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Letter to decision makers: Canadians with cystic fibrosis need the COVID-19 vaccine now /news/lettre-aux-décideurs-les-canadiens-atteints-de-fibrose-kystique-ont-besoin-du-vaccin-contre-la-covid-19-sans-plus-tarder

Letter to Provincial Health Ministers regarding access to COVID-19 vaccines /news/letter-to-provincial-health-ministers-regarding-access-to-covid-19-vaccines

Letter to the Honourable François Legault and Christian Dube /news/letter-to-the-honourable-françois-legault-and-christian-dube

Life Changing Treatment, Trikafta, is Advancing Through The Canadian Drug Approval Process /news/life-changing-treatment-trikafta-is-advancing-through-the-canadian-drug-approval-process

Life-changing Drug Trikafta Submitted to Health Canada for Ages Six to Eleven /news/life-changing-drug-trikafta-submitted-to-health-canada-for-ages-six-to-eleven-

Life-changing treatment, Trikafta, is coming to Canada /news/life-changing-treatment-trikafta-is-coming-to-canada

Living with Cystic Fibrosis /about-cf/living-with-cystic-fibrosis

MANITOBA BECOMES FINAL PROVINCE TO COMMIT TO LIST LIFE CHANGING CYTIC FIBROSIS DRUG /news/manitoba-becomes-final-province-to-commit-to-list-life-changing-cytic-fibrosis-drug-

Manitoba EXPANDS ACCESS TO TRIKAFTA, ENSURES LIFE CHANGING DRUG IS ACCESSIBLE TO THOSE WHO NEED IT /news/manitoba-expands-access-to-trikafta-ensures-life-changing-drug-is-accessible-to-those-who-need-it-

marche /pages/marche

Mental Health /about-cf/living-with-cystic-fibrosis/mental-health

Mental Health and Wellness /about-cf/covid-19-information-for-cf-community/mental-health-and-wellness

Mia Gaudenzi /about-us/cf-champions/mia-gaudenzi

monthly /pages/monthly

National Advocacy Network /our-programs/advocacy/how-to-take-action/national-advocacy-network

NEW BRUNSWICK EXPANDS ACCESS TO TRIKAFTA, ENSURES LIFE CHANGING DRUG IS ACCESSIBLE TO THOSE WHO NEED IT /news/new-brunswick-expands-access-to-trikafta-ensures-life-changing-drug-is-accessible-to-those-who-need-it-

New International Guidelines on Mental Health in CF /about-cf/virtual-education-program-for-patients-and-caregivers/new-international-guidelines-on-mental-health-in-cf

New Research Shows 15% Reduction in Cystic Fibrosis Deaths by 2030 If Trikafta is Made Available Now /news/new-research-shows-15-reduction-in-cystic-fibrosis-deaths-by-2030-if-trikafta-is-made-available-now

New standards of care made available today by Cystic Fibrosis Canada /news/new-standards-of-care-made-available-today-by-cystic-fibrosis-canada

NEW SURVIVAL MILESTONE FOR CYSTIC FIBROSIS IS CAUSE FOR CELEBRATION BUT NOT INACTION /news/new-survival-milestone-for-cystic-fibrosis-is-cause-for-celebration-but-not-inaction-

Upcoming Events

May 25, 2024

REGINA Ride for the Breath of Life Bike Run

On Saturday, May 25th, 2024 the South Saskatchewan Chapter of Cystic Fibrosis Canada is proud to be hosting their 40th Annual Ride for the Breath of Life.

We are so grateful for all of our riders over the years coming together to raise much needed funds. Since our first run we have raised over $824,595 for research, advocacy & clinical care for Cystic Fibrosis Canada, all because of YOUR support!

See details for more information on how to join us!

CF Champions

Kelly Ann Quinlan

Age 19, St. John's, Newfoundland and Labrador

My name is Kelly Ann Quinlan and I am 19 years old. I was diagnosed with cystic fibrosis at birth. My 24-year-old brother Michael also has cystic fibrosis, which is a challenge, as we both live in the same home but must live separately to a degree. We are very close to our parents and sometimes they struggle with the extra duties and constant cleaning that comes with raising two CF children.

Canadians with cystic fibrosis consume a large number of enzymes, about 20 pills a day, to help absorb nutrients from food