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...

My name is Ingrid and I am the mother of a two-and-a-half-year-old with Cystic Fibrosis (see the cutie below). I also host a podcast...

Magic Talk Interview with Carly Flynn 18th Sept 2021 chatting about life as a mum of a PWCF, Sweatember and Trikafta.

The podcast gets a mention on the AM Show Good News segment, 9th September 2021.

The Cystic Fibrosis community is part of the 100k people that submitted a petition to parliament to increase Pharmac funding. We are...

The first series of What The CF! A Cystic Fibrosis Podcast has been an amazing and emotionally exhausting project and I don’t regret it...

Ingrid chats to Eilís Moroney, the author of 'Our Baby Has 65 Roses' and mum of a little person with CF - two-year-old AibhÍn, about...

Eddie, Henry and David are all parents of little CFers. Ian chats to these dads about diagnosis, telling friends and family and what NOT to

Kelly explains what causes CF, what happens in your genetic counsellor meeting, and the options for couples wanting more children.

Sophie, Kayla and Jessica are all mums of little CFers born during the pandemic. We chat about Cystic Fibrosis and telling family.

Ingrid chats to Sue Lovelock, Southern Fieldworker for Cystic Fibrosis New Zealand. Sue has worked as a fieldworker for 14 years and...

We discuss the journey to diagnosis for our son Orson at six months old. From pregnancy and birth, tests, diagnosis and processing the...

Auckland couple launch a new podcast dedicated to Cystic Fibrosis - What the CF! A Cystic Fibrosis Podcast. Ingrid Grenar and Ian Wright...