Kevin Timms, PhD, Joins Ramsay Researchers Class of 2022!
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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?”
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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
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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
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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
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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
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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
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“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
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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
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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!
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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)
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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
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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,” […]