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.
Saturday, February 14, 2009
mri
Jailynn had her MRI they told me they would general anesthesia and no ventilator this time! We are waiting for results now, do no know how long that will take. They decided to stop the EEG. Jailynn has been awake today but not very responsive this morning.she is slowly responding a bit more. She does kinda respond to touch but she still isn't right. Jason and I are going to advocate for her to get her back on a plan to eat soon, atleast on clear liquids soon, she is trying to chew her lips and everything else. I am thinking we will not be in the picu much longer. My aunt called and she is going to bring us dinner
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