Distinguished scientist pens letter to Ardern govt: mRNA jabs have caused ‘Irreparable vaccine-induced harm’

The letter from Dr. Charlton Brown was shared by Dr. Robert Malone on his SubStack today.

Dr. Brown is a distinguished scientific researcher. Malone was one of the key scientists in the development of mRNA vaccines and a world authority on them. The two have known each other for decades, and Malone was not aware Brown was conducting a statistical analysis on the mRNA jabs, or that he was quietly working on research which demonstrated beyond doubt the extreme risks of mRNA vaccines, until today when Brown asked Malone to share the results.

The results take the form a letter addressed to the Prime Minister and all Ministers of New Zealand. The letter is titled, ‘Open Letter & Evidentiary Document sent to the New Zealand Prime Minister and all Ministers: COVID-19 negative vaccine effectiveness and harm evidence in New Zealand and overseas.’

It makes shocking reading, and begins:

‘In this Open Letter and evidentiary document, I share my research results on overseas government and Ministry of Health (MoH) [ie. New Zealand Ministry of Health] 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.’

Highlights:

• The statistical biases evident in the Ministry of Health and other healthcare agencies’ calculable unvaccinated COVID-19 case rates essentially eliminated the negative vaccine effectiveness harm signal from ready public view.
• 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).
• 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 previous combined 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, including New Zealand.
• Pfizer 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.
• Of grave concern for global public health is a gain-of-function origin to SARS-CoV-2 as indicated by its spike protein incorporating human infectivity and pathogenicity enhancing features unprecedented in nature while synthetic biology left its fingerprints.
• There is no evidence supporting a Wuhan Huanan market zoonosis because no virus progenitor or animal host was ever identified.
• 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.
• 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.

Dr Brown concludes his letter as follows:

You are requested to investigate:

• the New Zealand and overseas evidence for negative vaccine effectiveness, vaccine failure, and toxic vaccine lots,
• 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,
• the role of COVID-19 vaccination in exacerbating comorbidities most frequently associated with serious-severe COVID-19 outcomes,
• SARS-CoV-2’s gain-of-function origin while internationally championing a punitive global ban on gain-of-function R&D, and
• 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.”

Read Dr. Brown’s full letter here. Read Dr. Malone’s SubStack here.