We are here to help and support you.  Our group of caregivers and parents are from all over the world. We laugh, we cry, and CELEBRATE every milestone our little ones make together.  We are a FAMILY!  If you are a parent or caregiver of a child that has a SYNGAP mutation, please reach out to us. We are from all walks of life. We are from different cultures and different languages. The love and determination we share for these beautiful people bring us together. We welcome you and know that you are not alone!