A disturbing report published by Dr. Kevin McCairn, Ph.D., appears to have confirmed fears of the mRNA COVID-19 jabs impacting the health of offspring born to women who received the injections.
The case study involves a three-year-old child born to a woman who received the experimental COVID-19 jab during pregnancy.
“We report the presence of amyloidogenic fibrils in the peripheral blood of a three-year-old child with documented in-utero exposure to maternal mRNA-based SARS-CoV-2 vaccination,” McCairn wrote in the abstract.
“Using fluorescence microscopy and scanning electron microscopy (SEM), persistent fibrillar structures were identified that display amyloid-like morphology and autofluorescent characteristics,” he added.
“The child was born 1 week after mother’s 2nd Pfizer shot—no vital signs at birth, required resuscitation, and has been chronically ill since: recurrent infections, multiple surgeries, immune dysfunction,” Nicolas Hulscher of the McCullough Foundation noted.
BREAKING: Amyloid Fibrils Found in 3-Year-Old After In-Utero mRNA Injection Exposure
The child was born 1 week after mother’s 2nd Pfizer shot—no vital signs at birth, required resuscitation, and has been chronically ill since: recurrent infections, multiple surgeries, immune… https://t.co/m7eAaAIJeb pic.twitter.com/bBnvYC0dLM
— Nicolas Hulscher, MPH (@NicHulscher) June 3, 2025
Full post:
The child was born 1 week after mother’s 2nd Pfizer shot—no vital signs at birth, required resuscitation, and has been chronically ill since: recurrent infections, multiple surgeries, immune dysfunction.
At age 3, shows persistent amyloid-like fibrils circulating in blood
Confirmed by fluorescence microscopy & SEM—not typical clots or plaques
Fibrils exhibit cross-β sheet binding, prion-like folding, and autofluorescence
“This case represents a sentinel event that underscores the need for systematic, high-resolution evaluation of post-vaccine biology—especially in pediatric and developmental contexts that have the shadow of events being precipitated by biowarfare research. The persistence of amyloidogenic fibrils years after gestational exposure cannot be dismissed by outdated pharmacokinetic assumptions.”
In simpler terms, the same white, fibrous clots found in deceased vaccinated individuals by embalmers have been detected in a living child of a vaccinated mother.
“We conclude with a contextual analysis linking these observations to the origins of SARS-CoV-2 and its countermeasures, which emerged from biowarfare-linked research conducted within civilian academic institutions under the rubric of Dual Use Research of Concern (DURC),” McCairn wrote.
Anyone keeping up? THIS is the speed of science. @KevinMcCairnPhD and @Kevin_McKernan are shaking the foundations of @HHSGov @CDCgov @NIH https://t.co/JU0W0P0sHT
— KarmaDoc (@ERKarmaDoc) June 3, 2025
McCairn writes:
The presence of stable amyloidogenic structures in a child three years post in-utero exposure demands reevaluation of the safety assumptions surrounding mRNA-based interventions. The spike protein has been documented to form amyloidogenic epitopes, and its capacity for proteolytic resistance mirrors that of prions.
Recent findings by Hammerstom and Nyström (2021) have further deepened the concern. Their structural bioinformatics work identified never-before-seen amyloidogenic domains within the SARS-CoV-2 spike protein, which include attack surfaces aligned with known neurodegenerative and inflammatory mechanisms. These motifs—conserved in both the virus and the encoded vaccine spike—were propagated globally through a mass public health measure based on gene-transfection technology.
Given that over 13 billion doses of mRNA-based COVID-19 vaccines have been administered worldwide, and that global SARS-CoV-2 infection numbers surpass 770 million individuals, a substantial portion of the human population has been exposed either to the pathogen or the transfected antigen. Furthermore, the continued inclusion of mRNA vaccination in pediatric and booster schedules amplifies this exposure.
This raises alarming questions about the cumulative biological burden of such widespread contact with a protein that may harbor intrinsic misfolding and aggregation potential. The possibility that environmental spike exposure serves as a reinforcing mechanism for pre-seeded pathology—especially in developmentally primed systems—necessitates urgent scrutiny under the precautionary principle and renewed international bioethics standards.
Read McCairn’s full report on Substack.