@A MyEpilepsyTeam Member I find WebMD okay. This is the much better site for everything to do with medications https://www.drugs.com/

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A MyEpile...

@A MyEpilepsyTeam Member,
The only way I know I have had a seizure @ night is how I feel on the morning. I will go to bed not sore or stiff, minor headache (the norm (3)). When I awake in the morning my covers are all on the floor, my body aches everywhere, I feel like I’ve been in a fight or hit by a car. Blurry vision, Migraine above a (7), usually have stiff muscles in one of my arms, (usually my right). I have fallen off the bed once and the couch a time or two. I don’t recall how I felt so much as, being surprised and confused as to why I was on the floor. I live alone. I do know I don’t function as well on those days, when I have had a seizure at night. Most of the time I will sleep all day sometimes 2 days. I don’t eat or anything because I’m so exhausted.

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A MyEpile...

I have occasionally had nocturnal seizures but it's been a while now.
I always have tonic-clonic (grand-mal) seizures. There are a few ways I can tell if I've had one in my sleep.
I wake up immediately after the seizure has ended and I'll be super confused and disoriented. I also get body pain from my muscles seizing and sometimes I bite my tongue really bad.
Sometimes I only have one symptom, sometimes it can be a combination.
I don't usually have auras but I can usually feel a seizure coming on and get myself to a safe place. The one time I remember having an aura it was deja vu and it was so intense that it made me feel sick to my stomach.

Thank you all for your answers! I only had those two mornings in a row that I woke up with the headache and all of that body pain (and have had not any since and do not remember ever having any before this), so I unofficially believe that I have added nocturnal seizures to my collections of seizures.
NOTE: They really need a function on here to list the old and new name of the seizure type and the brand and generic names of the medications when we type in one.
Off course, since they are a non-profit organization with sites for Epilepsy and quite a few other -- you can find this out by researching them on the internet. I did this after the Epilepsy Foundation refused to mention them to people with Epilepsy because they told me that they are profiting in some way off of those of us on here. However, I have yet to find any proof of this on here because I have not seen any commercials and I have not received emails with ads for medical treatments and the like for seizures. H

Have any of you?

I have partial complex sezuires and take a daily nap every day at ththe same time which I never did when I was younger seeing I've had epilepsy so my life and started having sezuires at age 5 from a TBI. I have nocturnal sezuires, sezuires in my sleep and I get this information from my neroligest from my neropace reading when I have monthly visits or a issue. I've woken up with a headache and the whole day after a nocturnal sezuire which is every night am sluggish and very tired for the whole day and unmotivated and fatigued I may be sore all over and none of this this from falling as I sleep with a body pillow and my back towards the wall. So I know I've had a sezuire that night. And am also confused for most of the morning not wanting to get out of bed and sleep most of the day as my sezuires drain the life's blood from me and all my energy.