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Alport Syndrome Journey as a Patient, Mother and Nurse
Manage episode 287336904 series 2861129
Tammy Flynn, Tammy Flynn: podcaster, and Special needs advocate a에서 제공하는 콘텐츠입니다. 에피소드, 그래픽, 팟캐스트 설명을 포함한 모든 팟캐스트 콘텐츠는 Tammy Flynn, Tammy Flynn: podcaster, and Special needs advocate a 또는 해당 팟캐스트 플랫폼 파트너가 직접 업로드하고 제공합니다. 누군가가 귀하의 허락 없이 귀하의 저작물을 사용하고 있다고 생각되는 경우 여기에 설명된 절차를 따르실 수 있습니다 https://ko.player.fm/legal.
As we wrap up our Alport Awareness Series & support National Kidney & Alport Syndrome Awareness Month, I am so excited to welcome to the show, Cassandra Smith ICU Nurse and Volunteer Patient Advocate, Alport Foundation.
Cassie Smith, a Kentucky native, is a registered nurse and mom to three young children. She was first diagnosed with Alport syndrome in late childhood. Two of her three children were diagnosed in early 2019. Both her professional and personal experiences make her passionate about patient advocacy. Cassie recently accepted the opportunity to Co-Chair the newly established Emerging Leadership Council for Alport Syndrome Foundation. In this role, she is volunteering with others to better address the unique needs of Alport patients in the 25-35 year old age range.
Listen in as Cassie shares her journey of rare disease from the perspective of patient, parent and nurse.
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