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.
Friday, February 6, 2009
Going to see Jailynn
I called last night before bed and after waking up this morning. both times I was told by Jailynns PICU nurse that she was doing well and no problems. They have increased meds to make her stay still and not turn her head. they also retaped her head I have a few pics from yesterday