Many European Huntington’s Disease Associations work to help people living with Huntington’s disease to live a better life. They work to establish a community of “Huntingtonians” and to spread knowledge.

You can get in touch with your local Huntington Associations here or by looking at the pdf below.


Turn the page by using the arrows in the lower-left corner.

Save the date and join us at the EHA Conference!

We’re bringing together families, professionals, and supporters to strengthen the HD community 💙 You can also make a difference by joining our Teaming initiative, donating just €1 per month to support families affected by Huntington’s disease. Together, we get stronger!