Honoring People with ME/CFS for Invisible Disabilities Week
As we strive to make myalgic encephalomyelitis, otherwise known as chronic fatigue syndrome, or ME/CFS, more diagnosable and treatable, we are always aware that many people suffer with this disease […]
Advocacy Success! Florida Members of Congress Take Action for ME/CFS
Florida Members of Congress Take Action for ME/CFS Solve M.E. teamed up with local Florida advocates to launch a lightning advocacy action with huge success this week. Congressmen Gus Bilirakis […]
Big News in ME/CFS Research Funding
CDMRP Funding Announcement Comes Just 24 Days After Congress Opens Potential $350 Million to ME/CFS Researchers ME/CFS researchers can compete for 5 new funding streams and over 100 awards, up […]
Victory! Six Major Federal Wins for ME/CFS
Dear Friends, Throughout 2019, I reported on our advocacy gains for ME/CFS. Thank you for standing with me and our advocacy partners during a particularly turbulent year while we fought […]
