Karen’s story
It does not get easier, but it does get better.
From diagnosis to redefining daily life, this ALS caregiver shares how acceptance, creativity, and support helped her and her husband navigate life with ALS, one moment at a time.
Heather’s story
I wanted a space where I could speak freely and without judgment.
Heather reflects on caring for her daughter through ALS, the deep toll of caregiving, and how finding an ALS-specific grief support community helped her feel understood, supported, and less alone in her journey as an ALS caregiver.
Dave’s story
As I look ahead, I’m feeling hopeful for all that is possible.
Discover how Dave finds hope, connection, and strength while living with ALS in his third year. Your gift can be dedicated in memory or in celebration, helping to make a meaningful impact.
Hashem’s story
Even in the face of ALS, life continues to offer beautiful gifts.
Hashem’s story is one of resilience, family, and finding meaning while living with ALS. It’s a reminder that even in uncertainty, moments of love and connection still shine through.
Blake’s story
From a diagnosis to finding a community.
This story honours Blake Termeer, a devoted husband, father, and grandfather, and reflects on how the ALS Society of Alberta’s support and Equipment Loan Program made it possible for his family to stay connected and create meaningful moments.
Lorie’s story
ALS is not something anyone can face alone. But through walks like this, 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.
Help us make an impact.
Even the smallest donation can make a large impact on somebody affected by ALS.
