Long Covid: Research, Policy and Economic Impact (Session II)
Solve Long Covid Initiative, in partnership with the Global Interdependence Center, is conducting a year-long webinar and conference series exploring the pandemic’s long-term healthcare, policy, and economic impact, specifically the […]
“The Long Covid Bust” – A Working Caregiver’s Perspective
By Emily Taylor, Vice President of Advocacy and Community Engagement, Solve M.E. This essay was originally published as a blog for Cumberland Advisors Market Commentary “I just got a virus, […]
Solve M.E. Calls For Congressional Action After Budget Delays Thwart ME/CFS Research Centers
The National Institutes of Health (NIH) recently published a long-expected request for applications (RFA) for the Collaborative Research Centers (CRCs) for ME/CFS, announcing that the funding levels for the centers […]
Chronic Illnesses in Women: ME/CFS and Migraine
Join us for this event in which ME/CFS & migraine comorbid communities collaborate to bring together patients, researchers, and doctors to discuss ME/CFS, migraine disorders, and their impact on women’s […]
What Long Covid Means for Financial Markets
David R. KotokThu Feb 17, 2022 This article was originally published by Cumberland Advisors and can be viewed here. The business world is starting to recognize the economic impact of Long […]
Introducing Solve M.E. Advocacy Month!
We are so excited to announce that next year’s Solve M.E. 2022 Advocacy Week will be bigger and better than ever — and will now be Advocacy Month! For Advocacy […]
November is National Family Caregivers Month
November is National Family Caregivers Month, offering an opportunity to acknowledge the vital contributions made by family caregivers everywhere. In the ME/CFS community, we know the difference a loving caregiver […]
Watch our H.R. 7057 Town Hall Meeting
Watch now: The H.R. 7057 Legislative Cafe Chat Hosted by Emily Taylor Earlier this year, Representative Jaime Raskin introduced H.R. 7057, the Understanding COVID–19 Subsets and ME/CFS Act. This landmark […]
Solve M.E. Advocacy Director Emily Taylor Answers All Your Questions About H.R. 7057 in this Q&A and Town Hall!
Hi Solve M.E. Community! In case we haven’t met before, my name is Emily Taylor, and I’m the Director of Advocacy and Community Relations at Solve M.E. Over the […]
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 […]
Solve M.E. Announces 2020 ME/CFS Advocacy Week Virtual Transition in Response to COVID-19
Solve M.E. Advocacy Week activities this April in Washington, D.C., will be transitioning to entirely remote formats and our team will be cancelling in-person events to protect and preserve the […]
Victory! Six Major Federal Wins for ME/CFS
Dear Friends, Throughout 2019, I reported on our advocacy gains for ME/CFS. Thank you for standing with me and our advocacy partners during a particularly turbulent year while we fought […]
