In this season of gratitude, reflection and community, we wanted to share something special with you. The enclosed story is a real and unscripted account of one family’s experience at MUSC.
Jenna and Stephen Brown faced a devastating diagnosis for their unborn baby girl: the most severe form of spina bifida. They put their faith in a team of caregivers here at MUSC, and they allowed us to join them on their journey – from their baby shower to the delivery room, through little Harper’s spinal repair and on to life today. We wanted to share that journey with you to demonstrate in the most authentic way why your support matters so very much. Because without that generous support, experiences like Jenna, Stephen and Harper’s – experiences that happen every day across our campus – simply wouldn’t happen.