SRL- my pediatrician was the same way. first thing we did for both girls. With N she brushes herself to help calm... we have a swing set up in her doorway also.
Yesterday when we were at Occupational Therapist (OT) with N, she swang, spun, ate something, played with some sensory things, swang again, ate something and then was going to start swinging again and started losing her speech... so she came to me and started climbing on me. She needed physical contact.
WHat was interesting is that it was like a sensory cycle, all in an hour, she went through every sensory need, she even asked to turn down the lights, and at the end when she was really done her speech went also.. and she needed me.
Me and the Occupational Therapist (OT) found it very fascinating to watch, the full cycle of her little sensory wheel. It gave us lotes of insight as to whet she needs also.
Lots of vestibular, oral, tactile, but all in short amounts. Or she gets overwhelmed and falls apart....
Hopefully the schools will continue to accept this disorder...