When Dee was diagnosed with stage 4 CKD she decided to share her journey online, creating a vlog before moving into podcasting in 2020. To listen to the first episode of Diary of a Kidney Warrior Podcast now, click on the links below.
Dee Moore's kidney journey
Diary of a Kidney Warrior Podcast
Dee says: “Diary of a Kidney Warrior Podcast is a space for honest conversations about kidney disease. I explore the realities of living with CKD – including the difficult and sensitive topics – while always holding onto hope. My aim is that listeners feel informed, supported, and less alone on their own kidney journey.” DKWP is now created in partnership with Kidney Care UK.
Every episode of the podcast explores different aspects of kidney disease. Whether you live with kidney disease, or a family or friend does, Diary of Kidney Warrior Podcast will help you learn more.
Diary of a Kidney Warrior Podcast episodes
New episodes of Diary of Kidney Warrior Podcast are available to download every other Monday from Podbean, Apple Podcast and Spotify. You can also listen to episodes on YouTube.
Look through a listing of all available Diary of Kidney Warrior Podcast episodes below.
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Episode 156
Diagnosed with PKD at 10: living with hereditary kidney disease
What is it like to be diagnosed with polycystic kidney disease (PKD) at just 10 years old – and to know it runs through your family? Dee Moore speaks with Natasja about her experience of PKD, a hereditary condition that has affected multiple generations of her family and which can cause chronic kidney disease.
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Episode 153
Living with ADPKD: a polycystic kidney disease story
What is it really like to grow up knowing kidney disease runs in your family? In this powerful episode of Diary of a Kidney Warrior Podcast, Dee is joined by Jamie from Texas, USA, who shares her lived experience of Autosomal Dominant Polycystic Kidney Disease (ADPKD) – a genetic kidney condition that can affect multiple generations.
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Episode 128
Beyond the diagnosis: Carl's story of resilience, transplant and hope
Dee sits down with Carl, whose diagnosis of vasculitis at 15 years old led to an unexpected battle with chronic kidney disease (CKD). Carl takes us through his diagnosis and treatment journey, culminating in dialysis and a kidney transplant. He also shares his experience as a father with CKD and compares renal care in the UK versus Australia.
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Episode 114
Rare Kidney Diseases: Katie's Journey with Loin Pain Haematuria Syndrome
Katie Newell shares her journey with rare kidney condition Loin Pain Haematuria Syndrome (LPHS), discussing its impact on her health and mission to raise awareness around LPHS.
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Episode 90
Needling for beginners part two: Dan’s kidney warrior story
Needling for beginners part two. In this second part of a three-part series, Dan Waters joins Dee Moore to share his inspirational kidney warrior story.