hi rich

...sorry folks it's a bit long, due to personal experience.
the manifestation of emotional pain and fear definately has the ability to lower your seizure threshold. the mental state those memories bring is such a high level of stress, and with stress being one of the main sz triggers, it's not uncommon to break the threshold.
my first sz was a simple partial at 15, was horrid fear for about 40 seconds. however with good health and no one with epilepsy in my family, the psychologist diagnosed as post-traumatic stress disorder and i went on zoloft. tried taking myself off after one year b/c at that time i wasn't in agreement w/meds, though during that time (what were called episodes) went down, but not erased. in my late teens i had more and more, so went back on it, and lived my life accepting the condition i had.
age 25 was my first grand mal and e diagnosis followed after the 2nd one a few months later. didn't have another g.m. on carbamazepine for almost 5 years, but 'episodes' remained. not until age 28 found out they were seizures all along. case in point:
i was sexually abused by a young male babysitter at age 6, and due to fear and not knowing what to do my parents chose (tho they dealt with him

) to avoid counselling as i was so young and 'put it out of my head.' that worked for 9 years.
last year my new epi explained that b/c my e was found in my hippocampus, when the first s.p. hit at 15 it 'dug as deep in the memory bank that it could and found the most terrifying one buried.'
as the memory was of him putting me to bed that night, then turning around and coming back, that first sz brought back memory of what he did right down to the pyjamas i had on. hence my 1000+ partials have been fear-based.
i've read a number of journals on how similar epilepsy and ptsd can be, and how it's not an uncommon mis-diagnosis. had he got it right at 15 (by proper testing ie: mri) i would have been diagnosed with e and on meds way earlier in life. was very hard to accept.
for whatever (hugs) you're asking this, i can't say enough how we have to be our own advocates, and if you feel that further testing is necessary, demand. i am a classic example of them making a quick decision, and getting it wrong.
once the lesion was found in 2011 my doc requested the psychologist have a one-meeting sit down to discuss and open my file from 1994. he refused.