Ingrid Grenar
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.
top of page
Search
Ingrid Grenar
- Jul 11
- 1 min
Episode 17: WRESTLER Dustin Raynor AKA Dustin Bozworth
Ingrid chats to Dustin Raynor, better known as professional wrestler Dustin Bozworth, about living with cystic fibrosis.
Ingrid Grenar
- Jul 3
- 1 min
Episode 16: HOSPITAL
We update you on our CF hospital admission.
Ingrid Grenar
- Mar 28
- 1 min
Episode 15: BELLA POWELL
Ingrid sits down with Bella Powell, a young woman with Cystic Fibrosis who was the first in New Zealand to get Trikafta.
Ingrid Grenar
- Feb 26
- 1 min
Episode 14: PATRICK GOWER
Ingrid sits down with the well-respected and much-loved New Zealand journalist Patrick Gower.
Ingrid Grenar
- Jan 24
- 1 min
Episode 13: BACK TO SCHOOL
Ingrid chats school, camp and sports with Helen Ulyatt, mother to an active 9-year-old with Cystic Fibrosis called Sophia.
Ingrid Grenar
- Dec 4, 2022
- 1 min
Pharmac announce they will fund TRIKAFTA from April 2023
Pharmac announce they are to fund Trikafta in New Zealand for people with Cystic Fibrosis from April 2023.
Ingrid Grenar
- Nov 28, 2022
- 1 min
WTCF! nominated for NZ Podcast Award 2022
What the CF! A Cystic Fibrosis Podcast is nominated for Best Family Podcast as the NZ Podcast Awards
Ingrid Grenar
- Sep 6, 2022
- 1 min
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...
Ingrid Grenar
- Sep 5, 2022
- 2 min
Never Better is a witty must-see Covid-19 time capsule with a CF spin
We review Never Better by Julianne Fox.
Ingrid Grenar
- Aug 1, 2022
- 1 min
Episode 10: CF TODDLER
In this episode, Ian and I get to grips with life with a toddler with Cystic Fibrosis.
Ingrid Grenar
- Jul 12, 2022
- 6 min
‘People Say Really Stupid Sh-t To You When Your Child Has Been Diagnosed With Cystic Fibrosis’
This article was originally published on Capsule and reposted here with permission. When Ingrid Grenar founded ‘What The CF! A Cystic...
Ingrid Grenar
- May 18, 2022
- 1 min
Episode 9: TRANSPLANT
Lizzie McKay (Cystic Fibrosis NZ) shares her journey with Cystic Fibrosis and shares very candidly her journey to getting a lung transplant
Ingrid Grenar
- Apr 19, 2022
- 1 min
Episode 8: KALYDECO
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
Ingrid Grenar
- Mar 24, 2022
- 1 min
Episode 7: TRIKAFTA
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...
Ingrid Grenar
- Mar 17, 2022
- 2 min
A letter to Rt Hon Jacinda Ardern - I want hope for my son with Cystic Fibrosis
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...
Ingrid Grenar
- Sep 23, 2021
- 1 min
Interview on Magic Talk Radio
Magic Talk Interview with Carly Flynn 18th Sept 2021 chatting about life as a mum of a PWCF, Sweatember and Trikafta.
Ingrid Grenar
- Sep 16, 2021
- 1 min
The AM Show
The podcast gets a mention on the AM Show Good News segment, 9th September 2021.
Ingrid Grenar
- May 22, 2021
- 2 min
Andrew Little MP owes us an apology
The Cystic Fibrosis community is part of the 100k people that submitted a petition to parliament to increase Pharmac funding. We are...
Ingrid Grenar
- May 3, 2021
- 6 min
A message from a listener
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...
bottom of page