Let's make it an event to remember
You are a powerful player in the vital work of Cystic Fibrosis Canada. By supporting, fundraising or registering for an event, you help fund critical cystic fibrosis research and drive essential support for Canadians living with CF. All this and a heck of a good time too!
We love events here at Cystic Fibrosis Canada. And we love connecting as a community across the country. Check out our roster of inspiring community events, including webinars, conferences and town halls.
Shinerama is here!
Shinerama is a beloved part of campus life across Canada, bringing students together during orientation week to raise funds and awareness for cystic fibrosis.
From car washes and BBQs to trivia nights and drag shows, students get creative with fun events that make a real impact.
Check our website to see if your school is involved — or find out how to start!
Find out more!Find an upcoming event
Peer Connect Session: Self-Care for Parents and Guardians
Looking to connect with others impacted by cystic fibrosis? This session will focus on self-care for parents and guardians of people with CF!
2025 Fusion Gala - An Evening in London
Prepare to be delighted. Tickets and sponsorship opportunities are now available for the 2025 Fusion Gala - An Evening in London!
Peer Connect: Young adults (18+) living with CF
Looking to connect with others who understand life impacted by cystic fibrosis? This session will focus on Young adults (18+) living with CF and is open to those living with CF.
Royal Victoria Marathon 2025
Join Team CF Canada at the 2025 Royal Victoria Marathon!
Peer Connect: To tell or not to tell: sharing about your CF diagnosis with others
Looking to connect with others who understand life impacted by cystic fibrosis? This session will focus on discussing your CF diagnosis with others and is open to those living with CF.
Peer Connect: Connecting dads and father figures
Looking to connect with others who understand life impacted by cystic fibrosis? This session will focus on connecting dads and father figures and is open to parents or guardians of someone living with the disease.
Peer Connect Session: Traveling with CF
Looking to connect with other parents and guardians navigating life with cystic fibrosis? This session will focus on traveling with CF and is open to oarents or guardians of people with with CF.
Car Parade
Join us for a Halloween themed car parade in Support of Cystic Fibrosis Canada.
Halloween Piggy Banks
Are you a school or parent looking for a simple, fun, and educational Halloween activity? The Halloween Piggy Bank Campaign is a great opportunity to raise awareness about cystic fibrosis among children, while supporting the 1,200 CF families in Quebec.
Upcycle Christmas Craft Sale
Selling gently used and well-loved Christmas decor, along with decor that is crafted into new creations, giving these items a second life.
Défibrose 2026: The Kenya Experience
Led by parents of twins with CF, Quebec families will run 25 km in Kenya to raise funds for CF research—together, for a life without limits.
Organize an event
If you want to host an event of your own, or already have one in the works that could be a fundraiser for the CF community, then you’re well on your way to becoming a Change Maker.
Change Makers are fundraisers who rally local support to raise funds, create awareness and generate a lot of goodwill by hosting any kind of fundraising event - from lemonade stands to birthday parties to golf tournaments and everything in between. It’s easy! And lots of fun.
All About Change Makers
Shine Season is back — and it’s your chance to make an impact.
This summer, join CARSTAR locations across Canada in raising critical funds for cystic fibrosis through Shine Season, the company’s annual fundraising campaign running from June to September.
Points East Lighthouse Run
The Points East Lighthouse Run/Relay is taking place on Saturday, June 14, 2025! Sign up a team of four members or run the 29-kilometer course as a solo event.
Gear Up 4 CF
The 20th Annual GearUp4CF is an annual cycling event established in 2008 in B.C., that unites cyclists in a fundraising initiative for Cystic Fibrosis Canada. Pedal with us as we harness the power of community and collective effort to generate financial support for the CF community.
Lawn Summer Nights
When summer rolls in this year, don't miss out on the ultimate summer experience! Lawn Summer Nights has a spot waiting for you and your friends or colleagues: warm nights, cold drinks, good music and great people on the greens, all for a great cause!
Camp Fromaway Summer 2025
Camp Fromaway is a 5-day free virtual summer camp for youth aged 12+ living with cystic fibrosis. Cystic Fibrosis Canada is proud to be partnering with Upopolis to offer this incredible opportunity to our community.
Team Nicole 2025
A 212km adventure of hiking, swimming and cycling from Muskoka to Aurora, creating awareness, raising money, and connecting people. Come join us along the way!
Peer Connect: Living with CF and making the decision to have children or become parents
Looking to connect with others who understand life impacted by cystic fibrosis? This session will focus on living with CF and making the decision to have children or become parents and is open to those living with CF.
Peer Connect: Supporting young children with CF
For parents/guardians of someone living with CF: Looking to connect with others who understand life impacted by cystic fibrosis? This session will focus on supporting young children with CF and is open to parents or guardians of someone living with the disease.
Peer Connect: Navigating moving out of home for the first time
For adults (18+) living with CF: Looking to connect with others who understand life impacted by cystic fibrosis? This session will focus on navigating moving out of home for the first time and is open to those living with CF.
Shinerama
Since 1964, Shinerama is Canada’s largest post-secondary fundraiser in support of Cystic Fibrosis Canada. Over 20,000 student volunteers from Canadian universities and colleges come together every year to make a difference in the lives of those battling cystic fibrosis (CF).
Jogging for Jovie
Whether you jog, walk, cheer, or donate, join us as we're Jogging for Jovie.
Peer Connect: Self-care
For adults (18+) living with CF: Looking to connect with others who understand life impacted by cystic fibrosis? This session will focus on self care and is open to those living with CF.
Tour du Mont Blanc 2025
A dedicated group is embarking on the iconic Tour du Mont Blanc to support the fight against cystic fibrosis.
Peer Connect: Grief, loss, and survivor’s guilt in the CF community
Looking to connect with others who understand life impacted by cystic fibrosis? This session will focus on grief, loss, and survivor’s guilt in the CF community and is open to those living with CF.
Peer Connect Session: Supporting Young Children with CF
Looking to connect with others navigating life impacted by cystic fibrosis? This session will focus on supporting young children with CF and is open to parents and caregivers.
Peer Connect: Clinic days and talking to your CF care team
Looking to connect with others who understand life impacted by cystic fibrosis? This session will focus on clinic days and talking to your CF care team and is open to those living with CF.
KISS CF Goodbye #9
A night of live music, raising awareness and funds for Cystic Fibrosis.
Peer Connect Session: Self-Care for Parents and Guardians
Looking to connect with others impacted by cystic fibrosis? This session will focus on self-care for parents and guardians of people with CF!
2025 Fusion Gala - An Evening in London
Prepare to be delighted. Tickets and sponsorship opportunities are now available for the 2025 Fusion Gala - An Evening in London!
Peer Connect: Young adults (18+) living with CF
Looking to connect with others who understand life impacted by cystic fibrosis? This session will focus on Young adults (18+) living with CF and is open to those living with CF.
Royal Victoria Marathon 2025
Join Team CF Canada at the 2025 Royal Victoria Marathon!
Peer Connect: To tell or not to tell: sharing about your CF diagnosis with others
Looking to connect with others who understand life impacted by cystic fibrosis? This session will focus on discussing your CF diagnosis with others and is open to those living with CF.
Peer Connect: Connecting dads and father figures
Looking to connect with others who understand life impacted by cystic fibrosis? This session will focus on connecting dads and father figures and is open to parents or guardians of someone living with the disease.
Peer Connect Session: Traveling with CF
Looking to connect with other parents and guardians navigating life with cystic fibrosis? This session will focus on traveling with CF and is open to oarents or guardians of people with with CF.
Car Parade
Join us for a Halloween themed car parade in Support of Cystic Fibrosis Canada.
Halloween Piggy Banks
Are you a school or parent looking for a simple, fun, and educational Halloween activity? The Halloween Piggy Bank Campaign is a great opportunity to raise awareness about cystic fibrosis among children, while supporting the 1,200 CF families in Quebec.
Upcycle Christmas Craft Sale
Selling gently used and well-loved Christmas decor, along with decor that is crafted into new creations, giving these items a second life.
Défibrose 2026: The Kenya Experience
Led by parents of twins with CF, Quebec families will run 25 km in Kenya to raise funds for CF research—together, for a life without limits.