Every couple of years I have seizures then my Dr wants to try something new or ups the dosage. The meds I'm on now are making me dizzy and off balance

Apparently I've read through medical online case studies that covid 19 can cause Ataxia, movement disorders, and Epilepsy after infection .I wanted to add links here but it wouldn't work I find this an interesting thing to know about as I'm wondering could covid 19 infection be the reason for my symptoms the variables in diagnosis are a lot but still it's a possibility.

Will it set off with excessive motion.

I love listening to music and i have a few songs i listen to when it's a bad day. I'm looking for some newer ones if anyone has one.

I’m hoping to hear from folks who seizures began after they were Covid vaccinated, as is the case with my husband.

Did any of you have your first time ever seizure since you were Covid vaccinated?

I was told I have Grand Mal and other Seizure Disorders one of them called Pseudoseizures . Anyone else ever hear of this? I'm told it's hard to diagnose and often gone undiagnosed or is missed. My family and I was just grasping the Grand Mal Seizures now there's more to try and sort thru?

Hi everyone
My name is Mar, 31 years old female, im new to seizures and epilepsy, in Aug 2021 i started having partial seizures. I didnt know they were seizures, i initially thought im having panic attacks or something. Anyways, fast forward to sep 2nd, 2021 i had my first tonic clonic, my husband found me on the floor in my office seizing. Called 911, I had peed myself and bit my tongue which indicated that i had seizure. Anyways i spent 3 days in the hospital where they ran tests (CT scan,… read more

This is a general question of public opinion. I myself always assumed it was, but apparently it's not at least according to Social Security in Indiana that is. I finally decided to apply b/c someone else I know receives disability do to having seizures which started after an aneurysm they also happen to work as well. So I decided to give it a try and was denied b/c epilepsy was not a disability that would stop me from working. So opinions do you agree or disagree on Epilepsy being a disability?

Something some said got to me. Not all forms of epilepsy make tou loose consciensness. I am always alart and and aware of several of my triggers. My sezuires are either absent, mind staring or simple/conplex jerks (like a cold chill).

I have complex partial seizures. My neurologist and I have talked about my license as I have brought it up. He sees no reason to revoke my license and my diagnosis does not require them to be.

Anyone else still have their license?