Expertise · Regenerative Medicine & Longevity
Stem cell applications, NAD+ protocols and longevity interventions — a corner of medicine where the marketing consistently outruns the evidence, and where measuring the gap between the two is the expert's central task.
Regenerative and longevity cases turn on a question most experts are poorly placed to answer: what did the evidence actually support at the time the therapy was sold? These clinics operate in the space between promising early research and established practice — and their marketing borrows the language of the former while charging for the certainty of the latter.
As a clinician-investigator in longevity and regenerative endocrinology — and Director of the AI Academy at the Geneva College of Longevity Science — I can locate a given protocol precisely on that spectrum: what the trials show, what the regulators have said, what a careful physician would have disclosed, and where a defendant's claims crossed from optimism into misrepresentation.
Case Patterns
Unproven cellular products marketed for orthopedic, neurologic and cosmetic indications; infections and adverse events from unregulated processing; and consent documents that promise regeneration the literature has never demonstrated.
High-dose NAD+ infusions, vitamin drips and chelation programs administered without medical indication, screening or supervision — and the cardiovascular, renal and metabolic complications that follow when contraindications are never checked.
Subscription "optimization" medicine: panels of off-label prescriptions — hormones, peptides, metformin, rapamycin — bundled into protocols with no individualized assessment, sold on marketing claims that consistently outrun the evidence.
Physician oversight in name only: standing orders signed for patients never examined, non-physician injectors operating beyond scope, and supervision arrangements that dissolve under discovery.
Marketing vs. Evidence
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