On May 10, 2006, at only 6 months old, Sophie was diagnosed with Infantile Spasms...a RARE and CATASTROPHIC form of epilepsy. She continues to battle this disorder on a daily basis. Only after she had the majority of her left hemisphere of her brain removed (on May 29, 2009) has she had a relief in seizures (though she continues to show spiking in her EEG). She has shown much improvement in development since the surgery.
Sunday, September 16, 2007
Yet Another Medication Increase...
We increased Keppra on Saturday morning. Sophie now gets 125mg in the AM and 125mg in the PM. She was so completely out of it on Saturday. Luckily, it was just a fluke because she seemed to be in a better mood today.
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