Ingrid GrenarMay 171 minEpisode 9: TRANSPLANTLizzie McKay (Cystic Fibrosis NZ) shares her journey with Cystic Fibrosis and shares very candidly her journey to getting a lung transplant
Ingrid GrenarApr 191 minEpisode 8: KALYDECOChris 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 GrenarMar 231 minEpisode 7: TRIKAFTAWelcome 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 GrenarMar 162 minA letter to Rt Hon Jacinda Ardern - I want hope for my son with Cystic FibrosisMy 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 GrenarSep 22, 20211 minInterview on Magic Talk RadioMagic Talk Interview with Carly Flynn 18th Sept 2021 chatting about life as a mum of a PWCF, Sweatember and Trikafta.
Ingrid GrenarSep 15, 20211 minThe AM ShowThe podcast gets a mention on the AM Show Good News segment, 9th September 2021.
Ingrid GrenarMay 22, 20212 minAndrew Little MP owes us an apologyThe Cystic Fibrosis community is part of the 100k people that submitted a petition to parliament to increase Pharmac funding. We are...
Ingrid GrenarMay 3, 20216 minA message from a listenerThe 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 GrenarApr 26, 20212 minEpisode 6: BOOKIngrid 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...
Ingrid GrenarApr 12, 20212 minEpisode 5: DadsEddie, 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 GrenarMar 30, 20211 minEpisode 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 GrenarMar 15, 20212 minEpisode 3: MumsSophie, Kayla and Jessica are all mums of little CFers born during the pandemic. We chat about Cystic Fibrosis and telling family.
Ingrid GrenarMar 2, 20212 minEpisode 2: CFNZ FieldworkersIngrid chats to Sue Lovelock, Southern Fieldworker for Cystic Fibrosis New Zealand. Sue has worked as a fieldworker for 14 years and...
Ingrid GrenarFeb 15, 20212 minEpisode 1. DiagnosisWe discuss the journey to diagnosis for our son Orson at six months old. From pregnancy and birth, tests, diagnosis and processing the...
Ingrid GrenarNov 30, 20202 minWTCF! A Cystic Fibrosis Podcast - press releaseAuckland couple launch a new podcast dedicated to Cystic Fibrosis - What the CF! A Cystic Fibrosis Podcast. Ingrid Grenar and Ian Wright...