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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Blog
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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Life insurers’ new genetic test policy called an 11th-hour stalling attempt
The decision by Canada’s life insurers to stop requiring genetic testing for the vast majority of new policy holders is
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Canadian insurance industry pens rules on use of genetic test results
Canada’s life insurance industry has announced new measures that says it will protect consumers from genetic discrimination. But critics warn
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In the Know – January 2017
Volume 12, Issue 1 GENETIC FAIRNESS Laws needed to prevent genetic discrimination Postmedia Network – January 13, 2017 Many Canadians
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Celebrating Our Champions of Hope
As we enter 2017, the Huntington Society of Canada wishes to extend our heartfelt thanks to our Champion of Hope
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