You may have arrived at this page because you are the parent, family member or friend of a person affected with Cri Du Chat Syndrome, or some other anomaly of Chromosome 5. We hope that this site will provide you with information and encouragement.

While an unexpected diagnosis may feel frightening, we would like you to be inspired by the family stories that have been shared. When you feel ready, we encourage you to read the message for new parents written by the founding members of the support group. We do not profess to be experts, but we would like to share our experiences of Cri Du Chat Syndrome with you, and to extend a hand of friendship and support. Connecting with others can provide encouragement during times of challenge and times of celebration as your child develops. Your child is a beautiful and unique individual with so much to offer you and the world.