Hosted by Josh Axe
Written by a model from the transcript; not yet reviewed.
In this episode, the host and the guest, Brigham Buehler, discuss the flaws within the traditional healthcare and insurance model, exploring how corporate incentives and pharmacy benefit managers drive up prescription costs while limiting access to proactive preventative care. They examine advanced longevity treatments such as therapeutic plasma exchange, exosomes, and peptides like BPC-157, explaining how these tools can reduce inflammation and detoxify the body. The conversation also highlights the importance of individualized medicine, foundation lifestyle habits, and combining modern diagnostic testing with historical wisdom.
Josh Axe opens the show, setting the stage for a discussion on natural medicine and the challenges of the current healthcare system.
The hosts discuss how insurance often excludes cutting‑edge treatments like plasma exchange, IV nutrients, and peptides, forcing patients to pay out of pocket.
Brigham Buhler is introduced, and the conversation shifts to plasma exchange therapy and its role in detoxification and hormone balance.
Buhler shares case studies, including a chef’s fertility success and a high‑weight‑loss patient’s improved sleep and inflammation markers.
The conversation turns to cash‑pay labs and pharmacies, explaining how they bypass insurance barriers and empower patients and clinicians.
Buhler recounts his FOIA requests, FDA testimony, and the hurdles faced by peptides and other natural therapies in gaining approval.
The conversation explores advanced blood panels, genetic testing, and the importance of individualized protocols over one‑size‑fits‑all prescriptions.
The hosts debate the safety profile of peptides, the prevalence of gray‑market sources, and the need for regulated, clinician‑prescribed pathways.
Josh and Brigham wrap up by urging listeners to seek comprehensive testing, consider natural therapies, and advocate for patient‑centered care.
Discussion of how large pharmaceutical companies create barriers to entry and control drug approval and patents.
Eli Lilly’s attempt to reclassify a GLP drug as a biologic to extend patent life and limit compounding.
Debate over the safety and efficacy of peptides, including anecdotal evidence versus regulatory skepticism.
Therapeutic Plasma Exchange Originsinsight
Traditional plasma exchange machines were originally used in hospital systems to detoxify burn victims over 25 years ago, and are now being repurposed for longevity and blood filtration.
Microplastics and Testosterone Levelsstory
A chef with extremely high microplastics and a low testosterone count successfully raised his testosterone level above 800 without hormone replacement therapy after undergoing plasma exchange and detoxification.
The Hidden Costs of Insulindata
Up to 30 percent of the money generated from an insulin prescription is returned to insurance companies through rebates, which functions like a kickback.
Unnecessary Thyroid Medicationsdata
A Journal of American Medical Association study revealed that approximately 21 million out of 23 million women taking levothyroxine likely receive zero health benefits from it.
FDA Peptide Safety Review Datadebate
Despite submitting over 800 studies and data from 14 million patients showing minimal adverse events, the FDA released statements against peptides relying on old black-market certificates of analysis.
Patent Laws and Biologics Strategystrategy
Eli Lilly requested the FDA to reclassify their triple agonist retatrutide as a biologic to secure a 12-year patent and prevent legal compounding in the United States.
Glyphosate and Regional Cancer Ratesinsight
Regions in the United States where more glyphosate is sprayed experience higher cancer rates, matching its status as an endocrine disruptor across multiple species.
“Your health insurance is like car insurance. It's great if you total the car, but if you're expecting it to rotate the tires, change the oil and maintain the vehicle, you are going to be sorely disappointed.”
“The average American is now on four or more prescription drugs. Like you said earlier, we're one of the sickest countries in the world, but we spend more on healthcare than any other developed nation.”
“The FDA deemed all three of those as, as, what was the verbiage they used, not extreme, it was a major adverse event.”
“When you look at therapeutic plasma exchange, EBU, advanced red light therapy, nutritional IVs, all of these advanced therapies that have really incredible healing properties, insurance almost never covers them.”
“And the hard thing that people are forgetting is you can't patent something, like the patent laws in the United States say you can't patent something that's readily available in nature.”
“If patients are getting efficacy, they're using their cash.”
“You have diet, lifestyle, nutrition. Are you getting enough sleep? There are a dozen things that can move the needle for you, probably more than peptides or a medication.”
“We don't have double-blind placebo-controlled trials on parachutes, but I don't see anyone jumping out of a plane without one.”
“Thirty percent of medications are prescribed off‑label. I mean, almost 100% of the testosterone in America is being prescribed off‑label.”
Who decides which treatments you can access—and at what cost? Ways2Well founder Brigham Buhler joins Dr. Josh Axe to discuss pharmacy benefit managers, prescription pricing, and his fight for peptide access. They explore his FDA testimony, the debate over BPC-157 and GLP-1 medications, and his clinic’s use of plasma exchange and ozone therapy.
12,113 words · 2 speakers
Speaker names marked are inferred from speaking time and the show’s known hosts — they are not voice-verified.
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