
Urgent Action Alert: New CDMRP Legislation!
Congress slashed over 57% of funding from the Congressionally Directed Medical Research Programs (CDMRP), which

Congress slashed over 57% of funding from the Congressionally Directed Medical Research Programs (CDMRP), which

Myalgic encephalomyelitis (ME), also known as chronic fatigue syndrome (CFS), is a debilitating illness that

The federal government is considering eliminating the CDC’s only program dedicated to Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

Tell Congress to Restore Our Research! Reverse the 57% Cut to the Congressionally Directed Medical

We are proud to announce the selection of the 2025-2026 Lived Experience Taskforce (LET), a

Registration in now open for Solve M.E.’s 2025 Advocacy Week June 23-27! With a new

Along with nearly 240 other organizations, Solve M.E. enthusiastically endorses the SSI Savings Penalty Elimination

This week, the House will vote on a continuing resolution to fund government programs through

In 2023, the Long COVID Alliance (co-founded by Solve M.E.) established a new Infection Associated

Solve Board Member Cynthia Adinig has been selected as a member of the Health and

Solve recently had the honor of being invited to sponsor Long Covid Grand Rounds for

We are thrilled to announce that we are now accepting applications for our Lived Experience