"fake aspies" and self diagnosis. DISLIKE, sorry.
AardvarkGoodSwimmer
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Okay, I am Aspie self-diagnosed, and I think my mother is even further along on the spectrum than I am. If I could recommend one thing it's to try and be a bridge for your son, or rather try and build for him multiple bridges, rather than keeping him cloistered with you. My Mom sometimes acted like we were (are) best buddies. And while it is normal, and probably healthy, for mothers to be close to their sons who are age 12 and 13, she kept at it far too long.
And like so many things, it's not about clunk moves. It's not about suddenly shifting gears. It's more like if, say, it's more than 70% the cloistered model, then it's time to start thinking about and gently and matter-of-factly suggesting other social openings for you son and/or complimenting him as he develops his own interests.
My Mom also gave very clumsy social advice, as if a good skill works all the time, when of course it doesn't. Us human beings are just too complex! And I mean all of us, Aspie, 'Normal,' Different in Different Ways, all of us are just too complex for any one skill to work all the time in some kind of mechanical way. Well, I wish someone would have told me this (or better yet, model this). I had to largely figure it out on my own. And good social skills are heuristic, not algorithmic. And it's about medium touch. light touch the feedback is sometimes so small and indirect, it's hard to read what's going on. Medium touch, and graciously accept whatever feedback is there, that's where the person is at that time, and take it from there.
My husband and I are in the process of having our son evaluated to see if he is autistic or has aspergers.
If he's an Aspie then by definition he's autistic.
Thanks for the clarification. I was under the impression that Aspergers Was being removed from the Autism spectrum but I guess it hasn't happened yet. Does anyone have any useful information for me? If I had more time I wouldn't be asking. But I am desperate to find answers. I don't have time to wade through a lot of BS books. If anyone has a good book they would recommend let me know.
Aspergers is being removed as a diagnosis period, it's all just autism. But as I pointed out earlier Apergers is probably going to be used and/or understood for a while yet just like the term manic/depression for what would now be diagnosed as bi-polar disorder.
Well, to be precise, AS is being folded in as a subcategory of autism in the DSM-V, along with things like NVLD and PDD. An individual psych or neurologist might refer to "Asperger's" to distinguish a patient from someone with Kanner's autism, but it's all going to fall under the autism code in the Big Book O' Disorders.
Willard, that bit about Uncle Sam "taking care of his own" certainly sounds nice. But right now, I'm trying to get help just paying for the bills for this broken arm and subsequent physical therapy. So far, the state has turned me down because I'm not 65, I'm not blind, and without an official diagnosis, I'm not "disabled". Without that assistance, of course, I can't even get an appointment with a psychiatrist to diagnose my AS, or whatever other label they feel covers my various symptoms. The Social Security Administration doesn't like certifying people as "disabled" when they're missing limbs, and my problems can't be seen from a distance (for all that they keep me from getting past job interviews). So tell me, to whom do I turn at this point??
(Yes, I do have an application in with SS - but I've been told not to hope for anything.)
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He advice to go through low-income psych care for a diagnosis in the US is potentially quite bad advice. Those parts of the system are often entirely ignorant about developmental conditions in adults. And even the developmental service systems often don't know about any but the absolute most stereotypical autistic adults. I have an autism diagnosis but I have watched the local diagnostic process for poor people and most people, even those who clearly meet all the criteria for an AS diagnosis, end up getting diagnosed with depression, anxiety, or psychotic withdrawal, maybe a personality disorder or two because nobody here knows anything about autism in adults. And psych places look for psych conditions and don't tend to diagnose developmental conditions accurately (many knowing only stereotypes of autism).
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"In my world it's a place of patterns and feel. In my world it's a haven for what is real. It's my world, nobody can steal it, but people like me, we live in the shadows." -Donna Williams
(Yes, I do have an application in with SS - but I've been told not to hope for anything.)
I wasn't classified as disabled until after I was diagnosed with AS. When I went in to see a therapist for depression and overwhelming anxiety attacks, I was just unemployed, virtually homeless and suicidal. What I'm talking about is not related to Social Security. You don't need to go in armed with 'assistance' - that's the whole point, that you have nothing. No government wants more crazy homeless people living in their streets. Tell me I'm wrong all day long, I only know what I've experienced and it wasn't a miracle that fell out of the sky - it was a bunch of US government paperwork and a state agency that gets the majority of its funding that way helping me fill it out.
I don't understand what you mean by 'broken' arm and 'missing' limb, but if you're actually missing a limb, there's no way they could NOT classify you as disabled. Being a huge bureaucracy, however, the SS administration can take its sweet time getting around to a determination - it really helps to go through an attorney who specializes in SSI stuff. They can cut through the BS a lot faster and more efficiently with better results (like anything created by politicians, it's a paperwork game, amateurs have a hard time winning it), and a lot of them work NO WIN, NO FEE, so it won't cost you a cent.
I wouldn't count too heavily on that just yet. The DSM was supposed to have been revised nearly five years ago and they keep pushing the date back because they can't agree on all the changes. By the time the actual DSM-V actually gets published there may be no change in the classifications of Asperger Syndrome and HFA at all.
Last edited by Willard on 08 Jun 2010, 3:19 pm, edited 1 time in total.
sinsboldly
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Discuss
OK, since I am almost 60 years old a mature valid discussion sounds just great! I was 56 when I first heard about Asperger's Syndrome. I was taken up short by how much it described ME, and my supervisor at work was also shocked (as just an observer). As I continued to research it I identified more and more with the diagnosis and when I was 58 I had a psychological evaluation that confirmed I was, indeed Asperger's Syndrome - and not 'mild', either!
You can probably understand, at 56 I knew myself pretty well, knew my patterns and tendencies, etc. I had nothing to gain to see myself as Autistic, matter of fact, I had a lot to lose! There are a whole sub culture of undiagnosed Aspies old and elderly folks right here on WrongPlanet that isn't here because it is 'trendy' or 'cute' or 'special', but because this is the one time in our lives we finally figured out what was going on.
so . . .sue me!
Merle
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What I mean by "broken arm" is that about a month ago I fell off a skateboard in my garage and broke my arm. Reduction required minor surgery and the implantation of a metal plate in my wrist. The bills are mounting, but the state won't help because I get $704/month for watching my daughter, which to them means I'm capable of earning a wage and thus not deserving of assistance, and since I don't have the diagnosis of a disability, I'm not disabled - and the people at the local offices don't have the authority to decide that I'm disabled based on my own experiences; they need paperwork from physicians or psychiatrists in order to make the determination.
Without that paperwork, I can't get assistance to see a psychiatrist to get the paperwork. Catch-22. And they seem perfectly content to watch these bills drive me out into the street, if that's what I have to do to get assistance (currently, I live with my ex-wife and her husband - our relationship is, er, interesting, but we like it).
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Sodium is a metal that reacts explosively when exposed to water. Chlorine is a gas that'll kill you dead in moments. Together they make my fries taste good.
Honestly, even the most well-known AS professionals make mistakes.
Psychiatry isn't absolute science. There are some tests that are good, yes. However, testing can be expensive. People wonder why I did not get tested at school. Part of it was because I've feared the idea of being somebody's lab rat; I was a troubled kid, known to be rude to authorities and anyone else who happened to come near me. But another reason is because all the teachers really care about is your marks. If you do well in school, the teachers would often be willing to make exceptions for you because they can see that you're working really hard.
Also. There are other reasons why people don't get tested. Not everyone knows about AS, and sometimes, even though people can see that there's something off about you, they don't quite know what it is. The media's portrayal of AS/autism is very different from how it manifests itself in real people. Which really skews people's picture of what AS is.
In addition, many self-diagnosed people here are in their older ages. AS only entered the DSM in 1991. Therefore, it makes sense that they weren't diagnosed eariler.
I think the main thing is identifying with other people on the spectrum, as well as having people who are close to you offer their opinion. If the majority of them feel comfortable acknowledging that you have AS, then you probably do have it. I'm all for the self-diagnosed people seeing a professional. However, it can be expensive and thus unaccessible to some. I've also read some posts on here where people said that they prepared for their assessment so that they could come across as being more autistic. That is ridiculous, and a wrong diagnosis is entirely possible. And it is a shame. The whole point of it is to come across as yourself so that the right diagnosis could be granted.
And yes, it's ridiculous to make your decision based on reading some random articles on the Internet. But I do believe that not all self-diagnosed Aspies are fake.
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Leading a double life and loving it (but exhausted).
Likely ADHD instead of what I've been diagnosed with before.
Last edited by MathGirl on 08 Jun 2010, 4:04 pm, edited 2 times in total.
sinsboldly wrote:
Thank you. It's a little frustrating to have felt like a freak for so many years because you couldn't do or understand what everyone else does without a moment's thought and then to be told you just want an excuse or to be trendy. When I first found WP and started seeing myself again and again, I almost cried. I'm sure I'm not the only one.
CockneyRebel
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I really prefer just to take a person's word for it.
Who am I to accuse someone of faking? Who am I to add to anyone's personal pain by being holier-than-thou about my diagnosis? Further, even when somneone HAS a diagnosis, how does that suddenly become the gospel truth, written by the hand of God? How many of us (like me) had four or five incorrect diagnoses before we arrived at Asperger's? So, why are we claiming that someone else's doctor (or our own) MUST have been correct on this one?
I really hate threads like this. no matter the motives or intentions. People need support and they need their questions answered. They should not feel like outcasts their whole lives, just to come to an online community and feel like an outcast again.
That's shameful.
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"If you can't call someone else an idiot, then you are obviously not very good at what you do."
i didn;t mean it in a militious way, sorry if you took it like that. Also @Kiley they do an EEG to monitor brainwaves to check for seizures as I sometimes black out and they thought that was related to my Aspergers. I didn;t realise I'd offend anybody and I double checked by saying sorry in the title. ![]()
I apologize also if I was rash. I don't read much, I just go on rants.
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"If you can't call someone else an idiot, then you are obviously not very good at what you do."
Maybe it depends on the kind of self-dx'ed people you're seeing. If you're talking under 20 years old, there's probably some still coolness factor in pretending to have a psych diagnosis. As time goes on I'd expect that to end pretty rapidly, though. Psych conditions are highly stimagtized in most of the adult world.
If you're talking about older people, you have to remember that no one checked any kids for AS before 1994. And the checks that kids get nowadays are paid for with taxpayer money -- adults have to pay on their own. Your mentioning EEG's and such makes me think you had a really thorough and thus expensive assessment, even if you didn't pay for it. I saw someone on here yesterday say that the total cost of their assessment was about $5000 (holy sh*t).
Also, the diagnostic process doesn't seem to be standardized. If someone has an official dx you don't know if they got it through a 1-hour interview, or a lot more intense testing like you did. Do you also feel uncomfortable with people with the 'quicky' diagnoses?
I think we all tend to assume that our personal experience is the norm. I.e. if someone is diagnosed by asking their GP, and it's all realtively painless and simple, they assume that's how it is everywhere for everyone. There are endless stories here of GP's, psychologists, psychiatrists, and others telling people things like "you made eye contact once, so you can't possibly have AS." I was told by UCSF Medical Center that if you can dial the phone and ask about assessments, then you don't need one, because you can't possibly have an ASC.
As far as precison, and this is just IMHO: I understand, but my experiences in the world leave me with the thought that little in life is known "for certain." I've seen doctors engage in all manner of human folly and screw up with regard to health issues for 20 years. I don't see people with PhD's as gods, doctors are not automatically geniuses, and people with great credentials don't always know what they're doing. It's hard to live with that knowledge, always wondering if the ground you stand on is shifting sand. Certainty is so much more comfortable. But that doesn't necessarily make it more true.
