The Hybrid Harms: When Vaccines and Virus Collide, By Brian Simpson

Lerking in the annals of modern medicine, few chapters rival the COVID-19 saga for its blend of ingenuity, hubris, and unintended fallout. A lab-forged virus, born from risky gain-of-function tinkering in U.S.-China labs,meets its engineered nemesis: mRNA "vaccines" fast-tracked from DARPA blueprints. The promise? Swift protection, fleeting side effects. The reality? A toxic tango that's left billions exposed to chronic torment, sudden collapses, and death rates that defy the "mild variant" narrative. Enter the McCullough Foundation's bombshell paper, Compound Impacts of COVID-19 mRNA Vaccination and SARS-CoV-2 Infection: A Convergence of Diverse "Spikeopathies" and Other Hybrid Harms, freshly published in the Medical Research Archives. This 380-reference juggernaut doesn't just dissect the wreckage; it unveils the Hybrid Harms Hypothesis, a framework explaining how mRNA shots and SARS-CoV-2 infections don't just add harms, but multiply them, producing a global excess mortality crisis that lingers like a shadow pandemic.

For years, the establishment peddled a binary tale: vaccines save lives, infections kill. But as excess deaths pile up, 874,000 in the U.S. alone since rollout, per medRxiv analyses, the cracks widen. Omicron, hailed as "mild," synced with mortality spikes in highly vaxxed nations, not the unjabbed. Negative efficacy? Check: Cleveland Clinic, Japan, Israel, dose-dependent infection hikes. Long COVID or vaccine injury? Indistinguishable, with vaxxed "Long COVID" patients packing 7x the spike burden. This isn't coincidence; it's convergence. And the Hybrid Harms Hypothesis maps the mechanism.

At the heart lurks the spike protein, SARS-CoV-2's infamous spearhead, now mass-produced by mRNA jabs. But it's not solo: lipid nanoparticles (LNPs) ferry it body-wide, igniting inflammation; DNA contaminants (SV40 promoters included) whisper genomic sabotage. The paper's abstract cuts to the chase: "mRNA vaccinations create a persistent toxic milieu... amplifying morbidity and mortality risks commonly ascribed to SARS-CoV-2 infection."

Imagine priming a powder keg, then tossing in a match. That's hybrid harm: prior vax leaves a smouldering spike residue, detected up to three years post-jab, then infection reignites it, layering autoimmunity, clots, and organ failure on subclinical scars. Case reports scream persistence; autopsies echo spike in brains, hearts, placentas. Unvaxxed Omis? Mild. Vaxxed? Cataclysmic surges.

Forget waning protection; mRNA shots boost breakthrough risks. The paper spotlights an eighth study: dose-dependent infection hikes, from Cleveland Clinic's serial jabs correlating with higher odds, to Japan's Omicron waves drowning vaxxed cohorts. Qatar's data? Boosters tripled reinfection odds. UK/Iceland: same script.

Why? Immune imprinting, original antigen fixation blinds to variants, per Nature frameshifting fallout. Add IgG4 tolerance (non-inflammatory antibodies post-mRNA), and you've got viral free rein. Result: Omicron's "mildness" masked amplified harms in the primed, turning sniffles into strokes.

"Long COVID" is a catch-all for spikeopathy, be it viral or vax-derived. But the paper unmasks the fraud: vaxxed patients boast 11,356 U/mL spike antibodies vs. 1,632 in unvaxxed, without recent infection. Clinical overlap? Total: fatigue, neuropathy, myocarditis — indistinguishable. Yet, misattribution reigns: vax injuries labelled "COVID sequelae," inflating viral blame while burying iatrogenic sins.

Excess mortality tells the tale. Post-2021, vaxxed nations logged surges syncing with Omicron, not lethality, e.g., U.S. states with low vax saw convergence post-BA.1 via natural immunity, but high-vax hubs? Persistent peaks, 5x "faster" vaxxers' rates. Europe: slow boosters = 4.9 OR for death. Global? 1.47/100k excess in non-Omicron vs. Omicron's dip, but only where immunity balanced; vax-heavy spots? No reprieve.

The Hybrid Harms Hypothesis isn't alarmism, it's epidemiology's missing link. That 2–3 year "Window of Vulnerability"? Millions still wander it, each reinfection a potential detonator for layered pathologies. Unjabbed Omis? Near-zero excess. Vaxxed? 36% relative mortality risk post-two doses, per Milwaukee data.

This demands action, not deflection. Halt mRNA boosters pending genomic audits. Probe misattributions via spike assays in "Long COVID" cohorts. Fund autopsies for excess deaths, reveal the spike signatures. And accountability: DARPA architects, Pfizer execs, regulators who greenlit without biodistribution, face the tribunal.

The Hybrid Harms isn't hypothesis; it's harbinger. Ignore it, and the next wave—be it lab-leak 2.0 or mRNA 2.0, repeats the horror. Heed it, and we reclaim agency from the spike's long shadow. The body isn't a battlefield; it's a temple. Time to purge the poison.

https://www.thefocalpoints.com/p/breaking-publication-mrna-vaccines