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The health and well-being of our CF community is the highest priority for Cystic Fibrosis Canada during the outbreak of COVID-19. We’ve compiled resources to help keep you up to date with the latest information available for you. However, if there is anything further you would like to know please email advocacy@cysticfibrosis.ca
The resources currently available for you include:
Join us for a fun night of laughs on Thursday, June 17th at 8:00 p.m., just in time for Father's Day! Put the children to bed and pull up a chair for some good laughs about adulting. This show is virtual but NOT pre-recorded - it's live. We promise there will be NO bad Dad jokes!
*See event listing to learn more*
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My name is Mia Gaudenzi and I’m 12 years old. I was born a seemingly healthy baby until around 3 years old when I became ill with pneumonia regularly. Doctors just thought I was unlucky until I had my sweat chloride tests to rule out CF.
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