How are adults diagnosed with Aspergers helped?
Services are heavily skewed towards children and adolescents. "Help" comes from learning as much as you can about Asperger's and autism and applying it to your own situation.
Connection to the autism community is a good place to start.
_________________
When God made me He didn't use a mold. I'm FREEHAND baby!
The road to my hell is paved with your good intentions.
-Accommodations: You get get accommodations at work and school because of your diagnosis.
-Seeing specialists: Some counselors and such specialize in working with people with ASDs, without a diagnosis they're unlikely to take you on as a patient (because of having too many people trying to see them with diagnoses). It is sometimes possible to do this without a diagnosis, but much more difficult.
-Monetary help: Sometimes people can get disability payments for an ASD. This is dependent on otherwise meeting criteria for it.
-Vocational Rehab: If you're being unable to find and hold a job, state vocational rehab groups will work with you if you have a diagnosis of an ASD. The quality of this varies by location.
-Others understanding you better: Whether parents, friends, partners or whatever, a diagnosis gives people the reassurance that you are that way, and lets them research what they can do to help or what they can avoid. (It was not until my diagnosis that my dad stopped trying to pressure me to be on anxiety medication for traits of my Asperger's that were not due to anxiety)
And then there is of course just knowing what traits do match your weaknesses and working to minimize the negative effect of this on your life.
Having a diagnosis as an adult means for me:
* I have greater self-understanding (the diagnostician was able to tell me things about myself - e.g. about my mannerisms and about how I spoke - that I was not aware of)
* others whom I tell (my spouse, my boss, my friends) may have a better understanding of me (though that will also depend on their knowledge of AS and willingness to learn)
* my psychologist understands me better when working with me about emotions and sensory sensitivity
I qualify for health insurance cover in so far as I am referred by my GP for help with stress, anxiety, or depression. To the extent that having AS makes the risk of those things more obvious, having a diagnosis may help me a little with getting a referral for psychological services.
Right, I left that out.
In some places a diagnosis hurts you in the way of health insurance, in others it helps.
-I likely qualify for a secondary health insurance from the state (because of a disability + low income despite the fact I have other health insurance), that would help me pay copays.
-My health insurance now must cover things like Occupational Therapy if deemed medically necessary because I have a diagnosis of an ASD. I've been debating whether I want to take advantage of that because my sensory issues are huge (I feel that even though I consider sensory issues parts of ASDs, I have SPD on top of those).
I guess it depends on where you live and what services are available. But as wavefreak58 said, services are mostly aimed at children and adolescents (and adults at the severe end of the spectrum who were diagnosed as children). I hope that services for newly diagnosed adults will improve as surely there must be more and more of us.
For me personally, the only "help" I get are the sessions with my psychologist, and I'm getting them more so because I suffer from depression. I don't get any more because I have AS, although that would be very useful.
(ETA, my psych mentioned I could probably also get access to an OT to help with my clumsiness. I don't think it's necessary at this point though.)
Last edited by CheeseDeprived on 24 Oct 2011, 3:55 am, edited 1 time in total.
It surprised me a little that even here in Eastern-Europe (Hungary) they can provide help for adults like I am. Well, I'm not getting it yet, I have to finish the evaluation first. My biggest problem is with relationships with the opposite gender. I wonder what kind of help they can offer me, though...
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"Aut viam inveniam aut faciam." (Hannibal) - Latin for "I'll either find a way or make one."
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If you are high functioning - do not expect much.
I got "free" dental (reduced cost: "Högkostnadskort" in Swedish) for a few years since my teeth took severe damage from a depression i was in earlier. Most of it was fixed with my own money before i got the card, so - well, not much help there.
Then there are some social gathering (help groups) i can apply for, but they mainly focus on helping low functioning aspies how to cook, make their bed (etc)... not very useful for me at all.
What i really wanted was sort of help to form relationships, even a free membership on a dating site would be appreciated - even if they are the way they are.
_________________
"It is far better to grasp the Universe as it really is than to persist in delusion, however satisfying and reassuring" (Carl Sagan)
I have read a lot of comments so far that I definitely relate to on getting diagnosed with Asperger's as an adult. One of the biggest things for me was that I finally knew what it was that made me so different/eccentric all of these years. I then joined WrongPlanet and am continuing to learn more and more about the autism spectrum.
_________________
"My journey has just begun."
My experience so far is that if you've managed to survive without becoming homeless for many years, managed to get married and stay married for many years, and have managed to raise three children without anyone in the government feeling they would be better off somewhere else...
Yer screwed and on your own.
I do hear there are some groups though, and that depends a lot on where you are. I haven't looked into any in my own area yet, so I've no idea how much help they would be. I'm pretty accepting of who I am, so I really don't need much in the way of emotional support.
What I need is more in the way of a life coach, but without any funding to pay for it, I'm left to flail about. Not much fun I tell you, and a truly stupid waste.
I'm in subsidized housing, on Foodstamps, and all my kids are on medicaid because I cannot manage my life well enough to change this situation. I can guarantee that the cost of a life coach to help me improve my situation would, in the long run, cost a hell of a lot less that it has and will to continue on this course.
_________________
I'm not likely to be around much longer. As before when I first signed up here years ago, I'm finding that after a long hiatus, and after only a few days back on here, I'm spending way too much time here again already. So I'm requesting my account be locked, banned or whatever. It's just time. Until then, well, I dunno...
-Seeing specialists: Some counselors and such specialize in working with people with ASDs, without a diagnosis they're unlikely to take you on as a patient (because of having too many people trying to see them with diagnoses). It is sometimes possible to do this without a diagnosis, but much more difficult.
-Monetary help: Sometimes people can get disability payments for an ASD. This is dependent on otherwise meeting criteria for it.
-Vocational Rehab: If you're being unable to find and hold a job, state vocational rehab groups will work with you if you have a diagnosis of an ASD. The quality of this varies by location.
-Others understanding you better: Whether parents, friends, partners or whatever, a diagnosis gives people the reassurance that you are that way, and lets them research what they can do to help or what they can avoid. (It was not until my diagnosis that my dad stopped trying to pressure me to be on anxiety medication for traits of my Asperger's that were not due to anxiety)
And then there is of course just knowing what traits do match your weaknesses and working to minimize the negative effect of this on your life.
All of this, but unfortunately these services are not available everywhere, and when they are available, they cost an extraordinary amount of money.
That needs to change.
_________________
Given a “tentative” diagnosis as a child as I needed services at school for what was later correctly discovered to be a major anxiety disorder.
This misdiagnosis caused me significant stress, which lessened upon finding out the truth about myself from my current and past long-term therapists - that I am an anxious and highly sensitive person but do not have an autism spectrum disorder.
My diagnoses - social anxiety disorder and obsessive-compulsive disorder.
I’m no longer involved with the ASD world.
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