Wednesday, September 22, 2010
Double Day at Duke!!
Posted by The Burgess Family at 12:57 AM 0 comments
Monday, June 14, 2010
A sad day

Posted by The Burgess Family at 7:46 PM 0 comments
Wednesday, May 19, 2010
A Day at Duke
First we had to go to the Duke Eye Center to meet with Dr. W. and let him check on Chayse and her progress. Chayse's eyes have gotten no worse, but they have not gotten any better either. We did learn today that her glasses were made with the wrong prescription in them, which didn't hurt her at all, but they were not strong enough to help her either. So, we are now without glasses for a week while the lenses get replaced with the correct prescription. Hopefully once they glasses are replaced, she will be able to focus and see correctly.
Posted by The Burgess Family at 8:12 PM 0 comments
Thursday, March 18, 2010
Occlusion Therapy
Chayse seems to be adjusting well to wearing her patch during her therapy hours. It is something we are able to do here in the home so that has made this part pretty easy so far. The first few minuets she has it on are a little challenging but once she gets ajusted to it, she does ok. She has run into the furniture a few times but I think that will get better as she gets used to using her eye again! I also think that this gives her a little headache though as it is pushing her brain and eye to work together in ways that they have not worked in a
while, but is what we are wanting to happen!
Posted by The Burgess Family at 12:34 PM 6 comments
The gift of sight
Posted by The Burgess Family at 11:36 AM 0 comments
Saturday, March 13, 2010
Hope
Tonight, I find myself thinking about sweet baby Hope. I am sitting here, in my home, with two wonderful and loved children. I see them play and interact and in the midst of it, I think about Hope and the moments we never had with her. The hour she was here was so short and yet it went by so fast. I know had her time been longer it would have been a time filled with pain and suffering due to her organ defects but I still find myself sometimes wondering about her smile or her laugh... things we will never know. I look at these two miracle children playing at my feet and my heart overflows with love. While we have a void in our lives that will never be filled, our lives are so full from these children. And I wonder, how is that possible. How did we get so blessed. God... He is so good.
My cup runneth over.
My cup runneth over.
Posted by The Burgess Family at 5:18 PM 1 comments

