I know I hav'n't been about at all in hte last 6 months or so but I just thought I'd let you know how things have progressed since ds's diagnosis in march.
Got DLA middle rate after total brain melt down trying to fill out that bloody form. Think I have to do it again in December coz ds is going to be 5, oh joy.
Got a lot of help from 'contact a family'and a web site www.bhas.org.uk (I don't know how to do links)
Have a speech therapist helping ds out, but we were on the waiting list for 18 months.
We were not successful in getting a statement for him, I think because he was at a private nursery but we are going to go for it again because ds started reception class at the local mainstream school in September, and it is proving much more difficult than any one thorght. Ds will not sit on the carpet with all the rest of the children, he hides under tables or any available nook when he does not want to do something, usually group activities such as assembly, pe and carpet time. The teacher is doing as much as she can and genuinely seems to like him which I count as a massive bonus, and the headmaster also seems very supportive so far, they need a 1 to 1 person for ds and they are trying, they had one but she had to leave to go back to Australia, trained teacher and everything, big bummer. They have been using various interested 'mums'but they have their own stuff going on, and ds needs consistency. The head has assured us that he has found the funding for a 1 to 1 person for ds but he has to advertise and get the right person, so when this person will turn up is anyones guess.
I keep falling in and out of love with the school, because they really do give the impression that they want to be inclusive and are doing all they can to support ds, but it still seems that the only real progress being made is between the class teacher and us by concockting cunning plans to get ds to sit on the ruddy carpet.
The head apparently used to sit on the board that gives out statements and has sounded optomistic about getting one, but the senco at the school is rather more pessimistic as are most other people, since we have a diagnosis nad have still been refused so far.
We will see I guess, but at the moment it is day to day battle getting out of the house fully dressed, getting to school vaguely on time and then ds getting through the day avoiding stress as best he can, generally by hiding in a book, and then getting dragged off to after school club where he endures the noise and rowdiness of post-school mayhem. Finally being picked up by post work mum, dragged to dd's nursery to pick her up then supper, that he usually hates, followed by the melt down when bed time is first mentioned.
There you go, life so far,if any one has any good getting auti boys to sit down and listen techniques please pass them this way, any suggestions gratefully recived.