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Join Theresa in Building Hope for ME/CFS Research!

Imagine a life where your everyday dreams suddenly become a distant memory. For Erica, a vibrant young adult diagnosed with ME/CFS at just 14, the journey has been a relentless battle against fatigue, migraines, and cognitive dysfunction. Her aspirations for

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Personalized Treatment Trials: Video Update!

The Heart of the Matter   General practitioners (GPs) often trial different treatments with their ME/CFS and Long COVID patients.   In partnership with GPs, by studying the outcomes of each treatment, the patient’s lived experience, and the personal history

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Fran Haddock’s Candid Interview on ME/CFS!

Today, we are excited to share an exclusive video interview featuring Fran Haddock, a dedicated advocate for ME/CFS, chronic illness, environmental, and social justice causes. Fran’s profound six-year journey with ME/CFS took a significant turn after a COVID-19 infection, escalating

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Join Kim and Andrew in Transforming ME/CFS Awareness

Today, we’re thrilled to showcase the impactful work of Kim Eggers and Andrew Gifford, OMF supporters whose unwavering dedication to amplifying awareness and understanding of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is truly inspiring. Meet Kim Eggers Kim Eggers has had

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Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS) Post Treatment Lyme Disease Syndrome (PTLDS), Fibromyalgia Leading Research. Delivering Hope.Open Medicine Foundation®

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