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Wednesday, 8 April 2009

Info Post
The Curebie debate continues to rage and while it's not normally a thing I'd get involved with, there's quite an intelligent article from Tiff on Life on the Spectrum

The article is called;

Just Plain Fed Up
http://lifeonthes.blogspot.com/2009/04/just-plain-fed-up.html

It walks the fine line between curing and acceptance and advocates neither. If it advocates anything, it's an end to advocacy. There's no doubt about it Tiff would certainly investigate a cure if one came along but it's this line that makes her different;

I'm not shinning a positive light on autism, I'm shinning a positive light on my SON who happens to have autism. He has a lot of gifts and I refuse to walk around looking like I've just attend his funeral so people can throw money towards a cure

I'm not sure that I agree with a cessation of all advocacy. After all, it's advocacy that gets ideas off the drawing board and into real life. I do however agree with Tiff's sentiments. Those with the condition or those who are caring for a family member with the condition are best placed to present their "individual faces" of autism. Nobody is really up to the task of presenting a single unified "face of autism" because there is no unity. Everyone is unique.

The Cure
Right now, there is no cure for autism, just a bunch of dangerous and untested theories and therapies. There's no point in a curebie debate (to cure or not to cure) simply because there is no cure.

I'm also not terribly interested in throwing money towards the search for a cure because I'm not convinced that one will be found. I'm even less certain that I or my children would want it if it were found.

Of course, I accept that there are people out there who would do anything for a cure but lets face it. If they announced a cure tomorrow, it would still be ten years before it reached the common people and by that time, most of our affected children will be grown up and able to make the decision for themselves.

I'd much rather see the "search for a cure" money being put to use providing better facilities for the children and parents with autism. They need support now, not dreams tomorrow.

Acceptance
Tiff puts her finger on the crux of the whole thing. Acceptance. That's what makes the difference between a good parent and a great one. It's obvious that she's not only accepted her son's condition but is also able to enjoy the little touches that his unique gifts bring.

There's also great followup article on Saved Aspie, called;

The Cure Debate Continues
http://savedaspie.blogspot.com/2009/04/cure-debate-continues.html

This has some interesting real-life recollections about meeting the parents with the wrong attitude and it's well worth a read.

Normal is just so over-rated. Instead of trying to force your aspie to fit into the "normal box", why not try to see them for the amazing people that they are. There's a good reason why many aspies don't want to be cured.

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