epilepsy and disability?
has anyone's neurologist said that they're "not disabled" once they hit 12 months without a seizure?
I recently hit 12 months seizure free, and my neurologist said they'll no longer consider me "disabled" by my epilepsy which has left me feeling pretty down. I already really struggled with accepting that my epilepsy is a lifelong disability, then my neurologist said i'd no longer be considered "disabled" by my epilepsy which has left me feeling pretty weird??
epilepsy has taken so many things from me, like my career, memory, functional capacity and ability to do lots of activities I once enjoyed. it feels pretty disabling to me 😭
(I have focal epilepsy with tonic-clonic seizures, I'm on 2000mg keppra daily, this is the only dose of keppra where I haven't had a single seizure)
sending huge hugs to you all, epilepsy is so darn cruel 🫂