The adventures of a very special little boy. Thursday, January 15, 2015. He was so excited after his visit with the horses Jeremiah and Modock that he decided to adopt several rare and special little horses. They constantly watch over him and he is always happy to reach out and find one nuzzling his hand. So we are one big horsey-family. Saturday, April 26, 2014.

Thursday, October 24, 2013. Well my latest update is a new picture of the family. Oh my how we have changed and grown. Thursday, August 15, 2013. School will start again soon, but not soon enough for her, she is bored with mommy. So here is my big girl, in her new wheelchair with a matching pink cast. Not to happy about it! Sunday, February 24, 2013. php? We also received a .

Welcome to the Foundation for Children with Microcephaly! We have created this website. To help and inform parents and families of children who have been diagnosed with. Microcephaly, Lissencephaly, Polymicrogyria and other closely related neurological. If your child has just been diagnosed, you have a million questions and thoughts running. It gets really frustrating when no one has the answers to any of your. We are here to help! Contact a parent now. Just try to help our .

Wednesday, March 20, 2013. 3 years to the Day. He was put in a medical coma on 3-19-10. The pictures were taken 3-20-10. The bottom picture shows how bad of we knew he was. This is what ENT gave us on the way out the door. Tuesday, January 1, 2013. Yes he flopped over from sitting.

Wednesday, January 16, 2013. A week and a half ago Gavin went in for a sedated heart echo, and to have his pacemaker read. I usually get nervous before these visits. I spend time wondering if we will get good, or not so good results. After we got home, the boys were asking me how it went, and then Nolan and Caleb started reminiscing about the days that Gavin spent a lot of time in the hospital. We were separated so often.

We May Not Have It All Together, but Together We Have It All! Saturday, April 13, 2013. Dear Friends and Family,. Forgive us for the silence! But much has happened since our last post, including the miraculous birth of our identical twin girls, Adelynn and Sarah! So we just began a new and improved blog and vlog to celebrate the miracle of family online with you! Meet us there at allboysbutnine. com! Or even better see our youtube channel www.

Monday, September 3, 2012. Kelsea had a wonderful first year of school. Kelsea is very shy by nature and will barely speak when adults are around.

An ordinary mom sharing glimpses of her life, including transracial adoption, special-needs kids, and the typical stuff of life. Posted by Kelly in Inclusion. My friend and I watched silently. It was as though I had been punched in the gut. I could not breathe as I watched them walk by. And then the tears came. And I realized that all the nights I.

Thursday, August 19, 2010. LAST WEEK WE HEADED TO IDAHO TO TAKE MICHAELA TO EFY AND THE REST OF US TO ATTEND THE MURDOCH REUNION. MICHALEA GOT TO SPEND THE LAST NIGHT BEFORE WE LEFT. ALL THE KIDS TIE DYED SHIRTS. WE SPENT OUR TIME IN A BEAUTIFUL CABIN. YOU CAN SEE THE BEAUTIFUL TETON MOUNTAINS FROM THE FRONT WINDOW. MCKENZIE GOT TO SPEND TIME WITH HER COUSIN AMBER. MICHAELA AND HER FREIND FROM MESQUITE, APRIL ATTNEDING EFY.