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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.

Ingrid Grenar
Jul 29, 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
Mar 28, 20231 min read

Episode 14: PATRICK GOWER
Ingrid sits down with the well-respected and much-loved New Zealand journalist Patrick Gower.

Ingrid Grenar
Feb 26, 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
Jan 24, 20231 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
Dec 4, 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 24, 20221 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
Mar 17, 20222 min read
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