Second Annual PKS Family Reunion
Last year, we attended what was most likely the first ever international Pallister Killian Mosaic Syndrome gathering, with around 15 families meeting to discuss life with PKS among ourselves and a small group of medical professionals.
Based on that resounding success, a second gathering has been planned for early August in Columbus Ohio. Visit the PKS Support Yahoo Group for more info!
A Work of Art
Our children have been on many trips with us to help promote Mom’s artwork, but this father and son team has taken artistic collaboration to the next level.
Ben and his son Bennie’s creations, as well as Dad’s journal are available at benandbenniewaddell.blogspot.com
PKS In the News: England
The Press reports today about a young child with PKS who was recently diagnosed with another rare condition: Kawasaki Syndrome.
From the article: “He spent the next few days being closely monitored in hospital, but has now recovered enough to come home and will be checked for heart complications in two weeks.”
PKS Kids Logo
This weekend the PKS Board chose among the submitted logos, with this red and black design being the clear favorite among the 14 voters.
It’s a good design, and I’m sure once I learn to make the distinction between the recent non-profit and the larger PKS Support community, I’ll cause less trouble. 
Logo Ideas for PKS Kids
Here are a few logo ideas for the new foundation:
The circle logo is Veronica’s idea, but I added the exclamation.
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