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, […]
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. & 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,” […]
World ME Alliance calls on WHO Director General to recognize ME/CFS alongside Long Covid
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On Wednesday 12th October Dr. Tedros Ghebreyesus, Director General of the World Health Organization, wrote an op-ed in the Guardian. In it, he lays clear the devastation that Long Covid […]
Study Reveals First Genetic Links in ME/CFS, Could Accelerate Development of New Treatments
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Oxford-based biotech company PrecisionLife announced that their combinatorial analysis of genetic data links 14 genes to ME/CFS and identifies many patient subgroups. According to a press release, “This is the […]
Guest Blog: That Thing Called Pacing, by Ingebjørg Midsem Dahl
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Ingebjørg Midsem Dahl was born in 1979 in Oslo, Norway, where she still lives. She came down with ME acutely in 1983. Ingebjørg has done written information work for major […]
Solve M.E. Board Member Testifies at Congressional Hearing
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House Holds Hearing on “Understanding and Addressing Long Covid” This week, the Select Subcommittee on the Coronavirus Crisis held a hearing on understanding and addressing Long Covid and its consequences. […]
Guest Feature from Fiona Lowenstein: Chronic Illness Communities on Vaccines
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The following essay is a guest feature from our friend, journalist Fiona Lowenstein. Fiona is the founder of Body Politic, a grassroots health justice organization for individuals with Long Covid. In […]
New Hope for Diagnosing and Treating Post-Infection Illnesses: Lessons Learned from HIV/AIDS
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In this special webinar, Dr. Steven Deeks (Professor of Medicine-in-Residence at the University of California, San Francisco) will be hosted by Solve M.E. Medical Advisor Dr. David Hardy (former Director […]
Solve M.E. CEO Oved Amitay and Dr. Leonard Jason Write Letter to the Editor, Nature
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DePaul Univeristy Professor of Psychology Leonard Jason, PhD and Solve M.E. President and CEO Oved Amitay recently co-authored a response to a Nature article linking Epstein-Barr virus (EBV) and multiple […]
CDMRP for ME/CFS: Navigating the Grant Application Process
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Solve M.E. hosted special guest, Cecilia Dupecher, PhD Program Manager for PRMRP at the Congressionally Directed Medical Research Programs (CDMRP) for an informational webinar designed to better inform and prepare […]