Stories

COVID-19 and Cystic Fibrosis Cystic Fibrosis SA has compiled a list of resources to help people with CF with the COVID-19 (coronavirus) pandemic. Read story

Breathe | SALA 2020 Festival Online Exhibition Breathe is an online art exhibition part of SALA Festival by artists living with or having a close connection with Cystic Fibrosis. Read story

Camping and living with CF – Ben’s story Ben is 28, he loves to play board games and go camping and he lives with CF. Read story

Kryssy was gifted lungs and life began again Kryssy Pawlik-Discombe lives with CF and is celebrating 8 years since her life changing lung transplant (TX). Read story

How Jess got her groove back Jess is a Riverland born and bred, thirty year old who loves hanging with her dogs, staying fit, listening to… Read story