Episode 18: CFNZ Lisa Burns
Ingrid chats to CFNZ Chief Executive, Lisa Burns. They discuss what CFNZ does for CFers and their families throughout their lives and what the organisation's plans are for the future to make sure no o...
28 Jul 202333min
Episode 17: Wrestler
Ingrid chats to Dustin Raynor, better known as professional wrestler Dustin Bozworth. Dustin shares his story living with cystic fibrosis from childhood, to pro wrestling, to reality TV on ‘Stone Cold...
10 Jul 202329min
Episode 16: Hospital
Ingrid shares their journey during a recent hospital admission and Orson gives his views on the whole adventure
2 Jul 202328min
Episode 15: Bella Powell
Ingrid sits down with Bella Powell, a young woman with CF who was the first in New Zealand to get Trikafta thanks to the late Sir Bob Elliott – who gave her this gift of life during his final months b...
27 Mar 20231h 10min
Episode 14: Journalist, Patrick Gower
Ingrid sits down with the well-respected and much-loved New Zealand journalist Patrick Gower to talk about the part he played in highlighting the need for funding of Trikafta for New Zealanders living...
25 Feb 202354min
Episode 13: Back to School
Ingrid chats with Helen Ulyatt, mother to an active 9-year-old CFer called Sophia. They chat about how she prepped for starting school and all the fears and worries surrounding this milestone, as well...
23 Jan 202344min
Episode 12: Our diagnosis story
We discuss the journey to diagnosis for our son Orson at six months old. From pregnancy and birth, tests, diagnosis and processing the news. It's emotionally a highly charged episode but we end up lau...
19 Okt 202234min
Episode 11: Never Better
In this episode, Ian and I review the brilliant film Never Better and chat with its writer-director Julianne Fox. Julianne, who has CF herself, filmed Never Better in late 2020 and received great revi...
6 Sep 202240min
