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Links To Information On Huntington's Disease
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"The soul would have no rainbow if the eyes had no tears."
~Indian proverb
While your visiting, why not sign up for the National Research Roster of Huntington’s Disease Patients and Families?  This roster is an important nationwide information resource dedicated to assisting scientific research on Huntington disease.  Click here to read about the roster or learn how you can sign up->   Huntington's Disease National Research Roster or click here to print out their brochure -> PDF -  HD National Research Rooster Brochure Give the greatest gift to research and future generations. For information on donating a brain or storing DNA samples please see visit the Roster's website.
Today there are hundreds of websites where HD information can be accessed, unlike 8 to 10 years ago. Families from around the world are still struggling, daily, to find information to help them live with this devastating disease.  This website contains several links to very resourceful information on Huntington's Disease that I hope you find informational.
 
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