65 Roses Virtual Volunteer
On 65 Roses Day we paint the state with roses to raise awareness and funds for children and adults living…
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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…
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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…
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Message from the CFSA Board
Update from the CFSA board regarding the recruitment of the CFSA Executive Officer position
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Donate this Christmas
While you and I wait for COVID-19 to pass so normal life can resume, a family with cystic fibrosis never…
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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…
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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…
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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.
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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.
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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.
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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).
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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…
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