Faisons de cette activité un événement mémorable!
Vous jouez un rôle primordial dans le travail crucial de Fibrose kystique Canada. En apportant votre aide, en recueillant des fonds ou en vous inscrivant à un événement, vous nous aidez à financer des recherches cruciales sur la FK et à offrir un soutien essentiel aux Canadiens atteints de FK. Et tout cela en vous amusant!
Shinerama
Shinerama est devenu une institution sur de nombreux campus à travers le pays, jouant un grand rôle dans l’expérience étudiante. Cet événement encourage les étudiants de première année à rencontrer de nouvelles personnes et à redonner à leur communauté pendant la semaine d’orientation.
En savoir plusTrouver un événement à venir
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.
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).
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.
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.
Organisez une activité
Si vous souhaitez organiser une activité, ou si vous en organisez déjà une qui pourrait permettre d’amasser des fonds pour la communauté FK, alors vous êtes en passe de devenir un membre de L’escouade FK.
Les membres de L’escouade FK sont des personnes qui rallient les soutiens locaux pour recueillir des fonds, sensibiliser le public et générer beaucoup de bonne volonté en organisant toutes sortes d’activités – des ventes de limonade, aux fêtes d’anniversaire, en passant par les tournois de golf… et on en passe. C’est très facile et tellement amusant!
Tout sur L’escouade FK
65 Roses Gala
The 24th Annual 65 Roses Gala; Step back in time to an era of elegance and intrigue at the 65 Roses Gala, MasCUREade: Unmasking a cure for cystic fibrosis.
Wrapping for a Cure
Gift wrapping in exchange for a donation. Wrap your gifts with love and make a meaningful difference this holiday season. Visit the Gift Wrap Factory and add an extra touch of warmth and goodwill to your giving.
The Royal Ball
We are thrilled to welcome back The Windsor-Essex Royal Ball in 2025. This exciting event is aged for children 12 and younger and will take place on Sunday, January 5 at the Ciociaro Club in Windsor, ON. The Ball will encompass all of the features you have loved from previous years, and more.
Ultimate NHL Road Trip
Take a chance to win an NHL road trip of a lifetime by seeing 3 games in 4 nights! Open to residents of Atlantic Canada Only. Must be 19 years of age or older.
Cystic Fibrosis Curling Funspiel
Join us for the 1st annual Curling Funspiel for Cystic Fibrosis Canada in North Bay! Register soon - spots are filling up quickly!
Elvismania
Elvismania is back for its 7th year in support of CF Canada! Join us for an incredible concert featuring 8 Elvis Tribute Artists with the band Rudy & The Angels.
Spring 2025 Town Hall
Connect with the cystic fibrosis community, hear about impactful work being led by Cystic Fibrosis Canada, learn about a research or healthcare topic and opportunities to act on priorities to help Cystic Fibrosis Canada at this March 19 virtual Town Hall
Face Off with CF Gala
Join us on March 23, 2025 for another unforgettable night of giving and love. Together, we’ll raise awareness and funds to support those living with cystic fibrosis. 🌟 Let’s come together to make a difference! Save the date and let's make a lasting impact in the fight against cystic fibrosis during a night to remember!
$75 Tire Swap for Dante’s Journey to the Cure
Waterdown Collision is proud to announce our latest fundraiser supporting Dante's Journey to the Cure!
2nd Annual Cornhole Fundraiser in support of Cystic Fibrosis Canada
Get ready to toss some bags for a great cause! Join us for our 2nd Annual Cornhole Fundraiser in support of Cystic Fibrosis Canada!
Brews N Blokes
Brews N Blokes is a night of live music, great food and fun in support of Cystic Fibrosis Canada!
Dance for CF - Masquerade Ball
Come out to support the Dance for CF Masquerade Ball in support of Cystic Fibrosis Canada!
Outrun CF Durham
The 15th anniversary of Outrun CF is here!
Emera Blue Nose Marathon
Join Team CF Canada at the 2025 Emera Blue Nose Marathon!
Ottawa Marathon 2025
Join Team CF Canada at the 2025 Ottawa Marathon!
Walk To Make Cystic Fibrosis History
The Walk To Make Cystic Fibrosis History is CF Canada’s largest fundraising event taking place from coast-coast in local communities. Our 21st year of the Walk brings us together with one goal – fundraising to make an impact on the cystic fibrosis landscape and ensuring that no one is left behind.
65 Roses Fort McMurray Golf Charity Tournament
The 1st annual 65 Roses Fort McMurray Golf tournament with silent auction, raffle, golfing prizes and closing with a meal, will take place at the beautiful Vista Ridge Golf Course.
Servus Calgary Marathon 2025
Join Team CF Canada at the 2025 Servus Calgary Marathon!
The Robbie International Festival & Tournament
The Robbie is the world’s largest annual charitable youth soccer tournament. For over 50 years, The Robbie has donated to Cystic Fibrosis Canada to support life-extending research, treatment and education for those living with CF.
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.
Battle for Breath
Since its inception in 2016, Battle for Breath has been more than just a gaming tournament—it’s a platform for making a meaningful impact.
Strokes Fore Life Golf Tournament
We are thrilled to announce that the Strokes Fore Life Cystic Fibrosis Charity Golf Tournament will be returning to the gorgeous Oshawa Golf and Curling Club on Monday, June 9, 2025.
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.
Ride for the Breath of Life - Edmonton
The Ride for the Breath of Life - Edmonton 20th anniversary is taking place on Saturday June 14, 2025.
Community Forum: Spotlight on CF Research
Register now to attend Cystic Fibrosis Canada’s 2025 Community Forum: Spotlight on CF Research.
65 Roses Nanton Golf Tournament
The 65 Roses Nanton Golf Tournament presented by Century 21 Foothills Real Estate will take place on Thursday, June 19, 2025 at the Nanton Golf Club. This event has been organized to help raise awareness and funds for this genetic disease. Events like this help raise much needed funds for life changing medications, clinical trials for new medications, and the pursuit for longer, healthier lives for those living with cystic fibrosis.
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.
Vancouver Half Marathon 2025
Join Team CF Canada at the 2025 Vancouver Half Marathon!
9 & Dine for Cystic Fibrosis
Join us on the greens for a fun-filled golf tournament to raise funds and awareness for cystic fibrosis. Every drive, putt, and birdie brings us one step closer to a cure. Let’s tee off for a great cause!
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.
Superheroes Unite!
We invite you to be a hero in the fight against cystic fibrosis (CF) by supporting Superheroes Unite —a special fundraiser taking place in Windsor, ON this summer!
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.
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.