CJR
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Let me start by saying, "I'm SORRY!" No, I haven't fallen off the face of the earth...I've just fallen into the Twilight Zone! LOL. I guess I didn't realize how long it's been since I've popped in for a visit here. But now, I realize how much I've missed it!
I'll try to catch up on Shan's story some. She was diagnosed in Feb of '08. We spent the day after her 1 year anniversary at the ER yet again. I think this was our 5th trip with her. Before E she had NEVER been to the ER. Now, unfortunately, it doesn't even faze her. We have started Keppra XR and then reduced it due to severe agitation and then added Depakote ER back on. That is her current cocktail.
However, the Neuro told us that she is not controlled with this level of drugs. So my nearly 12 year old daughter said this to the Neuro, "I've been living with seizures all of my life without knowing it. What I did know was that I was flakey and different but that I was happy. I don't want to take higher doses of these meds because then I can't be happy. What is the point of full and total seizure control now, anyways? I can't drive a car...I'm a kid. Besides, with my hormones all out of whack because of puberty we aren't gonna get control right now, are we?" (proud mama moment::rock
The Neuro took a look at me and said, "How do you fight with her?" I answered, "I don't! I listen to her...She makes good points and she knows what she can handle better than I do." So the Neuro was convinced to let Shan call the shots...for now.
Now, if only I could convince the school that Shan and I know more about what she needs to be successful than they do. She has yet another 504 meeting tomorrow in which their personal physician consultant will give us a classroom evaluation of Shan's needs. I would like to believe that this will lead to better management of Shan's case (after all, it can't get much worse) but I have a sneaky suspicion that they're going to use this consultant to reduce their responsibility and/or the services that they offer Shan.
I'll try to catch up on Shan's story some. She was diagnosed in Feb of '08. We spent the day after her 1 year anniversary at the ER yet again. I think this was our 5th trip with her. Before E she had NEVER been to the ER. Now, unfortunately, it doesn't even faze her. We have started Keppra XR and then reduced it due to severe agitation and then added Depakote ER back on. That is her current cocktail.
However, the Neuro told us that she is not controlled with this level of drugs. So my nearly 12 year old daughter said this to the Neuro, "I've been living with seizures all of my life without knowing it. What I did know was that I was flakey and different but that I was happy. I don't want to take higher doses of these meds because then I can't be happy. What is the point of full and total seizure control now, anyways? I can't drive a car...I'm a kid. Besides, with my hormones all out of whack because of puberty we aren't gonna get control right now, are we?" (proud mama moment::rock

Now, if only I could convince the school that Shan and I know more about what she needs to be successful than they do. She has yet another 504 meeting tomorrow in which their personal physician consultant will give us a classroom evaluation of Shan's needs. I would like to believe that this will lead to better management of Shan's case (after all, it can't get much worse) but I have a sneaky suspicion that they're going to use this consultant to reduce their responsibility and/or the services that they offer Shan.