Every parent hopes for a healthy, bouncing baby complete with ten fingers and ten toes. Dreams of football players, future presidents or homecoming queens dance though an expecting parent's head.... Nothing is more devastating than when these dreams are taken away from you.
When a family discovers their child has Spina Bifida, the world quickly becomes consumed with fear of the unknown, fear for the future, and mourning for dreams that may never come true.
The SBAG has developed a program, though a team of volunteers, that helps move families past fear. New families are teamed up with our Guardian Angel parents willing to share experiences, answer questions and help guide new families through the complex world of having a special needs child.
If you are looking for support or would like to participate in this program as a mentor please email firstname.lastname@example.org