A physician with more than 25 years of experience, Dr. Mary Talley Bowden is board-certified in both Otolaryngology and Sleep Medicine. In 2019, she founded BreatheMD in Houston. Educated at the University of North Carolina in Chapel Hill, the Medical College of Georgia at Augusta University, and the University of Texas Medical Branch, Dr. Bowden completed her Residency at Stanford University.
She is one of the few direct care specialists in the U.S. who does not contract with any health insurance companies and strives to offer affordable care with clear pricing.
However, Dr. Bowden was targeted after speaking out against prescribed protocols for treating COVID-19 and the experimental COVID-19 vaccine. She has been a target of the Texas Medical Board, the U.S. Food and Drug Administration, and Houston Methodist Hospital for her early treatment of over 6,000 patients with COVID-19, despite her treatment record recording zero deaths.
Her results highlight the effectiveness of her protocol in direct contrast to the protocols hospitals were using. The protocols the hospitals are using are connected with countless deaths, hospitalizations, and adverse effects, according to the government data found on the Vaccine Adverse Event Reporting System (VAERS).
Following Dr. Bowden’s success with her protocols, the Texas Medical Board filed a formal complaint against her for violations of the Texas Medical Practice Act. Now, after a couple of appeals, her next hearing is scheduled to take place on April 29, 2024.
From early on in the pandemic, Dr. Bowden and other doctors, were using ivermectin, a medication which two scientists won a Nobel prize for working on, in their treatment protocols. In response, the FDA initiated an aggressive campaign against using ivermectin in treating COVID-19. The FDA used the famous “horse” message, stating, “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19,” emphasizing that it is a horse dewormer and should not be used on people. This message can still be found on the FDA website.
Dr. Bowden and two other doctors sued the FDA for overstepping their authority and making suggestions for patient treatments. Judge Don Willett agreed, declaring in his ruling that the “FDA is not a physician. It has authority to inform, announce, and apprise—but not to endorse, denounce, or advise.” Currently, this case is going back to the U.S. District Court in Galveston for further debate.
Dr. Bowden has also sued Houston Methodist for defamation. Although her case was dismissed, she appealed, and the judge reviewed the case on Dec 12, 2023. She does not expect to hear anything back on this case for over a year.
In the beginning of the COVID-19 pandemic, Dr. Bowden started using monoclonal antibodies to treat her patients and had great success. She explained that whenever she needed more, she could order them and they would be delivered the next day. However, the government took over the distribution of the monoclonal antibodies. When this happened, it became harder and harder for her to get them until the government just stopped shipping them. Dr. Bowden says this was to push the COVID-19 vaccine.
“The monoclonal antibodies were very effective and the patients would turn around the next day if treated early,” said Dr. Bowden, emphasizing that “early treatments lead to better outcomes.”
When she could not get any more monoclonal antibodies delivered by the government, she worried there would not be anything else as effective. However, she discovered ivermectin and hydroxychloroquine worked just as well.
In 2021, the attacks on ivermectin and hydroxychloroquine increased exponentially. Dr. Bowden and others believe that the more ivermectin, a generic prescription drug, threatened the lucrative pharmaceutical industry, the more enemies it accumulated.
At present, there are more than 17,000 physicians who support early treatment and the protocol Dr. Bowden uses.
Additionally, Dr. Bowden explained that there is now overwhelming data that the spike proteins in the COVID-19 vaccines are causing four major domains of disease; cardiovascular, neurological, blood clots, and immunological abnormalities.
Because of this, her priority is to do everything she can to get the COVID-19 vaccine off the market. “We need more political leaders to stand behind this,” she added.
Dr. Bowden advised citizens to “publicly confront your representatives, publicly ask the people running for office are you still taking these shots, are you willing to roll the dice with your selves or with own kids. If you have safety concerns, if you have efficacy concerns you need to speak up because if it is not safe for you, it is not safe for your kids, and it is not safe for your constituents.”
She is also very concerned with the pediatric vaccine schedule, which currently includes the COVID-19 vaccine. This is very scary, she explained, because most parents trust the doctors when they attend their children’s well visits and innoculate them according to the vaccine schedule. However, she believes parents have awoken since COVID to the dangers involved and is hopeful that even more parents will wake up.
In Dr. Bowden’s opinion, “there is no reason for children to get these shots … we have no long-term safety data.”
Dr. Bowden went on to say when she looked at her new patient appointments, over seven percent were for “ongoing chronic debilitating health issues” that developed following individuals receiving the vaccine.
She added that it is “very hard to diagnose myocarditis in a nonverbal child.” How can a child communicate that they have chest pain, the primary symptom of myocarditis?
Dr. Bowden fears these young children will get myocarditis—permanent scarring of the heart—and then one day they will collapse on the soccer field. “This is what we are looking at,” she emphasized.
Any other vaccine would have been pulled off the market a long time ago, according to Dr. Bowden. She explained that in the 1976 Swine Flu outbreak, they stopped giving the vaccine after 25 deaths. Currently, on VAERS, there are more than 36,000 deaths reported, which is believed to be only one percent of the real number, due to underreporting. Yet they are still advertising this vaccine.
There is also significant concern with the protocol the hospitals are using to treat COVID-19 patients. The CARES Act provides incentives for hospitals to use treatments directed solely by the federal government with the backing of the National Institute of Health. These incentives are financial and provide payments to the hospitals for the following: a diagnosis of COVID, admission to the hospital, use of Remdesivir (a drug shown to cause kidney failure in 25 percent of the people who take it), a patient being put on a ventilator, and if the patient dies and the cause of death is listed as COVID-19.
These incentives were not designed to treat patients and facilitate their health, but to aid in their demise, warned Dr. Bowden.
Now, the FDA is warning of a catastrophic drop in life expectancy. In just the last nine months of this year, over 158,000 more Americans died unexpectedly than in all of 2019—before the COVID-19 vaccine was introduced. To put that number in context, that is more American casualties than in all wars since Vietnam, combined.
Dr. Bowden expressed deep concern about what is happening to the medical industry. Doctors have lost their autonomy and are now employees taking orders from the government and administrators on how to treat their patients, she explained. Many are sheep, she said, who sit quietly and do what they are told, rather than what is right by the medical doctrine, “first do no harm.” She sympathized that they have families and mortgages, but said they cannot allow themselves to be controlled by nefarious forces.
