April 20, 2022


And this condition, Amyloidosis, is why Long COVID and the myriad conditions induced after exposure to the Spike Protein of SARS-CoV-2 has been so difficult to DEFINE.


Even under usual circumstances, the diagnosis of Amyloidosis usually takes visits to no fewer than FOUR individual specialists.

It is because ALL of the sequelae of SARS-CoV-2 infection (and exposure to the Spike Protein, via Spike Protein therapies) are AMYLOIDOSES.

I need not reference case reports and studies. They are all readily available via a simple search of the conditions listed combined with the terms COVID, SARS-CoV-2, and/or Spike Protein.

It is the DEPOSITION OF FIBRILS in Amyloidosis that causes damage to organs, and in the case of multiple organ involvement, this leads to multiple organ failure.

The Spike Protein, itself a highly inflammatory protein, induces these precise damaging fibrils when it encounters Neutrophil Elastase released from the neutrophils its presence recruits.


The Spike Protein travels via Extracellular Vesicle. Using different cellular models propagating prions or pathogenic Tau aggregates, we demonstrate that vesicular stomatitis virus glycoprotein and SARS-CoV-2 spike S increase aggregate induction by cell contact or ligand-decorated EV.

Disease-associated protein deposition usually starts locally, subsequently spreading stereotypically to other brain regions1. AD, the most prevalent neurodegenerative disease, is associated with the extracellular accumulation of Aβ amyloid and intracellular inclusion of misfolded microtubule-binding protein Tau as in neurofibrillary tangles.


But, in the case of Spike Protein Amyloidosis, the SPIKE ITSELF induces the fibrillary tangles. AND IT IS SYSTEMIC and affects ALL ORGANS.

Therefore, elite athletes are symptomatic before the general population. They already have hypertrophied hearts, which are further enlarged to a symptomatic state by the deposition of the Spike Protein fibrils. The general population, will, of course, follow.

The University of Vermont recently published a paper showing that the Spike Protein induces elevated microsatellite instability (MSI). They indicate it may foreshadow the induction of cancers. Which is true, however I believe they have missed the main point.


The Trinucleotide Repeats Subset of MSI result in proteins with expanded polyglutamine (polyQs) that tend to form amyloid-like fibrils abundant in β sheets, leading to dysregulation of transcription, impairment of the ubiquitin-proteasome system, mitochondrial dysfunction, and autophagy defects and thus induce cellular toxicity.


And the “clotting” being indicated as the cause of Long COVID? Yes, and no.

However, the main cause is that it IS due to Amyloidosis.


The most common causes of age-related progressive dementia include Alzheimer’s disease (AD) and vascular cognitive impairment (VCI), however, mixed disease pathologies commonly occur, as epitomized by a type of small vessel pathology called cerebral amyloid angiopathy (CAA). In CAA patients, the small vessels of the brain become hardened and vulnerable to rupture, leading to impaired neurovascular coupling, multiple microhemorrhage, microinfarction, neurological emergencies, and cognitive decline across multiple functional domains.

This is most likely why China has adopted such a strong Zero COVID policy. Any exposure to the Spike Protein may induce this chain reaction. Please note, China does not use any full Spike Protein vaccines.