Kevin Timms, PhD, Joins Ramsay Researchers Class of 2022!
We’re excited to share that Kevin Timms, PhD, is joining our Ramsay Class of 2022! Solve’s Ramsay Research Grant Program attracts new scientists to the field of ME/CFS and Long […]
Watch now! “Long Covid: What Will it Take to Accelerate Therapeutic Progress?”
Solve M.E. and BIO co-hosted a timely and informative event examining the emerging research in Long Covid and the existing body of data in other post-infection diseases such as ME/CFS. […]
FDA to Host Patient-Focused Drug Development Public Meeting for Long Covid
The US Food and Drug Administration (FDA) is hosting a virtual public meeting on Patient-Focused Drug Development for Long Covid on Tuesday, April 25th, 2023, from 10 a.m. to 4:00 p.m. […]
Just released! FY23 Peer Reviewed Medical Research Program (PRMRP) Funding Opportunities for ME/CFS
At Solve M.E., our advocacy team is dedicated to opening new government funding avenues for ME/CFS, Long Covid, and post-infection disease research and care. Thanks in part to these efforts […]
Announcing the 2023 World ME Day Campaign
We’re joining our peer organizations at the World ME Alliance again for World ME Day 2023. This year’s theme focuses on the hallmark symptom of ME/CFS: post-exertional malaise. The goal […]
Key Takeaways from the New Federal Budget
Dear advocates, allies, and friends: I’d like to take one last look back at 2022 before we leap forward into an exciting new year. Starting with the Omnibus Appropriations bill, […]
Long Covid After One Year: The Good News & the Bad News
“Mild Covid-19 disease does not lead to serious or chronic long term morbidity in the vast majority of patients” was the headline in most media coverage of an important study […]
An Evolving Landscape: Long Covid’s Impact on ME/CFS
It’s hard to believe that we’re well into the third year of the COVID-19 pandemic, which coincidentally overlaps with my time as Solve M.E.’s President and CEO. In this time […]
Letter for Medical Providers on Caring for People with Severe and Very Severe ME/CFS
Are you or a loved one bedbound or homebound as a result of severe or very severe ME/CFS, perhaps following COVID? Do you struggle to do basic activities like taking […]
Join Us For Solve M.E. Advocacy Week!
We are so excited to announce that next year’s Solve M.E. 2023 Advocacy Week will take place both virtually and in person throughout the week of April 17th to April […]
Solve M.E. Engages New Community Partners Through Lived Experience Taskforce (LET)
Building on our commitment to centering the crucial voices from our community in the leadership and decision-making at Solve M.E., we are transforming our Community Advisory Council (2019 – 2022) […]
Solve M.E. & Community Partners Denounce Misleading New York Magazine Article
The article published in NY Magazine on Nov 4, 2022, “Has Long COVID Always Existed? The pandemic might not have spawned a new chronic illness but rebranded an old one,” […]