The time is past due for Genetic Non-Discrimination Legislation
A Blog from our CEO – Bev Heim-Myers February 4, 2016 Less than 13 years ago there were 100 genetic
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A New Bill Tabled Addressing Genetic Discimrination
A Blog from our CEO – Bev Heim-Myers January 6, 2016 Last year was a very exciting year for the
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Helping families talk about HD
By Barb Horner, Nova Scotia and P.E.I. Resource Centre Director It’s never easy discovering that Huntington disease (HD) runs in
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Lighting it up in Edmonton
By Zach Foss The Huntington disease (HD) cause is really personal for me. My grandmother passed away from Huntington disease
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Seven years and going strong at Toronto’s Run for HD
On June 28th, the Toronto HSC Chapter held its seventh annual Run for HD. And what a run they had!
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Behind-the-scenes Volunteer
By Laurie Williams Supporting my family and other people affected by Huntington disease (HD) is the reason I volunteer with
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The HDSA convention: Take 2
By Valerie Mallock I had the privileged of being selected, with Katie DeLargie, to represent YPAHD – HSC’s youth chapter
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Dan Middleton: Running to finish HD
I didn’t know anything about Huntington disease when my sister-in-law Angela tested positive for the HD genetic mutation, but I
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Reflections on Winnipeg
There are moments in time that should never be forgotten. Moments when you know people have been touched; moments when
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We have good reason to be optimistic: An update from the Huntington Society of Canada
We are pleased to share some good news from the Society and provide you with an update on our recent
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