UPDATE 2: The Blood Supply Is Contaminated: BREAKING: Two New Studies Raise Alarm Over Potential COVID-19 “Vaccine” Contamination of the Blood Supply

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All the way back in September of 2022 this Substack warned…

…then a couple of years later in June of 2024 another warning was issued along with a potential cure…

…and now we have even more evidence that the entire blood supply is completely contaminated; to wit:

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We report nine unvaccinated blood transfusion recipients who experienced serious complications including blood clots, heart damage, multi-organ failure, and death.

by Nicolas Hulscher, MPH

A newly published two-part scientific study raises major alarms about an issue that has received remarkably little scrutiny: What happens when blood from COVID-19-vaccinated donors is transfused into another person?

Blood banks routinely screen donations for recognized infectious threats. Yet the current blood supply is not routinely screened for vaccine-derived mRNA, spike protein, plasmid DNA, amyloid, fibrin-microclot complexes, or other relevant vaccine-associated constituents.

Our newly published two-part series investigates this blind spot from two complementary directions. The two studies were authored by James A. Thorp, MD; Claire Rogers, MSPAS, PA-C; R. Clinton Ohlers, PhD; M. Nathaniel Mead, PhD; Nicolas Hulscher, MPH (myself); Kirstin Cosgrove, CCRA; Sierra Hamm, RN; David Speicher, PhD; and Steven Hatfill, MD, M Med.

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Part I: Serious Post-Transfusion Complications in Nine Unvaccinated Patients

Potential Implications of COVID-19 Vaccination for Blood Donation: A Retrospective Case Series and Literature Review—Part I of II

Part I presents a retrospective, hypothesis-generating case series of nine individuals who had not received a COVID-19 vaccine and subsequently experienced serious medical events after receiving blood transfusions.

Reported complications included thromboembolic disease, progressive clotting disorders, myocarditis, pericardial disease, disseminated intravascular coagulation, multi-organ system failure, and death.

We concluded that these cases, together with the existing literature, raise sufficient concern to warrant direct investigation of whether biologically active vaccine-derived constituents may be present in donated blood:

This study suggests that blood donated by COVID-19-vaccinated individuals may contain biologically active vaccine-derived constituents that could cause adverse clinical outcomes. The case reports and cited studies identify questions that warrant further investigation. All the pathogenic components of the COVID-19 vaccine or byproducts from it, have been found in several studies to be circulating in the blood of vaccinated donors. Healthcare providers must honor the ethical principles of patient autonomy and non-maleficence and support patients’ requests for autologous and directed designated donor blood. Screening blood donations for the presence of spike protein, amyloid, fibrin-microclot complexes, vaccine-derived mRNA, and plasmid DNA using quantitative assays and PCR-based methods should be considered for further evaluation by relevant public health and regulatory authorities, including the CDC and FDA.

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Part II: Extraordinary Blood, Clotting, and Neurological Safety Signals

Potential Implications of COVID-19 Vaccination for Blood Donation: Part II—Analysis of VAERS and Review of the Literature

Part II expands the investigation to the CDC/FDA Vaccine Adverse Event Reporting System, analyzing reports from January 1, 1990 through June 26, 2026 and comparing COVID-19 vaccines with influenza vaccines, DPT-containing vaccines, and all non-COVID vaccines combined.

The analysis identified statistically significant safety signals across every investigated endpoint, including reported rate ratios reaching:

Hemorrhage: up to 101-fold
Hemorrhage in pregnancy: up to 108-fold
Blood transfusion: up to 62-fold
Post-transfusion complications: up to 30-fold
Hypercoagulable biomarkers: up to 452-fold
Thrombotic events: up to 1,221-fold
Parkinson’s disease: up to 282-fold
Creutzfeldt-Jakob disease: up to 1,333-fold
Prion disease: 60-fold

These signals are particularly important because they overlap with many of the same clinical patterns observed in Part I, including thrombosis, hemorrhage, DIC, and multi-organ dysfunction.

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Part I identifies a series of serious post-transfusion events that demand investigation. Part II identifies striking pharmacovigilance signals involving many of the same biological systems, particularly clotting, hemorrhage, transfusion complications, and multi-organ dysfunction.

To preserve global blood-supply integrity, regulatory frameworks should move rapidly to implement direct quantitative spike-protein screening and high-sensitivity digital PCR testing for vaccine-derived genetic material across donor networks, while also investigating whether these constituents remain biologically active after donation, storage, processing, and transfusion.

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Actually, the situation is so beyond dire that there is now no possible way to preserve global blood-supply integrity whatsoever, and the only solution would be blood banks strictly sourcing unvaccinated blood tested for residual shedding to ensure purity and safety, having a network of unvaccinated friends with compatible blood types, or stockpiling your own blood for future use.

The very best therapeutics strategy for addressing VAIDS symptoms and the attenuation of the indefinite — more at ceaseless — production of “vaccine” induced spike protein (SP2) may very well be the following approach for both prophylaxis and treatment that also represents the ‘holy grail’ cancer cure that may also treat Alzheimer’s, mood disorders, Parkinson’s, Lyme Disease, Alpha-Gal Syndrom from Lone Star Disease, myocarditis, Hashimoto’s Disease, shingles (herpes), arthritis, Multiple Sclerosis, diabetes, leukemia, Lupus, skin conditions, various other “incurable” ailments, seasonal flu and even the common cold:

The Ultimate Disease Cure & Prophylaxis Protocol

• 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).

• CBD oil (1-2 droppers full [equal to 167 to 334 mg per day] under the tongue, 7 days a week) CBD-X: The most potent full spectrum organic CBD oil, with 5,000 milligrams of activated cannabinoids and hemp compounds CBD, CBN & CBG per serving.

• Fenbendazole (450mg, 7 days a week) or in the case of severe turbo cancers up to 1 gram — for MEGADOSE 1,350mg-2,000mg/day — for prophylaxis one 150mg tablet once or twice per week

• Ivermectin (24mg, 7 days a week) or in the case of severe turbo cancers up to 1mg/kg/day — for MEGADOSE 120mg-200mg/day — for prophylaxis one 12mg tablet once or twice per week

• Hydroxychloroquine (10mg/kg/day 7 days a week) - for prophylaxis one 200mg tablet once or twice per week

• Doxycycline (100mg, 7 days a week for 30-60 days)

• ImmunX immune support which also greatly increases the bioavailability of both Fenbendazole and Hydroxychloroquine (2 capsules per day) — for prophylaxis 2 capsules per day

• Removing sugars and carbohydrates (cancer food) from your diet and replacing table sugar with a zero glycemic index, zero calorie, keto friendly rare sugar like AlluX

• Ivermectin Cream (applied topically 2 times per day)

Do NOT comply.

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