Advocacy Director Emily Taylor On Sharing the Success of ME/CFS Advocacy Week
During Solve M.E.’s ME/CFS Advocacy Day 2018, 102 people with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)
May 31, 2021
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
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
Thank you for your patience and for standing with Solve M.E. and our advocacy partners
Tell Your Senator to SUPPORT INCREASED FUNDING FOR POST-VIRAL-DISEASE RESEARCH INTO ME/CFS! Thanks to your
Can you hear M.E. Now? Call Congress Today! We connected with over 47%
To watch the recording of the 2020 EmPOWER M.E. Roundtable: How to Navigate Disability Insurance
Looking for a way to make your social media account stand out? We’ve created ME/CFS
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