Solve M.E. and Bateman Horne Center Partner for Webinar Series: “Severe ME/CFS: Care, Rights, and Research”
In a continuing effort to support the ME/CFS community, Solve M.E. and Bateman Horne Center
September 13, 2024
In a continuing effort to support the ME/CFS community, Solve M.E. and Bateman Horne Center
Solve President & CEO and World ME Alliance co-chair Emily Taylor will be among the
Solve is proud to announce our partners for Advocacy Week 2024: #MEAction Black COVID Survivors
The global COVID-19 pandemic has created unprecedented awareness of the long-term health effects of infection-associated
As we approach World ME Day on May 12th, 2024, Solve joins the global community
The interactions between patient advocacy organizations and biopharmaceutical companies are critical, although often complex, and
Dear Solve Community, As Vice President of Advocacy and Engagement, I’m excited to share our
Today, Long COVID Alliance proudly announced it will begin establishing a new Infection Associated Chronic
The 2nd International ME/CFS Meeting at Charité Fatigue Center was held in Berlin on May
In December, we told you about a new Solve initiative, The Lived Experience Task Force
Solve M.E. and BIO co-hosted a timely and informative event examining the emerging research in
This article by Tom Popper originally appeared on Bio.com. While research into Long Covid is
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