PKS KIDS

A Forum For Those Touched By Pallister-Killian Syndrome

Gretchen & Simon

PKS Kids Face2Face 2010

Event Details

Time: June 24, 2010 at 6pm to June 27, 2010 at 12pm
Location: Mount Laurel Marriot and Coco Key Water Park, NJ
City/Town: Mount Laurel, NJ
Website or Map: http://www.cocokeywaterreso...
Phone: 1-877-231-7703
Event Type: medical, conference
Organized By: PKS Kids board
Latest Activity: Nov 29

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Event Description

Planning for our 3rd medical conference is underway right now. Although this is just to get us started (more emails and registration requests will be coming), please use the RSVP here to let us know if you're thinking of attending.

Please watch Ning, your email and the website for lots more details!!

We have rooms booked at the Mount Laurel Marriott and Coco Key Indoor Water Resort. Hotel rooms are $119.00 per night. If you are interested in booking at this time you may call Toll-free:
and ask for the PKS Kids reservation.

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Gretchen & Simon Comment by Gretchen & Simon on November 28, 2009 at 10:16pm
Susan, I can't wait to see Brian (and mom and dad!) again! :)
Susan Comment by Susan on November 28, 2009 at 10:07pm
Brian and his mom and dad plan on coming and will love seeing all of your young children. For those who haven't met Brian, he will almost be 28 years old then and he loves to travel.
Roxanne Garrigus-Case Comment by Roxanne Garrigus-Case on November 13, 2009 at 9:25pm
Of course the Case's do not want to miss it!! We will figure out a way to cross the continent!! Can't wait to see everyone and catch up!!!
Gretchen & Simon Comment by Gretchen & Simon on November 8, 2009 at 8:07pm
Sandra, we so understand what you mean! There may be more to come on this in the next few weeks. We'll let you know. :)
Sandra & Yara Comment by Sandra & Yara on November 6, 2009 at 3:02am
We'll try to come over, all the way from the Netherlands! We're looking for local sponsors who might help us getting there. So it's still unsure... But we'd like very much to come and hear all about PKS. Yara is only 6 months old and we want to find out everything there is to know about the syndrome.
Is there maybe a PKS fund that could support us (partially) in coming to the States? There are 2 more families in the Netherlands who'd like to come, but heey, finances.... :( Hopefully it will all work out for us!
Quist Family Comment by Quist Family on November 3, 2009 at 11:09pm
We are very much hoping we can attend. Will know more after the first of the year..Thank you SO MUCH for organizing this fantastic event again!
Gretchen & Simon Comment by Gretchen & Simon on October 30, 2009 at 2:50pm
YAY Beth! Hope all you ladies and your families can come :) It's SO MUCH fun!
Beth Berry Comment by Beth Berry on October 29, 2009 at 9:51pm
hoping to attend. Rilla will be a Berry by then, yeah!!!!
Noelle & Nasaya Coleman Comment by Noelle & Nasaya Coleman on October 29, 2009 at 1:53am
Would really like 2 attend as well.....will b working hard on it.
Abbey, Brayden, Cory Depoorter Comment by Abbey, Brayden, Cory Depoorter on October 28, 2009 at 6:22pm
we are hoping to go... we wil have another baby by then!!!!!

Attending (10)

Susan Roxanne Garrigus-Case Tom Amber and Shelby the zanes k Small Kate Elizabeth & Anthony Kelsey/ cammie Barclay family Gretchen & Simon

Might attend (10)

Christine (Airyn) Marcel en Liesbeth Austin (Amy Fulwiler) Sandra & Yara Quist Family Gina Smith Beth Berry Noelle & Nasaya Coleman Abbey, Brayden, Cory Depoorter Becky, Scott & Devon Gardner

Not Attending (2)

Natasha Goodman Madeleine Wilkinson

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