Neurological Disorders Chronic Fatigue Syndrome in the Best of the Web UK Directory

Neurological Disorders Chronic Fatigue Syndrome

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.

Association for Myalgic Encephalomyelitis

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

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.

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.

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.

Falcon Academy

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

Foggy Friends

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

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.

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.

ME Association

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

ME North East

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

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.

ME/CFS Parents

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

On Eagle's Wings: A Christian Perspective on ME

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

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.

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.

SupportME

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

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.

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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