Showing posts with label Autism. Show all posts
Showing posts with label Autism. Show all posts

Sunday, April 20, 2008

Putting it all in perspective

The key to all communication is knowing when to shut up. This blog entry illustrates that.

ISOLATION - Norma Desmond

My son needs the label of Asperger’s Syndrome so that people stop using inappropriate ones. There are many gifts that come with this condition. Difficulties arise from an inability of ‘normal’ society to understand or accommodate the way his brain works.
two sides to every story


Want to be a free thinker but still a nice person: Advice from a graveyard

I stopped at the grave of Victorian babies – I counted three dead and the mother taken in childbirth with the last one. Reflecting on that poor woman having to look into the chilly darkness of her children's graves put my modern problems into perspective. I didn't want to be careless with my own children's lives by doing something irrevocable simply because I was angry with my husband. The weight of what the mother had gone through gave me an anchor for the afternoon.

When I noted how many young people buried there had been brought down by cholera, malaria or some other condition we no longer worry about, I decided it's a privilege to live long enough to have problems exacerbated by a long life and marriage. I strolled past the grave of a girl 'who left us in her 13th year'. She was the same age as my daughter at the time. Her sad mother had written: 'The flowers appeareth on the Earth. The flowers fadeth.'

Walking home, I finally decided not to be a modern wimp, but to keep strong and fight for my family's future. I thought my friends in the graveyard approved, for as I walked away, the sun suddenly shone on a tombstone that I'd never seen before: "Whether we wake or sleep," the inscription affirmed, "we live together."

After finding the perfect photo to illustrate this story, I find myself with nothing to say that hasn't been said better in the caption for the photo.

This series is produced for a utata summer project - which aims to tell a story with six photos. My project tells the positives and negatives of having aspergers syndrome mainly to increase awareness of the realities and nit the myths surrounding the autistic spectrum

www.utata.org/show/speaks/dramaqueennorm a/1.php
the first six make up the story but the extras are ones with the same treatment that I still like very much.
I do too. The photo caption links to the set on flickr - please go comment. The quote links to the photo essay on utata - and that sure looks like something I need to pass around too.

As for the post excerpt, from which I was going to weave a post about anti-vaccine activists, perspective and cost-benefit ratios - all that now seems rather crass, and a disservice to both contributions. So, I will leave this as it is, and leave all the implications for each reader as they are, without further comment.


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Monday, March 31, 2008

Well, so much for the "Plague" eh?

celebrate neurodiversity.One of the "one in one hundred and sixty-six" statistic shares her experiences.

Asperger's: My life as an Earthbound alien - CNN.com: "ATLANTA, Georgia (CNN) -- Recently, at 48 years of age, I was diagnosed with Asperger's syndrome. For most of my life, I knew that I was 'other,' not quite like everyone else. I searched for years for answers and found none, until an assignment at work required me to research autism. During that research, I found in the lives of other people with Asperger's threads of similarity that led to the diagnosis. Although having the diagnosis has been cathartic, it does not change the 'otherness.' It only confirms it."
Please note that she is a manager for CNN. Not homeless. Not a burden on society. And certainly, considering her occupation, able to communicate quite well, thank you.

Oh, and her desire for a cure? Nonexistent.
Don't pity me or try to cure or change me. If you could live in my head for just one day, you might weep at how much beauty I perceive in the world with my exquisite senses. I would not trade one small bit of that beauty, as overwhelming and powerful as it can be, for "normalcy."
Like her, I've never wanted to be "the same." I would have loved to have been accepted for myself, rather than being punished and abused for it. I'd have probably ended up in some equivalent position too, so it was poor judgment on the part of educators and parents alike to try and "normalize me." Which they most certainly did, although I was not diagnosed as AS to the best of my knowledge.

What I really wish had happened was an education tailored to my learning style, my intelligence and, of course, all the things I have to actually learn that "normal" people seem to pick up from context. But I'm still pretty happy being me - and frankly, the parts that I'm unhappy about have mostly been the result of other people who could not or would not respond to me as I am.



Image Credit:


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Tuesday, February 26, 2008

Bad News/Good News/Better News

Bad News: I missed an opportunity to club another "autistic advocacy" group over the head.

Good News: I wasn't missed.

WONDERFUL news: It WORKED!


The Autistic Self Advocacy Network (ASAN) - Sections:

Victory! The End of the Ransom Notes Campaign
Hello everyone,

I am pleased to inform you that this afternoon the NYU Child Study Center announced that they will be ending the "Ransom Notes" ad campaign in response to widespread public pressure from the disability community. You can read that announcement here (at the NYU Child Study Center's website). The thousands of people with disabilities, family members, professionals and others who have written, called, e-mailed and signed our petition have been heard. Today is a historic day for the disability community. Furthermore, having spoken directly with Dr. Harold Koplewicz, Director of the NYU Child Study Center, I have obtained a commitment to pursue real dialogue in the creation of any further ad campaign depicting individuals with disabilities. We applaud the NYU Child Study Center for hearing the voice of the disability community and withdrawing the "Ransom Notes" ad campaign.

Twenty-two disability rights organizations came together to ensure the withdrawal of this advertising campaign. Our response to this campaign stretched continents, with e-mails, letters and phone calls coming from as far away as Israel, Britain and Australia. The disability community acted with a unity and decisiveness that has rarely been heard before and we are seeing the results of our strength today. Our success sends an inescapable message: if you wish to depict people with disabilities, you must consult us and seek our approval. Anything less will guarantee that we will make our voices heard. We are willing to help anyone and any group that seeks to raise awareness of disability issues, but those efforts must be done with us, not against us. This is a victory for inclusion, for respect and for the strength and unity of people with disabilities across the world. It is that message that has carried the day in our successful response to this campaign. Furthermore, we intend to build on this progress, not only by continuing a dialogue with the NYU Child Study Center and using this momentum to ensure self-advocate representation at other institutions as well, but also by building on the broad and powerful alliance that secured the withdrawal of these ads in the first place. We are strongest when we stand together, as a community, as a culture and as a people.

Thank you to all of you who have made this victory possible. Remember: "Nothing About Us, Without Us!"

Regards,
Ari Ne'eman
The Autistic Self Advocacy Network, President
http://www.autisticadvocacy.org
info@autisticadvocacy.org
732.763.5530


When you think about it, "Nothing About Us, Without Us" is a pretty damn good slogan for anyone. In our particular socio-political context - well, the Democratic Party springs to mind. The whole idea of "superdelegates" who's entire role at the convention is to suppress any outbreak of democracy is endemic of an authoritarian mindset.

Or if you prefer an apt literary reference - "All pigs are equal, but some are more equal than others." I'd agree - if you are speaking of porcine volunteers for the role of luncheon meat. If I WERE a member of the Democratic Party - and I have a rather too much self-respect for that - my driving goal at the moment would be to purge the party of every authoritarian sonofabitch who thought it was a good idea to "organize" it in the same way the Republicans organized theirs.

Personally, whether it's Mommy or Daddy claiming to know best - well, I got fifty years of experience and a millennium of well-documented history that says they don't. Yes, folks, I did indeed start learning this lesson in infancy.

The sine qua non of American Authoritarianism at it's purest and most simple-minded is NeoConservatism. So, let us look back on how well the "Republican Revolution" worked. Taking a party from oblivion to domination to extinction in thirty years is definitely an achievement of significance - in the sense of "whom the Gods would destroy, they first make proud." It's not an example to emulate.

And it all comes out of listening to people who say "trust us, we know what we're doing."


This is why no advocacy group - and that's what political organizations of all sorts are, whatever the breadth of focus - should be allowed to forget "NOTHING ABOUT US WITHOUT US."

Or the import of the Second Amendment.

When you think about it, it's the summation of the US Declaration of Independence and the Bill of Rights, with the second amendment being the underline and "or else;" the final resort when the cluebat breaks.

You may well wonder why the hell in our culture, with an express written constitution that literally enshrines and makes sacred the right to use force against those who believe they "know better" than you and I that we still have to do things like this, that we need any "advocacy groups" other than our elected representatives. But the fact that we do need the constitution is exactly why we NEED various advocacy groups that have the express purpose of sneaking up on the powers that be with nail-studded cluebats.

Remember that Alexander Hamilton was pretty much saying "it's just a scrap of paper" before the ink was dry. There are many nations and cultures that do not need such explicit standards - because, well, they are more civilized than this nation made up of cowboys, pirates, remittance men, fugitives and grifters. Don't think I'm disparaging our heritage - but I'm not blind to it's implications, either.

The Constitution was written by a very cynical group of men - including Hamilton - and while no doubt many of the did indeed agree with Hamilton that they "knew better," they were mutually aware that their visions differed enough that some enforced guidelines of mutual toleration were required, and that if they did not agree on some set of rules that permitted them to differ without violence - violence and barbarism would ensue. (Or "greater barbarism," as any of King George's advisers would have said. I suspect Franklin would have cheerfully nodded and asked him to pass the wench.)

So I suppose this is the real message. If you belong to ANY minority group - and you do - and it isn't soldered into unshakable connection with the Powers that Be - and trust me, it ISN'T quite proportionally to the degree you innocently assume it is - you need to support all us whining minority interests seeking our "special rights," as the social conservatives like to dismissively say.

There is no form of social conservatism and social conformity that can contain the range of people and the range of ideas needed to create and maintain a wealthy, expanding civilization. And more critically, there is no form of authoritarian, centralized government that can productively and usefully attend to our diverse and conflicting interests. Bluntly, a reliance on authorities - and particularly the sort of scum that rises to the top of OUR melting pot - is no substitute for individual self-governance and the excercise of one's rights in defense and advancement of one's individual rights both as an individual and as a collective of individuals with common interests.

This particular case illustrates that there is still a large gap in our culture between genuine disability and exclusion based on prejudice, for if it were not true, it would hardly be profitable to even consider pandering to prejudicial parental panic. And as such, it's a beautiful illustration of a particular instance of a deplorable degree of collective stupidity.

We are entirely too tolerant of routine intolerance, and far too forgiving of casual, institutional ignorance. Well-meaning ignorance is possibly the worst and most insidious form - and that's the sort that I'm sure this particular incident revolved around.

But the worst possible manifestation of such social norms is the panicked thought that it is somehow reasonable to attempt to camouflage or adapt children to the expectations of the stupid rather than expect other persons to live up to the minimal standards of mutual toleration and acceptance required of a diverse society.

To be especially blunt - this campaign assumed that parents of children with mental distictions should assume that their children would be brutalized unless they were somehow "cured" of being noticable.

I do have a very effective cure for that attitude myself. It's called "Martial Arts Classes."

Not only was the campaign appallingly offensive, but clearly, nobody involved in creating, deploying and funding the campaign noticed. That inevitably leads me to the assumption that they suffered from prejudice against the "differently abled" to a shocking degree themselves.

That sort of thing is bad enough when the folks involved are advocating against your interests, but when they are supposedly acting on your behalf - and sucking up money that damn well ought to be spend in your collective interests if it's going to be spent at all - it's not just offensive, it's injurious.

And whatever sort of minority you are, when the powers that be "act in your interest" in such a way - it's time to haul out the cluebat.

Attention, all minorities. Particularly Florida voters. Those who say "trust me, I know better" had best be required to prove it. And if they prove - spectacularly - that they do not, it's time to rid yourselves of them - or continue to suffer the price of their possibly well-meaning foolishness.


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Monday, February 25, 2008

The Life of a Free Range Aspie

Autism, Aspergers, PDD, PDDNOS are all conditions that exist on the Autistic Spectrum. All are classed as "disorders" in the DSMIV. That means they represent a billing code - and the world is filled with "cures" and advocates of "cures" for the whole range.

Inasmuch as there seems to be no serious consensus on what causes autism, or whether, in isolation, it's a problem outside of the extreme, (and those extremes do have protocols associated with them), the faint aroma of bubbling snake oil ought to be tickling your sinuses at this moment.

Some of us who are unquestionably on the spectrum do not see it as a "disorder" so much as a distinct difference with inherent communications difficulties - at least, when it's not in it's extreme forms. In many ways, it's social and personal impacts are similar to more obvious things, like blindness or deafness. And, as is well understood, any sensory deficit brings with it compensations that are arguably advantageous if the differently abled person finds a niche where they can bring that enhanced ability to bear.

(You know, I believe that's the first time I've ever used that PC phrase in a literally meaningful way.)

But I will say that "differently abled" is a much more useful way of thinking about aspergers, autism, and indeed almost all "disabilities." For the most point, the fact that such a person is unable to cope in the way almost everyone would requires they develop abilities that are comparatively rare by definition. And that - especially when those abilities are guided and developed with that idea in mind - is a valuable thing.

Unfortunately, groups like "Autism Speaks" are unwilling to comprehend that. Indeed, they are unwilling to even admit that autistics capable of communicating their preference to not be spoken for exist. As for aspies - well, there's nothing wrong with us that a few months in a skinner box couldn't fix. It's merely demoniacally inspired willfulness. It should not be particularly surprising that Autism Speaks and allied organizations are composed almost entirely of social conservatives; people for whom "not fitting in" is considered a crime of willful disobedience, or a disability of such crippling extent that any "cure" up to and including lobotomy or abortion is better than the "disease."

If you have stumbled across this almost unavoidable (and odious) viewpoint in a search for autism information, you might wish to trundle on over to autistics.org for the autie point of view, or you can drop by wampi.org for a mother's perspective on successfully raising a "free range aspie," without the "benefit" of most interventions and no aversives at all.

Todd is now in high school - and not a particularly aspie-aware one, despite our best efforts. And yet, while being more aspie than I am in many ways, he has friends, he's well liked, he's respected by his peers and his teachers, and this is all despite behavioral issues that one could easily label as "annoying."

Charitably.

The fact is, when everyone involved knows what's going on, it's a lot easier to avoid tripping the xenophobe circuits that lurk in our hindbrains. Our reptilian bits are convinced that what is concealed is potentially deadly dangerous - and there's been nothing in my conscious history that could argue with that first presumption all that effectively. Once we know that an annoyance is merely that - an inevitable and understandable consequence of a person being who they are, it's a lot easier on everyone involved. Particularly the aspie or autie who is no more immune to seeing themselves as being dangerously different than anyone else.

But of course, before you can be upfront about what you are, you have to understand it yourself. Alas, I had no words for what I was before my early forties - while Todd's mom knew from very very early on.

And, I should add with a proud grin, didn't much care. Nor did his dad (not I) - I will say with equally proud smugness. As a result, he's had appropriate accommodations his entire life - with no expectations whatsoever along the line of "fitting in to the world around him." That's an excellent thing, both philosophically and practically - if there's one thing a person on the AS spectrum is unlikely to be able to do effectively, it's "fit in" - and efforts in that direction will trigger pink monkey syndrome.

Trust me on that - my entire primary and secondary education was an exercise in tossing a pink monkey into the primate cage to see if he'll be able to pass THIS time.




It's hard on the pink monkey - and trust me when I tell you, it can end up with rather scuffed "normal" chimplets and primate attendants.

Of course, living in an area with larger catchment is a great thing; Todd was lucky in that he nearly immediately found his pink monkey posse and we-all just gutted it out as he geeked it up with his strange little friends.

I never, EVER want to hear the word "Pokemon" again.

And at the same time, I realized that with a shift in time, there I was geeking it up with MY strange little friends with the equally baffling Dungeons and Dragons - a bootleg first edition, actually. No, paperback.

Yeah, THAT old. Hell, I even wrote supplements. Todd's obsession never reached those heights - in regard to THAT topic. But the capacity will serve him well, since he didn't have parents who swatted him every time he wandered off into his head.

And yet, if you are concerned that you are doing the wrong thing as a parent, allow me to reassure you to a degree. I've come to the conclusion that in regard to my own personal configuration and nature, I had the worst parents possible. My mother was neurotic to the point of insanity (borderline, perhaps) and if my father was not a clinical sociopath - it was probably due to him being barely clever enough to avoid any significant attention.

So, aside from the obvious, the problem was that I could never rely on my parents to do the right thing, or even the predictable wrong thing. All I knew was that to bring an "instance" to their attention would raise it to the level of an outright "situation."

But nonetheless I managed to survive and find a niche. I am now fifty and content with my life - a fact that would probably baffle the hell out of an impartial neurotypical, for I have nothing of significance that most people would equate with proof of success. Me, I have all the proof I need.

I look at most of the things I'm supposed to want as "crap I have to dust." It's amazing how starkly different your values are if none of them involve impressing other people and expanding your social network. It's not surprising that many neurotypicals still see us as alien and therefore dangerous; there's absolutely nothing they think of as prime motivators that strike most aspies as being good things. Social dominance. Control of large, complex organizations. Having a full roladex. "Winning."

Todd LOVED t-ball until he discovered that winning meant someone else had to lose. Then he was done. He loved martial arts - as long as it wasn't a "sport." And he's one hell of a good fencer in particular and loves swordplay in general - but not at all interested in scored matches.

Like me, he's only interested in becoming better than he was last week. And like me, at some point, having had to come up for air, he will run head on into the fact that he's objectively as good as anyone else doing what he does - possibly better - and have no freaking idea what to do about it.

Fortunately, it appears that there's already a profession intended to deal with this matter.

We call them "agents." And pragmatically, that's the most significant accommodation needed for any aspie, whether they are literal agents, or simply family, spouses and partners that act in that way.

Pick any aspie of significance - like, say Einstein - and you will find that there was a person who is steering them toward the best applications of what they are, and steering others who need those talents toward them. I would not be horribly surprised to find that a large percentage of those persons have as rare a wetware configuration as our own.

But even left to our own devices, and having to cope with very nearly the worst possible combination of circumstances, I note that as we age, we tend to settle down and, as I said, find our niches. With help, we can probably find more impressive or lucrative niches - but I wonder to what extent that actually matters to us as aspies. It probably matters more to the people to whom we matter, frankly.

I think of myself as well-tested proof of concept.

My writing is distinctly aspie-style communication - something you may come to recognize as you go from place to place, reading what other aspies and auties have to say about themselves and their lives. I have little or no motivation to create other than the act of creation, whether it is writing or artwork. I love electronic media because it eliminates most of the out-of -pocket expense of being an artist or writer.

I've only lately really grasped that sometimes, in order for the effort to be meaningful, there has to be some objective proof of utility. Or, at least, that's my feeling. Lord knows, within the art world, I could point to exceptions. Nonetheless, those exceptions seem to get a lot of attention and attract commissions, so perhaps it's merely a different expression of my view.

Had I had different advantages - such as the upbringing Todd enjoys - I would very probably be ensconced in some comfortable tweed-lined academic niche. I'm not at all sure that I'd be more content than I am, and I'd only be as content as I am if I had people to cope with the things I could not cope with well or at all.

But certainly I would be of greater utility to more people and be making a broader, more lasting and I would hope positive impact on society.

On the other hand, with exactly the wrong set of circumstances - I could have been Karl Rove or Condi Rice. So all things being equal, I'll settle for the angels I have. I was on my way to achieving a niche of that sort when a parental idiocy sent me into a state of clinical depression that left me rather behind the curve.

But seeing as that diversion left me with an expertise and understandings I hope to ghu no more than a handful of other people can match, I am content - for I still have decades to apply it, goddess willing and the sky don't fall.

I think it's reasonable to state that whatever I think about the views parents in some factions of the autism awareness movement, generally parents wish their children to be as happy and as successful as they. And I'm here to say that no matter how badly you think you have screwed that up in your well-meaning way, that's probably still possible.

Whether you understand why they are as happy as they are, and think of themselves as successes when you don't is quite beside the point, really.

But of course it will be ever so much easier on everyone if you accept them for what they are. It could be worse, after all.

You could have a charismatic 89 IQ high-school linebacker with abnormally high testosterone levels and an addictive personality, doomed to a career in door to door appliance sales.

Frankly, I'd take Todd over even an average teenager. Some times Todd screws up, of course, like any other inexperienced human being. But the thing that relieves me is that he always errs on the safe side; he doen't take foolish risks and he does not seek out the company of people who do. I don't think I can think of an instance of him making the same mistake twice. I get to sleep at night, knowing for near certainty that there will be no emergency in his life that cannot wait for daylight - and it will almost certainly be deliberately caused by someone else.

Usually someone who thinks they "know better" and have a right to impose that vision upon us.

On such occasions, with such people. I find myself having no difficulty maintaining eye contact and smiling. None whatsoever. Oddly enough, they find it a lot less reassuring than all their theorizing says it ought to be.


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Friday, November 23, 2007

No, I haven't died, I got a (second) life.

I imagine that having died would be more comfortable. But don't take that seriously; I'm in the last stages of a med change and such thoughts are symptomatic of the lack of seritonin and/or dopamine, not a lack of meaning.

I've had a long and productive relationship with Paxil, but I'm afraid the relationship is over. Like many really long relationships, there's a period of withdrawal and readjustment. I'm feeling particularly autistic and multiple, with a good selection of involuntary movements and sensory issues thrown in.

Most critically, my judgment sucks, so for right now, I won't be saying much about much of significance until I'm stable again.

I need to obsess about something, but if I spent much time obsessed about society and politics under these conditions, I'd probably slit my throat. Right now it's almost impossible for me to take a deep breath and walk away, so I'm paying as little attention to current events as possible.

Instead, I've doing Second Life, climbing the learning curve and getting ready for what many think to be the next big thing; the 3-D web.

It's still an open question as to whether Lindon Lab's Second Life or one of a myriad of other such platforms, engines and combinations thereof will become the new http protocol, but it's an ...erm... virtual certainty that one will perhaps in time to materially affect the 2008 election. If not, it will affect the 2010 elections - or if there are no elections in 2010, make it rather difficult to impose an effective dictatorship.

Not that I've been doing anything on Second Life that involves politics.

It's all very fascinating and complex, but there's little that's worth sharing, or that I could share, since when I'm in this state I also tend to let my Id take me where it will, and you probably don't want to follow. For those that do, at some point I' MAY have something coherent enough to post to Erotic Truth.

But I'm holding onto that thought until my thought process is again supported with socially-approved chemical crutches. I'll be trying Welbutrin and with any luck, it will work and I won't have to spend any more time being undermedicated.

Speaking of Paxil, while I'm not a medical professional and not pretending in any way to have more authority than entirely too much personal experience; take this as a bit of practical advice. In the normal course of events, you should never, ever, ever take an antidepressant for more than a year, and certainly never without the ongoing support of a certified clinical psycopharmocologist. [Cue Laugh Track]

NORMAL people - those who have not had their neuro-chemistry permanently altered with a series of untreated clinical depressions - will not likely need to take any antidepressant longer than a few months so the following is intended for those who must manage depression like diabetics manage their insulin levels, adapting to the unpalatable reality that their mental health is largely dependent on direct chemical intervention.

In the realm of practical reality within these here United States, simply be glad that you can get a GP to prescribe antidepressants. Meanwhile, as someone who's had brushes here and there with mental health professionals - let me advise you that you owe you and your loved ones a sincere shot at becoming a gifted amateur specializing in you.

However, as I said, Paxil worked very well for me, for a long time, so well and so long that it's apparent worst downside bit me; it's a persistent med that you do become gradually habituated to. So you can't simply switch medications over a long weekend - the higher your dosage, the longer it takes to taper off, and the more uncomfortable it will be. There's a lot of information out there on the web about Paxil/paroxidine and like all medications, you need to balance the up sides with the down sides. Paxil has plenty of both, and like all such medications, what happens to you is something that really cannot be precisely predicted.

I'm utterly miserable and unfit for human company while unaccountably blessed that there are folks in my life that will tolerate me and and monitor my behavior. If that was not the case - and I cannot possibly underline this enough - it's urgent that you accomplish this in a mental hospital or clinic.

Still, six years of relative sanity and stability is worth a lot, even if it comes with a massive balloon payment at the end of the term, and I have nothing but praise for the wonderful boffins who came up with this magic pill. I just wish the ride could have lasted a little longer.


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Tuesday, June 19, 2007

1% is not enough, recruit, recruit, recruit!

Autism Diva: Where are these 1 in 166 autistics?:

"Where are these 1 in 166 autistics?
The increasing diagnosis of autism may be being accompanied by a decrease of other diagnoses, and it may be just that more people know what autism looks like now.

The largest part of the increase in autism among the California DDS numbers is in high functioning autistics, though the calamity howlers would have you believe that we have low functioning autistics coming out of our collective pores."
My analysis went in a parallel direction - given we are such a large threat to the status quo, I'd have thought we would be having a more profound effect. As far as I can tell, the only affect we are having is on fund raising efforts - and perhaps some impact on the overuse of mercury in medicine and industry. It probably won't change anything for us, but as Martha would say, "It's a Good Thing."

There are a total of 176,465 clients of all types in the Cal DDS system (cerebral palsy, mental retardation, autism and epilepsy are the main dxs) if you divide the total population of California by the whole case load of the California DDS you get 1 DDS client per 201 Californians.

We still aren't up to 1 in 166 now are we?

If you go to www.oddizm.com you can find links to more analyses of the stats that are badly abused to support a non existent autism epidemic. As usual with medical panics in the US, the media and advocates are in cohoots to create the most sensational story - and suppress the real one.


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Thursday, March 08, 2007

Even MORE Pokez in the eye - and insight as to why.


The Pokez incident that I first mentioned a week or so ago refuses to go away, and this story gives an idea as to why.

San Diego CityBEAT: "“This is coming from all over the world,” said William Cary, a former board member of the San Diego Autism Society. “Some people are calling for a boycott, but there are others of us who would like to go with our children, and see how they’re going to respond, or reevaluate how they treat people.”

The Centers for Disease Control estimates that about 4 million children are born with autism every year, and one in 152 8-year-olds are autistic. Cary believes the Pokez incident tapped a deep reservoir of frustration in the autistic community.

“Everyone has a horror story,” Cary said. “I once had a supermarket clerk ask if my son needed an exorcism.”

Glass filed a police report and has been in contact with the City Attorney’s office. At the moment, he doesn’t plan to sue, but that could change.

“What I really want out of this is an apology for David,” he said. “He needs to know he didn’t do anything wrong.”"
Both autistics themselves AND the parents of autistics need to know they haven't done anything wrong when some disturbed individual decides to target the day's frustration upon us or ours just because we are a visible target.

I'm Autistic, what's your excuse?
Frankly, this has more to do with the concepts of Civility, Civilization and Civil Rights than it does with Autism or the alleged lack of it by the experts in neurobiology at Pokez.

David did nothing wrong, Pokez has done nothing right; compounding a waitress's "mental moment" with a callus disregard for the family and the good opinion of civilized people.

I believe it's time - both specifically and generally - to insist on being treated with the same courtesy given whatever home-boys the easily amused hang with, whether they be grungy rock fans, as in this case, schoolyard bullies or fans of quack cures for visible differences.

It is all of a piece, symptomatic of deep dysfunctions in our society, depravities that we must no longer tolerate in the name of "trying to understand both sides." This is one of those cases where there IS only one side; where even the most biased retelling of the facts cannot conceal the malicious and casual indifference to the difficulties and pain of others that has permeated our society. To remain silent, or to patiently endure it is to permit evil to flourish.


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