Big Pharma and government-directed Medicine in the US and UK have shifted in the last 25+ years to a “one-size-fits-all” focus on profits and “protocols” over patients as individuals with unique needs and customizing treatments with various approaches to each patient.
US physician host DrLee4America and co-host Pharma expert Hedley Rees are joined by UK Physician, researcher, and international keynote speaker, Dr. Philip McMillan, Consultant Physician in the NHS, UK, with over 20 years of medical expertise and an innovative approach to COVID-19 and dementia reversal.
Since the COVID-19 pandemic started, Dr. McMillan has applied his research skills to understanding the pathological impact of the SARS-CoV2 virus.
In June 2020, in collaboration with top international ACE2 expert Professor Bruce Uhal at Michigan State University, Dr. McMillan published a unique theory of autoimmune response to ACE2 enzyme as the primary reason for such severe damage with COVID-19 illness.
In March 2021, he published a follow-up paper proposing a more detailed and comprehensive explanation of the symptoms associated with COVID-19 and “Long-COVID.” His presentation on “mystery clots” in COVID is here: Pathologist meets Embalmer: Cause of Mystery Clots: https://philipmcmillan.substack.com/p/embalmer-meets-pathologist-cause
For more on Dr. McMillan’s work, see his Substack: Vejon COVID-19 Review, a Comprehensive overview of COVID-19 research focusing on autoimmunity as the primary pathology of the disease.
Hedley Rees, based in the United Kingdom. Mr. Rees has been providing consultancy on developing, manufacturing, and distributing drugs fully compliant with the GMP requirements of 21 CFR Title 21 since 2005 through his company, PharmaFlow. Before that, he spent 16 years in senior roles in Big Pharma (Bayer) and ten years in biotech (British Biotech, Vernalis, and OSI Pharmaceuticals (now Astellas). Mr. Rees also authored Supply Chain Management in the Drug Industry: Delivering Patient Value for Pharmaceuticals and Biologics for Wiley, NJ 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.
Read more on Facts about SARS-CoV-2 Injections (aka DNA vaccines) and advanced therapy medicinal products (ATMPs): https://open.substack.com/pub/hedleyrees/p/facts-about-sars-cov-2-injections?r=xoehy&utm_campaign=post&utm_medium=web Watch Recent interview discussing the violations of manufacturing processes and regulations that are supposed to keep us safe: https://rumble.com/v1qe9nk-freeman-interviews-hedley.html.
Hedley joins Truth for Health Foundation Team: https://open.substack.com/pub/hedleyrees/p/hedley-joins-truth-for-health-foundation?r=xoehy&utm_campaign=post&utm_medium=web
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: https://rumble.com/v14gou4-drug-development-expert-sounds-alarm-over-rushed-to-market-covid-19-vaccine.html
For more information, go to Truth for Health Foundation website www.TruthForHealth.org. 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 the fight for medical freedom on all fronts.
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