Hi all,
As I read others' messages, I am noticing that everyone seems to be
on lower doses of meds than Megan is. And Megan still hasn't gotten
total control of her seizures. I realize everyone reacts differently
to medication, but do you think the high dosages that Megan requires
indicates that she might be better on a different drug? Or that they
might want to add a different drug to the mix? I have to add here
that I am extremely frustrated, as she used to have almost complete
control of her seizures when on depakote, even though she was not
always compliant on taking her meds. Now she has at least a seizure a
month..... and I know that may not seem like much to some of you, but
this is supposed to be one of the easier forms of epilepsy to control!
Take care,
Tammy
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