I found out a relation was on the spectrum, and at first I panicked, because I thought of Rainman, and I genuinely thought autism was this horrible disorder that trapped you in some other world. But me being me (and that is, total Aspie

), I wanted to find out everything I possibly could about autism. In the end, I suppose autism became somewhat of a special interest - I collected as much literature as possible, scoured every (sensible) website I could, and asked as many people as I could.
By this time, I'd started to recognise autistic behaviours in myself, and people close to me started to comment on it. Linsey said to me "when I met you, I thought you really were just different... but the more I got to know you, the more I realised that there was just
something... not not quite right, but that... you really
are different, and I could never put my finger on what exactly". I'd show people Aspergers traits, not telling them what it was, and ask them what they thought - I'd usually get "oh wow, you do that, you're like that..."
I do believe it seems to run in families - I think the idea of having an Aspie kid is quite cute (not that I have any intention of breeding an Aspie kid, a kid's a kid, its not an extension of my personality and life ambitions). Especially because I'd know, and I'd know how to deal with them. When I spoke to my mother about autism, and she started asking me about traits, my dad happened to come downstairs to make a cup of tea, and I saw the look she gave him, as if to say "ah..." Speaking to my dad's brother about my dad, he said "you're the double of your dad in every way, even your mannerisms, the way you speak, your sense of humour... there's no way he could deny you're his!" He showed me pictures of my dad around my age, and its pretty clear that he's got Aspergers - he's not smiling in any photo (even his wedding ones), and he just has that... vibe. If I hadn't been told by his brother that I replicate his mannerisms, I'd not be as certain, but seeing photos of him before the schizophrenia got to him, and that knowledge... its too coincidental. Oddly enough, I always felt that I had a stronger connection to my father than my mother - felt confident that if my dad was well, he'd 'get' me in ways my mother didn't. Which is probably true, but hey! Its good enough for me these days to know I'm
that similar to him, so I try to think "well, I'll live my life happily and fully now, because he can't, and I know this is what he would have wanted..."
Another thing that really struck me when reading about Aspergers is the part about echolia. I'm crap at doing accents, but if I'm around someone with a different accent, I've always absorbed it, without realising. When I was a kid, my accent flitted between Irish-American-Scots - I used a lot of American and Irish phrases, probably more so American. I just put it down to the fact I had an Irish gran, and lived in quite an Irish community, and the Americanisms I put down to the fact my dad was in the middle of emigrating there when he got ill. I have quite a few American relatives and people just assumed that I had an American parent (which I kinda, sorta do I guess... my dad was obsessed with American culture and was desperate to leave Scotland) - I used to say "mom" instead of "mum" (then it became this really twee "mother"; I used to say it the way Bambi says it when his mum got shot), stuff like that. Even now I don't have a true Glasgow accent, and I still use Americanisms and American pronouncations sometimes - I say 'vitamins' the American way for example, and I
hate being corrected for it. Its all bloody English and you know what I'm saying, so what if I say "vyte-a-min" instead of "vit-a-min"?? Jeez...
Also, the monologues................
I guess if you feel the diagnostic criteria fits, go with it. Its not hurting anyone, and if you're comfortable labelling yourself, I don't see what the problem is. Locally, you can self-refer to the ARC, they deal with adult diagnosis, but one of the adult Aspies I know told me there's a change in their funding. So basically they're only getting funding to diagnose the 'problem' cases, i.e. if your Aspergers is causing difficulty in day to day living. I think most people who work with Aspergers on that level (and this is just my personal opinion on the matter too) would be inclined to say Aspergers itself isn't the problem, its the range of co-morbids that
may present with it. I personally just see Aspergers as a different way of being, everyone has shortfalls as well as their good points. I'd probably be called hyperlexic, but also I'm convinced I have ADHD. I can pay a
lot of attention to something I find interesting, but if I find something dull, I can't muster any attention. My temper used to be vile too - I have to do things to stop it beginning to boil. And I get
really hyperactive spells, where I'm full of beans and literally cannot calm down. Most people do just find me funny in those spells, because all I do is make up my own languages, and amuse myself noisily for about an hour. I can't get a diagnosis though, because it doesn't impact greatly on my day to day living, and most people around me just say "Lorna, you're being ADHD again" if I do annoy them. I suppose I'm more suspectible to it as an Aspie, but its not a necessity. Thats why I don't buy into Aspie supremacy (although, as a geek, the X-Men comparison is always entertaining - "I WILL DEFEAT THE EVIL NT WARLORD WITH MY SUPERHUMAN JAVA PROGRAMMING ABILITIES").