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The Blood Supply Crisis: COVID Vaccines, FDA Policy, and Patient Rights


In this episode of Nurse Michele Talks Podcast, Michele is joined by R. Clinton Ohlers, PhD, Vice President and Director of Media Relations for SAFE BLOOD Donation. Together, they confront one of the most pressing—and deliberately avoided—medical freedom issues facing Americans today: access to safe, unvaccinated blood for transfusions and surgery.



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Since the December 2020 rollout of the COVID-19 vaccines, an overwhelming body of data has emerged from Pfizer and Moderna trial documents—data Pfizer fought to conceal from the American people for up to 75 years before a federal judge ordered its release on an accelerated schedule. Once public, those documents revealed that Pfizer was fully aware of serious adverse events occurring during clinical trials, yet continued to promote its product under the claim that it was “safe and effective.”

Despite these revelations, the vaccines were deployed globally under Emergency Use Authorization (EUA). Even more troubling, when Pfizer later claimed FDA approval, the product that was actually approved—Comirnaty—was not made available to the American public. Instead, Americans continued receiving EUA-labeled products while being led to believe they were FDA-approved. This distinction matters profoundly when evaluating risk, informed consent, and long-term safety.

The CDC’s Vaccine Adverse Event Reporting System (VAERS), a passive surveillance system, currently documents nearly 50,000 reported deaths following COVID-19 vaccination. Yet public health authorities have failed to properly investigate these deaths or communicate findings transparently. Compounding this failure is a 2015 Harvard Pilgrim study commissioned by HHS, which found that VAERS captures only about 1% of actual vaccine-related injuries and deaths. Even more shocking, in the ten years since public health officials acknowledged this catastrophic underreporting, no meaningful remediation has occurred.

If VAERS captures just 1% of harms, then the true scope of potential harms, injury and death associated with the COVID-19 vaccines may be orders of magnitude higher than officially acknowledged. If our public health officials are not properly investigating deaths… That may explain why data surrounding the anomalies found within the blood of the Covid vaccinated is being ignored as well. Thankfully, research is being published around the world. With global research openly documenting concerning findings in the blood of COVID-19 vaccinated individuals, public health authorities can no longer claim ignorance. Their refusal to acknowledge and disclose potential risks to the American blood supply is indefensible.

Meanwhile, independent researchers worldwide have published data confirming persistent spike protein, mRNA, DNA plasmids, and SV40 sequences in vaccinated individuals’ blood—lasting months to 750+ days after injection. Researchers at Yale University reported that in a subset of study participants with persistent symptoms following COVID-19 vaccination, SARS-CoV-2 spike protein was detectable more than 700 days after their last vaccine dose — far longer than the typical “few days” most studies expected. Investigators such as John Beaudoin Sr. have documented alarming increases in acute kidney injury following vaccination. Kevin McKernan has identified DNA plasmids circulating in vaccinated recipients. Even more troubling, SV40 sequences—flagged internally during Pfizer’s trials—were reportedly never fully removed.

These biological findings coincide with rising reports of aggressive, fast-progressing cancers—often referred to as “turbo cancers”—observed almost exclusively in COVID-19 vaccinated populations worldwide.

Yet despite this growing body of evidence, neither the American Red Cross nor U.S. public health authorities have separated the blood supply by vaccination status. This has created unique and devastating challenges for Americans seeking autologous (self-donated) or directed blood donations from family members or friends—options that were once considered standard of care.

History makes this refusal especially alarming. During the HIV/AIDS crisis of the 1980s and 1990s, public health authorities failed to adequately protect the blood supply. As a result, countless hemophiliacs and transfusion recipients were unknowingly infected with HIV and hepatitis. Many died before meaningful safeguards were implemented. The lesson should have been clear: once blood is contaminated, damage cannot be undone.

Yet here we are again.

Dr. Mary Bowden has publicly highlighted these concerns, noting that many patients fear receiving blood “poisoned by mRNA,” while citing an FDA information sheet that discourages directed blood donations as “not medically indicated.” Hospitals now rely on this FDA guidance to deny patients and families the right to choose their own blood donors—even in life-saving surgical and emergency situations.

This brings us to SAFE BLOOD Donation.

Dr. Ohlers explains that SafeBlood was founded after early evidence—visible as early as August 2020—suggested profound differences between vaccinated and unvaccinated blood. European clinicians and naturopaths predicted serious downstream consequences for the global blood supply. Those predictions were later confirmed by morticians, clinicians, and families reporting unexplained clotting, cardiovascular injury, and death following COVID19 Vaccination.

SafeBlood exists to restore patient choice, medical freedom, and informed consent. The organization maintains a registry pairing transfusion recipients with non-mRNA vaccinated donors, ensuring donors can be contacted when blood is urgently needed for surgery or emergency care.

Importantly, SafeBlood does not discriminate. COVID-19 vaccinated individuals are also eligible to receive unvaccinated blood—recognizing that vaccine-injured patients often wish to avoid further exposure to spike protein, mRNA, DNA fragments, or SV40 sequences already circulating in their bodies.


This issue affects 100% of Americans. Whether vaccinated or unvaccinated, everyone may one day need blood. Surveys now show that as many as 25% of Americans believe they know someone who died from the COVID-19 vaccine, and more than 50% believe they know someone injured or disabled by it. These are not fringe beliefs—they are widespread, lived experiences.

History has already shown the cost of ignoring blood safety warnings. The question now is whether we will act before history repeats itself once again.

What You Can Do Right Now

Readers are strongly encouraged to visit SafeBlood.com and register so their blood type is on record—for themselves, their loved ones, and their communities. Whether preparing for an upcoming surgery or simply safeguarding the future, being listed in the SafeBlood registry can make the difference between life and death.

👉 IMPORTANT:

When you sign up for any SafeBlood membership or Substack option, be sure to use the code NURSEMICHELE at checkout.

✔️ You’ll receive 10% off, and

✔️ You’ll directly support Nurse Michele Talks Podcast in continuing independent medical journalism and patient advocacy.

Medical freedom begins with informed choice—and safe blood is foundational to that freedom. Citations & Supporting Evidence

Foundational Science Behind SafeBlood

Early Blood Analysis (August 2020)

  • Comparative analysis of vaccinated vs. unvaccinated blood, showing visible differences.

Based on these findings, SafeBlood founder George Della Pietra, along with European naturopaths, predicted serious downstream consequences for the global blood supply.


Evidence Confirming Blood Supply Concerns

Morticians & Clotting Observations


Documented Patient & Case Reports

SafeBlood reports receiving similar accounts regularly, including outreach from physicians observing these patterns clinically.


Peer-Reviewed & Scientific Evidence

Persistence of Vaccine Components

Transferability Through Blood


Epidemiological & Insurance Data


Ongoing & Emerging Risks


FDA Policy & Blood Donation Restrictions


Additional Context


Resources & Follow-Up


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