Canadian insurers out-of-date on genetic testing, says non-profit group
The CLHIA’s opposition to the Genetic Non-Discrimination Act ignores lessons learned in other nations, according to non-profit group The Canadian
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The Adventure Continues…
We just completed 2 weeks or 325 km of our amazing adventure on the Camino de Santiago. Our best night
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Global HD Organizations Launch Collaborative Advocacy Group
Earlier today, it was announced that 3 global Huntington’s disease (HD) patient advocacy organizations have teamed up to create a
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Founders Walk raises nearly $24,000 for Huntington’s disease research, treatment
Efforts to find a cure for Huntington’s disease received a boost on Saturday, Sept. 16, as participants made their way
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Ready, set, go raise money
The 21st Annual Huntington Indy Go-Kart Challenge was a huge success. The Winnipeg Chapter was able to raise $20,000 for HSC’s
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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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WINDSOR HUNTINGTON SOCIETY RACES FOR A CURE
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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Why Insurers Are Wrong About Canada’s Genetic Non-Discrimination Law
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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In The Know – September 2017
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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S&K September 2017 – Volume 10 Issue 5
Travelling with Huntington Disease Huntington disease (HD) is a hereditary, neurodegenerative illness with physical, cognitive and psychiatric symptoms. This means
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