The Association provides a voice for the HD community to all areas of government and non-government to improve the lives of those people with or impacted by Huntington’s disease.
If you have a concern or issue and are not sure who to go to or how to get your voice heard, you do not need to do it alone. We can work through an approach with you and then we can advocate for you or we can support to you advocate for yourself.
We advocate for individuals or for groups with common issues. We also advocate proactively to agencies on new initiatives, legislation and trends that we can see will impact on individuals, groups or the collective HD community.