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Action for M.E. is the leading UK charity for people with Myalgic Encephalomyelitis (M.E.) and their carers. M.E. is a chronic, fluctuating illness affecting 250,000 people in the UK. It may be diagnosed as Chronic Fatigue Syndrome (CFS) or Post Viral Fatigue Syndrome (PVFS). Action for M.E. provides information and support, while campaigning for better services, more effective treatments and greater investment in research until our vision is achieved and M.E. is overcome.
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