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

Ingrid chats to Dustin Raynor, better known as professional wrestler Dustin Bozworth, about living with cystic fibrosis.

We update you on our CF hospital admission.

Ingrid sits down with Bella Powell, a young woman with Cystic Fibrosis who was the first in New Zealand to get Trikafta.

Ingrid sits down with the well-respected and much-loved New Zealand journalist Patrick Gower.

Ingrid chats school, camp and sports with Helen Ulyatt, mother to an active 9-year-old with Cystic Fibrosis called Sophia.

Pharmac announce they are to fund Trikafta in New Zealand for people with Cystic Fibrosis from April 2023.

What the CF! A Cystic Fibrosis Podcast is nominated for Best Family Podcast as the NZ Podcast Awards

In this episode, Ian and I review the brilliant film Never Better and chat with its writer-director Julianne Fox. Julianne, who has CF...

We review Never Better by Julianne Fox.

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

This article was originally published on Capsule and reposted here with permission. When Ingrid Grenar founded ‘What The CF! A Cystic...

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...