Downloadables & Webinars

We have created a leaflet that can be used to share information about the registry with families impacted by JoHD. Download it here.

 

Registry documents:

Participant Information Sheet.

User guides:

Setting up an account

Posters:

Newsletters:

 

Videos:

Juvenile-HD Impacts – Personal Perspective – https://youtu.be/A_6H38YppLI

Biology of JHD(Research) – https://youtu.be/y7q5H4d8u1c

HDYO Webinar – Juvenile-HD (Family, Research) –  – https://youtu.be/qnQk2N9g8TY

Managing Symptoms of JHD (Button in symptoms section) – https://youtu.be/lYw0a5RjpPw

Challenges with Diagnosing JHD – https://youtu.be/0oNc5NT4b0Q

Living with JHD – https://youtu.be/Sb6YjAfB1H0

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HDYO is the only organization who focus solely on supporting young people impacted by HD around the world. Will you help us?

Contact US

These goals cannot be done by just a few people by themselves. The JHD community needs as many partners working together as possible to reach families, encourage participation, help us develop resources and much more.