Nation-wide community based voluntary group who provide a range of services to people affected by severe ME. Includes newsletters, articles and news.

Providing information, advice and support to individuals suffering from the condition as well as to their family members and loved ones.

Charity for children and young people with ME/CFS. Features membership information, news and advice on education, benefits and other assistance.

Aims to increase awareness of ME and chronic fatigue syndrome as a real and debilitating illness. Provides news and campaign updates.

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.

Non profit organisation which provides tutor and mentor supported educational and life skill courses for people with ME.

Community forums and message boards for those suffering from Myalgic Encephalopathy, Post Viral Fatigue Syndrome or Chronic Fatigue Syndrome.

Funds osteopathic research into chronic fatigue syndrome, which in recent years has led to the scientific support of The Perrin Technique.

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.

Offers support, information and practical advice. Includes membership details and how to find local support.

Offering support and newsletters for people in the region affected by ME/CFS. Details fundraising efforts and events.

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.

Provides support and community features for parents, would-be parents and parents to be suffering from ME/CFS.

Discusses the experiences and response of a Christian suffering from ME.

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.

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.

An online resource for sufferers of ME. Includes guides and newsletters plus support contacts.

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.

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.