Well, meet with Dr. Pavkovic today but didn't get any answers. Jayen's lab results came back and we decided to up the depakote too. Jayen is now taking 4 topamax and 2 depakote pills every morning and night.
I really didn't get any questions answered. Every time I would ask something I would get the response, "It is really just too early to tell." The only thing I was given is a possible name. I was told if I had to have a name for it it would be called secondary generalized epilepsy. We are mainly focusing on controlling the seizures right now and will work more on the causes later.
I really wish Matt was here to help me through this. I think part of me dies every time I see Jayen having another seizure.
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