| |
Action for M.E
The UK's leading charity dedicated to improving the lives of people with M.E. They've been at the forefront of the campaign for more research, better treatments and services since 1987, and provide information and support to people affected by M.E.
|
Invest in ME
An independent UK charity campaigning for bio-medical research into Myalgic Encephalomyelitis (M.E.), as defined by WHO-ICD-10-G93.3. They have links nationwide and also internationally.
|
The M.E. Association
A national UK charity providing support, magazine and helpline to people affected by M.E./CFS which also funds research.
|
|
|
Parents with M.E
Dedicated to parents with M.E. with a message board and articles for advice.
|
BRAME (Blue Ribbon for the Awareness of ME)
BRAME helps and supports those living with M.E. and produces literature to help and educate people about M.E. besides raising funds through Blue Ribbon/BRAME campaigns worldwide to be used to create greater awareness and understanding of M.E./CFS.
|
Irish M.E. Trust
Established in 1989 for the purpose of trying to alleviate some of the hardship which was being experienced by M.E./CFS sufferers throughout Ireland.
|
M.E. India
Aims to lend a lifeline to the lives of people with M.E. in India and to provide information and support to people affected by M.E.
|
|
|
ME Free For All
An organisation for all those with an interest in M.E. - sufferers, their carers, doctors & researchers - to come together.
|
Sussex ME/CFS Society
Informs, supports and represents those affected by ME/CFS in East Sussex, West Sussex and Kent; and is also affiliated to the national patient organisation Action for ME.
|
|
|
ME Research UK
A source of research news, educational literature, and information on accessing social care services and support, as well as links to other information and groups on the web.
|
|
|
|
|
CFS Research Foundation
The aims of the CFS Research Foundation are three-fold; first, to gain a workable understanding of how the disease is caused (pathogenesis), and second, with that knowledge, to develop useful treatments which will lead to a cure in most cases. And thirdly, to develop a diagnostic test for the disease which is simple enough to be used widely and specific only to Chronic Fatigue Syndrome (CFS).
|
|
|
National Alliance for Myalgic Encephalomyelitis
The National Alliance for Myalgic Encephalomyelitis was established to address the issues of recognition and definition, and to raise awareness of this devastating neuroimmune disease that has afflicted nearly a million people in the U.S.
|
ME Training Company
The aim of METCo is to provide information and simple training packs for individuals and teams to raise the appropriate awareness needed, to effectively support people with severe ME in their own homes or in care homes or hospitals.
|
|
|