Pallister-Killian Syndrome - Guest Gretchen Peters

In recognition of Rare Disease Day February 28th, 2011 Tara talks with Gretchen Peters, mom to Simon, about his diagnosis of PKS and her involvement with PKS KIDS. A non-profit whose mission is 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). And to provide resources and support to families, therapists and caregivers of children with PKS.