Action for ME (AfME)

AfME was founded primarily as a campaigning Charity (No. 1036419).

We are a patients’ organisation with 8,000 members, largely run by and for people with ME.

We aim to help individuals individually and by influencing national policy.

We offer up-to-date information via a range of publications and websites – for patients and professionals and help people keep in touch with others with the illness. We also offer advice and support via our telephone helplines and through support of affiliated groups.

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In 1998 the Government’s Chief Medical Officer made the following announcement:

“I recognise that ME is a real entity. It is distressing and debilitating. It affects a large number of people and poses a significant challenge to the medical profession.”

Sir Kenneth Calman


He established a Working Group, due to report in 2001 which it is hoped will advise his successor on the diagnosis and treatment of ME. Action for ME is represented on the Group.

Too little is known about ME and AfME is keen both to promote research and disseminate research findings to lay and professional audiences.

AfME receives no government funding and is largely supported by donations, legacies and subscriptions.

[boxibt style=”success”]Enquiries, Membership and Administration
P.O. Box 1302

Telephone 01749 670799


[boxibt style=”success”]Headquarters and Press Enquiries
4 Deans Court
St Paul’s Churchyard

Telephone 020 7329 2299
Fax 020 7329 3600

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