News

This blog series is a place for the ALS community to learn about and stay updated on ALS Canada's advocacy efforts as well as relevant developments within the government. Please note that because ALS Canada…

On June 12, a diverse and passionate group of researchers, clinicians, ALS organizations, and people affected by ALS gathered in Toronto for the National ALS Research Summit. Hosted by ALS Canada, the day-long workshop marked a…

In this interview with members of the ALS Canada Research Team, David Taylor, Chief Scientific Officer and Colleen Doyle, Director of Canadian Research, both discuss the ALS Canada Research Program and building the foundation of ALS discovery in Canada.   …

Engaging with elected officials is a cornerstone of effective advocacy. Whether you are living with ALS, a caregiver, or someone who wants to see a better reality for people affected by this devastating disease, your voice matters. This blog post…

The ALS Society of Canada is honoured to welcome five new members to its Board of Directors. Their professional accomplishments, combined with a personal understanding of the impact of ALS from the perspective of a neurologist, caregiver, or people living…

ALS Canada expresses deep gratitude to four departing members of our Board of Directors who have completed their terms this year. Thank you, Dr. Ken Chan, Dr. Leslie Green, Dr. Wendy Johnston, and Craig Storey, for your dedication, leadership, and…

June’s ALS Awareness Month offers a critical opportunity to shine a light on a fatal disease that remains largely underfunded and under-recognized TORONTO – The ALS Society of Canada (ALS Canada) is calling on Canadians to unite in support of people…

Empowering post-secondary students affected by ALS in their educational goals while strengthening care and support of the ALS community For the third year, the ALS Society of Canada (ALS Canada), together with the family and friends of Kevin Daly, is…