Register now and get your friends and family members to be part of this iconic event! Help raise much-needed funds for cystic fibrosis! In Victoria, most of us have been in lockdown with only a limited time to enjoy the start of spring in Melbourne, while in NSW, things have been a bit more relaxed…. View Article
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When it comes to celebration, where there’s a will, there’s a way. In the time of the Great Depression, families hosted ‘potluck’ dinner parties as a way to remain connected, proving that a global crisis was not going to stop a party. This is why Cystic Fibrosis Community Care is working so tirelessly to plan… View Article
One of the hardest parts about COVID-19 is not being able to participate in activities we love like before. As the coronavirus crisis continues, schools everywhere are struggling to keep children healthy and connected.
Your feedback on what we do is highly valued and appreciated, so in addition to our regular ways of providing feedback, we have two ways that you can be involved and share your experiences and thoughts – focus group interviews (conducted via video conference) and an online survey.
Cystic Fibrosis Community Care is working to keep everyone in our community safe during the COVID-19 (coronavirus) pandemic. We have compiled a list of up-to-date resources on websites for you to visit, depending on what questions you might have.
Life with CF changes when you become an adult. The modern facilities, the Starlight Room and Clown Doctors become a distant memory as adult life arrives. CF Strong aims to bring back some warmth to the big kids, and to strengthen the adult community by enabling shared knowledge, advice and support.