I've worked for Cystic Fibrosis Tasmania since March 2010 and I'm extremely passionate about the work that we do.
The CF community deserves as much support as possible. CFT receives no Government funding and holds events and fundraising activities to raise enough funds to support our members.
I just can't imagine what it would be like to live with this condition, or to have a child who has it. There is no cure at the moment. The treatments and medication that a person with CF has to endure each day are time consuming and not great.
05 May 2018 - 05 May 2018
11 Aug 2018 - 11 Aug 2018
16 Feb 2019 - 13 Apr 2019
19 May 2019 - 19 May 2019