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
Living with ME/CFS is not only debilitating, but life-altering. This is especially true for a young adult planning for a normal future. It has been sixteen years since I was diagnosed with ME/CFS. At the time I was only 14
During OMF’s May Momentum campaign, we aim to raise awareness for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). Today, we are honored to share the story of Faten, a dedicated OMF supporter from France. Faten’s experience highlights not only the challenges faced by
Today, May 12th, we observe International ME/CFS Awareness Day. It’s a day to recognize and stand in solidarity with the millions of individuals worldwide impacted by this debilitating condition. Exclusive from OMF Directors What motivated you to focus your research efforts on
The Heart of the Matter Hormones impact the immune system and energy metabolism, which are both considered major parts of the biological cause of ME/CFS. Changes in hormone levels may impact the development of the disease and its severity. The
Every May, Open Medicine Foundation (OMF) unites with supporters worldwide to mark International ME/CFS Awareness Day on May 12 through our annual May Momentum campaign. This pivotal time allows us to spotlight the profound challenges faced by those living with
Imagine a world where your doctor can diagnose your disease and understand how to offer the right support. Open Medicine Foundation (OMF) and the Bateman Horne Center (BHC) created the Medical Education Resource Center to help patients and providers with
Exciting news! The 16th Invest in ME Research International ME Conference 2024 (IIMEC16) and 13th International Biomedical Research into ME Colloquium 2024 (BRMEC13) are set to take place 26-28 June 2024 in Cambridge, England! These events, hosted by the
If you know anything about ME/CFS and Long COVID, you know the painful reality of finding a healthcare provider that understands these diseases. There are countless stories of people spending limited energy to visit multiple providers only to learn they
Today, we are excited to share a new publication by Fereshteh Jahaniani, Ph.D., Ron Davis, Ph.D., & colleagues: “Longitudinal cytokine and multi-modal health data of an extremely severe ME/CFS patient with HSD reveals insights into immunopathology, and disease severity.” This
In the heart of our Open Medicine Foundation family, there are personal stories that bring to light the stark reality of living with ME/CFS and Long COVID. Today, we invite you to witness the profound narrative of Sean Henneberry, a
Time is running out! Our Hope Builder challenge ends soon, and we need your help to meet our goal of welcoming 30 new monthly donors by the end of March. Thanks to our community’s passion and generosity, we have already welcomed 17 incredible Hope Builders this
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