The Big News!

OK I can't contain it any longer (hehe), we are officially moving! We are moving downtown that is:) We will be right across from the Marshall Middle School in a beautiful old building that is amazing. We have already started to paint and remodel so I will be posting pictures soon. And we will be having a HUGE Open House TBD that you won't want to miss out on. I am so excited about our new space, there is so much room and we have really tall ceilings (Yay). Wait till you all see, there are awesome spots right in the building for Senior Pictures the architecture is beautiful, and I feel so blessed that this spot became available right when I started looking. Yippee!!!!! Anyways, I will have pictures to show you all of our progress so stay tuned.

In the mean time I will post some pictures of my beautiful niece Grace Elaina she is such a joy to our family and she has been a huge part of our healing process. Not to mention is she not the most adorable thing you have ever seen:) I am not biased or anything. Enjoy! Everyone have a great weekend!

There is a special one for her Daddy and the Shubert Family:)

Contest Winner!

Congratulations to Gretchen ! She won a $15 Gift Card to Starbucks for sending in this picture. Thank you to everyone who participated in the little contest it fun to see all the entries.

I wanted to take the opportunity to do a little shout out to Simon and PKS, Simon has a rare condition that effects only 200 children in the world! To find out more visit the website at www. pkskids.net . Also I am going to paste this email Gretchen has sent me about a fun fundraiser for PKS Kids!

Superbowl Football Pool to Support PKS Kids!!!!

Each square is $10 (Of your $10 donation, five will go towards the pool and five will go to PKS Kids.)

$125 will be awarded at the end of the 1^st, 2^nd, and 3^rd quarter, and at the end of the game (4^th quarter OR overtime).

$500 will be donated to PKS Kids in Simon’s name!

You may contact me by phone 269-781-9221 or email gpeters@pkskids.net

PKS Kids is a wonderful non-profit organization that supports all families of children with Pallister-Killian Syndrome throughout the world! Each year we work to bring together doctors who specialize in this rare condition and families affected by PKS at an annual conference. Your donation to PKS Kids will help make this event possible. PKS Kids is a 501 (c) 3 organization and your donation is tax deductible. Pallister-Killian Syndrome occurs when there is a duplication of the 12^th chromosome and affects approximately 200 children in the world. It happens at the time of conception for no known reason. Please visitwww.pkskids.net to learn more about Pallister-Killian Syndrome. Thank you for your support!!!

~Gretchen Peters