This section provides information on local/regional support
groups and organisations where you can find support and help.
M.E.
Association (England)
4 Corringham Road,
Stanford-Le-Hope,
Essex,
SS17 0AH.
Tel: 01375 642466
Fax:01375 360256 |
Founded in 1976, the M.E. Association has nearly 10,000 members,
and has a large number of local support groups. It offers several
useful services, including a 'listening ear' service by telephone
and advice on welfare benefits. Annual membership costs around £15,
and includes 4 quarterly journals.
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M.E. Association (N. Ireland),
Bryson House,
28 Bedford
Street,
Belfast,
BT2 7FE.
Tel/Fax:
01232 439831 |
M.E. Association (Scotland)
52 St.
Enoch Square,
Glasgow,
G1 4AA.
Tel: 0141
204 3822 |
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Action For
M.E.
Third Floor
Canningford House
38 Victoria Street
Bristol
BS1 6BY
Tel: Lo-call 0845 123 2380
or Membership:
0117 9279551
Tel support: 0845 123 2314
Welfare
rights helpline: 01749 330136
Fax: 0117 9279552
Email: admin@afme.org.uk
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Action For M.E. was founded in 1987 and has a strong campaigning
focus. It provides fact sheets, advice and is actively
involved in lobbying and other activities. Like the M.E.
Association, it has a large number of local support
groups around the UK. Annual membership is £15, and entitles
you to receive its magazine, InterAction.
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The
National M.E. Centre,
Disablement Services Centre,
Harold Wood
Hospital,
Gubbins Lane,
Harold Wood,
Romford,
Essex,
RM3 0BE.
Tel: 01708
378050 |
The centre, since 1990, a registered charity, aims to
provide specialist care for both in-patients and out-patients with
M.E./C.F.S.
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AYME Association of Young People with ME
(reg charity 1082059),
P.O Box 605,
Milton Keynes,
MK6 3EX.
Tel: 01908 373300
Email: info@ayme.org.uk
http://www.ayme.org.uk
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AYME (pronounced 'aim') is a UK-based independent
registered charity dedicated to giving help, friendship,
support and vital contact to children and young
people with Myalgic Encephalopathy (M.E) . AYME's
activities. It is run by the young members themselves,
overseen by their Director. |
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