-CoV-2’s gain-of-function origin and the mechanisms used to enhance infectivity and pathogenicity (https://grandsolarminimum.com/2022/12/01/covid-19-vaccine-harm-evidence/).
Download a PDF copy of this US Vaccine Adverse Event Reporting System (VAERS) study that investigated the evidence for toxic COVID-19 vaccine lots (Toxic COVID-19 vaccine Lots (VEARS, USA)) and the associated .zip file containing the VAERS data text files (VAERS_COVID-19-Vaccine_Death-Hospitalization_data_07122021_Archive).
Abstract:
According to this analysis of the US Government’s Vaccine Adverse Event Reporting System data (VAERS), one year of COVID-19 vaccine-associated deaths and hospitalizations (“adverse outcomes” by 07/12/2021) were equivalent in number to all other vaccine adverse outcomes in the USA over the last 32 and 20 years respectively. A small minority of vaccine lots was associated with the majority of these COVID-19 vaccine-related adverse outcomes. Furthermore, there was an uneven distribution of negative outcomes across vaccine lots (i.e., skewed and peaked). Most of these adverse outcomes were associated with a minority of lots sent to a larger number of states. This minority of lots had a significantly higher weighted mean and median of adverse outcomes per state per lot fraction sent to a State when lots were shipped to ≥11 states (deaths) and ≥19 States (hospitalizations) compared with those sent to state totals below these thresholds. These issues were replicated with all US COVID-19 vaccines. These results would imply the presence of significant differences in vaccine lot composition or specification, or there was targeted vaccine use in high-risk demographics (i.e., the elderly) coordinated via a central vaccine distribution mechanism. Ninety percent of all vaccine-related adverse outcomes were associated with mRNA gene-therapy-vaccines.
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