What advice would you give to someone who cares for a person with epilepsy?

I think the advice I would give would be to make sure that you are seeing the best possible doctor for you in terms of their expertise but also someone you can build a relationship and you can work with. I think I would urge a fellow parent to be as informed as possible, reading leaflets from the charities and things like that and possibly to join something like a support group of parents so that you've got someone to talk to and share your difficulties with.


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