Kyle’s Schizencephaly Blog

One more night!

July 27th, 2009

•   Today Kyle finished his last therapy session. He worked hard and was ready to get it over with. Wendy and Dr. Tony stopped to ask us what we thought about the stem cell treatments and they told me to be honest. I told them that I don’t know if the stem cells did him any good or the therapy, but it was a big accomplishment that he could pull himself into a sitting position. Dr. Tony seems to think that it is the stem cells. Whatever it is I plan on working him so he can continue to make more progress. Dr. Tony said that the stem cells have not settled yet and we should see results for the next several months. So that sounds good to me. I would much rather see the results at home with all of my family and friends. Now, our China family was very supportive as well. They know how important the little achievements are and they were not afraid to tell Kyle how proud they were of him. We will miss all of our new friends, but we’re so ready to get home.
•   We loaded up all of our stuff from the hospital and told everyone goodbye. Georgina cried and Lawerence said she does that everytime. We wish everyone at the hospital lots of luck! We came to enjoy our last night at the Holiday Inn. Although we don’t get to sleep late the sun still will not shine in at 4:30 because the curtains are so dark! We’ll also get to take a bath. We’ve been taking showers for a month so I’m going to soak in the tub and it’s so big Kyle will probably swim in it.

    So this is the last time I’ll post from China! Next you’ll be reading updates from Louisiana, and maybe Tennessee if we ecide to go on a good old American Vacation one day!

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