Dr. Stephanie Seneff & M Nathaniel Mead's recent publication (likely will be pulled down when Pfizer & Moderna puts muscle on Cureus) remind us of the devastation of the Malone, Bourla, Bancel, Sahin

et al. deadly mRNA technology under-pinning mRNA COVID injection! I have problems with how this abstract was written & I will follow up with another stack, too wishy washy, opens door to Malone deaths

https://pubmed.ncbi.nlm.nih.gov/38274635/

‘In the interim, problems with the methods, execution, and reporting of these pivotal trials (COVID vaccine insertion by me) have emerged.

Re-analysis of the Pfizer trial data identified statistically significant increases in serious adverse events (SAEs) in the vaccine group.

Numerous SAEs were identified following the Emergency Use Authorization (EUA), including death, cancer, cardiac events, and various autoimmune, hematological, reproductive, and neurological disorders.

Furthermore, these products never underwent adequate safety and toxicological testing in accordance with previously established scientific standards.

Among the other major topics addressed in this narrative review are the published analyses of serious harms to humans, quality control issues and process-related impurities, mechanisms underlying adverse events (AEs), the immunologic basis for vaccine inefficacy, and concerning mortality trends based on the registrational trial data.

The risk-benefit imbalance substantiated by the evidence to date contraindicates further booster injections and suggests that, at a minimum, the mRNA injections should be removed from the childhood immunization program until proper safety and toxicological studies are conducted.

Federal agency approval of the COVID-19 mRNA vaccines on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits. Given the extensive, well-documented SAEs and unacceptably high harm-to-reward ratio, we urge governments to endorse a global moratorium on the modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered.’