Description Our guest this week is Swapna Sasidharan, of Schaumburg, IL, a Vice President of Technology at ABCO Holdings, mother of two children, incuding one with POGZ, and founder of the Cure POGZ Disorder Foundation.  Swapna and her husband Sandeep are the proud parents of twoi 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 about rare diseases and inspired to find a cure for POGZ, the rare disorder her son has, Swapna is dedicated