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Register and start fundraising today for the 2024 Ride for the Breath of Life! We can't wait to hit the tarmac with you and #ridefurtherfor Canadians living with cystic fibrosis to fund research, treatment and care!
https://www.rideforthebreathoflife.ca/
DetailsJoin us for the CF Canada Community Forum: "Uncharted Territories," taking place on April 26 from 4 PM to 5 PM EST or 1 PM to 2 PM PST.
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Gillian Maramieri has been involved with Cystic Fibrosis Canada for 10 years and is a working mother of two boys. Her youngest, Matthew, has cystic fibrosis and was the first to be diagnosed with CF in the family. He was diagnosed at birth after Gillian’s doctors noticed an echogenic bowel 18 weeks into her pregnancy. Her first words after the diagnosis were, "Ok, now what do we need to do?"
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