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.
Wednesday, June 25, 2008
I left "more" and "wall" off the list. She also said "go" in therapy today. Oh, and she also says "ball" spontaneously. I knew I was forgetting something.