Well - Thursday is the day that we have our next MRI of the brain and see the neurosurgeon. We are hoping that the brain has grown and the fluid is decreasing. This is always a stressful visit and I am sure that I will not sleep tonight.
The good news is that she is making more noise and even laughing on the rare, sweet occasion. I want everything for this sweet little girl - I want her to be able to walk and crawl. I want for her to be able to look at my face and see me smiling at her. I want to hear her giggle as we play. These are the things I pray for each day. I know, one day at a time.
Thank you all again for all the prayers. We love you all!
Wednesday, February 3, 2010
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