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The Rare and Resilient - ONE in 5000 Podcast shares stories and information with members of the Imperforate Anus (IA) / Anorectal Malformation (ARM) global community. Produced by the ONE in 5000 Foundation, it is a resource for families, friends, teachers and health professionals to discover more about this relatively unknown condition and build a community of support and understanding for those living with it and their families. For further information, please refer to our www.onein5000foundation.org website. Podcast Disclaimer: This podcast series is presented for the purposes of sharing information and experiences with the IA/ARM community. The ONE in 5000 Foundation Inc. accepts no legal liability whatsoever arising from or connected to, the accuracy, reliability, currency, completeness of any material provided in this Series or the Interviews posted as part of it.
Episodes
Wednesday Sep 21, 2022
Wednesday Sep 21, 2022
For episode 36 we are joined by Nat from Melbourne, Australia, who is the mother of 18 month old Levi. She shares their journey of him being born with IA/ARM during COVID-19. Levi had his PSARP at only two months and his reversal at four months due to the uncertainty caused by Covid. Nat details how her family and medical team navigated their way through an incredibly difficult time with no access to family support due to lockdowns.
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