{"id":7269,"date":"2021-10-12T21:12:23","date_gmt":"2021-10-13T01:12:23","guid":{"rendered":"http:\/\/www.nutriciametabolics.com\/?p=7269"},"modified":"2025-06-20T02:38:54","modified_gmt":"2025-06-20T06:38:54","slug":"blog-caring-for-rare-podcast-season-1-episode-1","status":"publish","type":"post","link":"https:\/\/www.nutriciametabolics.com\/en-us\/blog\/caring-for-rare-season-1-episode-1\/","title":{"rendered":"Caring for Rare Podcast: Season 1, Episode 1"},"content":{"rendered":"\n

Raising Young Children With PKU \u2013 An Interview With Lacy Shaffer And Julie Bolduc Defilippo<\/h2>\n\n\n\n
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Left: Lacy (second from left) and her family. Right: Julie (back row, right) and her family.<\/figcaption><\/figure>\n\n\n\n

Nutricia North America\u2019s new podcast \u2013 Caring for Rare \u2013 explores what life is like with a rare metabolic disorder such as phenylketonuria (PKU), maple syrup urine disease (MSUD), and homocystinuria (HCU). Episodes feature families\u2019 personal stories of inborn errors of metabolism. Our guests on the show share their difficulties at diagnosis, changes they made to adapt to condition management, everyday joys, and more.<\/p>\n\n\n\n

Though these disorders are rare, it is possible to find community and support. We hope you\u2019ll feel comfort and connection in the stories of Caring for Rare.<\/p>\n\n\n\n

Listen now, or find Caring for Rare on Apple<\/strong><\/a>, Google Podcast<\/strong><\/a>, Amazon music<\/strong><\/a> and other podcast hubs!<\/h2>\n\n\n\n
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