LupaLuna wrote:
Luckily for me. I learned stimming etiquette at a young age. Had to. Although I was never punished for doing it. I did learn that it was not socially accepted behavior and was look down upon. As a result. I hated myself for doing it but I had to it or otherwise, I'd go stir crazy. I learned to treat my stimming vents a lot like going to the bathroom. If I needed to stim, I'd just leave and head to a private area and do my thing and nobody had to know what I was doing.
Mine has been like this. However while I do things I private that no one sees since my diagnosis I realize I do more in public then I realized.
Unfortunately taking the analogy to the OP's situation would be a person who is viciously mocked for peeing or defecating and that is abuse. All she do if moving is not an option is to find a private places to do what she needs to do.
Going to a psych or school counselor would be taking a risk. There is a chance it will help, but there is a good chance these "professionals" will agree with the mother probably not with her tactics but with the basic idea stimming is wrong. As the old saying goes "follow the money". The OP is from the USA and while individual states administer Obamacare there are many aspects the are mandated by the Federal Government. I noticed in my plan when my arm was broken 30 hours of psychical therapy were partially subsidized. I needed more and was forced to pay out of pocket for the rest forcing me to stop PT before I should have. If I was a kid in school Obamacare will pay for 180 hours of ABT to rid me of my Autistic traits. The "professionals" looking to supposedly "help" are quite aware of this.
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Professionally Identified and joined WP August 26, 2013
DSM 5: Autism Spectrum Disorder, DSM IV: Aspergers Moderate Severity
“My autism is not a superpower. It also isn’t some kind of god-forsaken, endless fountain of suffering inflicted on my family. It’s just part of who I am as a person”. - Sara Luterman