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Category: Myalgic Encephalomyelitis

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Action for ME (Myalgic Encephalomyelitis)

Action for M.E. takes action to end the ignorance, injustice and neglect faced by people with myalgic encephalomyelitis (M.E.) They do this by meeting need now to improve the lives of people with M.E. while taking action to secure change for the future.

Web:www.actionforme.org.uk
Telephone:0117 927 9551
Email:questions@actionforme.org.uk

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The ME Association

The Association aims to support, to help, to inform and to empower all those whose lives are affected by ME/CFS by:
(1) Providing information on ME/CFS to all who need it.
(2) Providing support for people with ME/CFS and their families on all ME/CFS-related issues.
(3) Increasing public and professional awareness of ME/CFS.
(4) Representing people with ME/CFS at every level of decision making.
(5) Fighting for, and attaining, equal rights for people with ME/CFS.
(6) Retaining ME/CFS as a high-profile issue.
(7) Finding a cure.
(8) Raising money to fund research into the cause(s) and treatment of ME/CFS.
(9) Gaining public support for fundraising to meet challenges ahead.
The Information Line is available during the hours 1.30pm - 4pm Mon.-Fri. This service is available to members and non-members alike.

Web:www.meassociation.org.uk
Telephone:01375 642466
HelpLine:01375 361013
Email:enquiries@meassociation.org.uk

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The ME Association (Staffordshire)

This is the local branch of the M.E Association. The Association's national contact is also provided below.

Web:www.meassociation.org.uk
Telephone:01785 816862
Email:n/a

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