Almost two years ago, I received a life-changing diagnosis—ALS. The journey since has been a rollercoaster of challenges, unexpected moments, and incredible support. Looking back, the signs were there. In February 2023, stepping onto a curb became difficult—something I dismissed at first. By spring, frequent falls raised concerns, and in May, I voiced them to my doctor. He reassured me it was aging, but I knew there was more.

Frustration led me to the E.R. in October, determined to be heard. A fourth-year resident took my concerns seriously, noting my family history—my mother’s ALS diagnosis in 2001. That moment changed everything. A referral to Neurology set things in motion. Just one month later, my sister and I sat across from Dr. Jewett as he confirmed what I had suspected: Familial ALS. From that moment, the ALS Clinic at South Health Campus became my lifeline.

Thanks to research advancements, and support from the ALS Society of Alberta, I have access to resources my mother never had—a comforting thought. Through it all, my friends and family are my greatest strength. What could have been a dark time is a reminder to embrace life. Inspired, I checked off a bucket-list adventure: an Alaskan cruise!

ALS has changed my path but not my spirit. With my community and the ALS Society of Alberta behind me, I move forward with gratitude. I’m honoured to be the 2025 Betty’s Run for ALS Ambassador and invite you to join me on June 8. Whether you walk, run, donate, or cheer, your support makes a difference. Let’s stand together for those living with ALS today and for a future without this disease.