The Solve M.E. 2026 Community Address: Shaping What Comes Next

On October 20th, Solve M.E. is bringing our community together for the 2026 Community Address: Shaping What Comes Next, a live conversation about how we are thinking about science and […]
We Won a Delay on OMB Guidance, Tell Congress to Finish the Job

Today, we’re saying a big thank you to our Members of Congress. By passing a continuing resolution that delays the proposed Office of Management and Budget (OMB) “Regulation for Federal […]
How to Submit a Public Comment on the Proposed Federal Grant Rule

What is happening? The Office of Management and Budget (OMB) has proposed new rules that would change how the federal government awards and manages every research grant in the country. […]
You Reached Out and Your Senators Showed Up for ME/CFS

Earlier this appropriations season, we put out a call to action asking you to contact your Senators in support of ME/CFS research funding, and so many of you responded. We’ve […]
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, […]
Government Shutdown Disruptions and Community Support

As of this week, the federal government has shut down, and the impacts are already being felt across systems and services our community depends on. Congress was unable to pass […]
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 […]
Solve and Allies Call For Pandemic Accountability

Solve M.E. and the Long COVID Alliance (co-founded by Solve) are among the dozens of organizations and experts that joined Marked By Covid in urging Congress to pass S.1489, the […]
Ask Congress to CARE!

We’re excited to announce our House and Senate asks for Solve M.E.’s Advocacy Week 2023! The two pieces of legislation are companion pieces to one another — we will be […]
Solve M.E. Board Member Testifies at Congressional Hearing

House Holds Hearing on “Understanding and Addressing Long Covid” This week, the Select Subcommittee on the Coronavirus Crisis held a hearing on understanding and addressing Long Covid and its consequences. […]
10 ME/CFS Organizations Join Solve M.E.’s Letter to Congress Recommending Priorities for Federal COVID-19 Relief Package

Last month, Solve M.E. identified yet another COVID-19 relief package funding opportunity for ME/CFS and worked with our friends on Capitol Hill to outline additional federal post-viral research and medical […]