A Win for All of Us
Now that our government has narrowly avoided a shutdown, I’d love to share some insights
October 6, 2021
Now that our government has narrowly avoided a shutdown, I’d love to share some insights
Each year on August 8, Severe ME Day, we reflect on the tremendous toll this
As part of the ceremonies marking the 31st Anniversary of the Americans with Disabilities Act,
In response to COVID-19, Solve M.E. co-founded the Long COVID Alliance (LCA), a network of
During Solve M.E.’s ME/CFS Advocacy Day 2018, 102 people with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)
In her U.S. News & World Report article, “In Long COVID, Advocates Battling Chronic Fatigue Syndrome See
The 5th Annual ME/CFS Advocacy Week hosted by the Solve ME/CFS Initiative (Solve M.E.). Advocacy
Advocacy Week Kickoff Event with Rep. Jamie Raskin (MD-08) The 5th Annual Solve M.E. Advocacy
Advocacy Week Welcomes Partners from Long COVID and Rare Disease Communities The 5th Annual Solve
Today, Solve M.E. warmly welcomes 50 new partners in the fight to return millions
The 5th Annual ME/CFS Advocacy Day April 20, 2021 The 5th Annual ME/CFS Advocacy Week
Last month, Solve M.E. identified yet another COVID-19 relief package funding opportunity for ME/CFS and
