2020 Postcard from Palm Springs
Highlights from the 2020 CHDI HD Therapeutics Conference are now here! This year’s Postcard covers HTT-lowering therapeutics, including an
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Bev Heim-Myers, Chief Executive Officer of the Huntington Society of Canada, received an Award of Distinction from HCCC. Click here to learn
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Photographer Meghan Andrews has HD. Meghan is raising awareness for HD through her photobook, Huntington Disease: Trials and Triumphs. Click here to
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John Stainsby has the genetic mutation that means he will one day develop HD. John is sharing his story. Click here to
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Marion Genoe’s father and three of her siblings had HD. Marion is raising awareness this month by sharing her story.
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Hedley Cullen has Huntington disease. Hedley is raising awareness this May during HD Awareness Month by sharing his story. Click here to
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My daughter, Erin Wade, has Juvenile Huntington disease. Growing up in Brockville, Ontario, Erin used to be an outgoing teenager.
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Together, with our Chapters, we officially launch the 2015 May HD Awareness Campaign. Let’s celebrate the best of our community!
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Erin Wade has Juvenile HD. Her mother, Cindy Moore, is raising awareness this May during Huntington Disease Awareness Month. Click here to
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May is Huntington Disease Awareness Month. HSC is spreading the word, educating Canadians about HD and how they can help.
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To celebrate National Volunteer Week (April 12-18) the Huntington Society of Canada is honouring the volunteer work of Rob Laycock.
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