"Let's Roll!" was the rally cry of Eddy Lefrancois as he faced 25 years living with ALS, a reality not afforded to most people diagnosed with ALS today. Help me to change that.

I'm challenging myself to do more for people and families living with ALS by participating in the first-ever ALS Canada Revolution Ride - a volunteer-powered, fundraising event held in support of the ALS community.

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 26, 2021 in Dundas, Ontario. I hope I can count on you for support.

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