Our dad and husband, Mark, was sadly lost to ALS last summer. For those who knew him, he was an avid and passionate cyclist, who was energized by the Tour de France, La Vuelta, and other worldwide events. If he was able, we don't see a world where he would not be participating in this Ride.

The ALS community needs our support to provide hope and help to families affected by ALS.

Amyotrophic Lateral Sclerosis (also known as ALS, Lou Gehrig’s disease, or motor neuron disease) is a disease that gradually paralyzes a person as their brain is no longer able to communicate with muscles that they are typically able to move at will. As the muscles of the body break down, someone living with ALS will lose the ability to walk, talk, eat, swallow, and eventually breathe.

I want to contribute to a future without ALS, which is why I’m gearing up for the Revolution Ride on September 22nd, in Dundas, Ontario. I hope I can count on you for support.

Please consider donating to my team fundraising page as we work towards a future without ALS.

Your support is needed now more than ever - we are stronger together!