Listen Score
LS 26
Global Rank
TOP 10%

ABOUT THIS PODCAST 🔗

Update frequency:
every 42 days
Average audio length:
38 minutes
Has sponsors
English
United States
17 episodes
since April 1, 2024
episodic

LATEST EPISODE 🔗

"Now what?" It's the question Valen asked 25 years ago as an 18-year-old newly under the care of nephrologist Dr. Terry Watnick, and it's the same question she's answering in this episode for anyone facing a new kidney disease diagnosis today. Valen reunites with Dr. Watnic…

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PREVIOUS EPISODES

In recent years, new KDIGO guidelines for both IgA nephropathy (IgAN) and PKD have been released – but what does this mean for patients and their loved ones? In this episode, Valen talks with Mike Spigler, Chief Program Officer and Vice President of Strategic Partnerships, Research and Education at…
Behind John Fluevog's decades of iconic shoe design is a personal story of kidney disease, transplant, and gratitude. Valen talks with John about his creative journey, his diagnosis of polycystic kidney disease, and the transplant that changed his outlook and inspired him to create shoes carry…
The future of rare kidney disease treatment is full of hope and innovation. Valen chats with Dr. Jill Green and Dr. Pranav Garimella about groundbreaking research and why the patient voice matters when working with advocacy groups and industry to shape future treatments. Leave feeling inspired and …
Patients are key to advancing rare disease treatment. IgA nephropathy (IgAN) patient Russ Roberts and his nephrologist Dr. Arnold Silva discuss the role of clinical trials in rare kidney disease research and how patients and providers can work together to shape the future of treatment. Get practica…
Strong relationships with your healthcare team are essential for managing complex care. Valen and her nephrologist, Dr. Adarsh Bhat, explore how patients and providers can collaborate, while transplant recipient Tristan Mace shares tips on managing a complex care team. Discover valuable tips on bui…
Strong relationships with your healthcare team are essential for managing complex care. Valen and her nephrologist, Dr. Adarsh Bhat, explore how patients and providers can collaborate, while transplant recipient Tristan Mace shares tips on managing a complex care team. Discover valuable tips on bui…
Caregiving is a shared journey. Valen is joined by mother-daughter duo Linda and Autosomal Recessive Polycystic Kidney Disease and Congenital Hepatic Fibrosis (ARPKD/CHF) patient Claire Bevec, along with Valen’s husband Noah, to talk about the evolving dynamics of caregiving. Hear advice and strate…
Caregiving is a shared journey. Valen is joined by mother-daughter duo Linda and Autosomal Recessive Polycystic Kidney Disease and Congenital Hepatic Fibrosis (ARPKD/CHF) patient Claire Bevec, along with Valen’s husband Noah, to talk about the evolving dynamics of caregiving. Hear advice and strate…
Advocacy starts with finding your voice. Valen and chronic rare disease patient advocate Swapna Kakani discuss how they discovered their purpose in patient advocacy and offer practical tips for anyone wanting to make a difference. Learn how to use your voice to drive change and support the rare dis…
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