Since being diagnosed, I’ve been having lots of confusing dreams, I can never work out what’s going on in the dream, or if I do I completely forget. I then feel really confused and sometimes have a sense of déjà vu .
@A MyEpilepsyTeam Member,
I never see the end of my dreams.
I used to never have (memorable) dreams. Now I do. People I don't know breaking into my apartment are the most vivid ones.
I think these dreams are residual effects of the Gabapentin I was administered when in the hospital. (It gave me hallucinations while I was still on it. I had never hallucinated before then.) I'm glad those have faded away.
I have a dream like this nearly every night now, for the first few weeks the dream was about me knowing where my phone is but not being able to get to it. I think this is because I was on the phone when my seizure began. It’s very strange, now the dreams are always a blur or I’ll remember faces at times.
I have a similar thing where it's basically like a dream will start but I only really see the end. I know it makes no sense. It's basically like your watching tv the show starts at 7 and goes until 8 and you jump in on the show at around 7:45-7:50.
It's dif per person, I do have strange dreams now and then, and I have a few good ones but once In a while I'd say, but I'll take it, I am ok with that, I am not complaining about it, I do try to make some sense of the strange ones, but a brief moment 3 min if that, a little bit longer if that is something I could find of some kinda use it and a message to the dream I had,if not I throw it out, my opinion here
A Neutral? As For And If You Dream, Do You Think It Has Something To Do With The Condition We Have And Meds Or A Natural Thing Combined?
I Have Right Temporal Lobe Epilepsy And I'm Currently On Vimpat. Anybody Out There Have Vivid Or Weird Dreams?