Functional dystonia and seizure questions
Hi FND friends! I have two separate questions so if anyone has advice for either that could help, that would be wonderful! Just in case **trigger warning** talk of seizure and dystonia symptoms
I apologize if this question gets asked a lot or has been answered: what helps your functional dystonia, specifically in your legs and feet? Mine is triggered typically the worst at night when I’m relaxing in bed and sometimes I’ve noticed when my legs are chilly. I had restless legs before my diagnosis and only ever found one thing that helped that but I struggle a lot with this later on in the day. It’s such a random problem for me that I really don’t have much advice picked up so anything is appreciated!
My second question topic is for my functional seizure friends. Do y’all have them bad when you sleep? I’m getting quite frustrated/annoyed because I’ve **known** I have nightmares and sleep issues but they aren’t happening much in the day anymore and now are like these things that I half remember but like **know** happened, if you feel me? I have to be slightly conscious when they begin but they “end” by me falling asleep. I used to have them very bad during the day. But how do you get a more restful sleep? I can’t really control them. Little side note: I’m not sure if I was having them in my sleep when I had my EEG, I can’t remember that entire hospital stay :/ but I assume they are functional? Idk lol. It would prob say in the EEG notes if any happened in my sleep, yeah?