hi all, I've got a 4 year old DD (developmentally sound) who was diagnosed with myoclonic epilepsy at around 2 years old (we've never really been told what kind and have been tested for Dravet which was negative). She had the odd eye flicker and head dip but not too many and reasonably well controlled with Epilim. She's 4 and a half now and due to start school in Sept. Her 'episodes' as we call them have been getting more frequent and more noticeable and the paeds have suggested Keppra which we are introducing slowly now over the last week. We've seen little improvement and whilst she's a normal functioning 4 year old apart from this I feel like this is taking over her life too much as she now refers to them as he funny turns. Does anyone have any experience of this, anyone know anything? I'm so googled out from the last 2 years that my head hurts. I am worried about leaving her in nursery, I worry all day about her at work and I'm pretty sure my one year old son would say that he get's not enough attention as mummy and daddy focus all their spare time on DD..
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