Cystic Fibrosis is still not a well‑known disease and that makes fundraising incredibly challenging.
Awareness, education and profile‑building are essential to helping people understand why support is urgently needed.
Experience has shown us that the more people that know about Cystic Fibrosis, the easier it becomes to raise the funds researchers need to develop new treatments and, one day, a cure.
Our annual Grand Ball and other community‑driven fundraising events have helped raise the profile of Cystic Fibrosis in Western Australia, but for many people it remains an unfamiliar and often misunderstood condition.
This gallery exists to change that.
These photographs tell the real story of Cystic Fibrosis, the children, young people, adults, families and friends who live with this disease every day.
They show the courage, resilience and hope that drive our mission.
We hope this gallery inspires you to learn more, share our message, and join us in doing everything we can to make a difference for those living with Cystic Fibrosis.
