Cyclists choose from 25 km, 40 km and 90 km routes in Jordan, Ontario, united by a shared goal to support people affected by ALS
JORDAN, ON, September 30, 2026 – On Sunday, October 4, cyclists will hit the road for the sixth annual ALS Canada Revolution Ride, choosing from three scenic routes through the picturesque countryside of Jordan, Ontario. This event raises critical funds that fuel the ALS Society of Canada (ALS Canada) mission to support people affected by amyotrophic lateral sclerosis (ALS) through trusted information and resources, advocacy, and investments in Canada’s most promising research.
Powered by devoted volunteers, the Revolution Ride offers three scenic routes through Ontario’s wine country, with 25 km, 40 km, and 90 km distances designed to welcome cyclists of all skill levels, whether they are looking for a leisurely ride or a greater challenge. Beginning and ending at Sue-Ann Staff Estate Winery, the event concludes with a post-ride gathering where riders, family, and supporters can recognize what has been achieved together and honour the people affected by ALS who bring the community together.
“The ALS Canada Revolution Ride is a deeply personal event for the ALS community,” said Tammy Moore, Chief Executive Officer of ALS Canada. “Whether they are riding alongside a loved one living with ALS, in honour of someone they have lost, or in support of the broader community, every participant is helping drive progress. Together, they are helping strengthen support for families affected by ALS and accelerating the search for better treatments and ultimately a cure.”
The Ride holds special meaning for Anika Brants, a former professional cyclist who competed internationally with Team Canada and stepped away from racing to be closer to home and support her mother, Tracy, following her ALS diagnosis in May 2025.
“Fundraising gives me something tangible that I can do to help my mom,” said Anika. “When so much of ALS feels out of my control, it gives me something to work toward and allows me to contribute to a world free of ALS. I know the money raised supports people and families living with ALS today and research that could change the future for families like mine. Just as important is the sense of community. Being surrounded by hundreds of people who understand what I am going through is incredibly comforting, and the ALS community has made me feel far less alone on this journey.”
ALS is a rare neurodegenerative disease affecting nearly 4,000 Canadians. There is currently no cure for this disease, which progressively paralyzes people as communication between the brain and the muscles breaks down. People living with ALS often experience loss of function, including the ability to walk, talk, eat, swallow, and eventually breathe. ALS carries a lifetime risk of 1 in 300 for each of us.
The Revolution Ride is virtually accessible through the Strava app for any supporters unable to attend the in-person ride. With this option, participants can customize their Revolution Ride from anywhere, on a date that works for them.
To show your support for the ALS Canada Revolution Ride, donate today at http://www.revolutionride.ca.
ALS Canada Revolution Ride Event Details:
When: Sunday, October 4, 2026
Location: Sue-Ann Staff Estate Winery – 3210 Staff Ave, Jordan, ON L0R 1S0
Start line times:
- 90km cyclists: Registration 7:30 a.m., start 8:00 a.m.
- 40km cyclists: Registration 8:00 a.m., start 9:00 a.m.
- 25km cyclists: Registration 8:30 a.m., start 9:30 a.m.
Post-ride celebration: Starting at 11:00 a.m. at Sue-Ann Staff Estate Winery, featuring food and drinks for family and friends to join the cyclists and celebrate post-ride.
About ALS and the ALS Society of Canada
Amyotrophic lateral sclerosis (ALS) is an unrelenting and currently terminal disease. It progressively paralyzes people because the brain is no longer able to communicate with the muscles of the body that we are typically able to move at will. Over time, as the muscles of the body break down, someone living with ALS will lose the ability to walk, talk, eat, swallow, and eventually breathe. Nearly 4,000 Canadians live with ALS and approximately 1,000 Canadians are diagnosed each year. Four out of five people living with ALS will die within two to five years of their diagnosis.
The ALS Society of Canada is working to change what it means to live with ALS. Grounded in and informed by the Canadian ALS community, we respond to the urgent unmet need for life-changing treatments by investing in high-quality research that will fuel scientific discovery and by engaging industry, supporting increased clinical capacity, and advocating for equitable, affordable, and timely access to proven therapies.
Responding to the tremendous need for current and credible ALS knowledge, awareness, and education, we empower Canadians affected by ALS to navigate the current realities of ALS, be informed consumers of ALS information, and advocate effectively for change. In Ontario, we provide direct community services to help people navigate ALS.
Founded in 1977, ALS Canada is a registered charity whose work is powered by generous donors who share our vision of a world free of ALS.
-30-
Join the conversation and connect with the ALS community online. Find ALS Canada on X, Instagram, or like our page on Facebook. Visit als.ca to find out more.
For more information
ALS Society of Canada
media@als.ca
437-703-5402
Support the cause
You can make a difference.
Donations provide crucial services and information to people living with ALS and allow us to invest in research and advocacy dedicated to improving quality of life.