PKS KidsTM was started by a small group of parents in 2006. Their purpose was to promote Pallister-Killian Syndrome and raise awareness through this non-profit organization.

Dawn lives in
Mike Zane, Vice-Chairperson
Michael is Vice President of Audience Development for CMP Technology, a
marketing solutions company serving the technology industry. He graduated from
the
Michael has been involved in the media business for over 17 years and currently
oversees a department of 32 people recruiting audiences for publications, live
and online events, email newsletters and gated online communities.
Michael lives in
involved in PKS KidsTM, and 3 kids. Jake, diagnosed with PKS is 3 years old. Jake
is the big brother to a sister, Kayla and brother, Brandon, who are 20 month old
twins.
Cammie Gray, Treasurer
Cammie Gray is married and has 4 children. Cammie worked eight years at a mental health insurance company and six of those years were spent in the Purchasing/Finance department. Her third child has Pallister-Killian Syndrome. After looking for 2 years for the reason her child was having problems and not knowing what was wrong, she knows the importance of educating the medical community about PKS. She has very high hopes for the success of this organization.
Gretchen’s youngest child, Simon, was born in 2004 with Pallister-Killian Syndrome. Not having informational resources to help her deal with the diagnosis, Gretchen was determined to help others navigate through the world of PKS. To update friends and family, she created a website for her son and she's thrilled to know that it has been the first point of information for several families. Not wanting to stop there, she hopes that PKS KidsTM will help to make information about Pallister-Killian widely available for those who are still searching. Gretchen lives in
Additional board members:
Medical Advisory Chair: Dana Paglia
Finance Chair: Cammie Gray
Education & Promotions Chair: Gretchen Peters
Member-at-Large: Kate Hettiger