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 […]
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 […]
Join the Fight for ME/CFS and Long Covid Funding!
Big news: The Senate Appropriations Committee is about to make some crucial decisions on the FY 2025 Labor-HHS-Education Appropriations bill. This includes funding that could be a game-changer for ME/CFS, […]
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, […]
Solve Appropriations Efforts Are Going Strong!
Last month, we shared big appropriations wins for our ME/CFS and Long Covid community members via the FY24 Department of Defense Appropriations Report from the House of Representatives, which included […]
July Advocacy Cafe
Advocacy Cafe is a community-favorite event that brings you more stories, inspiration, and conversations to connect and empower our advocates. This month’s session will take place 7/21 at 12 pm […]