The power of connection – one family’s experience with ALS

Throughout his lifetime, David Urlin has worn many hats. He has worked as a farmer, a businessman, a hotel owner and a deputy mayor, and in his spare time he used to play football, baseball, hockey, and racquetball. Then in 2016, everything changed. “David always did so much,” says his wife, Mag. “He cooked, he […]

Deanna Fennell: moving forward and giving back

For many years, the WALK for ALS has been bringing people together in support of a shared cause. Everyone has their own reasons for participating: some go to support a recently-diagnosed friend or family member; others focus on raising awareness, and some people WALK to honour the legacy of a loved one. “My mother was […]

Kristine Lee: making adjustments along the way

For the past decade, Kristine Lee has been progressively losing the ability to stand on her own. A wife and mother of two, Kristine has upper motor neuron predominant ALS, a form of the disease that typically progresses more slowly than others. A few weeks before her local WALK for ALS, she opened up about […]

Upcoming Webinar: The Canadian ALS Neuroimaging Consortium (CALSNIC)

Webinar: The Canadian ALS Neuroimaging Consortium (CALSNIC) Monday, April 24 at 12:00 PM Eastern Time: 30 minutes + questions Hosted by: Dr. Sanjay Kalra Click here to register for the Webinar During this webinar you can expect to learn how Dr. Kalra has built a team of researchers across Canada to develop the ability to […]

WALK for ALS early results: $3.9 million (and counting!) raised nationwide

Throughout the spring, summer and fall of 2016, Canadians showed they care about beating ALS, the devastating neuromuscular disease that gradually paralyzes people and takes away their ability to move, talk, swallow, eat and eventually breathe. In communities across the country – from Victoria, BC to St. John’s, NL, and from Windsor, ON to Whitehorse, […]