Special Fathers' Network Podcast

Our guest this week is Swapna Sasidharan, of Schaumburg, IL, a Vice President of Technology at APCO Holdings, mother of two children, including one with POGZ, and founder of the Cure POGZ Disorders Foundation. Swapna and her husband, Sandeep, have been married for 17 years and are the proud parents of two children: daughter Sloka (12) and son Ved (10) who has POGZ, a rare genetic disorder characterized by: developmental delays, cyclic vomiting, autism, microcephaly and gastrointestinal issues.Educated as an engineer, informed about the challenges of rare diseases and inspired to find a cure for POGZ, the rare disorder her son has, Swapna and the team at the Cure POGZ Disorders Foundation are dedicated to finding treatments and hopefully a cure for POGZ and other rare diseases.We’ll hear all about Swapna's background growing up in a traditional Indian family, about her career, her journey as a rare disease parent, her understanding about acceptance (the difference between surrender and acknowledgement) and her