I don't like the term "disease" that was used on the description---I view myself as a "difference." But as for the video---I liked it. There was a lot in it that sounded like me---the hair twirling (back when I was in junior high school I was damaging my hair), my hand rubbing (still do it---and finger flapping, etc.) And, I can't take very long at a social event either. I especially liked Clay Marzo's analogy of his social cup overflowing. Yes, that's me. I can only take so much too. It showed in a positive light how we with AS are---such as with our special intense interests/talents. But at the same time---yes, we can struggle socially. I have been to therapy too. I so appreciate my parents for not making me conform to the social norm...I spent hours locked in my room, "my world", at the organ/music, with roller coaster books, and house plans. Today, at 44 years old, in my music room, you will find a bunch of house plans/blueprints on the organ bench that I move every time I play the organ, and a large bag full of roller coaster blueprints beside my piano. I think most of us with AS can relate to Clay Marzo.
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"My journey has just begun."