Action for m.E. Was established for the relief of people suffering from the disease myalgicencephalomyelitis, (commonly known as m.E., or cfs/me), and to provide information, advice and support, and to promote public education, campaigning and research into the disease. On a day to day basis we provide telephone support to people with m.E., manage online m.E centre and publish 'interaction'.
Latest HighlightsFY 2025
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