
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

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

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

Solve CEO Emily Taylor and co-authors from esteemed organizations including the Bateman Horne Center; New

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

A special message from Solve M.E. President and CEO Emily Taylor With so much speculation

Solve President and CEO Emily Taylor recently penned an op-ed piece for Open Access Government

Solve is dedicated to opening new funding avenues for research and care for those with