The Clotastrophe Exposed – Clots and a Deliberate Cover-Up

The evidence is now overwhelming, but it continues to be ignored by the MSM and covered up by the State. Covid vaccines kill.

In June 2025, at the Tennessee Funeral Directors Association (TFDA) convention, a seismic acknowledgment occurred. Retired USAF Major Tom Haviland, invited by the TFDA President, presented the results of a survey of 28 embalmers and funeral directors. The findings were unequivocal and disturbing: 64% reported observing white fibrous clots in corpses, appearing in an average of 17 per cent of all bodies. Seventy per cent noted signs of micro-clotting – described as “coffee grounds” or “dirty blood” – while 39 per cent observed rises in infant deaths, averaging a 14 per cent increase over pre-2020 baselines. Multiple embalmers publicly raised their hands on video to confirm they had seen these rubbery, anomalous structures, many stating they had never encountered them before the COVID-19 era.

These observations are no isolated curiosity. They directly equate with the harrowing testimony detailed in the article “The Real Covid Catastrophe” in this magazine, featuring UK undertaker and embalmer John O’Looney in May 2025. In that compelling interview, O’Looney recounts how, after the mRNA vaccine rollout in early 2021, the embalming process revealed “little white clots… like calamari” in the drained fluids, rubbery and fibrous, unlike anything observed in decades of practice. Instructions were issued from on high to destroy them. Young people in their 20s and 30s, including athletes, began dying suddenly from clots, heart attacks, strokes, and aneurysms – phenomena virtually unknown pre-vaccination. Care-home deaths were systematically misclassified as “COVID” to inflate figures and justify the jab rollout, while hospital wards exhibited what O’Looney terms “medical malfeasance,” with pressure to administer drugs like Remdesivir (noted for its grim 53 per cent fatality rate in Ebola trials) and palliative protocols that hastened ends.

The parallel is unmistakable. Both accounts emerge from frontline professionals handling the deceased: O’Looney in the UK from 2021 onward, and the TFDA cohort in the US persisting into 2025. The clots are not ordinary post-mortem fibrin; they are white, fibrous, tentacle-like, protease-resistant structures appearing across ages, including infants. O’Looney’s “calamari” description aligns precisely with the “rubbery morphology” reported by Haviland’s respondents and earlier whistleblowers such as Richard Hirschman. The timing – absent pre-2020, exploding post-rollout – and the shared institutional pushback (O’Looney’s “destroy them” orders; public health agencies’ silence on Haviland’s repeated submissions to the FDA, CDC, and NIH) suggest continuity of the same phenomenon. This is no coincidence of infection or ageing demographics; it is a post-injection signature persisting years later.

Scientific scrutiny elevates these observations from anecdote to mechanism. Dr Kevin McCairn and colleagues’ intensive biochemical and microscopic analysis reveals the clots as amyloidogenic fibrin aggregates: abnormal, beta-sheet-rich protein structures formed through pathological remodelling of fibrin in the presence of spike protein. They exhibit dense rubbery texture, strong autofluorescence, positive Thioflavin T staining for amyloid, ultrastructural amyloid fibrils under electron microscopy, and PCR-detected human origin with markers suggestive of recombinant spike exposure. Elemental analysis confirms organic, protein-based composition devoid of typical blood markers (low magnesium, iron, potassium; elevated phosphorus). Critically, they test positive for prion-like seeding activity via RT-QuIC, indicating self-propagating misfolding capable of converting normal proteins. These are not mere thrombi but engineered-like amyloid fibrils resistant to plasmin-mediated fibrinolysis – the body’s natural clot-busting mechanism. In other words, these unusual white fibrous clots are not normal blood clots. They are abnormal, rubbery clumps made of misfolded protein, caused by the spike protein from mRNA vaccines. The clots are tough, resistant to the body’s natural clot-dissolving chemicals, and can trigger more misfolding. In short, spike protein turns ordinary fibrin into sticky, long-lasting fibres that the body struggles to break down.

Now, a landmark trilogy of scientific studies has comprehensively characterised these white clots, providing independent, multi-continental validation that elevates the phenomenon to a recognised pathological entity. Funded by New Zealand Doctors Speaking Out with Science (NZDSOS) and conducted by New Zealand-based researchers Dr Bruce Rapley and Dr Matt Shelton, the three-paper series analyses what they term “anomalous intravascular casts” (AICs). Dr Shelton stated: “NZDSOS has been at the forefront of raising concerns about these anomalous findings. This new three-part study, using international labs on three continents, describes their structure, elemental composition and protein makeup, concluding they represent a novel and persistent pathological entity.”

Paper 1 establishes that AICs are not ordinary clots. They are elastic, lumen-conforming, branched structures that form under active blood flow yet are strikingly devoid of intact red blood cells and platelets. Their rubberlike consistency and cohesive strength are incompatible with known pre- and post-mortem changes. Examination reveals elongated casts up to 25 cm in length, frequently branching and demonstrating elastic resistance atypical of conventional thrombi. These features differ markedly from both physiological thrombi and postmortem clots, indicating a distinct pathological phenotype.

Paper 2, the elemental analysis, reveals a bizarre chemical fingerprint impossible for a normal, protein-dominant fibrin clot. The clots are depleted in sulphur – a key marker of protein – and enriched in phosphorus, pointing to a hybrid organic-inorganic matrix. This composition underscores that AICs are not simple blood clots, but something fundamentally altered.

Paper 3 solves the protein puzzle. While the clots contain fibrinogen, the building block of normal clots, the chains are in an abnormal ratio. Critically, they are almost completely lacking in plasminogen – the enzyme required to break down clots – explaining their stubborn persistence. The protein profile also shows signs of inflammatory and immune system involvement as well as red cell destruction. Senior Researcher Dr Bruce Rapley states: “This is not just a big blood clot. This is a fundamentally different architecture. The profound deficiency in plasminogen is like building a structure impervious to future demolition – it’s designed to persist. The elemental data confirms it’s not just protein; it’s a hybrid material our bodies are forced to make but not equipped to clear.”

These findings hold profound health implications for the living as much as the dead. The researchers note that the formation of such persistent, obstructing material in blood vessels will lead to chronic oxygen lack, organ damage, pain, exhaustion, and cascades of inflammatory pathology. For an intelligent lay readership, this translates to the everyday horrors now reported: unexplained fatigue, brain fog, heart failure in the young, accelerating cancers, and “sudden adult death syndrome” – all potentially rooted in microvascular blockage that standard scans miss. The elastic, rubbery nature matches exactly the “calamari” pulled from veins by O’Looney and the TFDA witnesses, persisting four years after rollout because the body lacks the enzymatic tools to dismantle them.

Crucially, the NZDSOS-funded work does not shy away from causation. It highlights the covid injections as a crucial research direction and directly implicates the SARS-CoV-2 spike protein, whether from viral infection or, far more persistently and systemically, from mRNA vaccines that instruct cells to produce it continuously. Dr Shelton added: “This analysis puts substance to the observations our organisation has been highlighting for four years now. These are not ‘normal’ clots. This work adds to the scientific basis for the persistent symptoms and deaths since the (covid vaccine) rollouts and strengthens our many calls to halt the covid injections pending further investigation. Already these results are enabling rapid strides in showing how these harmful structures were predictable from first principles.”

International corroboration strengthens the case. Korean research provides vital population-level context. A large South Korean cohort analysis of excess deaths during 2020–2022 documented minimal excess in 2020 (0.3 per cent) but sharp rises thereafter: 4.0 per cent in 2021 and 20.7 per cent in 2022, coinciding precisely with mass mRNA deployment. Excess mortality hit younger cohorts and categories like endocrine/metabolic diseases, patterns consistent with micro-clotting and immune dysregulation. Complementary Korean work on mRNA-LNP effects on complement activation amplifies endothelial damage and clotting cascades. Japanese data showing excess deaths tripling US rates in 2023 despite high mRNA uptake echo unexplained mortality spikes.

Further evidence abounds. Haviland’s worldwide embalmer surveys (of 301 respondents in 2024: 83 per cent reported clots in 27.5 per cent of bodies) show no abatement into 2025. Infant death increases match O’Looney’s observations of sudden young fatalities. Micro-clotting reported by 70 per cent of TFDA professionals aligns with amyloid microclot literature, where spike exposure creates fibrinaloids impairing circulation. Autopsy series reveal overlapping pathologies: fibrin-amyloid hybrids and endothelialitis. The TFDA’s public hand-raising mirrors O’Looney’s 600 per cent thrombosis claim and discard orders. Public health agencies’ non-response, alongside media dismissal, constitutes gaslighting – or collusion in murder.

Equating the sources reveals a unified timeline. O’Looney documented the ignition in 2021: misclassified deaths as pretext, vaccine-induced thrombosis explosion, white calamari clots, and suppression. By 2025, Haviland and the TFDA confirm entrenchment. The NZ trilogy, published in 2026, supplies the rigorous, multi-modal proof – morphology, elements, proteins – that these are not artefacts but a novel, spike-linked pathology. The “Real COVID Catastrophe” was never the virus; it was the engineered solution; mRNA platforms delivering persistent spike that self-seeds clotting aggregates. Infection may initiate transient effects, but vaccination’s repeated dosing creates chronic production, biodistribution to ovaries, placenta, and brain, and transmissible misfolding.

For informed citizens in the UK and beyond, the patterns are unmistakable. Excess deaths persist globally; cancers accelerate in the young; fertility and infant metrics falter – all while official narratives pivot to “long COVID” or coincidence. The absence of pre-2020 anomalies despite decades of embalming, the refusal of regulators to fund independent autopsies, and Big Pharma’s continued promotion of mRNA (now in flu shots) despite signals point to deliberate omission. The NZ researchers’ call to investigate genetic platforms is not fringe; it is the logical endpoint of data from embalmers in Tennessee, undertakers in Milton Keynes, and labs in New Zealand.

The conclusion is inescapable and demands forensic accountability: these anomalous white fibrous clots are causally related to mRNA vaccines. The cover-up is orchestrated by Big Pharma government, and captured regulators (FDA, EMA, MHRA). All have stifled investigation, alongside the globalist elite whose pandemic frameworks (WHO, WEF-aligned policies) prioritised mass inoculation over safety. O’Looney’s “unlawful killings” via fraud and malfeasance find echo in TFDA’s 2025 data and the NZ trilogy’s 2026 warnings: ongoing, unaddressed, and escalating. Public health agencies’ silence is not incompetence but complicity. Embalmers’ courage – hands raised in Franklin, voices in the UK, scientists in New Zealand – pierces the veil.

The imperative is clear: demand independent inquiries, raw autopsy data, spike-detox research, and immediate suspension of mRNA platforms. The Clotastrophe is real; equating Tennessee’s confirmation, the “Real COVID Catastrophe,” and the NZDSOS landmark studies reveals not coincidence but causation. History will judge those who suppressed this as harshly as the architects. The bodies do not lie. Neither should we.