by c4cfadmin | Aug 14, 2023 | News
Cure4CF Update What makes Cure4CF Unique? The Cure4CF Foundation (Cure4CF) established in 2009 is part of the global community working to develop a cure for everyone with Cystic Fibrosis (CF). In Australia, we offer a unique approach to fundraising and supporting...
by c4cfadmin | Jul 6, 2023 | News
CF Parent Update Jen’s top tips for the early years as a CF parent Last month I sat down with our newest Community Ambassador Jen to talk about the things she wishes she had known in 2019 when she became a CF parent. Becoming a CF Parent Jen’s daughter Aveline was...
by c4cfadmin | Jun 2, 2023 | News
Research Update Exciting advancement in personalised treatment Cure4CF is funding a cutting-edge study in personalised bacteriophage treatment in CF, so what’s it all about? What are bacteriophages? Bacteriophages or phages for short, are viruses that specifically...
by c4cfadmin | Dec 19, 2022 | News
Trikafta Update Pharmaceutical Benefits Advisory Committee (PABC) Trikafta Outcome Cure4CF will not rest until there is a cure for everyone with CF. We are thrilled the Pharmaceutical Benefits Advisory Committee has recommended the inclusion of Trikafta on the...
by c4cfadmin | Oct 27, 2020 | Get Active Events
This year the 2020 Knight Frank Point to Pinnacle challenge to reach the top of Mt Wellington is open to everyone – worldwide! Join us from wherever you are on the planet in taking on the 1271m elevation challenge via Strava between the 14th and 20th of November – you...
Cystic fibrosis (CF) is what’s called an autosomal recessive condition. That means a person needs to inherit two faulty copies of the CF gene (one from each parent) to develop CF.
A chronic wet cough can be a warning sign of serious lung disease. Learn what your cough is telling you—and why early action matters for long-term lung health.
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