tbh, star, it's somethig I've long thought, but not wanted to articulate, iyswim?
the closest I have come to it before is by sayign I do not want dd as the "class pet" in MS school. That odesn't go down very well with LAs, but it is exactly what they are proposing when they say thingsllike "it will be good for her. and the other children will learn so much"
it certainly isn't a situation for the benefit of dd1, which is what should always be at the heart of decisions regarding her care/education etc.
there are honestly so many situations where I have ended upthinking "what on earth were they thinking of?!" thatit gets ridiculous. And, as you point out, I am not exactly shy at fighting her corner
there was a situation at her last school (the ASD one, who really should have known better) which happened twice - when, if they had listened to me, read her communication passport, and actually monitored her reactions, should never have happened at all.
I was angry the first time. The second, I was furious. I spoke (nicely) to the TA involved at pickup, and told her (nicely and patiently) why it should never have happened. She knew nothing of the background, and was shocked that shemight have been upsetting dd1 (I did beginto lose patiencea little at that point- dd1's reaction was not "normal", so howshe didn'tthink anyhting was amiss I'll never know, except of course, she was probably so steeled to ignore challenging behaviours, etc, etc, and so sure her course of action was right, that it couldn't be wrong)
I was told the following day (by the head)not to interfere with staff, and that I shouldn't tell them things which might confuse them, as the school had a way of dealing with situations which they always followed.
throughout all this, eveey day at home, I had dd1 tellingme she didn't like what was going on, and wanting me to sort it out for her, as she was unable to tell them she didn't like it.
I went in, and with dd1 with me, told the teachers concerned that they were not to do it again. that dd1 didn't like it, and she was very distressed by it. their response? "you shouldn't talk about these things in front of her - there is no quicker way to create a phobia"
ffs.
never mind they were gnoring she ALREADY had one, and was petrified of what they were going to do next.
as I said, it shouldn't have happened once, since I had told them about it all. BUt to then happen again, onceI'd reminded them - I can only assume that because she wasn't showing a "normal" reaction, then her fears did not count. (although I would dispute she wasn't showing a normal, small child reaction in the face of people she was supposed to be able to trust doing something that made her feel unsure - she froze completely, and withdrewinto herself - doesn't take a genius to work out something is wrongif you have a previously comfortable 4 year old suddenly (and consistently) withdrawing form a familiar situation, does it?)
Add in to that that I have had dctors dismiss her obvious discomfort at times with a breezy "well, hw do you know she is ill?", not ot mention thinking htat persistent rancid diarrhoea is ok - "oh yes, that is often found in autism" and not worht trying to sort out, the list really does go on.
I can only conclude that sometimes, some people do not see her as "worth" bothering with, or worth treating as they would any other person. and that is a truly horrifying thought.