"The increased availability of benefits and assistance is also no small factor - parents are more likely to push for a diagnosis if they think they’ll benefit in some way."
That is a disgusting thing to say!
All.of the parents of autitic children I know haven't "pushed for a diagnosis". We have all asked for our children to be assessed as we feel strongly that something isn't quite right.
The medical professionals don't diagnose it willy nilly you know! It's a very long process (2 years 4 months in my son's case) with your child seeing different professionals.
Plus DLA is exceptionally difficult to get. I didn't know anything about DLA until my daughter was diagnosed.
My son has been awarded it without diagnosis because of the difficulties he has.
Come and live a life with a couple of kids with ASD and then say it's "parents pushing for diagnosis" so they can get extra money.
That money doesn't even scratch the surface of the extra cost if having a disabled child. Every penny if my daughter's DLA goes on her therapy that the NHS refuse to provide, despite doctor's saying she needs it.
Forget the fact that I still have to fork out extortionate amounts on particular types of clothing, extra toys to try and get her to bath at least once a week (aged 11) and the extortionate cost of extra bed bath products to keep her clean when she finds a bath intolerable. The sensory toys she needs, the second hand £250 disability buggy that we sometimes have to use in order to get her out of the house. I could go on (and that's just one of my disabled children).
Then there's the fact that, due to their disabilities, they can't cope in childcare or cope too much with me working. I therefore have to work school hours only on piss all sleep because I'm regularly up.in the night with my 11 year old.
Even with the DLA we are living on the breadline despite being well educated professionals. I had to give up my £40k job due to my children needing me as they are disabled. Instead, I work for below minimum wage "work from home" jobs.