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.

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.

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...

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...

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...

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.

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