People with autism possess greater ability to process information, study suggests

People with autism possess greater ability to process information, study suggests.

I thought this was interesting. Some quotes:

Professor Nilli Lavie, from the Institute of Cognitive Neuroscience at UCL, hypothesises that this combination of the ability to focus and a susceptibility to distraction might be caused by a higher than normal information processing capacity.


Professor Lavie says: “Our study confirms our hypothesis that people with autism have higher perceptual capacity compared to the typical population. This can only be seen once the task becomes more demanding, with more information to process. In the more challenging task conditions, people with autism are able to perceive significantly more information than the typical adult.”

I wonder, then, how this would also affect those with ADD/HD and if maybe any subtypes would be more akin to autism than not. Distractibility and autism kind of go hand and hand along with hyperfocusing, both of which are also a part of ADD/HD.

As it is, I already believe that the two are too similar to be separate conditions. This just adds to that growing list of reasons why they probably should fall under the same diagnosis, as far as I’m concerned.

But as the article reads, it seems to me that we can extrapolate that ASD children have difficulty processing information because as children, they simply don’t have the higher functioning capabilities (i.e. maturity, age appropriate cognitive skills being too young) as the adults to properly organize that information they receive. Or we could extrapolate that they aren’t being given enough information. I tend to think the latter is probably not correct simply because developmentally, they couldn’t do much with more information anyway but I do think that the prior could be a very real issue. The article does state that while not all ASD children are savants, they are likely to have the same processing ability.

So maybe the processing issues we know ASD children have, stem from a lack of maturity and those processing issues correct as they get older and develop their non-typical skills that help them to process that information the way they do.

Certainly an interesting assertion. Maybe all us parents that are desperately worried about our kids’ processing for no reason (well, no reason might be stretching it but you know what I’m saying).  One thing we do know is that MR is not a symptom of ASD so processing disorders are always on the minds of parents of ASD children.

What do you think this could mean?


MMR II and Autism: Microcompetition the Missing Link?

MMR II and Autism: Microcompetition the Missing Link?.

Fascinating story. I hope there’s more to come on this front.

Allen Frances: DSM 5 Freezes Out Its Stakeholders

Allen Frances: DSM 5 Freezes Out Its Stakeholders.

Is anyone really surprised?

Should we even try to recover our kids?

I know, I promised a post on recovery and what it means but I got sidetracked and offer you this instead, which is sorta-kinda the same thing. But not. I still plan to post one on recovery, though. Pinky promise.

In response to Jim C. Hines’ review of The Speed of Dark, I’m posting this here because what I have to say really isn’t appropriate for his blog comments. I also thought that maybe some of my readers have read the book and might have something to add and would want to go to his blog to comment. I haven’t actually read the book so this is really in response to the question he poses:should we “cure” those with autism? There was a little more to it, and I’m not even going to touch the high vs. low functioning topic today, but that’s the basic question.

As someone that has a son that is mostly recovered from autism, it’s not something that I can understand as being something that changes one’s life to the degree that this kind of moral question asks. The book may be showing a “cure” in a different angle than real life, but in reality, there is already help. Not enough help, but some.

In real life, recovery is not a cure because autism is not a mental disorder that needs curing (something the NDers and biomed parents can all agree upon, but that’s as far as the agreement goes). It’s a bunch of biological inconsistencies and malfunctions that end up creating neurological symptoms. In some people, these symptoms can’t be corrected because the underlying condition can’t be corrected or found. I would venture to add that it’s not for lack of trying. Each child is unique in their issues. There are no two children with autism that present exactly the same way. But with thousands of kids recovering from autism every year, it’s hard to imagine that western medicine is right. A lot of people can be helped, and without the use of antipsychotics or antidepressants.

The real question is: what’s really going on with our kids? Why does the diet work for some and not for others? Why is it that treatments for other chronic illnesses, like CFS or Lyme or any of the other many things biomed parents and practitioners generally discuss, work on our kids, too? Has anyone ever noticed that even some people with depression seem to recover through biomed? Why has no one in traditional western medicine noticed the pattern? Or maybe they have and just refuse to acknowledge or explore it? Okay, so that’s way more than one question. You get my drift.

Not all kids can be treated the same. What works for one doesn’t necessarily work for another. It boils down to this: different biological issues for different children (and adults). But they all produce neurological symptoms.

Is it fair to expect that a child that has nothing but diarrhea doesn’t have something wrong with his/her bowels? They call it “normal” in autism instead of asking why. Prevacid is what you get. This is only one of may examples of what plagues these children. Sensitivity to sound. Why is it that when you treat a child for PANDAS, this sensitivity goes away? The OCD goes away? Why is it that when another child is treated for lyme, that child becomes completely and totally recovered?

Because there are really still very few cases of autism. It’s still as rare as it’s ever been, if it’s ever been at all.

Recovery doesn’t change who a person is. It gives them the chance to live life the way they want. Being able to not live life with an aching stomach doesn’t change the core of a person. It just means their stomach doesn’t hurt. Which in the case of developing children, many times means they can sleep better, eat better and focus better. Which amazingly enough, means they function better. Whoda thunk?

So is the question really about changing the core of a person with autism or is it about healing the medical problems they have? A person who thinks in pictures is still going to think in pictures. Having a healthy body isn’t going to change that. A savant isn’t going to suddenly stop being a savant because their vitamin deficiency was treated and they stopped scripting Thomas the Tank Engine.

My son went from moderate/severe autism to pretty much typical (I always say “pretty much” or “mostly” because he still has raging ADD – we’re working on it) and not once did it change him as a person – except when I gave him antidepressants but that’s another post. He is still the same lovable, caring and funny little boy he always has been. He’s thrived and become so much more. And he’s able to tell me exactly how what few issues he has left bothers him and makes him hate himself and frustrates him. I’m not going to lay down and allow him to grow up hating himself and then deciding he has to accept that this is him and he doesn’t need to change, all the while silently hating every minute of his life – nor will I let someone else convince him of that.

No matter what, he’ll be happy with who he is and I’ll encourage him and love him and teach him to love himself, but that doesn’t mean I won’t strive to help him become who he wants to become.

There’s a reason why autistic adults have a high suicide rate. If it’s hard for neurotypical people to watch and be around, if it’s hard for a mother to watch her son struggle, it’s 100 times harder to be the autistic person. Everyone wants to be happy and comfortable with who they are, including those with ASD.

Now, this whole argument is probably geared more toward the management of symptoms with antipsychotics, antidepressants and the like and I’ve kind of hijacked it for biomed. But that’s what happens when the argument is so vague. Could mean traditional medicine, could mean biomed. I dunno. And maybe those drugs do change a person. Like I said earlier, when I gave my son antidepressants, they definitely changed him. He was, quite literally, psychotic. At best, they are only meant to manage symptoms, and they do a very poor job of it. Still, some people do very well on them. I can’t argue with that.

But the recovery I’m talking about, the recovery us “crazy moms” are talking about, doesn’t change a person. It doesn’t change the way a person thinks or views life.

Wait. I’m wrong. It does change people. It makes them feel normal. Or maybe a better way to say it is not that they feel normal, for what is normal anyway, but that they no longer feel abnormal. It takes away the pain they aren’t supposed to have. Being in pain (physically or emotionally) doesn’t make a person special or unique. It just makes them in pain. To go through life needing to bang your head against a wall long after the bleeding started, is that really something you want to keep?