Nested in the annals of public health scandals, few revelations hit with the quiet ferocity of a November 18, 2025, peer-reviewed study buried in supplementary tables: 100% of COVID-19 vaccinated participants harboured amyloidogenic microclots in their blood. Not 80%, not 94% – every single one. In a cohort where 94% had received the jab, these fibrinolysis-resistant, Thioflavin T-positive anomalies weren't outliers; they were the norm, even among the "healthy controls." Framed as a probe into "Long COVID," the paper unwittingly unmasks what looks like Long Vaccine – a systemic vascular pathology driven by spike protein exposure, with no lab-confirmed SARS-CoV-2 infections to blame.
This isn't fringe speculation. It's data from fluorescence microscopy, proteomics, and in vitro experiments showing purified spike protein alone birthing identical amyloid clots. And it dovetails with a grim postmortem reality: those rubbery, white fibrous clots yanked from veins since 2021, now confirmed amyloidogenic by forensic labs. We're staring at a potential global health catastrophe – one that demands immediate, unflinching investigation. Here's why this microclot crisis matters and why ignoring it is a dereliction of duty.
The Pathology: From Micro to Macro – A Clotting Cascade Unleashed
Amyloid microclots aren't your garden-variety thrombi. These are rogue fibrin aggregates, misfolded proteins twisted into β-sheet structures that laugh at plasmin, the body's clot-busting enzyme. Detected via ThT staining (a gold-standard amyloid marker), they pack a toxic payload: neutrophil extracellular traps (NETs), myeloperoxidase, elastase, extracellular DNA, and inflammatory debris. In the study, small ones (<900 µm²) lurked in all vaccinated blood, but the "Long COVID" (read: symptomatic) cohort showed a 20-fold spike in larger beasts (900–1600 µm² in 98%, >1600 µm² in 60%).
Mechanistically? Spike protein – whether from infection or mRNA jabs – acts like a prion: it templates misfolding in fibrinogen, birthing insoluble, amyloidogenic clots that obstruct capillaries. Prior work flagged these in acute COVID plasma; now, they're ubiquitous post-vax. No wonder symptoms mimic vascular sabotage: brain fog from cerebral hypoperfusion, fatigue from muscle ischemia, dyspnea from pulmonary blockages.
This progression isn't theoretical. In vitro, spike alone replicates the mess; in vivo, it scales to horror.
The Smoking Gun: Embalmers and Forensics Paint the Postmortem Picture
Since 2021, embalmers have whispered about "calamari" – translucent, fibrous horrors unlike anything pre-pandemic. At the 2025 Tennessee Funeral Directors Association convention, former USAF Major Tom Haviland's survey blew the lid: 64% of 28 attendees reported white fibrous clots in 17% of first-half-2025 corpses. Seventy percent noted "coffee-grounds blood" (microclot sludge); 39% flagged a 14% infant death uptick. Video from the event shows hands shooting up – no hoax, just horror.
Enter Kevin McCairn, PhD: His team's forensic deep-dive on these clots (with McKernan, Kato, Rixey) reveals amyloid hallmarks – β-sheets, ThT fluorescence, dense fibrillar SEM ultrastructure, protease resistance, and human genetic material laced with spike/plasmid traces. RT-QuIC assays suggest prion-like seeding: these aren't inert; they propagate misfolding. In a gut-punch case, McCairn documented amyloid fibrils in a 3-year-old's blood after in-utero Pfizer exposure, the first such paediatric signal.
These aren't "normal" clots. They're end-stage microclots: the living's hidden burden manifesting as the dead's grotesque legacy. And with global vax rates at 70%+, we're potentially looking at billions with subclinical vascular sabotage.
The Stakes: A Public Health Reckoning Long Overdue
Why does this matter? Because amyloid microclots aren't benign. They're a stealth driver of:
Cardiovascular Collapse: Silent emboli fuelling unexplained strokes, MIs, and sudden deaths (up 20–30% post-2021 in VAERS data).
Neurodegeneration: Brain amyloid echoes Alzheimer's; spike's prion mimicry could accelerate tauopathies.
Long-Haul Hell: Explains the 10–20% "Long COVID" rate, but in a vax-dominant world, it's likely vaccine-induced endothelial injury.
Generational Risk: In-utero exposure? An amyloid legacy for kids, priming autoimmune and clotting disorders.
Economically? Trillions in lost productivity, healthcare overload, and a shadow epidemic of disability. Ethically? A rushed rollout without long-term safety nets has left billions as unwitting guinea pigs. The study's authors, silent on the vax link, exemplify institutional blind spots; no infection verification, yet "Long COVID" stamped on spike-driven pathology.
No More Excuses: Demand the Investigation Now!
Launch dried-blood-spot screening for amyloid burden (protocols exist via Synaptek Labs). Replicate McCairn's forensics on scale. Halt spike-based platforms until cleared. Fund reversal therapies: nattokinase, bromelain, or anti-amyloid monoclonals repurposed from Alzheimer's.
This isn't anti-vax hysteria; it's pro-truth science. The microclot signal – from lab benches to embalming tables – screams for transparency. Five billion doses later, we owe the vaccinated, the bereaved, and the unborn, nothing less than full disclosure. Ignore it, and history will judge us as the generation that let a clotting apocalypse unfold in silence. Time to clot off the denial, and demand the purge.
https://www.thefocalpoints.com/p/breaking-study-anomalous-amyloid