Wednesday, October 31, 2018

erased fiscal intersection by SPMI peer advocates in 2003 followed by autistic self advocates since 2007




  No more consumer-survivor rejection of prescription medications (and the medical model of disability) without cognizance and activism supporting Medicare for All as a universal buy-in additional health insurance choice to individuals, not a requirement to enroll,

and demanding an end to private insurer and taxpayer greed that cuts funding and doctor networks to improve individual mental health that improves long term outcomes if the individual receives LTSS, delivered in HCBS, after progressive public budgets overcome the austerity of the waiting list.




   Stephanie Mencimer took 8 years from 2003 until the publication of her 2011 Mother Jones article


 about Jared Loughner, killer of child Christina Green, born on Sept. 11, 2001, Federal Judge John Roll and wounded ex-AZCD8 (AZCD2 after 2012 election cycle redistricting seat held by R-Martha McSally 2014-18) Democratic member Gabrielle ‘Gabby’ Giffords among other victims, for Mencimer to make the connection to shifting money, from paying for institutions and their drugs and devices, prescribed by doctors financed by profit-greedy insurance companies managed 'one size fits all for efficiency' care. 


    For-profit and nonprofit private insurance companies, if they buy into the growing consensus that health care is a human right, must have their contracted benefits follow the person as payment for person-centered, community services instead of the consumer/survivor ‘community’ receiving some leadership of peer-run programs without the money following the person, including persons never institutionalized, from the institutional model to the community-based, person-centered model.   Human medical needs aren't a total production cost divided into unit costwidgets’ in b-school economics classes
as a way of developing social safety net (health and human, social services) budgets at all government levels.   The Judge David Bazelon Center throughout its history ignores the role of money except to close institutions not keep people who are out of them, but at risk of placement if they lose a job, housing or have another life transition, included in community. 



   Fuller Torrey in this 1998 Brain Storm article (reprinted from the Washington D.C. City Paper) called out managed care 'one size fits all for efficiency for profit' practice of medicine and even United Health Care CEO Bill McGuire’s $6.1 million 1 year  ($1 Billion in UHC CEO career) salary.



Over the course of two hours, Torrey rails against federal funding schemes for mental health care and attacks civil liberties lawyers for preventing sick people from getting well. He takes some potshots at John Mack, the Harvard psychiatrist who bills insurance companies for psychotherapy treatment for people who've been abducted by aliens. He skewers "mangled care" companies for paying CEOs multimillion-dollar salaries at the same time that they deprive the mentally ill of treatment. After noting that in 1994 William McGuire, CEO of United Healthcare, received $6.1 million in compensation, Torrey says, "If any of you think William McGuire is going to give back $1 million to open a clubhouse [a successful day program for the mentally ill], see me afterward and I'll give you a prescription for Haldol."


    Peer (consumer-survivor) advocates were fighting to end stigmatizing language in a 2003 article (The Sick and The Dead by Stephanie Mencimer) while safety net, publicly funded, inclusive, community-based services to one population (people with SPMI/mental illness and substance abuse disorders) were being devastated as similar services to another population (people with ID/DD formerly known as MR/mental retardation before 'Rosa's Law' rewrote federal laws) were cut to a lesser extent.  

    Peer consumer-survivor advocates erased (ignored) the fiscally intersectional questions of whether a person living with mental illness was receiving treatment or not

Untreated serious mental illness is a huge risk factor for violent crime, particularly among those released from mental hospitals. A 1992 study by Dr. Henry Steadman, now the chair of the national advisory board of the Center for Mental Health Services & Criminal Justice Research, found that 27 percent of released patients reported having engaged in at least one violent act within four months of being discharged. Those findings mirror older research suggesting that discharged patients had arrest rates for violent crimes 10 times that of the general population. Another study, published in the American Journal of Public Health in 2002, found that about 14 percent of adults with severe mental illness (schizophrenia and bipolar disorder) had been violent within the previous year. Not surprisingly, then, 16 percent of jail inmates are estimated to be mentally ill, according to the Justice Department—some 300,000 people, or four times the number who are in mental hospitals today in the United States. 



, and how to pay for adequate treatment if the individual could not, in their 2003 protest letters.   Autistic 'self-advocates' still ignore the same fiscally intersectional question 'who pays the costs' of 'autistic community' goals of inclusion and acceptance if individual autistics cannot pay the costs.  

  

  The MacArthur Foundation study, quoted by 2003 mental health advocates in their letters,













 may have also left out the distinction between treated and untreated, and implications for law and budget policy in assuring access to high quality, community based, treatment, in measuring the risk of person living with mental illness committing a violent crime. 


  The demands of one of the 2003 anti-stigmatizing language protest letters for more funding for better quality independent living services for individuals living with mental illness,

signed by American Association of People with Disabilities AAPD President and CEO Andrew Imperato in 2003 






were completely ignored by 2007.



   The ARC and Special Olympics (Disability Policy Collaboration) in their no 'r-word' campaign that led to Rosa's Law
 

rewriting the text of all federal law to replace "mental retardation" with "intellectual disability," after passing laws in states, also were less inclusive in their rhetoric than in the demands for money to pay the costs that their constituencies could not.  Shameful exclusion by the intellectual/developmental disability and physical disability self-advocate operated community-based organizations that is less cross-disability than their inclusive rhetoric makes them appear.

   Self help and actualization movement


that informs the consumer-survivor and self-advocate movements are inadequate replacements for inadequately-funded systemic change that, if the budgets are democratically made more fiscally liberal, will do the most good for the most people with disabilities at the most equitable (as individuals need help) pace. 













   Critics of the self-help and positive psychology movements like this book are a needed corrective to prevent positive psychology from legitimizing regressively worse income and wealth inequality by helping 99% of people accept declining living standards and busier lives working harder (not ‘smarter’) for less income.  





Failures of the self help and positive psychology that has informed the I/DD and SPMI/consumer-survivor disability rights movements are still documented  by what in 2018 is called a 'depression crisis' shown by self-medication with addictive substances from alcohol to opioids and other issues the '12 step' movement has, for almost 90 years since the book "My name is Bill W." was published, attempted to solve with supported (individual-sponsored) abstinence.
 

Disability Integration Act and more 1974 Rehab Act CIL funding can help more #PwDs more quickly than 'self-advocacy' 'community'



   A NJ Republican Jewish family, headed by Lee Solomon, finds their class privilege threatened by one autistic son with questionable ability to support himself and younger son with opioid addiction starting with father inadequately securing his painkillers from son.

 (Read part of image of article under sub-headline "I really liked them")





  Father, and New Jersey Republican party candidate supporter, Lee Solomon intervenes with opioid addicted son by reminding him who will care for (support financially in the absence of intergovernmental partnerships appropriating and authorizing tax receipts to pay for a social safety net) AJ’s brother on the autism spectrum.


   More DEA-paid for and locally-administered unused prescription drug take back days like these 






 could have helped Lee Solomon dispose of his unwanted 360 Oxycontin (opioid) pills (180 pills each with two different dosages) and prevented son A.J. from taking them recreationally and becoming addicted. Family economic security for the Solomon family could have been strengthened to support A.J.'s brother diagnosed (before the 2013 erasure of the diagnosis) with Asperger's Syndrome now diagnosed as autism spectrum disorder ASD. 


   ADAPT (Americans Disabled for Attendant Programs Today and Americans Disabled for Accessible Public Transportation two names same acronym) was less inclusive in effect than intent in building support for the 1990 ADA.  The Independent Living movement started in Berkeley, CA by the late Ed Roberts used similarly inclusive rhetoric for exclusive benefit to demand passage of the 1974 Rehab Act that pays for over 2,000 Centers for Independent Living CILs.  Expand the funding structure already in place to help more PwDs more quickly. 



  Both organizations and the Independent Living movement should support a reintroduced Disability Integration Act

in future Congresses and expansion of 1974 Rehabilitation Act funding as rustedaspie wrote last year


(quoted text in brackets to prevent reader confusion and make sentence in the current post comprehensible)


[  Demands for social change were always more exclusive

There now exists over 2,000 Centers for Independent Living in the United States alone. The core Service provided under the Rehab Act include, transition for people leaving nursing homes and youth, information and referral, independent living skills training, peer counseling, and advocacy.



 than the inclusivity of the rhetoric, used to organize people, by groups like the Berkeley, CA CIL, and ADAPT (Americans Disabled for Accessible Public Transportation and Americans Disabled for Attendant Programs Today), as well as the EnDependence Center of Northern Virginia.  ]


 to designate consumer-survivor and self-advocate run organizations as independent living centers to help more PwDs receive supports to live in communities of their choosing. No more fiscal austerity-based wait lists that hide electorally unpopular budget cuts by making the services harder to qualify for

and mental health consumer-survivor and intellectual/developmental disability self-advocate ‘communities’ severity contests/oppression Olympics. 



  No more diversion of demand away from safety net programs (based on a medical model of disability) by self-advocates like Autism Network International former organizers of autreat, its event planning successor Association for Autistic Community organizing autspace since 2014 with no event 2015 and 2017, aascend in the Bay Area of California, an autistic adult support group in Portland, OR, Autistic Self Advocacy Network ‘community building/political activism’ and aagw.net in the DMV (District, Maryland, Virginia). 

  Organizational missions of autistic self-advocate run groups listed in the above paragraph are all based on 'members' buying in to the meme (to replace the social safety net with peer to peer help)  'someone is always worse off than me' of hypothetical anonymized pity representing the social model of disability applied 

 to autism

by calling autism a personality 

 (summed up by this comment from user name Trogluddite)

9 months ago
For me personally, many of my traits do not seem at all like aspects of personality - though certainly, having grown up with them, they have contributed to the development of my personality.  In addition, having spent most of my life so far forcing myself to "pass as normal", there is a big question mark over whether the personality that I project to other people is entirely my real personality, rather than an false persona adopted for ease of interaction with other people.
To take one example.  I may be perceived by other people as having an "asocial" or "shy" personality.  However, much of my reticence to speak up socially has nothing to do with lacking the desire to do so.  There are aspects of my condition which make the process of communicating more difficult regardless of how much I would prefer to be more outgoing...
  • My processing of speech is very slow.  This often leaves me with little chance to express my true opinion.  I can choose between somebody else taking the next turn to speak before I get the chance, or to react quickly but say something which doesn't really capture what I really think or misunderstands information that I haven't processed yet.
  • Reading eye contact and body language are not simply a matter of having too little practice.  My senses get overwhelmed easily, and my ability to avoid distracting stimuli so that I can focus on the right thing at the right time is limited.  I do well at identifying facial expressions when it is explicitly tested, but in real life, I just don't see them in the first place because of these sensory issues and problems with attention.
  • Having to consciously attend to reading body language and expressions is a huge extra load on my brain relative to having an instinctive response for them.  As well as being very tiring, it also distracts me from hearing what is said accurately and processing its meaning.  It is hard to find the right thing to say when so much contextual information is missed.
  • Understanding social situations also calls for a lot of explicit analysis, again a further stress on an already overworked brain.  Trouble with judging the appropriateness of what I'm going so say leads to anxiety and self-censorship (often "playing it safe" by simply being agreeable whether or not I truly feel that way.)
  • Too much sensory input can simply overwhelm me to the point of shutting down.  If I feel that this is imminent, I have to remove myself from the situation, regardless of how much I would like to spend more time with the people present.
I do agree that the above, as with any other trait associated with autism, exist on a continuum, without any distinct boundary at which they become a disability or dysfunction.  However, I feel that the above are purely perceptual and cognitive traits.  Rather than being part of my personality, they are actually hurdles which impair my ability to express who I really am.  I would prefer that I could communicate with people more and feel more connected to them, and it frustrates me when I cannot, particularly when it gives other people a false sense of who I am or how I feel about them.
A similar argument could be made for the executive functioning issues which I experience, which can sometimes prevent me from initiating an action even when I desire it, can clearly see the benefits of it, and have all the necessary resources at my disposal.
In fact, this is largely how I define which of my autistic traits I consider to be disabilities - they are the parts which hinder me from acting on the needs and desires of my true self, or from negotiating reasonable compromises with the world around me.  However, by this definition, it is also perfectly reasonable that not all autistic people need identify themselves as disabled (or even as autistic at all), as their personality and their autistic traits may be in harmony with each other.


trait.

 Keeping an ambiguous 'boundary' between when an individual independent living problem becomes "a disability or a dysfunction" triggering (qualifying for) publicly-funded social services

I do agree that the above, as with any other trait associated with autism, exist on a continuum, without any distinct boundary at which they become a disability or dysfunction.

helps ration demand for expanded publicly-funded social services such as job development and retention, and housing, food and utility bill payment assistance to only the 'truly most needy' or 'vulnerable' (formerly known as low functioning) individuals with disabilities that even people with disabilities have been shamed out of seeking services in favor of 'workarounds'   that shift the costs of inclusion from the community to the individual mostly in time trying to create a 'workaround.'  

   Reducing the demand for information and referral back to the social safety net (funded by taxes and based on residence within the taxing state or local jurisdiction boundary to be found 'eligible') to ‘unofficial,’ individual, peer to peer relationships built within confidentiality-protected group spaces helps leave what little services and authorized tax revenues are left for the increasingly more intense need (formerly known as lower functioning) autistics unable to build peer to peer relationships because of urgency to meet immediate survival needs.  Self-advocacy perpetuating this situation that uses words like 'inclusive' or 'welcoming to all' is simply inclusive rhetoric for exclusive benefit.