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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Doing Something Positive
By Allison January 26, 2016 Less than two years ago, we found out my mother has Huntington disease (HD).
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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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A Fair Chance
A persuasive essay by Kaitlyn Neuman. We are taught in school to be accepting of everyone, regardless of their skin
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Confessions of a first-time Amaryllis Grower
Ok. I have a few confessions to make. Up until 4 weeks ago, I’m pretty sure that I have never
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Lighting it up in 2016
By Jamie Walters People who know me know I think big. Earlier this year I figured what better way to
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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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