Let's Handcuff the Elderly, Then Take Away Their Medicine, etc.

Dozens Arrested As Seniors And Activists Occupy Chicago Over Cuts
(Huffington Post)
November 7, 2011

CHICAGO, ILLINOIS– [Excerpt provided by Inclusion Daily Express] More than 1,000 senior citizens and their supporters marched from Chicago's Federal Plaza to the intersection of Jackson and Clark Street Monday morning to protest proposed cuts to Medicare, Medicaid, Social Security and Housing and Urban Development. At the intersection, more than 40 protesters, 15 of them seniors affiliated with the Jane Addams Senior Caucus, stood or sat in the street, arms linked, blocking traffic. 

Amid chants demanding that the cuts be forestalled — with suggestions for alternatives, including tax hikes — 43 demonstrators were escorted from the intersection by police and issued citations for pedestrian failure to "exercise due care," or for blocking traffic. Those cited included four protesters using assisted mobility devices and at least one centenarian. 

Judy Moses said she was glad to receive the citation–her second in her quest to maintain funding for programs that benefit seniors, following an arrest for blocking traffic in December at a similar protest.

Before the traffic-stopping demonstration, an estimated 1,500 people turned out for a rally at Federal Plaza, where community members and activists spelled out the damage that individuals, and the greater Chicago community, stand to bear if funding is cut from welfare programs that benefit seniors. After decades of payments into social security with the expectation of returns, Chicago's senior citizens expressed shock that the federal support they rely on could be reduced.

Entire article:
Seniors Join Occupy Chicago, Protest Cuts To Medicare, Social Security

http://tinyurl.com/cx7gatm
Related:
Occupy Chicago, seniors arrested for civil disobedience (Examiner)

http://tinyurl.com/cd7ksnp


 

Disability and the Clock

Baba Yaga

 

This morning I am hurrying. I am not alone in this. The clock says: “The only thing now is not to disappear.” In this way the clock is opposed to instinct, opposed to the body, even opposed to nature. The folk poetry of the world (pick anyplace) tells us that disappearance is imminent. There’s a witch coming, she’s dressed up like a shack and she runs on chicken legs and she’s going to devour you because you were minding your own business. Which gets me to my point: Marxists will say that the clock was given its exceptional power in the Industrial Revolution, but those of us who are forced to hurry, like geese before the rod, know that the clock is just trying to tell us that the witch with the chicken legs is coming. Keep moving. Keep rolling. Keep blinking. Keep limping. Erving Goffman understood the stigma of disability but he left out this insight: able bodied people see, in people with disabilities, and far down in their collective unconscious–see people who won’t outrun the witch dressed like a shack and running on her chicken legs. When people who do not currently have a disability see pwds they worry about running from the Baba Yaga. Trust me on this. Meanwhile, I have to get going, just like you my friend. The lines of the day are fuzzy. Where are my gloves?

 

 

Beyond Stigma: Mental Health Empowerment on Campus

See the announcement below:

 

Dear Colleague:

We write to announce the launch of the Campus Solidarity Campaign (CSC), a research program with the primary objective of investigating best practices to promote an environment of solidarity and support on college campuses for students with mental health concerns.  Grounded in research, it is our hope that this campaign will have a meaningful impact on campus climates, contributing to an increased ability of college students with mental health concerns to achieve their life goals, including completing their post-secondary education.  This program will utilize a social marketing approach to target key groups within campus communities to achieve this objective.  To find out more about the research program and the CSC, please visit the CSC website (http://www.stigmaandempowerment.org/campus-solidarity-campaign).  You can also keep abreast of the research and social marketing work of the CSC by becoming a fan of the CSC on facebook (http://www.facebook.com/pages/Campus-Solidarity-Campaign-CSC/139031809528703).

 

Kristin Sokol, MS, CRC, LCPC

 

 

Patrick Corrigan, Psy.D.

 

National Consortium on Stigma and Empowerment (NCSE)

Illinois Institute of Technology

College of Psychology

3424 S. State Street, First Floor

Chicago, IL

60616

Visit the NCSE website at www.ncse1.org.

 

Traveling Shoes, Traveling Dogs

In the last few days I have found myself once again traveling extensively and as usual, experiencing the highs and lows of disability travel. In Chicago where I was speaking at The University of Illinois Chicago campus about blindness in the 21st century I got yelled at by a mean spirited doorman who didn’t like the fact that I was letting my dog take a pee in the dead flowers outside the hotel. Trust me, there was no other place to go. His mean spiritedness was the issue. It’s not uncommon as a person with a disability to find yourself in a hieratic and miserable state of diminishment–it’s a caste system implicit in American social circles. The people with the disabilities can still be treated with contempt at the drop of a hat. Or use your own favorite cliche: whenever the mood strikes. 

 

Because of this spontaneous contempt factor I always wear a suit and tie when I travel. My costume (for that’s what it really is) is designed to say, “It’s Mr. Disabled Guy, to you, buddy.” I wear the proper getup for citizenship. No dirty tee shirt and bad haircut for this blind guy. I’m serious. I’m dead serious. Watch out. I might just be a professional person you stinker, you. 

 

Meantime, despite the bad reception from the doorman, I had a police officer at O’Hare airport hail me a cab–that is, he offered to hail me a cab. Then told me his cousin is losing his vision and his hearing owing to Usher’s disease. I told him about Guiding Eyes for the Blind which trains guide dogs for people with Usher’s disease. We had a human talk, a moment of soulful contact. We also talked about the Chicago Cubs. That was an uplifting moment. It was also a moment made entirely possible because of my disability. This is the flip side of the homunculus doorman. People with disabilities can tell you tons of stories that reflect this up and down dynamic of physical difference and social attraction-repulsion. It’s possible to argue that this is the same up and down dynamic we all face, regardless of physical difference–that is, if you’re just a normal looking person (whatever that might mean?) and someone treats you poorly at the supermarket checkout, you might then find, just moments later a person who does something kind for you. My point is not that disability makes for a different experience of the social circle, but that it simply intensifies the experiences. This is because of the inherent stigma associated with physical defect on the one hand, and the compensatory decency of civilized people on the other hand–but both principles involve something heightened, a mode of human activity that’s spurred by symbolism. God Almighty, one gets tired of it.

 

In New York City I had a limo driver (who I had paid to pick me up in advance) throw a fit when he saw my guide dog. He wasn’t going to take me to the airport. I had told the limo company about the dog. But they didn’t tell him. He was from India. He thought the dog was unclean. He was snotty. Eventually he took me to the airport but it was a frosty ride to say the least. 

 

And yet, just the evening before, while walking my dog near Central Park, a young Latino policeman came up to me and said how much he admired my dog and my ability to work with her. A nice moment to be sure. A human minute. Something that harkened back to our earliest times on earth when we had to be social creatures. 

 

This up and down business of disability is always heightened by travel. No wonder some people would rather stay at home. But compensatory judgements are always wrong. People are most often better than we suppose. I think that’s right. I think it’s right most days. I say so it’s so. My dog agrees.

 

 

No ideas but in things…and national parks

  —Say it, no ideas but in things—   nothing but the blank faces of the houses   and cylindrical trees   bent, forked by preconception and accident—   split, furrowed, creased, mottled, stained—   secret—into the body of the light!

via lancemannion.typepad.com

A great post this morning from Mr. Lance Mannion!

Huffington Post: AL FRANKEN: Net Neutrality Is Under Attack… Again

See Al Franken's important message at Huffington Post:

  This week, the free and open Internet millions of Americans have come to depend on is under attack.

AL FRANKEN: Net Neutrality Is Under Attack… Again

I've said that net neutrality is the most important free speech issue of our time. It's true. If Republicans have their way, large corporations won't just have the loudest voices in the room. They'll be able to effectively silence everyone else.

 

Sent from my iPhone

Chicken Pox Lollipops

The following story at Huffington Post convinces me that the utter decline of our nation has already occured, that we're living in the greasy and smeared streets of what once was a decent nation:

Here's the opening of the Huff Post article:

"KPHO in Phoenix reports that a Facebook group is offering parents the opportunity to receive lollipops in the mail that have allegedly been infected with chicken pox. The parents seeking these disease-riden sweets want their children to get chicken pox when they're young so they can become immune to the disease and avoid getting it later in life.

KPHO also found parents looking for people to send measles, mumps and rubella."

 

 

 

 

Judge Rotenberg Center Banned From Using Electric Shock on People with Disabilities

 

 

JRC Banned from Shocking New Admissions
 
 

Dear Supporters,

This week we can celebrate a major victory against torture of people with disabilities in the United States.   The Massachusetts Department of Developmental Services (DDS) adopted new regulations last week that greatly restrict the intentional use of pain as a form of treatment – including the use of electric shock, seclusion, and restraints on young children and adults with disabilities. As documented by a recent report by Disability Rights International (DRI), Torture Not Treatment, The Judge Rotenberg Center (JRC), based in Canton, Massachusetts, has used these practices, called "aversive treatment" for decades.

Facilities licensed by the DDS in Massachusetts can no longer subject new admissions to severe behavioral interventions including electric shock, long-term restraint, or aversives that pose risk for psychological harm – in other words, mainstays of JRC's "treatment" program. 

 

No other institution in the country – or the world, as far as we can tell – uses such barbaric practices. DRI's investigation found that the pain caused by this is so severe and outside accepted professional norms, that these practices constitute nothing less than torture. By permitting such treatment, the United States violates its obligations under international law, as defined by the UN Convention Against Torture. DRI filed our report, Torture Not Treatment, in 2010 as an urgent appeal to the United Nations. The top official on torture at the United Nations agreed with DRI, and when asked by ABC Nightline if the practices were torture, he declared, "Yes…I have no doubts about it. It is inflicted in a situation where a victim is powerless…a child in the restraint chair, being then subjected to electric shocks, how more powerless can you be?"

 

We applaud Massachusetts Governor Deval Patrick on taking a courageous stand by issuing an executive order for the Massachusetts DDS to review their policies regarding electric shock and other severe aversives.

The resulting new policy puts an end to the use of JRC's electric shocks on new admissions.But we can't declare success yet. While hundreds of children will be spared from JRC's behavioral experiments in the future, the new policies do not stop JRC from shocking and causing psychological damage to children already placed in the center. These children and young adults remain prisoners in a very dangerous environment. The center has been repeatedly investigated for suspicious deaths and physical abuse. JRC has been fined for identifying some clinicians hired by the school as psychologists, when in fact, they were not licensed psychologists. And as a result of an investigation into a case of abuse at the facility, JRC's director was forced to resign earlier this year after being charged with misleading a grand jury about the investigation.  

 

DRI is encouraged by the bold statement by the US National Council on Disabilities, a federal advisory body, which cited DRI's report, as well as the international definition of torture, to call for the use of painful shock aversives to be brought to an end. 

 

DRI urges the Department of Justice and the Obama Administration to fullfil its obgligations under the UN Convention Against Torture. DRI calls for a blanket ban on the use of electric shock as aversive treatment for children or adults with disabilities across the nation. There is nothing stopping JRC from shocking kids already in their center — or moving their facility to a different state to avoid the new Massachusetts regulations. The Department of Justice has an open investigation into the treatment of children at JRC. We ask you to  write a personal appeal to the investigators to help ensure that this torture is put to an end once and for all, and is never allowed to be duplicated anywhere else in the United States.

 

We are one large step closer.

Thank you for your continued support, 

Laurie Ahern,

President

 

 

 

Eric Rosenthal,

Executive Director

   

 

 

 

 
 

   
This email was sent to kantera@law.syr.edu by info@disabilityrightsintl.org |  

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