Suicidal ideation and seizures.
Brief background. I went to see a psychiatrist because I thought my “spells” were a scary sign of mental illness. I would have this sudden sense of deja vu followed by an overwhelming and unpleasant 10-30 second event. The psychiatrist told me she thought I was having seizures. I just about fell out of my chair. What??? The more I read, the more I realized she was right. Unfortunately, the neurologist I went to see disagreed. When I described my “spells” she said my symptoms were not indicative of seizures. It took two years before she walked into my hospital room and said: you have epilepsy. I was diagnosed with temporal lobe epilepsy. One of the medicines I was taking caused me to have double vision. The neurologist sent me to see three different eye doctors before conceding my symptoms might be from my Rx. Naturally, I have lost a lot of faith. Fast forward…I began to have sudden acute suicidal ideation. It comes on with the suddenness of a seizure. It lasts for about 10-30 seconds and it is followed by what I believe is a postictal phase of tearfulness. I’ve made my husband aware, because I am actually afraid that I might act before I can figure this out. We have had several conversations about this. Last night he said: “I dont think you should be left alone.” My response was, a very pouty, “I have to get sandpaper tomorrow.” I’m in the middle of refinishing a chest of drawers and I ran out of sandpaper. My husband was a counselor for years I have a bachelors in nursing. We have enough experience to know this shows I am future oriented. We have enough experience to know what a true suicidal state looks like. I am not suicidal. I believe I am having seizures. I dont believe I have the luxury of waiting for two years or seeing three different psychiatrists before my neurologist explores the possibility. As I said, I believe I am having seizures and I am concerned what a change in presentation could mean.
Interested in more discussions like this? Go to the Epilepsy & Seizures Support Group.
Jake
It is a nice thing to throw those seizure diaries out. You just want to throw those seizures out!
Laurie
Dear Jake:
I apologize for the spelling error, I need to review my spelling, etc. before posting it.
Laurie
Hi Leonard (@jakedduck1)
I apologize for asking you this question regarding the seizure diary. In another discussion, you have already mentioned that you are seizure-free for already some time 🙂 🙂 🙂 I forgot about that when sending you my last message. My memory is not the same anymore. I am sorry!
Anyway, thanks for sharing your past experience with seizure diary!
I am curious to know what kind of seizure diary other members of our group use. Anything to share?
Kind regards
Santosha
Hi @jennsprung
Thanks for sharing this experience of your seizures !!! I have very much identified myself with your focal seizure experiences. My experiences are pretty much the same, I also have TLE.
I know, it is difficult to find words to describe them. I first also called them vision and later on my short movies (it felt like a short movie I have already seen many times before). They were all very clear during the seizure, but after it is over I can not remember them. When I was younger, I could tell my mother “the movie is starting” at the start of a seizure. Nowadays, I can not warn through words anymore, but gestures. In the past, some seizures gave me a good sensation, like a feeling of relief. Nowadays, not anymore. In your post, you have mentioned that your seizures are terrifying. Would you mind telling me more about it?
Thanks again!
Santosha
@jennsprung
Hi,
Do either of you wonder? If so could you explain further?
I generally have generalized seizures but I wondered some. Nearly walked into the Grand Canyon & into a highway. I am also interested in hearing how your seizures are frightening. Thank you for asking that question Santosha.
Jake
@isittll
Don’t give it another thought. I’ve been called worse.
I knew it was a typo.
Take care,
Jake
Hi @santosha
You asked about the kind of seizure diary people use. I just use a small calendar, pocket size, and put a / over the date for each seizure I have. In the blank area I write any special note(s) about the seizure.
Best
Laurie
Hi Laurie, Good Morning @lsittll
Thank you for sharing this with me.
Does anyone use an e-diary of seizures?
Have all a nice day!
Santosha
@jakedduck1
Hi Leonard,
I could not understand well your question "Do either of you wonder?" Could you detail it more to me, please?
It is a pleasure to share my experiences with this group!
Thank you!
Santosha
I’m sorry I just saw this now- trying to get used to the mayo format! I’ll type something out in a bit! You want to know how I find them frightening?