The idea that somehow autism is a money maker baffles me. It is underfunded almost everywhere and most parents who deal with this suffer financial hardship. People lose their houses over this and somebody is claiming they are in it for the benefits?

We currently pay $100/hour of speech therapy that is funded, but that's about to drop off in three months when my son turns six.
Now one of Savage's arguments was AGAINST early screening. Not early diagnosis, screening. Personally that would have been a huge blessing for us. Our son was diagnosed at the age of five, one year before his funding cuts. And why? Because he was our first child, none of our friends have kids, and the difficulty I had toilet training him kept him out of preschool until he was 4.5 so nobody that knew about it saw him. We knew he was high energy and he did some things that my gut reaction was "that's creepy" and had an amazing memory when it came to movies, but I had no idea that's what autism looked like, and actually didn't believe anything was wrong with him at first. Of course watching him at a playground with his class sit and drop rocks closely in front of his face while humming instead of joining with the group I was shown the stark difference between him and the other normally developing kids. I was shocked how clear their speech was, how good their grammar was, how easy it was to just SIT with them, how well they could hold a crayon. Ironically his differences kept him at home away from other kids I could have compared him to. Screening would have been a God send for him.
So the result of that is he ending up with very little therapy because nobody caught it early. I look at the tapes of him at two when I'm trying to get him to look at me for around 10 minutes while he just stared at a napkin in a restaurant (oddly enough at
Disneyland) and it was obvious if you knew what it was. What would be so wrong with the doctors asking a couple questions at a checkup? My son wouldn't have added to the stats, he would have gotten more help and probably had a brighter future.
When his funding is cut next year we have absolutely no way to pay for what we were getting. We are the parents who "take what they can get" because I can't see how financially killing our selves is fair to the rest of our family. I'm sure my other son deserves to go to college and not support his bankrupt elderly parents. I would have to work 10 hours to pay for 1 hour of speech therapy. I'm not sure that one hour is worth my absence for 10 (before tax so it's probably more like 14), so I will be working with him instead.Fortunately our School District has been wonderful with him. And his big goal for grade one, saying hi back to somebody when they say hi to him instead of turning away and quoting a movie. Your damn right I'm taking what I can get.
As for the diagnosis. It's NOT easy to get. It took a referral from his preschool teacher, 20 hours of classroom observation, a doctor's referral, 2 hours of pediatritian's apointments, 3 hours of speech assessment, and 7 hours with a pediatric psych. Any one of the people looking at him could have stopped it if nothing was there. It's not like kids who are fine are going to be diagnosed after that.
I have yet to meet anyone who would WANT this. Hell autism is becoming the replacement word for mentally retarded in a lot of circles. To have your kid called retarded and have parents complain that he shouldn't be in a class with theirs (despite the fact he brought an aid in that helps out the whole class and he's probably smarter than a large portion of the kids in there) adds salt to the wounds. I'm sure people are just scrambling to have that stigma attached to their kid.