Stories

Cultural reportage
and personal essays.

Published intermittently. Always cultural, never prescriptive. Subscribe to the monthly letter to get the next one in your inbox.

All stories.

Analysis · Regulatory + policy

The DEA shadow over peptide reclassification.

Everyone is watching the FDA. But the agency that could turn a gray-market vial into a felony is the DEA — and the reason it has stayed out is the most revealing fact in the whole story.

8 min read · June 24, 2026
Analysis · Regulatory + policy

Why the FDA suicidality signal from 2023 still hasn't been resolved.

In 2023 the FDA opened an investigation into GLP-1 medications and suicidal ideation. In 2026 it's technically still open. What the data actually shows — and why "unresolved" is doing a lot of work.

8 min read · June 22, 2026
Analysis · Regulatory + policy

The orforglipron timeline: what we know, what we're guessing.

The story has changed tense. A year ago the question was whether Lilly's oral GLP-1 pill would work. Now it's when it ships — gated by the FDA clock, the label sequence, and factory capacity, not by biology.

7 min read · June 19, 2026
Analysis · Regulatory + policy

The compounded GLP-1 crackdown: actual timeline, actual losses.

Not a ban — the expiration of a temporary legal exception written into a 1997 statute. Who actually lost: not the drugmakers, but the telehealth layer and the patients paying $199 instead of $1,999.

7 min read · June 15, 2026
Analysis · Regulatory + policy

FDA's peptide reclassification, explained piece by piece.

The 2026 FDA action closed a grey market that was never technically open. Understanding what changed — and what was always illegal — matters for understanding where this goes next.

8 min read · June 12, 2026
Analysis · Clinical data

SELECT: the cardiovascular trial everyone misapplies.

SELECT showed a 20% relative risk reduction in serious cardiac events. But the trial only enrolled patients with established CVD and no diabetes. Here is what the numbers actually say — and for whom.

8 min read · June 10, 2026
Analysis · Clinical data

Discontinuation rates: the data the press release skipped.

The pivotal trials ran 68 weeks. Real-world persistence data shows 23.7% of patients still filling prescriptions at 12 months. The gap between those two numbers is the whole story.

8 min read · June 8, 2026
Analysis · Clinical data analysis

STEP-4: the trial everyone misquotes.

Bulls say it proves the drug keeps working; skeptics say you gain it all back. Both misread the same withdrawal design — and the truth in between is the whole point.

8 min read
Analysis · Clinical data analysis

The body composition data buried in the SURMOUNT trials.

Everyone quotes 20.9%. The body-composition substudy underneath it quietly settles the "muscle loss" panic — and I think almost everyone reads it backwards.

8 min read
Analysis · Clinical data analysis

Retatrutide: the five numbers everyone is ignoring.

Everyone repeats 24%. I think it is the least interesting figure in the Phase 2 data — and the five that matter are what the TRIUMPH readouts will decide.

7 min read
Essay · New

The third way. A cultural letter on the year the body conversation changed.

For a century the equation had two terms: diet and exercise. Then a generation woke up and the sentence had a third. An essay on what that third sentence does to a culture.

9 min read
Cultural · Essay

The "Ozempic personality" — what the science actually says about mood and behavior.

The cultural phenomenon, the honest read on the neuroscience, and what it means for how we talk about pleasure and motivation in the medicated era.

13 min read

One thoughtful letter, once a month.

The cultural essays, the reading recommendations, the conversation behind the next piece. First Sunday of every month.

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