The ME Association
 United Kingdom  |  Health/Medical

We provide information, support and practical advice for people who are affected by ME/CFS/PVFS (Myalgic Encephalopathy/Chronic Fatigue Syndrome/Post Viral Fatigue Syndrome), their families and carers. We also fund and support research, and offer education and training.

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The ME Association (The MEA), founded in 1976 funds and supports research and provides information and support, education and training. In this role, we benefit people with ME (myalgic encephalopathy)/CFS (chronic fatigue syndrome), professionals and all others interested in the illness. The Ramsay Research Fund is the research arm of The ME Association – the UK’s longest-established national ME/CFS charity. It is named after Dr Melvin Ramsay, an infectious diseases consultant who documented a major outbreak of the illness at London’s Royal Free Hospital in 1955. Current research projects include a scheme to set up a central ME tissue bank in a UK hospital.

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