This is one of the major problems with the autism community and the diagnosis. Someone who doesn't make eye contact and perhaps fixates on certain topics (maybe comp Sci) has the same diagnosis as my child who will require lifelong care and never live independently.
We need the public to understand both sides. To some autism is considered a 'gift', and this study suggested 46% of their numbers were at or above average IQ. What they didn't highlight is that 31% have low IQ and are the ones (as I mentioned earlier) that will require lifelong care and put an unimaginable burden on families.
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The problem with classifying autistic as "intelligent" and "obsessive" and "introverted" hides the truth that there are the other half of autistic people on the low-functioning end of the spectrum cannot live independently. And no, they're not exceptional at counting cards at Blackjack table either.
Young autistic children require many hours of direct speech and behavior therapy everyday just to get them to basic level of communicating what they want. This is the only known effective treatment for autistic children, but it has to happen every day for years, and it is extremely expensive. Trivializing autism causes insurance companies to put caps and limits on covering direct therapy because they don't see it as essential, but parents of autistic kids know that direct intense therapy is essential and makes a big difference.
As I've said elsewhere in this thread, when the CDC chooses to highlight (1) that 46% of these kids are average to above IQ, it says "don't worry". Why didn't the CDC choose to highlight "31% of these kids are severely impacted, unemployable, and will require lifelong care at an incredible expense to their families (financial and emotional) and taxpayers"? 46% is not even a majority, yet the CDC chose that group to mention as a highlight.
Why would the CDC make that choice?
My girlfriends brother has autism and he is smart, but will watch "finding nemo" for two months on repeat (he's 8 btw). A classmate of mine (who is extremely intelligent) also has autism, but functions normally, besides running everywhere and not making eye contact. Clearly, there is a large difference between the two and they have drastically different traits and I would argue different disorders.
If this is the case, the autism spectrum should be split into different disorders. This would provide more information to parents, and teachers about what particular traits the child has.
Using the example above, my kid is closer to paraplegic. But being in the community, I know kids with the sprained ankle too. Based on the comments in this thread, it seems many here think that most in the community have a sprained ankle. From this one study 54% are below or average IQ, with 31% definitely below. These 31% are the ones that will require lifelong care.
We need to change terminology to differentiate, so the debates about whether an increase is actually an increase don't happen. The CDC provides stats on several diseases in real time - autism numbers came out this week for kids born in 2002 and diagnosed before 2010. Doesn't anyone question why this is?
Autism is a spectrum. It's not just Asperger's and wholly unemployable. There is lots of room in the middle.
This is reasonable in regard to high-functioning Aspies, but remember that ASD covers a wide range. I think it would be better to retain the separate label for Asperger's, because it is distinguished by normal or better intelligence and language ability (while sharing other traits with classic autism) -- however, even within the Asperger's category there is a wide range.
Another aspect that is often underappreciated is that the HF aspie, if smart enough, can learn to adjust to normal society to such a degree that he/she can often pass for normal, so that a diagnostician would place him/her at a different point on the spectrum at different stages of life.
If you have the ability to say "I don't need fixing" to the autism organizations, rest assured that they aren't referring to you.
And on second thought, it may make sense from a public health perspective to abandon labels for subtypes, unless the experts think the subtypes have different causes. But AFAIK the causes of ASD are unknown.
The burden on families and society is quite different for these groups, and further classifications are necessary. There are also several related health patterns (digestive, allergy, etc.) with many who are usually more severely impacted which will likely lead to more research on causes. Some advocate for an additional medical diagnosis instead of just referring to the neurological. Down the road there could be a separate diagnosis for those.
It really depends on the severity of the symptoms, and whether the individual has developed effective coping strategies.