I’ve had epilepsy pretty much all my life. I’m curious for those who have had epilepsy for all their lives if it gets easier mentally or do you still feel frustrated with your disability.
I ask this because as someone who has lived this more than 25 years, I’ve gotten past the acceptance phase eons ago but I do get frustrated with the reality of what I can and can’t do in life. I’m just wondering if it’s just a phase or does this kind of stuff go on even as you get older.
I have had tonic-clonic seizures since 1981. I considered my seizures mostly controlled - 1 seizure every 3-4 years. I feel they have made me a stronger person and able to handle the bumps in the… read more
Did you know Beethoven, G.F. Handel,
Niccolo Paganini Peter Tchaikovsky, Robert Schumann all had epilepsy
When did you get it?
1950s
1960s
1970s
1980s
1990s
2000s
1959 is when I was diagnosed at age 7.
I had a conversation with a few people here. We all have had difficulties speaking. Getting confused, slurring words, dyslexia getting worse, not being able to put sentences together properly, etc.
If that’s a seizure, what type of seizure is it?
Or is it more likely just side-effects of medications?
Thanks.
@Pamale6
I always had trouble speaking clearly when I was having an aura, which is a warning sign for a seizure.
I've been on 9 so far. You think by that point that they would just let me smoke and leave me alone dude 😂
Should try edibles when going to bed
I’m curious to find out your perspective on epilepsy. If someone who is newly diagnosed with E asked you if there was any hope of gaining seizure freedom, what would you say? Would you fill them with hope that they would be successful in achieving freedom, tell them that not everyone gets « cured » or something else altogether?
It is possible I guess all you have to do is ask your doctor and see if that would be possible.
does rescue medications used in emergency for seizures work on non-epileptic seizures.
I mean the ones they use in hospitals to stop recurring seizures.
My son has rescue meds administered after 1 min due to apnoea. He goes blue very quickly. He was moving after the tonic clonic phase had subsided. He digs his heels in and slides along the floor on… read more
It hasn't even been 2 years yet and I've had grand mal, then nocturnal, now absence. Getting tested for autoimmune and now doctor wants to test me for MS too.
Luckily I have only had tonic-clonic seizures, but I know that could change at the drop of a hat.
I'm new to epilepsy & this site. My 17yr old son was diagnosed in February. How do the mommies / parents deal with teenagers , epilepsy & school? Most days i'm not sure to keep my son at home or send him to school? its at a point where i am considering home schooling. Plse advise? I need help
Thanks for the hug.
I have been a teacher for 24 years. But last week, for the first time, I seized in front of my class. I was in the middle of a lesson. My kids were amazing. I have prepared every class on the first day of school with a just in case procedure, and they were rock stars. But for 23 years it was never needed. School seemed to become a safe haven from my seizures. I had them very infrequently over the years but never in school. I hit my head and have been sporting a black eye trying to teach these… read more
I was a sub up until 2 years ago. I never had a grand mal in front of students. I did, a couple times, have petit mals firing off one after the other in front of them. When they went to lunch a… read more