I'm not sure how to describe this ...
I posted first on primary education about my son's teacher bringing me into the classroom at the end of the day and telling him off in front of me. I felt that she was a bit too brutal. She ordered him to look at her and ordered him to stop smiling. He never is able to look at me when I am cross and often smiles in a nervous way when told off. I felt so scared of the teacher myself that I couldn't say this at the time.
This really is a long story and I can't go through explaining it all again (if you want to know the whole story then its all under 'Should I speak to the teacher?' on primary education).
However after lots of discussion on there I have been advised that my son should be getting more support from the school and that I should organise a meeting with the teacher and Senco.
DS has hemiplegia, which is a form of cerebral palsy. He has a statement of special needs - level D.
I am not yet sure whether his behaviour is affected by his brain damage - is there a way of finding this out? - I was under the impression that there wasn't, but people suggest on the other thread that there is a way.
The school has not provided a 1-1 support. I am doing his physio for an hour in the morning before he starts school. Actually I am happy with both of these things. I know that DS would be driven mad by a 1-1 person hovering over him all the time. He does need extra help, but not all the time. Probably not even 50% of the time.
I would much rather do the physio myself (he starts late in class in the morning) as I know that a TA would not have the knowledge or inclination to do it as perfectly as I do - I mean that tongue in cheek and kindly - its just that I have four years experience of knowing what to do and am DS's mother - of course I want him to do the exercises as well as he can.
This is not a very good opening post. I am sorry. I suppose I just want to know what I should be asking for and what is on offer in schools. I have found the school (which I chose because I've been told they are brilliant with SN) to be very closed in its approach to me. They don't seem that keen on talking much about my son and what he needs. I have initiated a few meetings but there have been none since he started in September.
I'll stop there. If anyone has anything to say, I'll add more later.
Thank you for reading.