Making each day with ALS the best day possible.
We achieve our mission by providing support, facilitating the provision of care, promoting awareness, helping find a cure, and advocating for change.
Did you know?
About 300 – 400 Albertans and 3,000 Canadians live with ALS today.
It’s a rare disease, but its impact is devastating and far-reaching. Last year, the ALS Society of Alberta supported over 450 clients and their loved ones.
Dealing with a diagnosis? We can help with equipment and support.
Through our provincial Equipment Loan Program, we are able to assist people living with ALS by lending power mobility devices, assistive communication devices, and other medical equipment. The Equipment Loan Program is free of charge to ensure support is readily available when our clients need it most.
In order to make each day the best day possible for people living with and affected by ALS, we provide home visits, support groups, information, referrals and support for youth through The Debi Lefaivre ALS Youth Champions Fund. The ALS Society of Alberta also provides services in the Northwest Territories when required.
More than support,
a community.
You can help us make an impact.
When you make a financial donation to the ALS Society of Alberta, you are directly supporting Albertans living with ALS in their time of need.
Lorie’s story
We’re building something powerful: a community rooted in hope, action, and care.
Lorie lives with ALS and is dedicated to raising awareness, funds, and hope for a future where people affected by ALS feel heard, seen, and supported. She made an impact at the Lethbridge Walk on September 6, 2025, to take steps together toward new treatments and a cure.
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Help us make an impact.
Even the smallest donation can make a large impact on somebody affected by ALS.