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The 25% Me Group
- Nation-wide community based voluntary group who provide a range of services to people affected by severe ME. Includes newsletters, articles and news.
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Association of Young People with ME
- Charity for children and young people with ME/CFS. Features membership information, news and advice on education, benefits and other assistance.
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Blue Ribbon for the Awareness of ME
- Aims to increase awareness of ME and chronic fatigue syndrome as a real and debilitating illness. Provides news and campaign updates.
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CFS Research Foundation
- Aims to understand how CFS is caused, how it can be treated and to develop a diagnostic test. Provides a history of the foundation plus details of its papers, publications and research funded.
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Falcon Academy
- Non profit organisation which provides tutor and mentor supported educational and life skill courses for people with ME.
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Foggy Friends
- Community forums and message boards for those suffering from Myalgic Encephalopathy, Post Viral Fatigue Syndrome or Chronic Fatigue Syndrome.
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Fund for Osteopathic Research into Myalgic Encephalomyelitis
- Funds osteopathic research into chronic fatigue syndrome, which in recent years has led to the scientific support of The Perrin Technique.
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Help with ME
- Provides an active support forum for ME sufferers, plus information on aids and coping strategies.
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Invest in ME
- Charity campaigning for bio-medical research into Myalgic Encephalomyelitis; features event calendar and information on conferences, plus personal stories from people with ME and their families and carers.
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Living With ME
- Offers up to date news, recovery details and related links of interest.
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ME Association
- Offers support, information and practical advice. Includes membership details and how to find local support.
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ME North East
- Offering support and newsletters for people in the region affected by ME/CFS. Details fundraising efforts and events.
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ME Research UK
- National charity funding biomedical research into Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Details current studies and provides a research database and information on how to support the charity.
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ME/CFS Parents
- Provides support and community features for parents, would-be parents and parents to be suffering from ME/CFS.
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The National CFS Diagnostic and Rehabilitation Service
- A multi disciplinary team in Queen’s Hospital, Romford, Essex offers care and evidence-bsed treatment for patients, and support for their families and carers; includes details of their national CFS inpatient and outpatient service.
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Network ME
- Charity supporting those affected by ME/CFS in London and surrounding counties. Features information on events, treatments and advocacy training.
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On Eagle's Wings: A Christian Perspective on ME
- Discusses the experiences and response of a Christian suffering from ME.
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The Perrin Clinic
- Clinic which treats CFS/ME by osteopathic draining of toxins from the central nervous system. Includes video lecture, plus information on finding a practitioner or training to become one.
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Sophia and ME
- Documents the story of Sophia, a young woman who died from ME in November 2005 and became the first person in Britain to have it listed as an official cause of death. Includes news of the family's campaign to avoid having ME treated as a mental health issue rather than a physical one.
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SupportME
- An online resource for sufferers of ME. Includes guides and newsletters plus support contacts.
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Tymes Trust
- Charity supporting children and young people who have ME and their families. Features downloadable magazines, celebrity and political endorsements and information on the charity's publications.
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Welsh Association of ME & CFS Support
- Aims to provide a united voice in Wales for people with ME or CFS. Provides links to local Welsh support groups plus a wide variety of downloadable documentation.
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