Pallister-Killian Syndrome

PKS is a rare chromosomal disorder. PKS Foundation of Australia is a not for profit organisation aimed at generating awareness about the disorder within the general community and medical professionals; supporting kids and families of those affected by PKS achieve a better quality of life, through therapy and equipment support and generating sufficient resources to fund research into many of unknown facets of this disorder.

Donate Online

To make a secure online donation, please click on the "Make a Donation" image below.

PKS Family Fun Run/Walk

The NSW branch is organising its First PKS Family Fun Run/Walk on the 28th of July at Lane Cove National Park to generate awareness about the disorder and raise funds. Download Registration Form. For more information about the event, please click here.