My 4 year old has drug resistant focal epilepsy she’s tried several AEDS none of which work they started her on epilim and took a horrible reaction which the hospital have told me can not be because of the medication as they’ve never heard of anything like it they say now they’re running out of options and they’re speeding up the process to see if she’s a candidate for surgery does anyone have any insights or similar experiences please I’m at my wits end and I’m seriously scared for my baby she’s been through so much in her little life I just want to be able to help her