Most Canadians Still Think Lyme Disease Is a "Rural Problem"

It isn't. I've met people who picked up a tick in their own backyard in Ottawa, in a city park in Halifax, on a golf course outside Winnipeg. That myth is exactly why Rideforlyme.ca exists — and why, every summer, a growing group of cyclists pedals across this country to change the conversation.

My name is Nina Hudson. I spend most of my working hours untangling complicated health data and turning it into something a tired parent or a worried patient can actually use. Somewhere along the way, Lyme disease research pulled me in and never let go — partly the science, partly a friend whose two-year misdiagnosis still makes me quietly furious. I don't ride the full routes myself (my knees have opinions about that), but I've crewed enough rest stops to know exactly how much a cold water bottle and a kind word can mean at kilometre 80.

What You'll Find Here

• Straightforward guides on how our cycling fundraisers work and where the money goes
• Real stories from riders, patients, and the volunteers who keep the wheels turning
• Practical tick-prevention tips that don't rely on scare tactics
• Simple ways to donate, register, or organize a local route in your own community

A Note on Riding Responsibly

Fundraising should never mean pushing anyone past sensible limits — physical, emotional, or financial. We ask riders to train realistically, listen to their bodies, and give what they can without strain. Awareness works better as a steady habit than a single dramatic gesture, and that's the pace we try to keep here.

Have a look around, ask a question through /contact, or browse past routes on the /events page. Thank you for caring enough to read this far — that curiosity is exactly how change starts.