Cindi Rogers is the mother of two sons with Full-Mutation Fragile X Syndrome, ages 29 and 31. Jake, her oldest son was diagnosed in 1991, just days after her youngest son was born, at which time he was also diagnosed. After some years of grieving, she and her husband, with the help of many experts in the Fragile X field, found ways to create a manageable, productive, and relevant life as a family. It has been her personal mission to share these strategies in hopes of generating ideas that families can implement in their own lives, while living with Fragile X Syndrome. Thus her book Becoming Mrs. Rogers: Learning to Live the Fragile X Way was written! You don’t want to miss the incredible wisdom and encouragement that Cindi Rogers shares with us!