My name is Holly. I created this blog to document my now 4 year-old daughter Jailynn's journey with ACC, cortical dysplasia, and epilepsy. Also her brain surgery (hemispherectomy)and recovery.
Thursday, February 26, 2009
6th floor
yesterday maybe 6 or 7 pm, Jailynn was moved out of PICU to the 6th floor. Once there she began running a fever. She is in good spirits but sleepy. My dad insisted that he was staying the night with her. He had caught a bus early in the morning yesterday and spent hours getting here from Pennsylvania. So finally he convinced me to go home so i would get some sleep. I did but my sleep was filled with crazy scary dreams all about Jailynn. I am waiting for jason to finish packing the coolor with his lunch and stuff and then we will head bak to the hospital. I called after we woke up and they said she was fine. Her neuro said yesterday she can possibly go home friday.
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