A Quick Guide to Advocacy Week 2026
Solve M.E. and #MEAction are joining forces for a week of coordinated action designed to move ME/CFS from optional knowledge to the standard of care in clinical training — and […]
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 […]
2025 Advocacy in Review: What You Helped Push Forward
This year, you made the difference. In a year filled with gridlock for biomedical research and public health, your voice kept ME/CFS on the agenda. You showed up, spoke out, […]
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 […]
Solve’s Advocacy Paves Way for ME/CFS Research in $500M Women’s Health Funding
Solve is dedicated to opening new funding avenues for research and care for those with ME/CFS, Long Covid, and infection-associated chronic conditions and illnesses (IACCIs). Each year, we specifically advocate […]
Solve M.E.’s Appropriations Efforts for 2024
At Solve M.E., our mission is to drive research and advocacy efforts for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), Long Covid, and other infection-associated chronic conditions and illnesses (IACCIs). This year, […]
Just released! FY23 Peer Reviewed Medical Research Program (PRMRP) Funding Opportunities for ME/CFS
At Solve M.E., our advocacy team is dedicated to opening new government funding avenues for ME/CFS, Long Covid, and post-infection disease research and care. Thanks in part to these efforts […]
