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Open letter to the MHRA
Subject: Notification: Findings Regarding mRNA Vaccine Vials
To: Defective Medication Reporting Centre (DMRC)
To the regulators at the MHRA,
Please be advised that this is an open letter intended to inform both yourselves and the public.
I write to you with a pressing concern surrounding the contents of the mRNA vaccines, which were presented to the FDA by Mr. Kevin McKernan on June 15th, 2023. Mr. McKernan possesses significant expertise, with 25 years in the genomic space, an extensive history working with the Human Genome Project at Whitehead MIT, over 57,000 citations, and several patents on PCR and sequencing.
Mr. McKernan reported the discovery of expression vectors for the mRNA vaccines remaining in the vials. The unexpected presence of the expression vector exceeds the stipulated guidelines set by both the EMA and the FDA. Mr. McKernan underscored the grave implications of this discovery, referencing potential risks such as interferon responses and the possible DNA integration into the genome. Please refer to page 116 of the official FDA document for a transcript of the presentation, alternatively you can review the presentation as it was live streamed.
These findings of DNA contamination have since been replicated by another scientist, Phillip J. Buckhaults, Ph.D., who presented his results to the South Carolina Senate in September of this year. Through his investigation, he too found that the Pfizer vaccine contained unexpected plasma DNA fragments. Buckhaults’ work suggests this DNA contamination is from the vector used as a template for creating the mRNA vaccine. A testimony of his presentation is available for review at the following link.
Buckhaults suggested that this DNA might lead to some rare yet serious side effects, including death from cardiac arrest. He also mentioned the potential for this DNA to integrate into a person's genome, especially in long-lived cells like stem cells, which could lead to future health issues, including cancers.
Further to this, discovered in late August, a German laboratory became the third lab to confirm the DNA contamination findings. The Magdeburg Molecular Detections laboratory tested five still sealed batches of BNT162b2 vaccine. All five batches examined contain plasmids, between 83 and 354x above the EMA limit value. Below is a screengrab of the report.
On September 18th these findings were presented to the Bundestag by Dr. Jürgen Otto Kirchne. An official link to the presentation is available at the link below. Please skip on to the 2 minute mark to find the relevant section.
During his presentation to the FDA, Kevin McKernan advised this work can be reproduced with “in 60 minutes with a microliter of the vaccine 1-3 hundreth of the dose for less than $10”. Given the gravity and implications of these findings, I urge the MHRA to undertake a comprehensive review of these reports and conduct independent verifications.
Can you confirm that the MHRA is immediately looking to confirm or rule out these findings? Have any tests of this kind been done subsequent to the approval of these products? Can you please share any information you have on this matter.
Your prompt attention and actions in this matter would be greatly appreciated
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