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News

We deliver information that you can trust, informing you about the latest advances in ALS research, as well as upcoming events.

    Advocacy

    Ontario Provincial ALS Program: Enhancing care and quality of life of people living with ALS

    January 17, 2024
    In Canada, what the provincial health care systems provide does not always match the needs of people living with ALS. This statement rings true for Ontario, where the current ALS care and support landscape in the province presents people living…
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    Research

    Negative results from Phase 3 ADORE clinical trial of Oral Edaravone (FAB122) in ALS

    January 12, 2024
    Updated on: January 31, 2024 Pharmaceutical company Ferrer has announced topline results from the ADORE (ALS Deceleration with ORral Edaravone) clinical trial in ALS. The Phase 3 study, conducted in Europe, investigated the efficacy of an oral formulation of edaravone…
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    Fundraising Events

    You can support ALS Canada & enjoy tax benefits!

    December 22, 2023
    As we bid farewell to 2023, we want to take a moment to celebrate YOU. Your dedication throughout this month, and indeed the entire year, has been nothing short of inspirational. As a community, you have rallied together to show…
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    Press Releases

    All provinces are listing RADICAVA Oral Suspension (edaravone)

    December 18, 2023
    The province of Manitoba has listed RADICAVA Oral Suspension on the Manitoba Pharmacare Program (Exceptional Drug Status) as a treatment for ALS. With this announcement, all provinces and territories across Canada – as well as Veterans Affairs Canada and Indigenous…
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    Advocacy

    ALS Canada Advocacy Update – October-December 2023

    December 12, 2023
    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 government. Please note that because ALS Canada advocates federally and provincially within Ontario,…
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    Fundraising Events

    We’re closer than ever…but we’re not there yet

    December 07, 2023
    A letter from Tammy Moore, ALS Canada’s Chief Executive Officer Let me start by saying thank you. Thank you for standing beside us throughout the year, driven by our shared vision: a future without ALS. Today, I want to…
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    Fundraising Events

    An exciting GivingTuesday announcement!

    November 25, 2023
    Double your impact this GivingTuesday When it comes to fundraising for ALS, next Tuesday (November 28) is the single most important day of the year, and to help us celebrate the day, we have an exciting announcement. Does this sound intriguing?…
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    Press Releases

    ALS Canada and Brain Canada invest more than half a million dollars in the future of ALS researchers with the 2023 Clinical Research Fellowship and Trainee Awards

    November 10, 2023
    On World Science Day, the latest ALS Canada-Brain Canada research awards, with support from Fondation Vincent Bourque, highlight the importance of funding early-career researchers and clinicians   Toronto — In recognition of World Science Day, together with Brain Canada,…
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    The Standards Program Trustmark is a mark of Imagine Canada used under licence by the ALS Society of Canada. Registration No. 10670-8977-RR0002.

    2026 Amyotrophic Lateral Sclerosis Society of Canada

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