tethersend, no of course I wouldn't. because of course someone who lives it 24/7 is going to know more about it than someone whose life is only peripherally touched by SN.
My brother is likely HFA (but of course I saw that form a very different perspective), and my uncle is disabled too. I had a profoundly deaf girl in my close circle of friends at school, so my life was not untouched by disability.
But i think I would always have tried to understand, which is something I don't always get the feeling happens on here (and I don't mean absolutwely everyone by that, but just the clear-thinking, un-ignorant posters). Sorry ot keep harping on about it, but the bus thread really did change something for me - the OP had put everyhtig in her post, and still got vilified for daring to be only 10 minutes early for the school bus.
there was precious little horror at what had happened, and virtually no support for her being angry with the bus company - but lots of ridiculous posts about how she shouldn't leave her front door unlocked, and shoud always be available at all times in case the school decides to send her dd home a bit early, etc.
and, tbh, I would be horrified if a bus company shoved my NT dd through the door without checking I was there and/or ok, tbh.
just a moment's thoguht, to try to understanfd why she was shaking with anger, and what hideous thoughts must have been going through her mind.
as I said earlier, MN on the whole has a reasonable awareness of SN - we are more "visible" if you like - adn yet hundreds of posters glossed over the salient facts.
that's quit depressing - to me it signalled that in their haste to have an online barney, disability got overlooked. like disability is always overlooked.
Stewie - sorry to hear about your dd. i hope you don't have to wait too long to hear. dd2 was assessed for CF too, on account of manky mucousy bowel movements, and a stubborn chest infection (as well as generally bein FTT and a couple of other things). It is a stressful wait.