Since April 2000 the mission of the HDLighthouse Families Web site is to present and explain the latest research findings so that families afflicted by Huntington's disease can become proactive in their care, have hope for the future, and make good decisions in the present. Additionally we provide information that is vital to the the support of HD families. Where possible we will direct you to specialists in the your area of concern, but if we are able to provide better or more current information then you'll find it here.

Webcast, Patient Power, to discuss <i>&#8220;Huntington&#8217;s Disease: Understanding Illnesses of the mind and body,&#8221;</i>

Wednesday, January 23rd WHAT: Webcast – “Patient Power” with Andrew Schorr at In this special Patient Power program, we will focus on understanding Huntington’s Disease: a degenerative neurological illness of the mind and body. According to the Huntington’s Disease Society of America (, HD affects males and females equally and crosses all ethnic and racial boundaries. While there is no cure for Huntington’s disease
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