Media and Podcasts, Whistleblower Report

Yeadon and Rees on ‘The End Game’ for mRNA Gene Therapy Vaccines

Two career Pharma insiders expose the end game agenda with the gene therapy COVID shots unleashed on the world in a massive rollout of experimental mRNA and Lipid Nanoparticle technology that Big Pharma knew more than 20 years ago had serious toxicity in animal models and humans. Dr. Yeadon as an immunologist, exposes the damage to the immune system with the mRNA shots and also the critical fact, rarely discussed for the public, that Pfizer’s research on this mRNA technology from the beginning showed they could not even make it work in the research laboratory.

Hedley Rees describes the impossibility of manufacturing these experimental gene therapy shots to create a stable, reliable, and safe product for people. He explains how Big Pharma manufacturers have covered up these manufacturing failures and pushed unsafe products onto an unsuspecting public in their insatiable quest for the next big blockbuster drugs to generate massive profits. You can’t afford to miss these new revelations that could save your life.

According to our guest Pharma insider Whistleblower:

“Highly credentialed scientists and doctors have written numerous research papers explaining the dangerous mechanisms of action underlying mRNA/DNA “platform” technologies. The papers are meticulously researched and depict, correctly, in my opinion, many terrifying consequences of the technology that breaches the innate protective mechanisms of human cells.

Furthermore, these theoretical papers are validated by the observed outcomes, such as, for example, increases in all-cause mortality in high correlation. With increases in rates of vaccination in a given territory, unprecedented increases in the adverse events and deaths recorded by various passive reporting systems, astonishingly high reports of the adverse events and deaths from the pharmas’ own pharmacovigilance systems, and autopsy findings in vaccinated post-mortem showing the mechanisms of mRNA technology damage in histopathologic evaluations.”

So why doesn’t everyone have serious complications or die after the shots if they are so dangerous?

One plausible answer from our Whistleblower as to why there is such a discrepancy in the reactions people have to these experimental shots: “The mRNA shots do not conform to their label specifications. In practice, both “blank” and “lethal” vials and anything in between is produced.”

Good Manufacturing Practices (GMP, GLP, GCP, GDP) standards and pharmacovigilance oversight have been flagrantly ignored by the SARS-CoV-2 injection manufacturers, and FDA/EMA/MHRA has waved the evil jabs through, which is horrifying. The catastrophic death and disability happening to people around the world after receiving the COVID shots are directly related to US, European, and other countries’ regulators completely abdicating their safety and quality oversight function and duty to the public. For more on the potency variation and lack of safety and manufacturing quality oversight, read Failure to Scale: Covid-19 Injection Vials Must be Independently Tested for Conformity to Label. –

For more information, go to Truth for Health Foundation website Download our Vaccine Injury Treatment Guide, file a Citizens Vaccine Injury Report, check our medical and legal resources for help, sign up for newsletter alerts and join in the fight for medical freedom on all fronts.

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Mike Yeadon, Ph.D. immunologist and former Pfizer Chief Scientist worldwide for respiratory pharmacology and product development, speaks from a thirty-year career in pharmacological research and development, new product development, and as a Biotech entrepreneur. He has been a courageous Whistleblower since the fall of 2020, warning about the damage to pregnancy development due to the spike protein, similarity to a critical placental protein, and lipid nanoparticle damage to the ovaries and testicles. He is also Chief Scientific Advisor for Truth for Health Foundation and an expert witness on damage from the COVID gene therapy injections. His warnings two years ago are clearly being played out in the damage to people we are seeing now. He brings a global perspective to the vaccine injuries and overall agenda with the COVID shots.

Hedley Rees, based in the United Kingdom. Mr. Rees has been providing consultancy on the development, manufacture, and distribution of drugs that are fully compliant with the GMP requirements of 21 CFR Title 21 since 2005 through his company, PharmaFlow. PBeforethat, he spent 16 years in senior roles in Big Pharma (Bayer) and 10 years in biotech (British Biotech, Vernalis, and OSI Pharmaceuticals (now Astellas). Read more on Facts about SARS-CoV-2 Injections (aka DNA vaccines) and advanced therapy medicinal products (ATMPs) Watch his recent interview discussing the violations of manufacturing processes and regulations that are supposed to keep us safe:

Mr. Rees also authored Supply Chain Management in the Drug Industry: Delivering Patient Value for Pharmaceuticals and Biologicsfor Wiley, NJ, in 2011. His expertise is in the area of anything to do with manufacture through the three phases of clinical trials (and preclinical if required) and ongoing distribution of the commercial supply. Where regulations have been breached, he has a duty to bring this to the attention of regulators, as has been happening with the frozen vials of COVID shots that were shipped only part-way finished. Follow Hedley Rees on his Substack column, INSIDE PHARMA, where he shares all he can to expose the lies and deceptions that are costing lives and jeopardizing public safety. Watch one of his many interviews here:

Read more: Hedley joins Truth for Health Foundation Team.

Whistleblower Report with the Truth For Health Team on America Out Loud Talk Radio can be heard on weekdays at Noon ET. Listen on iHeart Radio, our world-class media player, or our free apps on AppleAndroid, or Alexa. Listen to other episodes of the Whistleblower Report, available on podcast.

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