Meet Sara - Preparing Rare Disease Patients for School

This week Taylor and Liz are really excited to have Sara join and share the story of her journey with her son who was born with Imperforate Anus. Sara shares her journey in finding care for her son's rare condition. Additionally, Sara provides details on key information for families sending their rare disease kids back to school. Click here if interested in learning more about Imperforate Anus. Thanks for joining us, Sara!

Looking for updates or a way to connect with Taylor and Liz? Look for us on Instagram at the NotSoRarePodcast as well as on Facebook at the NotSoRarePodcast. Also, feel free to message us at notsorarepodcast@gmail.com. We love to hear from all of you!