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 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
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
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
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...
Ingrid Grenar
Apr 13, 20212 min read
Episode 5: Dads
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
Ingrid Grenar
Mar 30, 20211 min read
Episode 4: Genetics and Cystic Fibrosis with Kelly Sullivan Genetic Counsellor
Kelly explains what causes CF, what happens in your genetic counsellor meeting, and the options for couples wanting more children.
Ingrid Grenar
Mar 2, 20212 min read
Episode 2: CFNZ Fieldworkers
Ingrid chats to Sue Lovelock, Southern Fieldworker for Cystic Fibrosis New Zealand. Sue has worked as a fieldworker for 14 years and...
bottom of page