The journey of Schuyler Rummel-Hudson began with a pediatrician's inquiry about her speech development, leading to a diagnosis of bilateral perisylvian polymicrogyria, a rare neurological disorder. This revelation provided her family with clarity about the challenges they faced, navigating a complex landscape of medical uncertainty, emotional turmoil, and fluctuating hope. The narrative explores their resilience and the ongoing impact of this diagnosis on Schuyler's life and her family's journey.
