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 […] The post Senate Appropriations: Big Wins for ME/CFS — Thanks to Your Advocacy appeared first on Solve ME/CFS Initiative.| Solve ME/CFS Initiative
From June 23–27, Advocacy Week 2025, over 200 fierce, compassionate advocates came together from all across the country to make sure one thing was clear: ME/CFS, Long Covid, and related conditions will not be ignored.| Solve ME/CFS Initiative
One of the cornerstones of our annual Advocacy Week program is the EmPOWER M.E. roundtable. Panels of patient advocates, professionals, and scientists share their expertise on topics relevant to the quality of life for people with ME/CFS and Long Covid and their caregivers. This year the EmPOWER M.E. topic is “Pacing: Power In Slowing Down.”| 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
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