Join the Fight for Federal Research Funding and Medical Education for ME/CFS
Appropriations season is moving fast this year, and we are proud to share that Solve M.E. has submitted our FY27 appropriations letters to both the House and Senate Labor-HHS and […]
Advocacy Update: Three Crucial ME/CFS Federal Budget Wins
Hi all, I wanted to circle back with a quick update: the federal funding bills covering Labor, Health and Human Services and the Department of Defense are now final. This […]
Keeping ME/CFS in the Fight on Capitol Hill
Hi friends, It’s Monique here, Advocacy Director at Solve M.E., with a progress update on the budget process. We’re right in the thick of appropriations season — when Congress decides […]
Senate Appropriations: Big Wins for ME/CFS — Thanks to Your Advocacy
Because of your persistence, advocacy, and shared determination, Congress is finally starting to listen. This year’s Senate Appropriations bills include some of the strongest support for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome […]
ME/CFS Research Roadmap Approved by the NIH NANDS Council
In an effort to move the ME/CFS field toward translational studies and clinical trials, the National Institute of Neurological Disorders and Stroke (NINDS) ME/CFS Research Roadmap was approved this week […]
NIH ME/CFS Research Roadmap Series: Nervous System
The first ME/CFS Research Roadmap webinar will take place on August 25, 2023, from 10:00 am – 2:00 pm ET. Focusing on how ME/CFS impacts the nervous system, presenters will […]
