new and testing the waters

Hi, my online name is Sophist. I am 25, female, have Asperger's Syndrome and undiagnosed Neocortical Temporal Lobe Epilepsy, and am a psychology/neurology FANATIC. I am currently in undergrad getting my bachelors in Psychology and then plan to move onto grad school for my doctorate in Experimental Psychology (no worries to any animal activists out there; I have NO intention of ever using animals in my research). As for my epilepsy, my TLE is very very mild and I am able to keep it under control without medications. Since all my triggers are auditory (my main trigger is actually a lack of noise and dead quiet) I almost always have on some fan or something for white noise to keep my seizures from coming on (this works pretty well). Also, if one comes on even with the white noise, I am able to put on headphones and listen to some music and it magically stops. My seizure symptoms include: *head buzzing (almost like an electric current running through my brain) *tinnitus *vertigo and dizziness *blurry white flashes of light *color spots of red, purple, or yellow (very rare) *motor tics in my left arm, hand, and shoulder *knocking/slapping sounds My "aura" is almost always the head buzzing and the tinnitus. I don't know whether I have CPSs or not. If I do, they are only momentary (which as I understand it would be unusual for CPSs) which is why I'm not certain. At most I can definitely conclude I have Simple Partials. On occasion I will also have the motor tics occur alone without any sort of aura and they do not generally turn into anything more than that. My seizures are brought on by a change in my energy level (brain waves), and more specifically, when I'm tired. So unless I'm really stressed and worn out, I rarely have any seizures out of the confines of my bed. This is another reason I don't seek diagnosis or treatment because they are not impairing my life much. And since I've realized my triggers and ways of heading off or stopping my seizures, my seizures since they first started about a year and a half ago, have decreased in severity. This is good because a frequent worry for epileptics who are also autistic (as I am) is that with time, the seizures more often get worse; which is just the opposite of nonautistic epilepsy as I understand it. Welp, I guess that's about it for now. Nice to meet you all. :)