I've been mulling this one over for weeks, please can anyone give me their opinion as i don't know what to do for the best, I am trying to be really objective but it's difficult, will try to be as brief as poss..
DS1 is almost 3 and has a language delay of approx a year, approx 300 words, mainly nouns, few verbs, very few phrases but these are just starting. We suspect HFA, or a language disorder with autistic like symptoms. There aren't any behavioural or sensory issues, or need for routine.
He's been going to a local Child Development Centre since Feb, and they say they've only heard him speak the most basic words "car" and "egg" for example. They have no idea he knows his letters, colours and numbers, despite him enjoying pointing them out to me everywhere we go, and the feedback I've had from them has been fairly negative - along the lines of he wouldn't cope in a regular pre-school, they wouldn't know how to handle him, he wouldn't take anything in, etc. They also don't seem at all interested in my input, I told them this week that we'd discovered what a massive effect juice had on him, and when I later collected him, he was as high as a kite due to all the juice, chocolate and crisps that they'd given him for their end of term party.. When I tell them something new he's done (I'm not a boasty mum, but surely if I can share things anywhere it should be there..) they give the impression that they'll roll their eyes the minute I'm gone. It's all so strange.
The thing is, he can and does cope really well in a nearby mainstream preschool, where the staff seem to know him much better than the CDC. Our SALT and the SENCO have both been in to observe him there and verify that yes he does speak (using some words I haven't even heard him use at home) and does interact comparatively well with staff and other children. They also reported how tolerant the other children were with him, which I credit the staff with, to some extent.
CDC want DS1 there 4 mornings a week from September, I'm really reluctant given his total lack of progress there. He is supposed to see their resident SALT there one day a week but he's been going since Feb and only ever met her twice.. if we pulled him out, he'd receive therapy at least once every six weeks which is more than he does there.
It's a really hard one as I know they're experienced professionals and I was all up for him going there originally, but there's just something about the environment that I don't feel is right for DS1 - it's total sensory overload, and although he doesn't seem to have sensory issues, I don't see how he can be expected to concentrate on interaction when they have tv screens blaring in the background and toys from floor to ceiling. Tellingly, our SENCO has a fantastic reputation in the area, and told me that the lady running the CDC which DS1 attends could be quite "pressurising." She was at pains to reassure me that if we pulled him out, he'd still get SALT and the help he needed at school. Really strange, help, don't want to turn down professional help for him but something doesn't feel right..