Debra Gilcrease resides in Fort Worth, TX. She is the mother of Bobby whom the story is about. Bobby was diagnosed with LGS (Lennox-Gastaut Syndrome) at 12 months old. Since his passing in 2012, Debra has dedicated herself to write about what an extraordinary child, young man and young adult he became. Her hope in writing this book is to share the joys, laughter and experiences with other children so they can see that having a brother or sister with special needs is no different than anyone else.
