Ask the Doctor · Roundup #1 · July 2026

Your questions, answered plainly.

The first Limitless roundup. Real patient questions, anonymized — answered by the physician who reads your labs, with no marketing fluff and no overselling.
Joshua Hare, DO · 6 min read · 2026-07-13

This is the format: you submit a question through the "Ask the Doctor" box on the homepage, and selected ones are answered here — anonymized, signed, and free of anything designed to sell you. Where the honest answer is "we don't know yet," that is the answer you'll get.

Question 01 · Peptides & the FDA
"Are BPC-157 and the recovery peptides legal right now, with the FDA meeting coming up?"
— Founding member, Dalton

The FDA's Pharmacy Compounding Advisory Committee reviews several peptide categories on July 23–24, 2026. That is worth watching, but here is the part the headlines will blur: a committee vote is a recommendation, not a rule. Even a favorable vote would require the FDA to publish a proposed rule, run a second public comment period, and issue a final rule — a process that typically runs more than a year — before any peptide's durable status under the 503A framework actually changes.

What that means for you is simple. At Limitless we prescribe only what is lawfully compoundable under current FDA categorization, sourced through licensed 503A or 503B pharmacies with full documentation — never research-grade or gray-market product. Nothing on your protocol changes on the day of the vote. We publish a dated tracker of exactly where this stands on our PCAC Watch page, and a plain-language explainer of what the vote does and doesn't do.

Question 02 · Testosterone & the heart
"I'm on TRT. Does the 2026 cardiovascular data mean it's finally safe long-term?"
— Male, 51, Chattanooga

The large randomized cardiovascular safety trial (TRAVERSE) did not show an increased rate of major adverse cardiac events in men treated for genuine hypogonadism compared with placebo. That is genuinely reassuring, and it retired a decade of fear built on weaker, older data.

It is not a blank check. The reassurance applies to men who actually have a deficiency, treated to a physiologic target, with monitoring. On every TRT protocol we track hematocrit, blood pressure, and your broader cardiovascular risk picture, and we adjust accordingly. Testosterone at Limitless is a therapy for a diagnosed condition — not a performance supplement dosed to a number you saw online. The full read is on the low-testosterone page and the hormone therapy overview.

Question 03 · NAD+
"Is NAD+ actually worth it, or is it just an expensive drip?"
— Female, 47, Calhoun

Both things are true at once, and I'd rather you hear both. NAD+ is a central coenzyme in cellular energy metabolism, its availability declines with age, and it stays on my personal standing recommendation for nearly every adult patient. That is the case for it.

The case against the hype: the boldest marketing claims — reversing aging, curing this or that — run well ahead of the human clinical evidence, which is early and mixed. The honest position is that NAD+ is worth doing for the mechanistic rationale and the quality-of-life response many patients report, described accurately and not oversold. I wrote the long version, including what the 2026 news cycle actually showed, in the NAD+ clinical evidence brief.

Question 04 · The GH-axis
"Every clinic near me advertises CJC-1295. Why does Limitless lead with tesamorelin instead?"
— Male, 44, Knoxville

Because the evidence and the law both point the same direction. Tesamorelin is the one growth-hormone-axis peptide with an FDA approval, a 26-week pivotal trial, a 2026 multi-RCT meta-analysis showing visceral-fat and lean-mass effects, and an NIH-funded cognitive endpoint trial. CJC-1295, by contrast, is not currently legal for 503A human compounding — clinics still advertising it are ahead of the law.

When one option has asymmetric evidence and a clean regulatory status and the other doesn't, the standing protocol should reflect that. We restructured the GH-axis menu around tesamorelin (with sermorelin as the alternative where indicated) and published the full reasoning in the GH-axis substitution brief.

Question 05 · Daily tadalafil
"You put daily tadalafil on the standard protocol. I don't have ED — why would I take it?"
— Male, 39, Ringgold

Fair question, and the short answer is that erectile function is only one of five reasons it's there. Daily tadalafil 5 mg is on the standard adult-male Limitless protocol as a default — unless contraindicated — for its endothelial (blood-vessel) effects, its established benefit for lower-urinary-tract and prostate symptoms, a modest blood-pressure effect, and downstream circulatory benefits, in addition to sexual function.

"Default" does not mean "automatic for everyone." Whether it belongs on your protocol is a physician decision made against your labs, your blood pressure, and your medication list — nitrate use, for example, is an absolute contraindication. The five-system evidence is laid out in the tadalafil brief.

Have a question for the next roundup? Submit it through the Ask the Doctor box on the homepage — anonymized, never published with identifying details.

Joshua Hare, DO, founding physician, Limitless Performance Medicine
These answers are general medical education, not medical advice, and do not create a physician–patient relationship. Peptide and hormone therapies are prescribed only after evaluation, appropriate lab work, and ongoing monitoring, and only where lawfully compoundable under current FDA categorization. Individual response varies. For a protocol calibrated to your biology, book a consultation.
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