65 Roses Virtual Volunteer On 65 Roses Day we paint the state with roses to raise awareness and funds for children and adults living… Read story
A Tough Pill to Swallow…ACCESS DEFERRED Trikafta was not recommended for reimbursement by the Pharmaceutical Benefits Advisory Committee (PBAC). Having seen the outstanding clinical trial data… Read story
Identifying Vascular Disfunction In CF – Childhood To Adulthood Our deepest and warmest accolades are for Andrew Tai, Paediatric CF Centre Director and researcher at the Women and Children’s… Read story
Message from the CFSA Board Update from the CFSA board regarding the recruitment of the CFSA Executive Officer position Read story
Donate this Christmas While you and I wait for COVID-19 to pass so normal life can resume, a family with cystic fibrosis never… Read story
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… Read story
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… Read story
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