European Huntington Association

Thinking about getting involved in the HD community but not sure how to start?
Here's the short version:

→ Find your national HD association
→ Send them a message, introduce yourself
→ Start with something small and see how it feels

That's really it. No experience required, no minimum hours, just a willingness to be part of something bigger than yourself.

Want to hear from people who've done it? Read their stories here: https://eurohuntington.org/2026/06/02/what-does-volunteering-for-the-hd-community-actually-look-like/ 💙

Today's the day! 🧬 Join our open webinar with Roche this evening for a deep dive into the Phase I POINT-HD Trial.

🕐 6:00 PM CET
📋 Register: https://us02web.zoom.us/meeting/register/3mWWkORVRti7iBS0F9WBzg

If you have any questions or topics you’d like to see addressed during the session, you can let us know in the registration form or send us a message.

See you there! 👋

🧬 Upcoming Webinar: Phase I POINT-HD Trial

Join us for an open webinar with Roche to dive deep into their latest ongoing research programme.

🗓️ Tuesday, May 26th
🕐 6:00 PM CET
🔗Register here: https://us02web.zoom.us/meeting/register/3mWWkORVRti7iBS0F9WBzg

We are pleased to have Patrik Brundin, MD PhD, Therapeutic Area Leader for Movement Disorders, and Peter McColgan, MD PhD, Global Development Leader at Roche, sharing this research update with the HD community.

Don't miss this opportunity to hear directly from the scientists shaping the future of HD research in Europe.