PKD and the Gift of Life, feat. Patient Advocate Valen Keefer episode artwork

EPISODE · Aug 30, 2024 · 40 MIN

PKD and the Gift of Life, feat. Patient Advocate Valen Keefer

from Wait, How Do You Spell That? A Rare Disease Podcast · host Patient Worthy

In this episode of the podcast we speak to Valen Keefer, a professional speaker and patient advocate who was diagnosed with polycystic kidney disease (PKD) at age 10. Valen has faced a number of challenges in her journey, including a double organ transplant, and now inspires other PKD and chronic illness patients by sharing her story.  Connect with Valen Keefer: Website - Podcast -  Facebook - Instagram - X - LinkedIn Editor's Note: Chronic conditions and rare diseases don’t discriminate. Patient Worthy and our partners are interested in amplifying the voices of those from all identities and backgrounds. If you have a story to share, learn more about how your voice can help spread awareness and inspire individuals from all walks of life here: https://shorturl.at/sPV02

Episode metadata supplied by the publisher feed · Published Aug 30, 2024

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PKD and the Gift of Life, feat. Patient Advocate Valen Keefer

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This episode was published on August 30, 2024.

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