The Huntington's Disease Advocacy Center's purpose is to provide answers to the many tough questions that patients with Huntington's Disease and their caregivers will face.

A disease that attacks the members in a family from generation to generation, this disease eats away at a person's nervous system.

The Huntington Society of Canada is a national health charity, consisting of volunteers and professionals united against huntington disease, an inherited genetic disorder.

HDA Online provides news of fund raising events, health care information and details of research into curing Huntingtons Disease ...

Caring for People with Huntington's Disease This page is meant to be a source of information for those with Huntington's disease, those at risk, their families, caregivers and those just wanting to know more. It is best viewed with Netscape or Microsoft Internet Browser. If you have visited here before and things do not seem to look right or work, try reloading the page. Huntington's Disease is ...

INTERNATIONAL HUNTINGTON ASSOCIATION The International Huntington Association (IHA) is a federation of national voluntary health agencies that share common concern for individuals with Huntington's Disease (HD) and their families. Each agency promotes lay and professional education; individual and family support; psycho-social, clinical and biomedical research; and ethical and legal ...

Help eradicate Huntington's Disease by funding medical research to find a cure for this genetic illness which is killing over 100, 000 individuals and destroying their families.

Huntington's Disease information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).

Huntington's Disease Society of America Illinois Chapter P.O. Box 8383, Rolling Meadows, IL 60008 Phone: (630) 443-9876 Announcements 3rd Annual State Conference, Huntington's Disease Society of America, Illinois Chapter Join us for a full day of information, education and fellowship for individuals with Huntington's Disease, their families, care providers, and health care providers. Saturday, ...

Site hosted by: Lakewood Public Library Welcome (313K) from Barbara Boyle, National Executive Director/CEO, Huntington's Disease Society of America Chapter Information and Announcements HDSA Northeast Ohio Chapter Board The Northeast Ohio Medical Advisory Committee HDSA Approved Genetic Testing Centers in Northeast Ohio Support Group For information about the support group call Don Barr, Family ...

The lighthouse of old stood as a beacon to provide navigators with cutting edge information. The purpose of this web site is to provide you with information for your consideration in making choices.

Describes the effect that Huntington's Disease has had on his family, includes details of the help available in the UK for those who came into contact with HD.

Internet Resources for Huntington's Disease Information (Formerly Links to Outside Resources) This document has been replaced by Electronic Resources on Huntington's Disease, 1990- The URL of this page is http://www.lib.uchicago.edu/~rd13/hd/outside.html Created and maintained by Renette Davis. Send comments to: rd13@midway.uchicago.edu Last updated: May 2, 2000 Return to: Huntington's Disease ...

Nutrition for People with Huntington's Disease Introduction | Resources By Renette Davis with assistance from people on the Mailing List for Huntington's Disease Introduction Dysphagia is the most common cause of death in HD, either directly from suffocation or aspiration, or indirectly from starvation. (From A Physician's Guide to the Management of Huntington's Disease by Neal G. Ranen, M.D., ...

The Mid-Michigan Chapter of the Huntington's Disease Society of America has merged with the Southeastern Michigan Chapter. The new web site is at www.qix.net/~bergdd Write to us at: hdsamich@iserv.net This page was revised: Sep 29, 2000 ...

Splash page for Australian Huntington's Disease Association (NSW) Inc. Website ...

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Welcome, Guest - Webring Home - Help/Support - Sign In THE HD WEBRING Home Health & Wellness Support Illnesses Genetic Disorders About this Ring This Webring is for all people who are connected in some way with Huntingtons Disease. For carers and caregivers, sufferers and families affected requiring support and advice. It may also be useful for the medical profession requiring research ...

Our organization is dedicated to assist families living with Juvenile Huntington's Disease, & ultimately help find a cure.