From Clinical Trials to Histopathological Analysis: Evidence Shows COVID-19 “Vaccine” Products in Widespread Distribution Have Detrimental Effects on the Heart.

1. Cardiovascular warning signs were present in clinical trial subjects at six months. The cohort that received Pfizer’s BNT162b2 had more cardiac deaths than the non-BNT162b2 group.

https://www.preprints.org/manuscript/202309.0131/v1

2. Pfizer document 3.5.6 indicates autoimmunity as the etiology (cause) of myopericarditis following BNT162b2 vaccination.

3. The government warning system signal has been and continues to be strong. Myopericarditis peaked in the year of maximum “vaccine” dosing and not in 2020 when the more potent SC2 variants accounted for COVID-19 illness.

Myopericarditis from COVID-19 Vaccines

[https://openvaers.com/covid-data/myo-pericarditis]
 

4. The excess mortality signal from population-level data is disconcerting.

https://phinancetechnologies.com/HumanityProjects/Projects.htm

5. Sudden Adult Death Syndrome (SADS) has become almost a daily news event.

https://open.substack.com/pub/makismd/p/fitness-enthusiasts-are-dying-suddenly

https://open.substack.com/pub/markcrispinmiller/p/in-memory-of-those-who-died-suddenly-96a

6. Histopathology data from multiple sources identified the causal relationship between the COVID-19 “vaccine” products and sudden death from heart disease.

https://link.springer.com/article/10.1007/s00392-022-02129-5

The pathological mechanisms of injury have been defined by Dr. Burkhardt’s Group using specialized post-mortem analysis.

Spike protein from the “vaccine” was differentiated from COVID-19 infection spike protein using special staining procedures.

The Burkhardt group tied the COVID-19 “vaccine” products to heart disease and Sudden Adult Death Syndrome.

Cardiac failure has now been tied to destructive cellular processes that occur in phases from inflammation to destruction to scarring.

Four pathological processes were identified.

Normal heart muscle is on the left and is characterized by orderly fiber bundles with a single cell nucleus. A late acute/subacute case of myocarditis is seen on the right in which the muscle bundles have been destroyed and abnormal cells have invaded the tissue.

At one year, the inflammation lingers, but most of the damaged heart muscle has been replaced by scar tissue causing loss of cardiac output (ejection fraction) in some cases or irregularity (adynamic) in the contractility of the scarred areas.

7. Myopericarditis should not be ignored or minimized.

“…almost 40% of the affected patients died within the next ten years, most of them from a cardiac cause, one in ten suffered sudden cardiac death.”

“The current data is from the years 2002 to 2008, so it does not take into account infections with the SARS-CoV-2 virus. The virus most frequently detected in the biopsy at the time was parvovirus B19.”

It is not known whether mRNA/spike protein myopericarditis will prove to be better or worse than post-viral (not COVID-19) myopericarditis.

Early indications are that complications from COVID-19 “vaccines” will be significant. Cho, et al. reported 17.7% ICU admissions out of 480 “vaccine” myocarditis patients, 7.8% fulminant, 4.4% fatal, and one heart transplantation.

https://pubmed.ncbi.nlm.nih.gov/37264895/

8. Inexplicably, more modRNA (synthetic mRNA) “vaccines” are in the pipeline.

 https://open.substack.com/pub/petermcculloughmd/p/dr-mccullough-responds-to-bidens

https://www.modernatx.com/research/product-pipeline