The 2016 Wish List

For me to not be a hopeless autistic, I would love the following

  • Better accountability to the professional class once and for all – Anyone who works with special needs, or is in management or acts as “leader” has traditionally gotten away with ether abuse, slander/libel, Federal corruption, etc.
  • Redefining “Self Advocacy” Self advocacy today is an abusive practice, by enabling the professional class and not empowering the individual. People should be driving off the George Washington Bridge to get what they want. No parent or even individuals should have to go so far to get what they need.
  • Educating the Public on the Welfare system The welfare system is a very broad spectrum of service delivery, and sadly everyone wants to get rid of Medicaid, but the unintended consequences would hurt people with various disabilities to get through their day to day lives. I’ve had a right wing nut job of a school secretary tell me that I have more of an Asperger’s case and accused me for “smooching with the government.” I’m very bright till I go into a classroom and be threatened to death by some inexpierenced professor…
  • Changing and Modifying the adult systems. Hey guess what? Your kids’ autism won’t go away when they turn 21, so stop believing you can fully “cure” your kids autism. Also what will happen when your kid graduates on their birthday? Have you ever thought of “falling off the cliff”? What if you live in Manchester, that notorious area agency will give you a 100% promise that you may never get any services unless you cry and whine your bleedy hearts by that point give you at least some minimal supports.
  • Educate the educators I’ve talked about misinformation since the inception of this site, and sadly the “experts” often inappropriately teach people things to make them scared to even work with them. Where has that gone? Nowhere!

That’s all I ask for this year.

 

Transitions? OMG That’s an Awesome idea…

…but why are you 10 years behind the 8 ball?

I sit on a planning committee of an annual conference for families who live in my state -the state I live in, and I sit and have to listen to a couple hours almost every month about people presenting ideas about transition planning.

And I sit there quietly like a wallflower.

I sit like I have severe autism.

I remain quiet.

I don’t like to come off as threatening or combative.

I just sit there.

And hopefully people of the intellectual class and the professional class gets their heads out of their rear ends and understand that while this is good for the second or third generation of autistics (or developmentally disabled people) in my state, the state I live in – what about the thirtysomethings who are limping around the system just trying to get through a day? Some may not be able to verbalize because they can’t put their concerns into words, or they have been severely manipulated by a bunch of racist psychologists who think its OK to ruin a child’s brain at their teenage years, and screw them off as they become adults and not have any clue what unintended consequences they do to these people.

Excuse me for being crass: I could care less about the goddamned spoiled rotten brats in special ed! Who gives a flying bleep about “the children!” What about the goddamned adults that the professionals could care less about?

I wished I wasn’t a monster, but I sadly became one in many ways thanks to the goddamned idiots running SAU 12, GLEC and dare I say “Doctor” Teresa Bolick who with all their failures caused me to become a scary person. Now I know why people run away from me. It’s these nitwits that should be on death row!

The controlled rants are over. 🙂

If you’re new to this site, let me be clear: I live in a state where we were the first in the nation to close a statewide “school” for autistic like people; but its also the same state where people have pushed “progressive” agendas that have resulted in “regressive” actions. I also live in the most richest towns probably per capita and those communities have absolutely zero tolerance for people with developmental disabilities (if you are under the age of say 21.) You (or your child, your “friend” from elementary school, or family member) has basically been hopeless since entering middle school; and some of these people have been hopeless as early as the end of the 20th Century. 

Help from a Doctor that Knows Adult Autism!

2017 Preface: These sets of concerns had dated over a year before, hence it sits in the 2014 category.

Unlike Asperger’s Syndrome types who claim they have “Aspergers by self-diagnosing”, I for one won’t stoop down such levels. I’ve tried to find a therapist, a doctor, (an MD or dare I say a “PhD”) and there hardly is anyone skilled with autism for adults.

Everything is for “the children” but adults with autism are being just treated the same exact way as the first generation (births between 1987 to 1992/3) because for whatever reason there is a lack of resources for adults. They know what’s happening to “the children” because when the said groups become adults – this is what they will be expecting. So if that is the case, why not wait? And why are you letting the first generation suffer? Why in the hell in 21st Century, could autism been the first case of civil rights of progressive actions unlike Down’s (which took too many centuries too long) to address? And, with all the technology in the world (the Web, Internet, PCs, cable networks, etc.) are we still addressing like its the 1960s, of slow actions, misleading information in the media; why does society have regressive radical opinions like how the 60s was in general?  

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