Still Going Strong
By Ellie, Isla, Anne and Marlene We are really doing it! It is Day 6 of walking and we just
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By Ellie, Isla, Anne and Marlene We are really doing it! It is Day 6 of walking and we just
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The 14th annual event raised more than $14,000 for Windsor-Essex families coping with the effects of Huntington disease. Click here to
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Canada was the last member of the G7 to pass its own genetic discrimination law, Bill S-201, in May. It prevents
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Volume 12, Issue 9 GENETIC FAIRNESS Why Insurers Are Wrong About Canada’s Genetic Non-Discrimination Law University of Guelph News –
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Travelling with Huntington Disease Huntington disease (HD) is a hereditary, neurodegenerative illness with physical, cognitive and psychiatric symptoms. This means
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By Ellie, Isla, Anne and Marlene Bags are packed and we are making our way to Saint Jean Pied de
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September 4, 2017 The big day that we have all been waiting for has finally arrived! Tomorrow, Ellie Smith, Anne
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A new exciting chapter in Huntington’s disease (HD) treatment is just beginning – WAVE Life Sciences have announced PRECISION-HD1
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There are still spots available to race go-karts around the track for the Huntington Society of Canada. The 22nd
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Return to Homepage Observational
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