Hi tta
If you don't have a statement you wont get a place at a special school until you do have one and the process takes around six months so you would have to try mainstream first when you move back.
I would definitely try ms first anyway. Your ds wont have ft support before statement anyway so you will go through the process of school action and school action + which will provide some school-funded support. If the statement is successful, and I hope that it will be, it sounds as though your ds needs lots of support, that will be the time you will be able to consider a ss. By then you will have had more experience of the UK system and what is right for your ds.
The statementing process will take the opinions of several specialists into account who will look at different areas of his development. They will be looking at what is preventing your ds from accessing his education, and suggest ways that he can be helped. It may be that these suggestions can be carried out successfully in ms, or it may be that his needs are too complex for the ms environment and to reach his full potential he will need specialist support in a ss.
My eldest ds is 14, in year 9. He suffers from behavioural problems with emotional, social and attention difficulties. He coped well in infant school with support from SA+. In junior school he struggled more and was considrered 'difficult' and 'naughty'. We tried to get him a statement in year 6 but as he was academically doing ok we were refused. With hindsight I should have pushed that further but didn't know I could.
In year 8 he was permanently excluded for constant low level disruption and then we were successful with obtaining a statement for him. He started at a ss for behavioural difficulties half way through year 9. It is a 'tough' school with some very difficult pupils. I was concerned as he is more 'vulnerable then villainous' (in the words of the ep) but we had come to the conclusion that he would never cope in ms. A ss for more specific disabilities was not right for him and particularly not for the pupils that attend there as they may have been placed in a vulnerable position with him there. (He can be violent).
He has settled very well in his new school. He said he feels he belongs here and that the staff understand him. He has always felt as though he doesn't fit in and that always bothered him greatly. The staff are very understanding and take his difficulties into account, something ms school simply don't have the time for.
I do think if he had been given more support at a younger age he would not be in this position now and could maybe have continued with ms.
He is under a paediatrician but with no formal diagnosis.
My younger ds is 3 and starting school in September. He has global developmental delay (meaning he is delayed in all areas of his emotional, social, intellectual and physical development) and a speech and language disorder. He uses Makaton to communicate but his speech is coming along slowly. We have his statment in place and he will be having reasonable support (20 hours a week atm but we are appealing for more and have been told last week he will get more hours but not yet how much more)
He has had amazing support from a variety of professionals - EP, paediatrician, SALT, physio, OT, play therapist, Family Support Worker, Specialist Teacher. The pre school received full time funding for 1to1 support and they have also been great.
He is coming on really well with all the support and we are trying ms for him but are keeping open-minded about the long term outlook. We have been told that he may well need to move to a ss in a few years, but that's not definite.
He is 'officially' classed as having a severe learning disability by the health professions and severe SEN by education.
ds1 however is not classed as having any learning disability by health professionals but severe SEN by education.
Do you have a diagnosis for your ds?
My advice to you would be, when you get back to the UK, see your GP as soon as possible. Take any reports or letters regarding your son's difficulties with you and ask to be referred to a paediatrician. Seek out the school nurse (often working with the health visiting team) local to you and speak to her. My school nurse has given great advice in the past.
When you are deciding on a school, speak with them frankly about your ds. Chose a school that is sympathetic to your ds's needs. Tell them you are considering applying for a statement. The process is much easier if you and the school are coming form the same place.
Push for the support you feel your ds needs and do it when he is younger, I believe he will benefit so much more than if you wait.
There's some amazing people here who offer sound professional advice and who can support you through the roller coaster of everything you have ahead. Certainly wrt diagnosing and statementing.
WRT to EP's tests. The do some specific testing so they can gauge developmental stages and levels but do observations too, their reports contain both statistical data and opinions after observations.
Obviously different areas work differently and this is purely based on my experience.
I hope some of this has been useful, I'm aware it's VERY long but i thought an outline of my experiences might be useful.