A recent report from Michael Palmer, MD and Sucharit Bhakdi, MD “summarizes evidence from experimental studies and from autopsies of patients deceased after vaccination.”
Their collective findings demonstrated:
- mRNA vaccines don’t stay at the injection site by instead travel throughout the body and accumulate in various organs,
- mRNA-based COVID vaccines induce long-lasting expression of the SARS-CoV-2 spike protein in many organs,
- vaccine-induced expression of the spike protein induces autoimmune-like inflammation,
- vaccine-induced inflammation can cause grave organ damage, especially in vessels, sometimes with deadly outcome.
We note that the damage mechanism is which emerges from the autopsy studies is not limited to COVID-19 vaccines only but is completely general—it must be expected to occur similarly with mRNA vaccines against any and all infectious pathogens. This technology has failed and must be abandoned.
While clinical case reports (e.g. [1,2]) and statistical analyses of accumulated adverse event reports (e.g. [3,4]) provide valuable evidence of damage induced by mRNA-based COVID-19 vaccines, it is important to establish a causal relationship in individual cases. Pathology remains the gold standard for proof of disease causation. This short paper will discuss some key findings on autopsy materials from patients who died within days to several months after vaccination. For context, some experimental studies are briefly discussed as well.
Bullet points from the report include:
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Most of the evidence presented here is from the work of pathologist Prof. Arne Burkhardt, MD
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Pfizer’s own animal experiments show that the vaccine quickly distributes throughout the body
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Expression of viral proteins can be detected with immunohistochemistry
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Expression of spike protein in shoulder muscle after vaccine injection
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Coronavirus particles contain two prominent proteins: spike (S) and nucleocapsid (N)
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Infected persons express the nucleocapsid protein (and also the spike protein)
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Injected persons express only the spike protein, which implicates the vaccine
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Expression of spike protein within the walls of small blood vessels
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Endothelial stripping and destruction of a small blood vessel after vaccination
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A crack in the wall of the aorta, lined by clusters of lymphocytes, leading to aortic rupture
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Healthy heart muscle tissue, and lymphocytic myocarditis
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Lymphocytic infiltration and proliferative inflammation in lung tissue
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Vaccine-induced expression of spike protein in a bronchial biopsy nine months after vaccination
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The Pfizer vaccine mRNA gets copied (“reverse-transcribed”) into DNA and inserted into the cellular genome
The report’s summary reads:
The evidence presented here clearly demonstrates a chain of causation from vaccine injection to
- rapid distribution of the vaccine through the bloodstream,
- widespread spike protein expression, prominently in blood vessels, and
- autoimmune-like inflammation and organ damage.
Vaccine-induced vascular damage will promote blood clotting, and clotting-related diseases such as heart attack, stroke, lung embolism are very common in the adverse events databases [4,12].
In addition to autoimmune-like inflammation, other disease mechanisms, including prion-mediated CNS degeneration [13], aberrant vascular protein deposition (amyloidosis) [14,15], and lipid nanoparticle toxicity [16], are plausible but require further study and corroboration. Overall, these vaccines can no longer be considered experimental—the “experiment” has resulted in the disaster that many medical doctors and scientists predicted from the outset [17]. The vaccination must be stopped, and all approvals and authorizations of their use must be revoked.
Read the full report at Doctors for COVID Ethics.
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