Ingrid chats to CFNZ Chief Executive, Lisa Burns. They discuss what CFNZ does for CFers and their families throughout their lives.

We update you on our CF hospital admission.

In this episode, Ian and I get to grips with life with a toddler with Cystic Fibrosis.

Lizzie McKay (Cystic Fibrosis NZ) shares her journey with Cystic Fibrosis and shares very candidly her journey to getting a lung transplant

Chris Macleod is a Candian with CF who was one of Canada's first patients on Kalydeco ten years ago. He’s now 52 and has advocated for CF ov

Welcome to Season 2 or What the CF! We're so happy to be back and ready to share lots of CF stories about treatment with you. If you're...