A Win for All of Us

Now that our government has narrowly avoided a shutdown, I’d love to share some insights about next year’s federal budget and how we are helping to shape it today. A key goal of Advocacy Day 2021 was to circulate Chairwoman Eshoo and Representative Lofgren’s “e-Dear Colleague” letter, requesting an additional $10 million for the chronic […]

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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 Solve ME/CFS Initiative (Solve M.E.) in authoring a powerful letter urging Congress to fund millions of dollars in new National Institutes of Health (NIH) and […]

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National Institutes of Health Conferences Demonstrate ME/CFS Progress: How Far We’ve Come and How Far We Need to Go

Solve M.E.’s Chief Scientific Officer, Dr. Sadie Whittaker, introducing a clinician panel discussion with Solve M.E. Research Advisory Council members Tony Komaroff (moderator), Dr. Lucinda Bateman, Dr. Susan Levine, Dr. Jose Montoya, Dr. Peter Rowe, and Simmaron’s Dr. Dan Peterson at the NIH conferenceLast week, people with ME/CFS, researchers, and clinicians gathered at the National […]

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