The largest-ever genetic study of ME/CFS has just revealed its first results — and they could change how we understand the disease. DecodeME’s groundbreaking DNA analysis points to both the immune and nervous systems as key players, offering fresh clues to the roots of this complex condition.| Solve ME/CFS Initiative
The Solve ME/CFS Initiative (Solve M.E.) is a non-profit organization that serves as a catalyst for critical research into diagnostics, treatments, and cures for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), Long Covid and other post-infection diseases.| Solve ME/CFS Initiative
The Medical Research for Our Troops Act (H.R. 3906) would restore the full $859 million cut by the fiscal year 2025 Continuing Resolution and fund all 35 CDMRP programs at their FY24 levels, including ME/CFS as a continued topic area. Tell your Representative to sign on as a cosponsor today.| Solve ME/CFS Initiative
Solve M.E. is a non-profit org focused on myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), Long Covid and other post-infection diseases.| Solve ME/CFS Initiative
With a new Congress and administration, we have a unique opportunity to introduce ME/CFS, Long Covid, and associated conditions to new decision-makers and build relationships that will shape the future of research, healthcare, and support for our community. By working together, we can create champions in Washington who will help drive meaningful change. Register today for Solve M.E. Advocacy Week 2025!| Solve ME/CFS Initiative