Episode

#41 Cracking the genetic code of complex chronic illness with Steve Gardiner, PrecisionLife

Podcast
Make Visible: ME/CFS, Long Covid, POTS, EDS, Fibro & MCAS Explored
Published
Sep 7, 2026
Duration seconds
3165
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not_requested
Canonical source
https://madevisible.podbean.com/e/41-cracking-the-genetic-code-in-mecfs-long-covid-with-steve-gardiner-precisionlife/
Audio
https://mcdn.podbean.com/mf/web/kqbctuijwt6ajn7i/Visible_S1_Ep41_Steve_Gardner.mp3
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/v1/public/podcasts/make-visible-chronic-illness-explored-7015207/episodes/41-cracking-the-genetic-code-of-complex-chronic-illness-with-steve-gardiner-precisionlife
Markdown
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Summary

PrecisionLife are cracking the genetic code on ME/CFS (myalgic encephalomyelitis/chronic fatigue syndrome) and Long COVID. Through large-scale studies with DecodeME, the LOCOME Project, Sano Genetics’ Gold dataset, and the All of Us research programme, PrecisionLife have identified hundreds of genes associated with Long COVID and ME/CFS, revealing distinct patient phenotypes and pointing to how each might be treated. This week, PrecisionLife CEO Steve Gardner explains why these findings mark a transformational point for ME/CFS and Long COVID. He covers what the genetics reveal, why stratification is essential in clinical trials, and the 42 repurposed drug candidates identified so far. Steve believes this represents a profound shift in how we understand, diagnose and treat ME/CFS and Long COVID, made possible through collaboration with the Complex Disorders Alliance, Action for ME, Innovate UK and the Metrodora Institute.