In Review: A Year of COVID-19 in the U.S.
This year the one-year anniversary of the first confirmed case of COVID-19 in the United States. It’s difficult to overstate the impact the COVID-19 pandemic has had on the world […]
Chronic Disease Stakeholders Join Solve M.E. in Push for Federally Funded Research into Long COVID
December 4, 2020 Jointly authored letter serves as a warning about the increasing number of COVID-19 patients experiencing post-viral complications. LOS ANGELES, CA — Twenty leading chronic disease stakeholders joined the […]
Journal of the American Medical Association (JAMA) article brings awareness to Long Covid and Solve M.E. Registry as a tool for research
A recent article about COVID-19 “long haulers” in the peer-reviewed medical journal The Journal of the American Medical Association (JAMA) referenced Solve M.E. and our You + ME Registry and […]
Watch Now! The Congressional Roundtable on Women’s Chronic Illness During a Pandemic
Watch now! The Congressional Roundtable on Women’s Chronic Illness During a Pandemic Last week, as part of our collaboration with the Congressional Bipartisan Women’s Caucus, Miles for Migraine, and the […]
ME/CFS and COVID-19 Long-Haulers: Read Our Op-Ed in The Guardian
Solve M.E. Chief Executive Officer Oved Amitay and Solve M.E. Research Advisory Council Member Dr. Anthony L. Komaroff (Professor of Medicine at Harvard Medical School and Senior Physician at Brigham […]
Senate Advocacy Action: $60m for ME/CFS Research
Tell Your Senator to SUPPORT INCREASED FUNDING FOR POST-VIRAL-DISEASE RESEARCH INTO ME/CFS! Thanks to your hard work during ME/CFS Advocacy Week, the U.S. Senate is currently circulating our request to include […]
ME/CFS Advocacy Week Continues: Can You Hear M.E. Now?
Can you hear M.E. Now? Call Congress Today! We connected with over 47% of congress yesterday. But we’re not done yet! Today we’re focusing on phone calls to […]
Leveraging the You + M.E. Registry to Study COVID-19
While COVID-19 has changed where we work, it has not stopped how hard we work on behalf of the ME/CFS community. Following several months of development, user testing and partnership […]
Magnify your voice! Make a gift to Solve M.E. and Support ME/CFS Advocacy and Research today!
“First I would like to say thank you for finding a way to make Advocacy Week happen despite the challenges we all now face. It is amazing what Solve M.E. […]
