Hi sprouts,
Sorry I was out at the swings there. I have three kids, DS(7) DS2(asd 5) and DD(2). I knew for a long time before I actually admitted to myself that there was something wrong. DD was 8 days old when I eventually got to the point where DP and I both had to say it out loud.
We were surrounded by people placating us with "All kids develop at different rates" and "he'll talk when he's ready" and for ages I just wanted to believe them. Every 6 weeks or so though I'd ask DP or DM or anyone if they thought there was anything 'wrong' with DS and of course they'd say of course not.
It's a hard situation as you don't want to worry anyone by suggesting there might be anything there but in my experience it's better to know early and get the right intervention asap. IF and I do mean IF the outcome is ASD which it really might not be. So don't jump ahead but if it is then help is there.
The help I've had from educational services has been brilliant. I'm on the west coast of scotland so I'm imagine it'll be similar in edinburgh. Same government etc. He really has came on leaps and bounds since we got a diagnosis last year.
Nursery have been fantastic and you really NEED them to be sympathetic and really get to know your child's quirks or any wee issues he might have. I'd perhaps look into other nurseries. Go speak to a few of them and just be candid- explain the situation and that you don't feel supported by them and that you are looking for an alternative.
You are correct, he should be in with his peers as this is the only way that children learn social norms so well done for fighting that.
Regarding DH, he's probably just sticking his head in the sand a wee bit and is being fiercely protective of him. I have been the same at points. I totally understand that no on is writing him off but the whole situation of a speech delay is a hard thing emotionally to deal with.
You have a baby and you just assume that everything will be perfect then suddenly there's a wee question mark on the horizon. A wee unknown. It's a complicated thing to work out.
I won't lie, it's a hard shift having three of them. DS1 misses out on things as we can't take ds2 to certain places due to sensory issues. Taking all three of them to the park on my own is a nightmare. You just really need to play it by ear I think. Could you put having more children off for a few years until you see how his progress develops?
On the flip side, Ds2 definitely benefits from having a brother and a sister. He is pretty much forced to be social all the time. We live in a tiny house and there is no space so he has to share, take turns, interact at a table, be kind, be semi quiet and moreover he demonstrates love to his siblings which my home visiting teacher tells me is quite unusual. I sometimes think that if he had been an only child then he would have turned our house into a wee dictatorship. He has that type of personality.
To be honest, from what you have told me I think you should get it investigated further. Just purely to put your mind at rest. A professional will be able to tell you more.
There are also two great books that i'd recommend getting to help with his speech
Hanen- It takes two to talk (for speech delays)
Hanen- More than Words (for kids on the AS) this one is brilliant. There's a great section at the beginning highlighting all the differing symptoms of the Autistic Spectrum. It can be so varying, it's baffling initially. My speech therapist sent me on the More Than Words course which was excellent. Ask around and see if they are running one in your area.
If you have any other questions then just ask.
Sorry this was a massive essay. :)