🚨 BREAKING: mRNA Technology Triggers a Chain Reaction of Biological Destruction
VIR-X 25% OFF FLASH SALE ENDS TONIGHT!
Not that any additional proof is required as to the deadly and deliberately democidal nature of the Modified mRNA slow kill bioweapon “vaccines…”
"The greatest fear among vaccinologists is the creation of a vaccine that is not only ineffective, but which exacerbates disease. Unfortunately, CoV vaccines have a history of enhancing disease..."
This article was originally published by this Substack on December 6th, 2021, and is now revised.
…and yet additional horrifying proof unrelentingly keeps pouring in…
Two landmark studies map the "Cascade of Harm"—from transcriptomic chaos to proteomic errors, systemic stress, and catastrophic clinical outcomes.
Two landmark studies now converge to expose the Cascade of Harm unleashed by COVID-19 mRNA injections—a stepwise progression from molecular chaos to clinical catastrophe:
Synthetic mRNA Vaccines and Transcriptomic Dysregulation: Evidence from New-Onset Adverse Events and Cancers Post-Vaccination
Clinical and Proteomic Associations of SARS-CoV-2 Infection and COVID-19 Vaccination in Multimorbid Patients: A Cross-Sectional Observational Study
Together, they reveal the full biological Cascade of Harm—unfolding from molecular instability, through systemic damage, to catastrophic clinical consequences:
Tier 1 — Transcriptomic Dysregulation
The foundation of the cascade lies in gene expression chaos:
Thousands of genes dysregulated following mRNA injection.
Disruption of ribosomal function, triggering nonsense-mediated decay.
Evidence of mitochondrial collapse — threatening cellular energy production.
This molecular storm destabilizes the body at its most fundamental level.
Tier 2 — Proteomic Abnormalities
The transcriptomic dysregulation translates directly into protein-level pathology:
Aberrant protein folding and production.
Distinct changes in fibrinogen, actin, and amyloid proteins detected.
These abnormal proteins serve as seeds for clotting, misfolded aggregates, and chronic tissue stress.
Tier 3 — Biochemical Systemic Stress
The proteomic disruptions manifest in blood as measurable biochemical distress signals:
↑ proBNP → cardiac strain and risk of heart failure.
↑ carbamide → renal dysfunction.
↑ CRP and ferritin → markers of systemic inflammation and immune overactivation.
These markers represent the body’s SOS signals — clear warnings of organ-level damage.
Tier 4 — Clinical Outcomes
The final stage is where patients suffer the consequences:
Myocarditis and pericarditis
Hypercoagulability and clotting disorders
Profound fatigue and immune dysregulation
Turbo cancers
Death
Much more
The cascade, beginning with hidden molecular chaos, ends in visible disease and loss of life.
These two new studies do more than highlight isolated harms—they connect the dots, mapping the full stepwise progression of damage unleashed by mRNA technology: from transcriptomic dysregulation, to proteomic corruption, to biochemical distress, and finally to devastating clinical outcomes.
This is a coherent, mechanistic picture of harm that can no longer be dismissed. The biological evidence has crystallized into an undeniable reality—one that demands urgent recognition, immediate action, and true accountability.
In other words, what we are witnessing is a genetically modifying “vaccine” that induces VAIDS, or gmVAIDS, or simply GMV.
And they always knew this would be the outcome for their Great Depopulation.
Thankfully, these GMV clinical outcomes may be treated, and, in certain instances, prevented by administering the following repurposed compound approach:
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Tocotrienol and Tocopherol forms (all 8) of Vitamin E (400-800mg per day, 7 days a week). A product called Gamma E by Life Extension or Perfect E are both great.
Bio-Available Curcumin (600mg per day, 2 pills per day 7 days a week). A product called Theracurmin HP by Integrative Therapeutics is bioavailable.
Vitamin D (62.5 mcg [2500 IU] seven days a week).
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Fenbendazole (300mg, 6 days a week) or in the case of severe turbo cancers up to 1 gram
Ivermectin (24mg, 7 days a week) or in the case of severe turbo cancers up to 1mg/kg/day
VIR-X immune support (2 capsules per day) greatly increases the bioavailability of Fenbendazole, and itself has powerful anti-cancer properties, among many other immune benefits, not limited to spike protein attenuation
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These studies need to keep being done.
However, the vaxxed simply don't believe them.
A while back, Ed Dowd asked one of the AI programs how long it would take people to accept that the vaxx was bad. The answer, at least for the general public, was 10 years. Many will be dead by then.
Do vaccinologists have fears?