Dr Kevin McCairn

21 April 2025

Warning: Global amyloidogenic health disaster with Dr Kevin McCairn

Dr Kevin McCairn latest laboratory findings and research should be the biggest news story out there right now because it affects every single person in the world.

He has established, by very sophisticated and expensive scientific equipment and his decades of experience in scientific research, the mechanism of harm for C19 and that we have a global amylogenic health crisis of misfolded fibrin causing multi-organ dysfunction, nuero-degeneration, cancer, heart disease, sudden death, strokes, vax injuries, long covid, etc…

These amyloidgenic prion triggering epitopes and peptide are also seeded in the environment as well as in living organisms.

Link to interview on Bitchute
Do watch our previous interview (if you haven’t already), which is linked below the description; an excellent utility video on prions, c19, biowarfare, historical context of prion diseases, animal models.

Link to previous podcast

We discuss his analysis of unusual fibrous white clots, retrieved from the deceased and how he determined their composition to be diseased, proteinaceous tissue; primarily misfolded fibrin that is highly amyloidogenic.

A systemic amyloid type disorder is considered on the hospital scale one of the most serious conditions that you can develop. There is very little in the way of treatments and as people progress through the illness, the light chain amyloids penetrate into their organs and the organs shut down because they become gummed up with this amyloidogenic peptide.

This is very concerning because after the initial seeding there is an amyloidogenic cascade that leads to the manifestation of disease as we understand it. It is not just the immune system dysregulation at this point, but the peptide itself is causing this build up of toxic peptides in the body itself.

The fibrous white clots were analysed under the microscope at low to high magnification and observations discussed. Very abnormal structural properties were observed that are consistent with protein misfolding and staining these samples also confirmed the result that it is misfolded fibrin.

The body contains significant amounts of fibrinogen that can potentially be converted to misfolded fibrin. The evidence of misfolded fibrin is prima facie. It cannot be disputed.

We discussed two important papers. Fibrin drives thromboinflammation and neuropathology in COVID-19

https://www.nature.com/articles/s41586-024-07873-4#:~:text=Fibrin%20promotes%20neuroinflammation%20and%20neuronal,lungs%20independently%20of%20active%20infection.

To establish that via infection, transfection or vaxxination this amyloidogenic process is causing thromboinflammation and neuropathology.

The second paper, discusses how the thrombo-inflammation and neuropathology sequence motifs of the SARS-CoV-2 spike protein appear to have been engineered into the virus

https://zenodo.org/records/14559752

The bioweapon was a binary attack with the virus itself and the gene transfection of the toxic peptide that was distributed in a co-ordinated lockstep event globally modelled on SPARS 2025

https://centerforhealthsecurity.org/sites/default/files/2022-12/spars-pandemic-scenario.pdf

Dr Kevin McCairn concluded that that the pathophysiology of long covid is based on the insertion of spike protein motifs with Zika nomology that mimics HIV GP120 spike protein properties and these features were designed features in the synthetic assembly of SARS-COV-2, a deliberate insert into the biowarfare agent to initiate a specific effect, the targeting of fibrin such that a person develops the sequelae of long COVID, which is characterized by extreme fatigue and neuropathy.

We discuss the chemical properties of the clots, data, excess deaths that included UK data showing the severe impact on younger cohorts between 25-50, which is an assault on any country and society.

From mass spectroscopy we moved onto raman spectroscopy that also established amyloidogenic peptides. We then moved onto RT-QuIC stands which is a highly sensitive assay used to detect prion proteins, that came with a strong signal for prions.

As a consequence of this research, Dr Kevin McCairn is confident that most blood products post COVID are contaminated with misfolded fibrin. We discuss the implications of this and the infected blood scandal, where more than 30k people in the UK were infected with HIV and hepatitis C after being given infected blood and were recently compensated but in Australia, victims are still fighting for recognition and compensation.

Ninety percent of blood sent to Dr Kevin McCairn have these amyloidogenic peptides and it is very concerning that clots taken from the body of the deceased still contain prions with a very strong signal months after they have been removed from the body.

We discuss the detection of amyloid burden through blood samples that you can send to Dr McCairn’s lab, from anywhere in the world, if you have any concerns or if you would simply like to submit a sample for research purposes. These tests can be given to your doctor, in order to get a treatment plan and also can serve as a way of determining if treatment is working by doing further tests after treatment to determine if the amyloid burden has improved or not.

We discuss ongoing research including how infective these peptides are to cause disease and counter measures that have been used to deal with the harm caused by the bioweapon and how his research will benefit finding effective treatments.

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To send blood samples for report or research visit