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YPAHD Day is a one-day conference hosted by youth for youth who are affected by Huntington disease.

Registration is now closed!

Will you be joining us?

November 18, 2017: Kelowna, Toronto and Moncton

Across the country, youth aged 14-35 will be gathering to learn about using social media to build awareness and generate funds, discussing grief and guilt, practicing different care strategies, hearing the latest in research updates, and thinking about event planning during the round table discussions.


Looking for more information? While registration is closed, download the registration packages for more information:

Click here for the Kelowna registration package.

Click here for the Toronto registration package.

Click here for the Moncton registration package.

Have questions about YPAHD or YPAHD Days 2017? Contact!

 YPAHD Day 2017 is brought to you by:

Missed YPAHD Day 2016?

In 2016, YPAHD Day was held in Halifax, Nova Scotia just before our National Conference.
To see photos from previous YPAHD Days, visit our Facebook page here.

History of YPAHD Day

In 2012, our youth chapter created a one-day youth conference (YPAHD Day) in conjunction with the HSC National Conference. Last year, in 2015, we hosted YPAHD day at multiple venues (Calgary, Halifax & Toronto) for the first time! YPAHD day attendees appreciate the fun and crazy antics, as well as needed education and support.


YPAHD helps youth think about and discuss things like genetic testing, family life, and dating with HD, and supports them in their struggles of being affected by the disease. This group gives young people someone to relate to, talk to, and lean on. This support system can be incredibly important during this stage in life and beyond.

The youth of the HD community are fun, energetic and resilient people. Young People Affected by Huntington Disease (YPAHD) began in 2008 and strives to:

  • Provide a community and support network for young people affected by HD
  • Increase public awareness thereby enabling others to understand the disease
  • Raise funds to deliver services for those living with HD and to further research in order to slow and prevent HD.
  • Listen to and advocate for the needs and goals of young people affected by HD through the communication mechanisms provided by the Huntington Society of Canada



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