My 23 year old, disabled son had a seizure a few days ago, he started taking Zoloft about 3 months ago, with the dosage increase after the first 6 weeks.
What I find really interesting (the disturbing kind of interesting!) is the number of people that have posted here that were the exact same age TWENTY THREE... By my count, I'm the ninth poster on this subject and the fourth, for the people who mention their age, to mention specifically 23. (I did catch that some people were younger at the onset of problems, but it really appears that there is a 2 year window that really needs to be looked into.)
Also, as a 43 year old woman and a medical professional with 20+ years experience, I know a seizure when I see one. But, like many, if not all of the other posters here, the doctors at two emergency rooms are insistent that he did not seize, but simply passed out due to dehydration/stress/behaviorial issues/low or high blood sugar/electrolite imbalance... take your pick because they were all said within the first few hours, and all withdrawn or reversed (ie: His electrolites are fine so we know he didn't have a seizure/The jerking movements can be caused by his electrolites being off.)
In the end, they transfered him across town to get rid of me and my demands for more than standard blood work, a chest x-ray and an EKG (you read that right, they checked his heart instead of his head!) And fighting his discharge after less than 4 hours of obsevation and about 90 seconds face to face with the first doctor. Before transfer, they did go ahead and run a CT scan on his brain and a do a quick urine dipstick after I started insisting, but ONLY because he had rolled down a small flight of stairs when he fell and because I told them that if they didn't do the dipstick, I would. In order to get him transfered, it took the help of one super nurse and I had to leave so they could do nothing but keep him, transfer him or set him out on the sidewalk. He was still discharged after being at the second hospital for only 6 hours, another round of blood tests, a bag of saline, a cheeseburger and, because I didn't come when they called me - thus the cheeseburger, saline and extra 4 hours. In the meantime, his "observation" and "care" consisted of never having him move or even stand up from the stretcher I put him on at the first hospital, not giving him his normal meds, no EEG, no neuro eval, ignoring everything we (my other teenage kids were there too) and he said about twitches, tremors and other odd movements - even when they happened WHILE THE DOCTOR WAS IN THE ROOM and almost got kicked. They went as far as to say that his chewing water, while he was confused, was NOT unusual, because, "If it had been a seizure he should be sleeping." Then going on to explain that because he has no history, wasn't sleeping (post-dictal), he had no mouth injuries and he had not urinated (though his bowels did release, which they also didn't notice then refused to acknowledge when I brought it to their attention) There was no reason to believe that he has any type of seizure.
Sorry to go on so long and give so many details, I guess I'm still in shock from the experience. And now finding this forum and the information that, despite the small number/sampling, seems to be showing a definate pattern that, at the VERY least the doctors should be aware of and looking at has been both eye opening and even more disturbing.
Thank You for taking the time to share and the best of luck!
Psyche