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When Geeks Meet, Are They More Likely To Have Autistic Kids?
An anonymous reader writes "Psychologist Simon Baron-Cohen thinks scientists and engineers could be more likely to have a child with autism, an idea that is fairly common currency in Silicon Valley. But many researchers say the proof isn't there yet. From the article: 'Baron-Cohen proposes that systemizing ability can be inherited — and that in information-technology (IT) enclaves such as Silicon Valley, where hypersystemizers are more likely to meet, pair off and have children, the result is a higher incidence of autism. Back in 1997, for example, he concluded that fathers of children with autism were more than twice as likely to be engineers as were fathers of non-autistic children. But autism researchers ... found that fathers of children with autism were more likely to work in medicine, science and accountancy, as well as engineering, and less likely to have manual occupations. They suggested that these fathers were simply more likely to have reached a higher level of education. Baron-Cohen says that when he reanalysed the data and controlled for education level, he found that fathers of children with autism were still more likely to be engineers, although the difference was smaller.'"
Isn't this a dupe?
Wasn't it a terrible story the first time around?
When I was a kid 24.679 years ago I had 4 kids in my 9am class with special needs, 2 in my 10 am class, 6 in my 11 am class, and 5 in my noon class. I had an average of 4.25 kids with special needs in my classes. There was only a 0.003% mention of incidence of autism on a daily sliding window basis but that didn't matter because we all got the same number of pencils, exactly 1 per week for the school year for 36 weeks of school, but on leap years we didn't get an extra 0.00555 pencils which I thought was wrong, nor did anyone take into account the total length of carbon trace each of us used or the exact pressure each of used pushed with.
When I was a kid we didn't have autism.
AC because I don't remember my login credentials and lost the associated email address years ago. If someone can mod this up to at least 1 or 2 so people can see it, I'd appreciate it.
I am an engineer, my wife is an astronomer. We have an ASD child. Around 18 months we definitely noticed odd behaviors, all red flags. She wouldn't respond to her name. She'd line up objects of the same color. She'd stack identical objects precisely, not the typical stacking you see from toddlers. She'd walk on the balls of her feet. Her speech was delayed. She wouldn't make eye contact. She'd arch her back away from hugs or other physical contact.
The initial diagnosis was PDD-NOS, pervasive developmental disorder, not otherwise specified. Our daughter's behavior didn't map precisely to an autism diagnosis, but she was on the spectrum. I will readily admit that I did not want that diagnosis. I wanted someone to tell me that my daughter was just a late bloomer, that the language delay was because we are a bilingual household, that all of the autistic behaviors weren't really autistic. It threw us into a very unfamiliar world of speech therapy, occupational therapy, physical therapy, insurance coverage, insurance denials, out of pocket expenses, sensory integration equipment, weighted vests, sleep disruptions ... the list goes on.
It's not easy. Sometimes I feel sympathy for the parents of neurologically atypical kids when they say "sometimes I wish my child just had cancer" because that's something that can hopefully be treated, hopefully be cured, as opposed to having to wrap your brain around the fact that your child is autistic, and you just. don't. know. if she'll ever be able to live independently, if she'll be able to be a productive member of society, if she'll be able to tell you that she loves you.
I didn't seek out the diagnosis. I didn't want her to get one at first, but it's true that having one has made it easier to open doors to certain treatment options. It's also closed other doors to certain treatment options -- "Oh, we only cover 20 occupational therapy visits per year, but none for developmental disabilities, and we consider spectrum disorders developmental issues, so ... yeah, sucks to be you!"
It's been over a year since that dx, and since then, thanks to aggressive early intervention we're seeing improvements. My wife has put her career on hold to devote herself full-time to this -- the window of opportunity is closing, and we're fortunate that this was caught early on, so we need to make the most of these early years -- and spends her days dealing with children's hospitals, therapists, early education from the school district, sleep specialists, insurance companies who give you a different answer every time you call. The last time we saw the developmental pediatrics specialist, he changed the diagnosis to high functioning autism. We're making progress but it'll be with us forever.
Still, when I can get a "papa, up" from her as I lift her into her bed, I tell myself that hopefully it'll be ok.