Information about Huntington Disease and HD support services available in Victoria.

Offers support for families living in the Australian states of New South Wales and the Australian Capital Territory. Includes resources and information about NSW.

Gives disease information, services available in Queensland Australia and links.

Information about caring for people with Huntington's disease, for patients, families and professionals.

A charity site aiming to spread awareness, information, and news about Huntington's disease.

Consumer health resource center providing information on the causes, symptoms, and treatment.

Building a camp and advocacy programs for children and families of Huntington's disease.

Contains general information about Huntington's disease and specific information about this chapter's fund raisers and events.

Links to overviews, clinical trials, case reports, diagnosis, treatment, research programs on Huntington's disease.

The clinic provides care from several perspectives for individual(s) with HD as well as their families.

The clinic provides care from several perspectives for individuals with Huntington Disease (HD) as well as their families. Based at the University of British Columbia, Vancouver, Canada.

An information sheet compiled by NINDS, the National Institute of Neurological Disorders and Stroke.

Information, questions and answers, problem-sharing, personal experiences and articles on Huntington's disease.

Supports people affected by the disease and provides information and advice to professionals.

Weblog with the latest information on research and news.

Information on Huntington's disease, research, and its management.

Huntington's disease facts listed concisely.

Information for all families living with this disease including people with HD, caregivers, those at risk and young people.

Comprehensive resource on Huntington's disease.

Services of the Huntington's disease program of the University of Connecticut Health Center.

Research, assistance, and education.

Federation of national voluntary health agencies.

A personal website with the story of a family affected by Huntington's disease (UK).

Information for families with a child with juvenile HD or one at-risk. Includes at-risk, genetic testing/testing of children, related JHD and HD symptoms and how to recognize/help, types of therapies, various medication and drug searches, surgeries, procedures used in testing, suicide, divorce, disabilities, assisstive technology, support links, and benefits/insurance.

Introduction to Huntington's disease, and an ask a doctor forum.

Nutritional information, and resource links on aspects of nutritional care for people with Huntington's disease.

Current information on treatments, drugs, support and patient resources.

A personal website detailing how Huntington's disease has affected Tony's family and friends.

Services of the Huntington's disease program of the University of Connecticut Health Center.