We provide information, support, education and training to benefit people with ME (myalgic encephalopathy), CFS (chronic fatigue syndrome) and PVFS (Post viral fatigue syndrome); professionals and all others interested in the illness. The aim is to support people with ME/CFS through all stages of their illness.– ME/CFS is hard to accept. And those who do not accept their illness rarely recover. So we help people understand and come to terms with their illness.– We help people get the diagnosis and medical help they need.– We help people struggling to cope practically, emotionally and financially. We work to shield them from remedies that offer false hope.– We help people explain their illness to disbelieving relatives, colleagues and friends.– We campaign and speak out for those who can’t defend themselves.ME Connect is our flagship helpline service offering support and information to anyone affected by M.E.
People affected by M.E.throughout the UK, including their families, carers and the health and social care professionals who support them.
Anyone can contact us directly.
The ME Association7 Apollo Office CourtGawcottMK18 4DF