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Pierre Robin Network is comprised of parents, caregivers, family members, medical professionals and adults with PRS. The purpose of our group is to share experiences with each other to ...(more)

For parents of children born with cleft lip and/or cleft palate. Our list is open to all to freely express their feelings, get support and to learn in a positive environment. We have a ...(more)

Welcome to CLAPA's Left Clip Forum for young people with an interest in cleft lip and/or cleft palate. This is a place where you can exchange ideas and opinions on anything from ...(more)

CleftClub.com is for providing information and support for those dealing with cleft lip and/or palate, whether you were born with it, are parents of a cleft child, or are a relative or ...(more)

Welcome to the Jaw Distraction/Craniofacial Surgery Discussion Group! This group is for all whose lives have been affected by a craniofacial difference or anyone who has an interest in ...(more)

Welcome to the Crouzon Support Network! An online support group for individuals and families who are dealing with Crouzon Syndrome and other craniofacial anomalies. A place to share ...(more)

I wanted to begin a message site for children. My son has microtia, a deformity of the ear, and I have had a hard time finding chat groups for children with facial deformities. Please ...(more)

This club is I guess, intended for but not limited to teens with a cleft palate and/or lip. Anyone is welcomed to join and talk about anything... I am 16, with a cleft lip and palate, ...(more)

I am the mother of a child with Muenke syndrome, and have had difficulty finding other families who are dealing with this as well. I am hoping by putting this group up I can meet other ...(more)