VSRF LIVE TONIGHT: Episode 218: Dr. Mary Talley Bowden, M.D.
Thursday, March 12: 7pm Eastern | 4pm Pacific
Tonight on VSRF Live, I am delighted to welcome back our friend, and VSRF Board Member, Dr. Mary Talley Bowden.
A Stanford-trained physician and founder of BreatheMD in Houston, Dr. Bowden treated more than 6,000 COVID patients using early treatment protocols that helped keep people out of the hospital. When she publicly challenged hospital vaccine mandates and restrictions on treatment, Houston Methodist suspended her privileges. She didn’t back down.
Her legal fight helped force the FDA to remove widely criticized messaging discouraging doctors and patients from using ivermectin.
Dr. Bowden has now written a new book, Dangerous Misinformation: The Virus, the Treatments, and the Lies, about what really happened inside medicine during the pandemic.
Today she treats patients suffering from injuries following the COVID-19 mRNA shots. Based on what she is seeing firsthand, she has become one of the most outspoken physicians in the country calling for the COVID-19 mRNA vaccines to be taken off the market pending full safety investigation.
We’ll also talk about Mary’s ongoing battles with the Texas Medical Board (TMB), her lawsuit against the Federation of State Medical Boards (FSMB), and her growing role in health freedom efforts.
Please join us tonight, and bring a friend.
Steve
PS: PLEASE SHARE OUR SOCIALS!
She is smart, beautiful, strong and we are so fortunate to have her on the right side of truth.
"pending a full safety investigation" is putting it mildly. It is absolutely essential to find out why these criminals were allowed to avoid having their deadly products escape rigorous examination through the appropriate gene therapy regulators. This would have also required a public review period enabling skilled members of the public an opportunity to make submissions, addressing the dangers/potential harms from these unnecessary experimental genetic products. We should also be given a reason as to why the known conventional proven, early, cheap, safe and effective products were restricted or denied to the public. (banning conventional known effective treatments has enabled their objective to use EU in order to coerce these dangerous substances upon the public), most likely to achieve a depopulation agenda. These products should have been immediately rejected, before they went into a single arm. It is also known the FDA was aware that these mRNA jabs were not tested to prevent transmission or infection from a virus around November 2020, hence..... it was a known fraud and assault on humanity from the beginning.