Family members share their experiences living with Huntington’s disease in this webinar from the Huntington’s Disease Alliance.

Over the past few months, family members affected by Huntington’s disease from across the UK and Ireland have recorded a series of short interviews about their experiences of living with Huntington’s disease.

The Huntington’s Disease Alliance invites you to join this ‘Family Voices’ webinar, where you will have the opportunity to watch these interviews. They offer first-hand insight into what it is like to live with Huntington’s disease as a family member.

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Huntington’s Disease Association - We improve care and support services for people with Huntington's disease, educate families and professionals, and champion people's rights across England and Wales.

Scottish Huntington’s Association – The Scottish Huntington’s Association provides expert and personalised support for those impacted by Huntington’s disease.

Huntington’s Disease Association of Northern Ireland - HDANI works throughout Northern Ireland, providing support, information, advice and social connections to those living with the impact of Huntington’s disease.

Huntington’s Disease Association of Ireland - HDANI works throughout Ireland, supporting you to access the health and social services you need, providing information to you and your health professionals, and championing your rights.