PKD And The Gift Of Life, Feat. Patient Advocate Valen Keefer Wait, How Do You Spell That? A Rare Disease podcast

コンテンツは Patient Worthy によって提供されます。エピソード、グラフィック、ポッドキャストの説明を含むすべてのポッドキャストコンテンツは、Patient Worthy またはそのポッドキャストプラットフォームパートナーによって直接アップロードされ、提供されます。誰かがあなたの著作物をあなたの許可なく使用していると思われる場合は、ここで概説されているプロセスに従うことができますhttps://ja.player.fm/legal。

Wait, How Do You Spell That? A Rare Disease Podcast »
PKD and the Gift of Life, feat. Patient Advocate Valen Keefer

15d ago 40:10

MP3•エピソードのホーム

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

72 つのエピソード

#Fitness #Rare Disease #Patient Worthy