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 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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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 1
By Katie DeLargie Thanks to YPAHD, (Young People Affected by HD), Valerie Mallock and I had the chance to go
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Genetic fairness in Canada moved a significant step forward
CEO Update June 16, 2015 Genetic Fairness in Canada moved a significant step forward last Tuesday, June 9, 2015. Bill C-68
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You Talked, Canadians Listened!
You did it! You made 2015 HD Awareness Month a HUGE success! WOW, what a month! As of Friday, media
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More than half of woman’s family dead from Huntington’s disease
Huntington’s disease has killed Brenda Wasylow’s grandfather, her mom and all but one of her mom’s four siblings. To read
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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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Strength in the Community
A Word From our CEO June 17, 2014 Bev Heim-Myers If you want to know more about the upcoming Durham Walk
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