Raising awareness for ALS while supporting ALS families and critical ALS research.
Helping Families Face ALS — and Heal After
At ALS Double Play, we support and connect families during their battle with ALS and beyond. We understand that ALS affects more than just the individual — it impacts the whole family, and that support doesn't end when a life does. That’s why we stand with both those living with ALS and those who carry on, determined to make ALS history.
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We raise awareness, fund critical ALS research, and foster community so that no one faces ALS alone. In 2025, we’re launching new mental health support to help families navigate the emotional toll of ALS — because healing is a lifelong journey.
Over $400,000 invested in ALS research to find a cure.
Dozens of families connected through outreach and peer support.
1,000+ community members engaged through events, talks, and awareness campaigns.
Launching in 2025: mental health support for families affected by ALS.
Our Mission & Vision
Our Mission
To be a connection for people living with ALS. Through their stories, we raise awareness, connecting communities to support the search for a cure.
To raise funds to donate to Canadian charities that are researching better treatment methods and looking for a cure for ALS.
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Our Vision
To make ALS history.
What is ALS?
Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's Disease or Motor Neurone Disease (MND), is a progressive neurodegenerative condition that affects nerve cells in the brain and spinal cord. ALS leads to muscle weakness, loss of mobility, and eventual paralysis.
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This fatal disease currently has no cure, but with increased awareness, research, and support, we aim to change the future for those living with ALS.
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What people are saying about ALS Double Play
Barb R.
In the spring of 2016—less than six months before we lost Christopher—we partnered with a production company to help share his story. For Christopher, and for our family, it was important to put a face to amyotrophic lateral sclerosis (ALS). We didn’t know how little time we had left, but we’re grateful we captured this moment. The result is a short, ten-minute film that speaks volumes about strength, dignity, and what’s still possible—even in the face of a terminal illness.