High Amyloidogenicity in Post-Mortem 'Calamari' Clots
Kevin McCairn With Greg Harrison and Richard Hirschman
mRNA / Prion Simplified Overview
Open Letter of Concern
The video presentation above is a simplified overview of the scientific and fully referenced Open Letter of Concern below. It is intended for those less scientifically minded, or as a preview to get an overall feel of the topic prior to reading the full Open Letter of Concern. It is based on the Simplified Overview pdf document located on this page that will open a new window to be read or downloaded.
Date: 27th July 2023
To:
1. Dr Christine Middlemiss BVMS, M.R.C.V.S., Chief Veterinary Officer at DEFRA & VMD
2. Abigail Seager, Director and CEO, VMD
3. Gavin Hall, Deputy CEO and Director of Authorisations, VMD
4. Julia Drown, non-executive Director VMD
5. Timothy Riley, non-executive Director VMD
6. Philippa Hardwick, non-executive Director VMD
7. David Catlow, M.R.C.V.S., non-executive Director VMD
Background
Following the authorisation of the first veterinary "mRNA particle" type "vaccine" - Sequivity for pigs in the USA, it is reasonable to expect that Merck/MSD Animal Health will seek authorisation for it in the UK if they aren’t doing so already. The paper mRNA Vaccine Development for Emerging Animal and Zoonotic Diseases1 published in the Viruses Journal in February 2022 indicates the general intention to develop further mRNA gene therapy products in a variety of different animal species.
Given the announcement of a partnership between Bayer and BioNTech announced in 2016 with the declared aim to produce veterinary mRNA gene therapies2, we must assume that it is only a matter of time before one or more products are presented to the Veterinary Medicine Directive (VMD) for authorisation.
There has also been mention of swapping current animal vaccinations to this mRNA technology. We find it interesting that it is only now when the novel mRNA technology is being pushed that so many weaknesses in current vaccination modalities are revealed in the mRNA Vaccine Development…1 paper, and yet the narrative and justification for mass vaccination of our animals has always been how safe and efficacious they are.
The first report of the successful use of in vitro transcribed (IVT) mRNA in animals was published in 19903. Since then, biotech companies had poor results testing mRNA drugs for cardiovascular, metabolic, and renal diseases, cancer, and rare diseases, with most finding that the adverse side-effects of mRNA insertion were too serious. Concern with severe adverse reactions of mRNA vaccines is reflected in the history of vaccine development. This was the very reason for many companies to abandon their development efforts. To now contemplate fast-tracking equivalent products within 8-12 weeks as happens with Sequivity, without long term safety testing and monitoring, is reckless at best.
Firstly, mRNA products of the type referred to as vaccines are nothing of the sort. As recognised by BioNTech in their official SEC filing (bottom of p.14), the FDA regards these mRNA products as gene therapies. Changing the definition of what a vaccine is to include these mRNA products does not make them vaccines, especially when the FDA definition of a gene therapy has not altered to exclude them. We can only assume that this change in the definition of a vaccine occurred in order to facilitate and fast-track authorisation of these novel products in order to bypass the usual trials and safety net required for non-vaccines because there is sufficient evidence to understand that these mRNA products are potentially inherently unsafe, such that they should only be licensed for use in individual life-saving situations where a congenital genetic disorder exists that so significantly shortens and/or impairs the quality of life that giving gene therapy is worth any risk that the gene therapy represents.
For the reasons set out below, to introduce such novel technologies into animals, especially those destined for the human food chain, exposes meat consumers to a variety of known dangers. This includes humans, our pet carnivores, and captive carnivores in zoos, laboratories etc and wild animals that have access to farmed meat products…(continued)
High Amyloidogenicity in Post-Mortem Calamari Clots With Greg Harrison and Richard Hirschman
Introduction
Mass Spectrometry Data
Analyzing Clots
Nanobot Nonsense
RT-QuIC Data, Amyloid Cross-Seeding
Blood Analysis
Issues With Obtaining Proper Testing / Analysis
Clots and Stem Cells
Deep Vein Thrombosis (Leg) Post-Vax
Cardiologists Secretly Calling for No more ‘Vax’
Analyzing Clots Part 2
Cerebral Amyloid Angiopathy
Psuedouridene and Misfolding Proteins. Intentional Bioweapon?
Shills, Disinfo & Muddied Waters
Post-chat wrap up / viewer Q&A
Related
Amyloid Signals, Vaxxed vs Unvaxxed Blood
Prions as Bioweapons? Much Ado About Nothing; or Apt Concerns Over Tiny Proteins used in Biowarfare
Transcript errors generate amyloid-like proteins in human cells
Fibrin drives thromboinflammation and neuropathology in COVID-19
Long COVID Breakthrough: Spike Proteins Persist in Brain for Years
Spike Protein Lingers in Brain, Fuels Long COVID
Amyloidogenesis of SARS-CoV‑2 Spike Protein
Plants can take up CWD-causing prions from soil in the lab. What happens if they are eaten?
Plants as vectors for environmental prion transmission
This Brain Disease Is Set To Double Worldwide By 2050. Are We Prepared? What Scientists Say.
The Fastest-Growing Brain Disease Is Set to Double – Are We Prepared?
Experts warn virus that almost all of us have caught may dramatically raise risk of young dementia
Do infections have a role in Alzheimer’s disease?
Prion Research Market Growth
Incapacitating Agents
Bioweapons Convention and Private Research
Amyloid Burden (‘Vax Injury’) Testing
Ways to connect
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Greg Harrison and Wayne Crouch have come up with a hoax about how they supposedly discovered new hidden ORFs in the genome of SARS-CoV-2: https://sars2.net/clot.html#An_Unholy_Triad_and_mystery_ORFs.
The hoax seems to have been inspired by a Twitter thread by Patent_SUN, who wrote about analysis by the Japanese Twitter user mbi92710920. When mbi ran ORFfinder on the Pfizer plasmid sequence that was uploaded to GenBank by McKernan, the spike ORF was numbered ORF11 and the long ORF on the reverse strand was labeled ORF19. Patent_SUN also pointed out how ORF19 had 23 matches to GXXXG, which he called a "prion motif".
This year Greg Harrison started to say that ORF19 was an ORF of SARS-CoV-2 and not the Pfizer vaccine, but it still had 23 "prion motifs", which he said made it extremely dangerous. He posted an AI-hallucinated image he said was a "plasmid map" of SARS-CoV-2, where there were 4 segments at different parts of the genome labeled ORF19. But in reality SARS-CoV-2 is not even a plasmid, and an ORF is a single contiguous region of the genome so there cannot be multiple ORF19 segments scattered throughout the genome.
Greg posted an AI-generated table of data about fake ORFs 11, 19, 29, 85, 43, 60, and 100. It showed that the Q/N and R/K content percentages of all ORFs were divisible by 5. For example ORF85 was 28 aa long and it had 15% Q/N content, but there is no integer you can divide by 28 that produces 15% when rounded to the nearest integer. Also ORF29 was 60 aa long and it had 50% Q/N content, even though there's 59,448 possible 60 aa segments of Wuhan-Hu-1 in all 6 frames, but the highest Q/N percentage in any of the segments is only about 27%. When I tried generating a similar table of fake ORFs with Perplexity, the Q/N percentages were all divisible by 2 or 5.
Greg's co-conspirator Wayne Crouch wrote that Greg discovered the secret ORFs by decoding secret Chinese and Russian military reports, and he released a series of AI-generated videos about the ORFs called An Unholy Triad. The first video in the series said that ORF19 went back to PLA virology studies based on "research logs from 1999 to 2005", and ORF29 traced back to WIV experiments based on "military reports from 2003 to 2008". But none of the research logs or military reports were actually shown in the videos.
In one Twitter thread Greg showed images that supposedly came from a secret Chinese report, but they clearly looked like AI-generated images with garbled text. But he said that he garbled text was some kind of a secret code that was used by bioweaponeers, so that for example one piece of text that looked like "Hetnody Ane Uadeeanchounsylnfrtn" was actually code for "Cytokine-Anchored Systemic Inflammation".
Last year Laura Kasner published a PDF by Greg Harrison's group which described the results of their supposed mass spectrometry analysis. The PDF included a photo with the caption "Worm-like fibrous clot from a patient who died from COVID disease". But the same photo was included in a paper published in 2019, which said it was a clot from a tube for removing lung fluid.
Greg Harrison is also supposed to have done an HPLC mass spec analysis of the calamari clots, but he only published the results of the analysis as simple pie charts that showed the percentage of each protein among the top 21 proteins. Me and Kevin McCairn have asked him to publish his raw HPLC data, but he has refused to publish it, because he came up with various excuses like that it would have identified the laboratory that did the research, that the PhD student who did the analysis signed an agreement with the university that they were not allowed to publish the raw data, or that the data was in a foreign language. When I asked him to even publish a more detailed table of the results with more columns, he published a simple table with 5 columns that might have all been generated from the percentages that were shown in his pie charts, and his table didn't even show what the column headers were. When I asked him what the columns meant, he said he couldn't answer because it was "proprietary information".
Two months ago after I busted Greg's ORF hoax, he posted a tweet that said: "And at this point in time, wish to retract my ORF 'rantings' due to our lack of credible evidence that any of our ORF stuff actually exists." [https://x.com/Greg21143362/status/1908007680406589892] However later he started pushing the story about the ORFs again.
McCairn told me this about Greg's hoax on his Discord: "I've reamed him out for it and how fucking stupid it is to be amplifying LLM hallucinations." And he told me: "And now I'm aware of the LLM nonsense, I have told them there will be the strictest scientific standards applied, and I will not have nonsense like that as an attack vector".
Tom Haviland wrote that he was in contact with a team that was analyzing Hirschman's clots in a lab, whose "lead scientist" was Greg Harrison. [https://laurakasner.substack.com/p/a-horrifying-breakthrough-in-the] About a month after Greg Harrison had announced that he had retracted his ORF rantings, Tom Haviland posted a comment at Substack that said "Decades of bioweapons research by the Soviets, Chinese, and Americans have developed nefarious ORFs that code for proteins that promote blood clotting, help viruses replicate faster, and help viruses evade the immune system". [https://www.thefocalpoints.com/p/new-study-pfizer-recipients-face/comment/113177574]
So far Greg Harrison has suffered little consequences even though he was busted producing transparent disinformation, and he's still going on podcasts with Hirschman and Haviland. If Hirschman and Haviland were sincere, they would probably want to break ties with Harrison, but I think they are both in on the scam.