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.
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Ingrid Grenar
Jul 11, 20231 min read
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, 20231 min read
Episode 16: HOSPITAL
We update you on our CF hospital admission.
Ingrid Grenar
Mar 28, 20231 min read
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, 20231 min read
Episode 14: PATRICK GOWER
Ingrid sits down with the well-respected and much-loved New Zealand journalist Patrick Gower.
Ingrid Grenar
Jan 24, 20231 min read
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, 20221 min read
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, 20221 min read
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, 20221 min read
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, 20222 min read
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, 20221 min read
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, 20226 min read
‘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, 20221 min read
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, 20221 min read
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, 20221 min read
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, 20222 min read
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, 20211 min read
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, 20211 min read
The AM Show
The podcast gets a mention on the AM Show Good News segment, 9th September 2021.
Ingrid Grenar
May 22, 20212 min read
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, 20216 min read
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...
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