PKS Kids is a non-profit organization aimed at helping all people involved with Pallister-Killian Syndrome. For parents and other family members of loved ones with PKS you can expect to learn all about PKS while interacting with other families from around the world. Doctors and caregivers can expect to educate themselves about PKS by reading the latest research and connecting with doctors who have seen the syndrome first hand.
One mission of PKS Kids is providing hope and help to families. Whether it's sharing information and support or providing grant dollars for equipment and therapies, we want to help.
To promote research, provide education, and raise awareness within the medical community in order to ensure early diagnoses of children with Pallister-Killian Syndrome (PKS). To provide resources and support to families, therapists and caregivers of children with PKS.
Our vision is to ensure that no family receives a diagnosis without hope and up-to-date information. Our aim is to provide answers and resources and connect families for support and friendship.