Message from the CFSA Board
Update from the CFSA board regarding the recruitment of the CFSA Executive Officer position
Donate this Christmas
While you and I wait for COVID-19 to pass so normal life can resume, a family with cystic fibrosis never…
Twenty years ago today, CFSA unveiled our very own rose
On this day...On 20th of October 2000, during the International Rose Festival, our very own rose was officially launched by…
On this day – The Gene for Cystic Fibrosis Found
On this day 23rd August, in 1989, international news reported that the gene responsible for Cystic Fibrosis had finally been…
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.
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.
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.
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).
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…