A Life in Stop Motion: A Film Animator & Research Chemist Shares her Battle with ME / CFS My name is Inga and I’m an Myalgic Encephalomyelitis / Chronic
“While Our Bodies Are Weak, Our Spirits Are Strong” My name is April Thompson. I am an Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS) sufferer and OMF
As someone aware of the impact of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS), you understand, as we do, that there is an urgent need to improve
Today Open Medicine Foundation launches its third annual #MayMomentum, our fundraising campaign in solidarity with May 12th ME / CFS International Awareness Day and dedicated to the
President of the CFS/ME Italian Association Opens up About her Battle with Illness. My name is Giada Da Ros, I am the president of the
Life Before ME / CFS: From Exciting Opportunity to Limited Capacity. My name is Elisabeth. I am 39 years old and became ill with Myalgic Encephalomyelitis / Chronic Fatigue
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