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2: Raising young children with PKU - an interview with Lacy Shaffer and Julie Bolduc DeFilippo
Manage episode 303617693 series 2989272
Caring for Rare: Stories of Rare Metabolic Disorders and Nutricia North America에서 제공하는 콘텐츠입니다. 에피소드, 그래픽, 팟캐스트 설명을 포함한 모든 팟캐스트 콘텐츠는 Caring for Rare: Stories of Rare Metabolic Disorders and Nutricia North America 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.
Moms Lacy and Julie: Raising children with phenylketonuria (PKU)
Forming community is essential for many people and caregivers living with rare metabolic disorders. In this episode, moms Lacy and Julie, who didn’t know each other previously, tell their stories of bringing up children with phenylketonuria (PKU). They cover navigating their children’s special diets with family and friends, dealing with feelings of isolation, as well as the joys of watching their children grow from babies to personality-filled kids!
This episode was produced by Alletta Cooper, Ulrike Reichert, and Kate Miley for Nutricia North America. The music featured in this episode is Look Inside by Sirus Music, and Sunbang by Elephant Music.
Contact us at NutritionServices@nutricia.com or NutriciaMetabolics.com
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