Days
Hours
Minutes
Seconds
Countdown finished!

On May 26, make your steps count.

Days
Hours
Minutes
Seconds
Countdown finished!
Young boy with walk bandana smiling at the camera.
A group of walkers makes strides down a path.
An older couple link arms at last year's event.
A little girls sits on top of her father's shoulders as they walk at the event.
Graphic map of Canada - over 40 locations from coast to coast

20 Years of Making History

Join thousands of Canadians who are making their steps count on May 26 by participating in our 20th anniversary of the Walk To Make Cystic Fibrosis History. Our largest fundraising event takes place in local communities across Canada and brings us together with one goal – taking a step toward creating a life unrestricted by CF for ALL Canadians living with cystic fibrosis.

JOIN US!
Graphic map of Canada - over 40 locations from coast to coast

2o Years of Making History

Join thousands of Canadians who are making their steps count on May 26 by participating in our 20th anniversary of the Walk To Make Cystic Fibrosis History. Our largest fundraising event takes place in local communities across Canada and brings us together with one goal – taking a step toward creating a life unrestricted by CF for ALL Canadians living with cystic fibrosis.

JOIN US!

And it’s as easy as 1. 2. 3.

Little girl holding up the number 1 with her hand

1.  In Person or Virtual?

Decide if you want to participate virtually or in person on Sunday, May 26

Woman holding up the number 2 with her hand

2.  Location?

Choose an event location close to home and register.

Man holding up the number 3 with his hand

3.  Ready. Set. Go!

Set up your fundraising page and get your (fundraising) party started!

We walk...

In memory of those we’ve lost and in honour of those we continue to support.

To invest in research and find new breakthroughs in treatment.

To ensure access to CF medicines so no one with cystic fibrosis is left behind.

Chanelle wearing her Walk 2023 event t-shirt.

I’ve participated in a few local CF Walks with friends and family as a team bringing awareness for CF. My favourite memories, at the Walk, are seeing the amount of involvement from the community. It was always comforting and brought some hope to the matter.

READ CHANELLE'S STORY

We keep walking so that every Canadian with CF can live a full, healthy life.


We walk, for people like Chanelle who doesn’t want to be left behind. 


Your participation can help to change the cystic fibrosis story in Canada, driving our important work funding CF research, programs and services to lengthen and improve the lives of all Canadians living with cystic fibrosis.


Will you walk with us this year?


REGISTER TODAY
Sebastian and his mom Vicky wearing their Walk gear at the event.

The Walk is part of our family's advocacy efforts...

We walk to raise awareness and help find a cure for rare mutations of cystic fibrosis. We want the public to know that there are kids like Sebastian living in Canada who are at risk of being left behind. Trikafta and other modulators are not accessible to all. Sebastian and others who could benefit from these breakthrough medications have the right to try them because the last 5-10% of people living with rare mutations deserve a chance at a longer and healthier life trajectory too.


- Vicky M, Toronto Walk

All kids should have dreams. 

My dream is simple. I dream of a future when CF no longer stands for Cystic Fibrosis but rather stands for “Cure Found”.


- Lauren A, Toronto Walk 

An older woman and her granddaughter wearing Walk tees smile for the camera
A young girl with CF sits on her couch with her cat as she received CF treatment

CF Canada works tirelessly...

Thanks to CF Canada and all of their hard work, in 4 short years we have gone from not knowing what the future would hold, to finding hope through gene modulator therapy with the introduction of Trikafta. CF Canada works tirelessly to make medications, like Trikafta, accessible. They support those living with CF and their families. They encourage awareness of the disease. They are also a small organization, and a very small staff team ensures that donations actually help the cause.

> Alissa M, Niagara Walk

Share by: