WTCF! A Cystic Fibrosis Podcast

WTCF! 
A CYSTIC FIBROSIS
PODCAST

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    Episode 9: TRANSPLANT
    Ingrid Grenar
    • May 17
    • 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
    Episode 8: KALYDECO
    Ingrid Grenar
    • Apr 19
    • 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
    Episode 7: TRIKAFTA
    Ingrid Grenar
    • Mar 23
    • 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...
    A letter to Rt Hon Jacinda Ardern - I want hope for my son with Cystic Fibrosis
    Ingrid Grenar
    • Mar 16
    • 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...
    Interview on Magic Talk Radio
    Ingrid Grenar
    • Sep 22, 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.
    The AM Show
    Ingrid Grenar
    • Sep 15, 2021
    • 1 min

    The AM Show

    The podcast gets a mention on the AM Show Good News segment, 9th September 2021.
    Andrew Little MP owes us an apology
    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...
    A message from a listener
    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...
    Episode 6: BOOK
    Ingrid Grenar
    • Apr 26, 2021
    • 2 min

    Episode 6: BOOK

    Ingrid chats to Eilís Moroney, the author of 'Our Baby Has 65 Roses' and mum of a little person with CF - two-year-old AibhÍn, about...
    Episode 5: Dads
    Ingrid Grenar
    • Apr 12, 2021
    • 2 min

    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
    Episode 4: Genetics and Cystic Fibrosis with Kelly Sullivan Genetic Counsellor
    Ingrid Grenar
    • Mar 30, 2021
    • 1 min

    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.
    Episode 3: Mums
    Ingrid Grenar
    • Mar 15, 2021
    • 2 min

    Episode 3: Mums

    Sophie, Kayla and Jessica are all mums of little CFers born during the pandemic. We chat about Cystic Fibrosis and telling family.
    Episode 2: CFNZ Fieldworkers
    Ingrid Grenar
    • Mar 2, 2021
    • 2 min

    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...
    Episode 1. Diagnosis
    Ingrid Grenar
    • Feb 15, 2021
    • 2 min

    Episode 1. Diagnosis

    We discuss the journey to diagnosis for our son Orson at six months old. From pregnancy and birth, tests, diagnosis and processing the...
    WTCF! A Cystic Fibrosis Podcast - press release
    Ingrid Grenar
    • Nov 30, 2020
    • 2 min

    WTCF! A Cystic Fibrosis Podcast - press release

    Auckland couple launch a new podcast dedicated to Cystic Fibrosis - What the CF! A Cystic Fibrosis Podcast. Ingrid Grenar and Ian Wright...
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