Genetic anti-discrimination law protects patient privacy without sacrificing research
An unusual vote in the House of Commons that saw Liberal backbench MPs defy the prime minister and his cabinet
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CHEX Speaks to Peterborough Chapter President
On the Morning show, CHEX sits down with Heath Sterling, President of the local Huntington Society Chapter. They talk about
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Giving Back
March 14, 2017 Jim Wiswell learned he had the HD gene in 1995. It was tough news to come to
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In the Know – March 2017
Volume 12, Issue 3 GENETIC FAIRNESS Press Release: Genetic Fairness One Step Closer to Canadians Making Informed Decisions About Their Health
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S&K March 2017 – Volume 10 Issue 2
Living At-Risk for Huntington Disease Huntington disease (HD) is a hereditary, neurodegenerative illness with physical, cognitive and psychiatric symptoms. To date,
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Uniting for HD
February 15, 2017 By Natalie Marnica Do you ever wonder what it would be like to be around people who
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In the Know – February 2017
Volume 12, Issue 2 GENETIC FAIRNESS Bill S-201: The Beginning of the End to Genetic Discrimination in Canada Rare Disease
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Champions of Hope important to the Huntington Society
January was the Champions of Hope Month at the Huntington Society of Canada (HSC). Champions of Hope are donors that
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2020 Amaryllis Photo Festival
Our annual Amaryllis Photo Festival kicks off in December and we are excited to receive some great pictures and stories
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S&K January 2017 – Volume 10 Issue 1
Feeding Tubes As Huntington disease (HD) progresses in a person, typically there are issues with weight loss, involuntary movements, diminished coordination, and difficulty
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