WTCF! A Cystic Fibrosis Podcast

When our son was diagnosed with Cystic Fibrosis at six months old we were shocked and devastated. From the first moment seeing his foggy little lungs, we knew this was gonna be a rollercoaster and we weren't wrong. What the CF! was born out of a curiosity to learn more, support others, and share experiences while we navigate our own CF journey. We want to tell the stories of others and answer the FAQ's that come along with a diagnosis. We'll seek the knowledge of experts and those living with CF to help to paint a well-rounded vision of what living with Cystic Fibrosis.

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Avsnitt(20)

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 knows all too well the pain and fear of diagnosis, the heartbreak ...

1 Mars 202126min

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 news. It's emotionally a highly charged episode but we end up lau...

15 Feb 202135min

TRAILER - Ep. 1 - Diagnosis

Check out the trailer for the very first episode of What The CF! A Cystic Fibrosis Podcast - COMING SOON - episode 1, we chat about our journey to getting a diagnosis for our son - just prior to the...

8 Feb 20211min