Disability News Service, Resources, Diversity, Americans with Disabilities Act; Local and National.

Saturday, June 25, 2011

The Coffee Klatch : Interview with Temple Grandin : enjoy...

The Coffee Klatch is an interactive forum on Blog Talk Radio and Twitter bringing you expert guests from around the world.



Temple Grandin (born Aug. 29, 1947, Boston, Mass., U.S.) American scientist and industrial designer whose own experience with autism funded her professional work in creating systems to counter stress in certain human and animal populations.

Grandin was unable to talk at age three and exhibited many behavioral problems; she was diagnosed as autistic. Her parents, rejecting a doctor’s advice to place her in an institution, instead sent their daughter to a series of private schools where her high IQ was nurtured. A 1970 graduate of Franklin Pierce College in New Hampshire, where she majored in experimental psychology, she went on to earn a master’s degree at Arizona State University in Tempe and a doctorate at the University of Illinois at Urbana-Champaign, both in animal science. Since 1990 she has taught that subject at Colorado State University in Fort Collins, where she also runs Grandin Livestock Systems.

Diagram of Temple Grandin’s conveyor system for humane animal processing. Among Grandin’s …Aware that intense fear, born of a hypersensitivity to sound and touch, is common both to autistic people and to animals, Grandin has devoted her life to devising systems to alleviate the anxiety of both groups. While still in high school she designed a “squeeze machine” to relieve her own nervous tension, modeling it on a chute fashioned to hold animals in place during branding and other procedures. Improved versions of her machine are widely used not only in schools for autistic children but also by autistic adults. The main focus of Grandin’s career has been the design of humane livestock facilities that eliminate pain and fear from the slaughtering process. Her designs enable workers to move animals without frightening them. Grandin is the author, coauthor, or editor of several books, including Genetics and the Behavior of Domestic Animals (1999), Thinking in Pictures and Other Reports from My Life with Autism (1995), and Emergence: Labeled Autistic (1986).

# For The Coffee Klatch Interview with Temple Grandin, go to: http://thecoffeeklatch.com/group/temple-grandin/ 

Illinois 21st Annual ADA Celebration: Keeping the Promise of Equality: Chicago July 14, 2011

State of Illinois
Department of Human Services

ADA Keeping the Promise of Equality
Join Us In Commemorating the 21st anniversary of the Signing of the Americans with Disabilities Act

Sponsored by the Illinois Department of Human Services in cooperation with numerous State Agencies and Councils

Where
James R. Thompson Center
100 West Randolph Street, Chicago
(Between Lake and Randolph & Clark and LaSalle Streets)

When
July 14, 2011
10:00 a.m. to 3:00 p.m.

Featuring:
Interactive and informational workshops on ADA issues
Supported in part by Equip for Equality, Great Lakes ADA Business and Technical Assistance Center and the Illinois ADA Project
Art Exhibit (July 11-15) featuring artists with disabilities
Hands-On Art activities
Coordinated by Sharon Hyson
Three-on-Three Wheelchair Basketball Tournament/Sports Activities
Supported in part by the Northeast Special Recreation Association (NEDSRA) and Chicago Park District
ADA Help Table
Exhibits from federal, state, and local organizations
Entertainment provided by performers with disabilities
The entire event is free and accessible
For more information
312-793-0034 (Voice)

888-614-2385 (TTY)

E-mail: DHS.ADACelebration@illinois.gov

Special Olympics Flame of Hope for 2011 World Summer Games in Athens : video : June 9


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Uploaded by SpecialOlympicsEE on Jun 13, 2011

On Thursday, 9 June 2011 at 10:00 am (Athens time), the Flame of Hope for Special Olympics World Summer Games Athens 2011 was lit during a formal torch lighting ceremony. In keeping with tradition, this ceremony will took place along the lines of the original torch lighting of the Olympics, at the Sacred Sight of Pnyx, opposite the Acropolis in Athens, Greece where the flame will be lit by the sun's rays. The lighting of this flame formally launched the Law Enforcement Torch Run® (LETR) Final Leg that precedes Special Olympics World Summer Games Athens 2011, that was just 16 days after this ceremonial lighting with an official Opening Ceremony on 25 June. This lighting ceremony will began a journey of the Flame of Hope across all of Greece, as well as Turkey and Cyprus, before returning to Athens to begin the Games.

# For Special Olympics website, click headlines or go to: http://www.specialolympics.org/

Stone–Hayes Center (CIL) that helps folks with disabilities, future of a Illinois non–profit could be on the line.: June 2011

CBS4 : Quad Cities, IL

Quad Citians with disabilities could end up on the streets. If Illinois doesn't anti–up, the future of a non–profit could be on the line.

Stone–Hayes Center for Independent Living in Galesburg helps folks with disabilities live on their own. The state has not only cut from its budget, but owes money. A lack of funding means a lack of services.

About ten years ago Deborah Williams was diagnosed with multiple sclerosis, soon after, she became legally blind. She said before finding Stone–Hayes, "I just had to stumble around and figure it out by myself."

Now, Williams is not alone. Whether it's help with housing, food, or other needs, Stone–Hayes points folks with disabilities in the right direction

"We give services from birth to death at no charge," explained executive director Dale Parsons, "so many people have disabilities and their families don't want to accept them."

However Stone–Hayes may not be able to continue its mission much longer if the state doesn't pay up. Illinois already owes 50 thousand this year, and has cut nearly that amount next year. Stone–Hayes fears what will happen to the people they help if the money never comes.

"They're going to be in the hospital, jail, nursing home or on the streets," Parsons said.

Williams said it would be devastating to lose the place, not just for the services, but for the emotional support.

"Every Tuesday we have peer mentoring, and it's great to meet people in my situation so I don't feel so alone."

Stone–Hayes leaders said they can still operate for a couple of years, but it's going to be tight and changes will have to be made.

"Wretches & Jabberers": Stories From The Road | Chapter Four : video : June 2011


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"A Small World After All": Larry, Tracy, Harvey & Pascal take to the road to promote the new documentary "Wretches & Jabberers" by Gerardine Wurzburg. This week, Tracy invites Henna and Antti to join him at his monthly task force meeting at Community Developmental Services in Barre, VT.

For more information about the "Wretches & Jabberers" tour, to sign up for our newsletter or see extra footage from the film, follow us on Facebook at "Wretches & Jabberers" or visit our website: wretchesandjabberers.org!

About the Film :

:In Wretches & Jabberers, two men with autism embark on a global quest to change attitudes about disability and intelligence. Determined to put a new face on autism, Tracy Thresher, 42, and Larry Bissonnette, 52, travel to Sri Lanka, Japan and Finland. At each stop, they dissect public attitudes about autism and issue a hopeful challenge to reconsider competency and the future.

Growing up, Thresher and Bissonnette were presumed “retarded” and excluded from normal schooling. With limited speech, they both faced lives of social isolation in mental institutions or adult disability centers. When they learned as adults to communicate by typing, their lives changed dramatically. Their world tour message is that the same possibility exists for others like themselves.

Between moving and transformative encounters with young men and women with autism, parents and students, Thresher and Bissonnette take time to explore local sights and culture; dipping and dodging through Sri Lankan traffic in motorized tuk-tuks, discussing the purpose of life with a Buddhist monk and finally relaxing in a traditional Finnish sauna. Along the way, they reunite with old friends, expand the isolated world of a talented young painter and make new allies in their cause.

From beginning to end, Thresher and Bissonnette inspire parents and young men and women with autism with a poignant narrative of personal struggle that always rings with intelligence, humor, hope and courage.

* every Saturday there will be another post of this 11 part series

2nd Man Charged With Prostituting Disabled Woman; Chicago : June 24, 2011

Chicago Sun-Times : June 24, 2011

CHICAGO (STMW) — A second man is in jail Friday after being charged with kidnapping a mentally disabled woman and forcing her to perform acts of prostitution while holding her against her will for four days.

Chester Nelson, 36, of the 1700 block West Albion Street was arrested June 10 and charged with involuntary servitude.

And on Thursday, Carlos Mitchell, 34, of 1925 S. 21st Street in Maywood was also charged with involuntary servitude, a Class X felony, Cook County State’s Attorney’s office spokesman Andy Conklin said.

Mitchell was ordered held on $250,000 bond Friday, Conklin said. Nelson is also being held on $250,000 bond, and both will appear for a preliminary hearing on July 1.

The crime happened over a four-day period from June 6-10, prosecutors allege. The 20-year-old Crystal Lake woman was in Chicago visiting a friend when Mitchell picked her up, according to prosecutors, who said she is mentally handicapped with the mind of a 12-year-old.

Mitchell allegedly took her to a hotel and demanded the victim strip, but she refused. She wanted to go home, but Mitchell told her she couldn’t leave until she made him some money, prosecutors claim.

He then took her to another hotel at 92nd and Stony Island Avenue, where his girlfriend, allegedly a prostitute, had her to set up a party line message. But no one came to the hotel room for sex that night, prosecutors said.

The next morning, Mitchell ordered her to stand naked in the hotel room for two hours. Nelson later arrived at the hotel to pimp out girls, and arranged for the victim to have sex with two men.

At some point, the woman told someone she was being held against her will. That person tried to give her a bus pass, but Nelson took it away, court records said.

Nelson was arrested June 10 after the victim was able to call her father and tell him what happened. The woman then jumped out of Mitchell’s car when she saw police and flagged them down.

Police located Mitchell on June 22 and he was tackled and subdued after a brief chase. A police officer suffered a shoulder injury during the struggle, court records indicate.

Mitchell was identified by the victim and three other witnesses, including his co-defendant Nelson, prosecutors said.

# More on report at: http://chicago.cbslocal.com/2011/06/24/2nd-man-charged-with-prostituting-disabled-woman/

Friday, June 24, 2011

Special Olympics World Summer Games Athens 2011: OPENING CEREMONIES LIVE :SAT JUNE 25 1-4 pm ET: ESPN3

ESPN Corporate Outreach today announced plans to cover Special Olympics World Summer Games Athens 2011 on two ESPN media entities. The Games are being held June 25 through July 4 in Greece. ESPN3.com will be the exclusive live media home for the opening (Saturday, June 25, 1 – 4 p.m. ET) and closing ceremonies (Monday, July 4, 1 - 4 p.m.) in the United States.

In addition, throughout the competition, ESPN.com will be providing information and an up-close perspective of this unique and inspiring event, reporting directly from the venues in Athens. The coverage will be featured prominently in ESPN.com’s The Life section (http://espn.go.com/espn/thelife/) and will be promoted throughout the site. This coverage will be available on ESPN.com as well as ESPN3.com online and via ESPN on Xbox LIVE and on mobile and tablet devices through the Watch ESPN app.

“Special Olympics became ESPN’s first charity of choice in the early 1980s,” said Rosa Gatti, senior vice president, corporate outreach. “We are delighted to have leaders of these two ESPN entities commit their time and resources to provide coverage of this global event. Team ESPN’s long relationship of volunteering at Special Olympics and Unified Sports programs has been extremely rewarding for our employees and their families.”

The 13th Special Olympics World Summer Games is the largest sporting event held in the world in 2011 and the first major sporting event in Athens since the Olympics were held there in 2004. Special Olympics Team USA will be joining 7,000 fellow athletes and teams from 180 nations around the world in Athens, Greece. Special Olympics athletes of all ability levels will compete in 22 different Olympic-type sports including: aquatics (swimming), athletics (track and field), badminton, basketball, beach volleyball, bocce, bowling, cycling, equestrian, football (soccer), golf, gymnastics, handball, judo, kayaking, powerlifting, roller skating, sailing, softball, table tennis, tennis, volleyball and the Motor Activity Training Program (MATP). Throughout the competition June 25 - July 4, athletes will display their athletic skill, determination and courage to the world, uniting people of all abilities through the power of sport.

About Special Olympics

Special Olympics is an international organization that changes lives through the power of sport by encouraging and empowering people with intellectual disabilities, promoting acceptance for all, and fostering communities of understanding and respect worldwide. Founded in 1968 by Eunice Kennedy Shriver, the Special Olympics movement has grown from a few hundred athletes to more than 3.7 million athletes in over 170 countries in all regions of the world, providing year-round sports training, athletic competition and other related programs. Special Olympics provides people with intellectual disabilities continuing opportunities to realize their potential, develop physical fitness, demonstrate courage, and experience joy and friendship. Visit Special Olympics at www.specialolympics.org. For information about the upcoming Special Olympics World Summer Games Athens 2011, visit the Games’ official website at www.athens2011.org.

About Team ESPN and Special Olympics

Throughout the years, ESPN has provided volunteers and financial and in-kind contributions to Special Olympics Connecticut and similarly at other office locations. ESPN is a sponsor of the Unified Sports school-based program in Connecticut. Unified Sports® is a registered program of Special Olympics that combines approximately equal numbers of athletes with and without intellectual disabilities on sports teams for training and competition. All Unified Sports players, both athletes and special partners, are of similar age and matched sport skill ability. Unified Sports teams are placed in competitive divisions based on their skill abilities, ranging from training divisions (with a skill-learning focus) to high level competition.

About ESPN3.com

ESPN3.com is ESPN's live sports broadband network, a 24/7 online destination that delivers thousands of live, global sports events annually. It is currently available at no additional cost to fans who receive their high-speed Internet connection or cable TV video subscription from an affiliated service provider. It is also available at no cost to approximately 21 million U.S. college students and U.S.-based military personnel via computers connected to on-campus educational networks and on-base military networks.

# For ESPN3 (online) click headline or go to: http://espn.go.com/espn3/#

"Campaign for Real Choice" Illinois disabilities advocate closes campaign but continues fight: June 24 2011

The Newa Gazette : by Julie Wurth : June 24 2011

Rights advocate closes campaign but continues fight for those with disabilities

URBANA — A statewide campaign founded in 2004 to promote "full inclusion" for people with disabilities is shutting down, but the co-founder says she will continue its ground-breaking work through other venues.

Barbara Pritchard of Urbana created the grass-roots Campaign for Real Choice in 2004 with her husband, Lester Pritchard, a leading advocate in the disability rights movement in Illinois.

Mr. Pritchard, who had cerebral palsy, died in 2009, and his wife, who is visually impaired, said it's been difficult to replace his insight and gift for bringing people together. The campaign's latest organizer also took another job recently, so she decided not to replace him.

The campaign pushed the state to fund community-based services that allow people with disabilities, both physical and developmental, to live in their own homes rather than institutions. The Pritchards had the resources to buy an accessible home in Urbana and wanted others to enjoy that independence.

Their campaign organized a "freedom ride" in 2005, evoking the civil rights spirit of the 1960s, to push for an end to institutionalization. It fought alongside other groups to close large state-funded institutions, such as Howe Developmental Center, and give people with developmental disabilities more choice about what they want to do with their lives.

Pritchard said the landscape has changed in the last seven years for people with disabilities, with new advocacy groups emerging to lead the fight for independent living and state officials adopting many of the same goals.

"There's different leadership in this state," she said.

In response to a class-action lawsuit, the state also signed a consent decree expanding community living opportunities for people with developmental disabilities. The state now has six years to move people into the community who choose not to live in large facilities, she said.

"By no means is it done. If Lester was still alive, the campaign would be up and battling. But it's hard to be an organization of one," Pritchard said.

"People are starting to fill in some of the gaps that the campaign was starting to do. What I want to do is lend my support to those groups to continue their work," she added.

Pritchard cited the Illinois Self-Advocacy Alliance for Change, founded in 2009 by Jennifer Knapp, the campaign's first organizer, to bring together advocacy groups for those with developmental disabilities. It wants the state to develop more "self-directed" support programs, so that people with disabilities can be more involved in decisions about their lives — where they should live or whether they should work in a sheltered workshop, take a class at Parkland or volunteer at an animal shelter, Pritchard said.

Knapp said the Campaign for Real Choice re-energized the independent living movement and connected groups working on behalf of those with developmental and physical disabilities. The campaign, and Mr. Pritchard in particular, taught people to "hope again and have a vision of what the lives of people with disabilities can actually be like and to believe that we can make changes in Illinois," she said.

Pritchard recently filled Mr. Pritchard's seat on the Illinois Council on Developmental Disabilities and will continue to serve on the statewide Independent Living Council. She is former director of Persons Assuming Control of Their Environment, an independent living center in Urbana.

She will also continue working with a task force monitoring a new state managed-care program for low-income seniors and those with disabilities in Chicago's collar counties, which privatized their medical services through two HMOs.

The Campaign for Real Choice initially fought against the privatization, then pushed to include people affected by the change on an evaluation team and a task force created to sort out problems with implementation.

"I'm not going to go away," she said. "I feel like I still have more to give, and there's still problems. I need to do it in a different way that fits me.

"I'm comfortable in that it's the right decision at the right time, but it doesn't make it easy. To me it's like letting go of one more thing that was Lester," she said.

Illinois Study Highlights Importance of Improved Medicaid Program : June 23 2011

The Huffington Post : by John Bouman

On June 17, Dr. Karin Rhodes and her colleague Joanna Bisgaier of the University of Pennsylvania released a report on access to sub-specialty doctors by children covered by Medicaid in Cook County, Illinois. The authors also published an article about the study underlying the report in the New England Journal of Medicine.

Dr. Rhodes undertook and was paid for the study pursuant to a contract with the Illinois Department of Healthcare and Family Services, the state's Medicaid agency. The study was part of the department's compliance with a 2005 consent decree in the case of Memisovski v. Maram, which followed a 2004 federal district court ruling that the state was not in compliance with Medicaid Act requirements that children receive recommended levels of preventive care and treatment of diagnosed conditions, and that they receive care at least to the same extent as children covered by other forms of insurance.

Following the consent decree in Memisovski, Illiniois has undertaken very significant reforms of the primary and preventive care system for children on Medicaid. It improved the rates paid for office visits to primary care doctors and dentists, and it held the processing time for those services to a reasonable level, even during the recession (when all other state bills were being delayed for many months). It launched a statewide "medical home" initiative designed to match children up with primary care doctors, which has had considerable success. Other strategies to improve primary care have been launched, and the overall effort continues.

The consent decree was less specific with respect to access to specialty care to diagnose conditions or especially to treat diagnosed conditions. It provided that the department undertake a study to examine the extent of access problems, and it left the remedies for any such problems to be determined after the study was completed. However, Illinois was not idle on this front. It enacted a round of rate increases for some pediatric specialists, and it included children in a disease management program for people with chronic illness.

The study released last Friday, however, shows that there is a very serious problem with access to specialty care for children covered by Medicaid and other public insurance, particularly as compared to children covered by other forms of insurance (mostly employer-based private insurance). Using a "secret shopper" methodology, the investigators posed as parents seeking care for a child, saying in one call that the child's coverage was Medicaid and in the next call that the same child's coverage was Blue Cross Blue Shield PPO (which dominates the market in Illinois). The Medicaid-covered children had very significant disadvantages for almost all sub-specialties in both the ability to get an appointment and in the waiting time for the appointment if it was granted. The one exception was psychiatric care, where there was a severe access problem regardless of type of insurance.

At the time of the original court order and consent decree, Illinois authorities were dealing with an inherited problem resulting from decades of underfunding and neglect of access issues in the state's Medicaid program. They have been working to comply with the decree and improve the program, in spite of the grinding recession-driven budget crisis in the state. Representatives of the children in the case look forward to working in cooperation with state authorities to find and implement solutions to these newly documented problems with specialty access.

Meanwhile, the study has resulted in media coverage, and some commentators are attempting to use it to bolster current attempts by conservatives to cut spending on Medicaid or relieve states of the duty to comply with Medicaid's federal rules guaranteeing children access to all needed care. Medicaid is not "broke"; it is underfunded. The underfunding causes it to fall short on its ability to deliver the kinds of quality health care that, over the long term, would save money by supporting healthier people. And Medicaid is not "broken"; it is falling short of its full potential. It provides plenty of essential health care to millions of children, working adults, people with disabilities and seniors. Cutting them off of Medicaid would hurt them immeasurably. And starving the program of funds would only exacerbate the problems with access and the efforts to expand the health care workforce needed to provide adequate care to all beneficiaries. Just because there are flaws in the program does not mean the program must end for millions of beneficiaries. If we scrapped every governmental program that has flaws that need fixing, where would the armed forces, roads, or schools be? Medicaid is essential, but it can and should improve, especially on this issue of access to needed care.

Pilot for Frontier Airlines Has Quadriplegic Passenger Removed: June 21, 2011

Reuters : By David Parker Brown at Airline Reporter

A pilot with Frontier Airlines, denied a quadriplegic passenger from taking his flight stating there were safety concerns. John Morris, 24, had recently flown from Denver to Dallas for a family wedding with no issues. It was when he was trying to make his way home that the disabled passenger and his family were told the captain would not allow him to take his flight.

His mother states that when a flight attendant saw John strapped in, using a seatbelt extension to secure his legs and chest, she stated she would have to have the captain’s approval. When the captain was informed of the situation, he explained that John would not be able to fly. Even after protests from John’s family and other passengers seated around him, the airline called the police and three officers boarded the aircraft. The mother states the police were sympathetic, but did nothing because he was not posing a threat to the plane or passengers. John and his family were then removed by the airline.

“The pilot did what he thought was best for the safety of this disabled person and the party, as well as the airplane, there was no wrong done here,” Frontier spokesman Peter Kowalchuk told 7News in Denver. “I don’t believe that his rights were violated. We’re in the process now of conducting an investigation.” He stated the pilot had concerns that the seatbelt extensions could be used to safely restrain the passenger and made the call to not let him fly. ”The pilot is the CEO of that aircraft, if you will,” said Kowalchuk.

John and his family were allowed to take the next flight since the captain had no safety issues. In the Department of Transportation policy on disability and air travel it states (thanks to 7News for finding this):

“If the carrier’s reason for excluding a passenger on the basis of safety is that the individual’s disability creates a safety problem, the carrier’s decision must be based on a ‘direct threat’ analysis. This concept, ground in the Americans with Disabilities Act, calls on carriers to make an individualized assessment (e.g., as opposed to a generalization or stereotype about what a person with a given disability can or can’t do) of the safety threat the person is thought to pose.”

The guidelines also state that a captain is, “in command of the aircraft and crew and is responsible for the safety of the passengers, crew members, cargo, and airplane. Taken together, this means that a carrier has the legal authority to refuse to transport an individual on the basis of safety. However, this does not mean that an airline, including the pilot or other airline staff, can discriminate on the basis of disability. If the Department finds that an airline’s decision to refuse to transport an individual with a disability was not related to safety, then it will take action against the carrier. The Department will also review the airline’s actions to see if the carrier followed the required process/procedures by providing the person who was refused transportation a written statement of the reason for the refusal within 10 days.”

When asked if the airline followed the rules, Frontier’s spokesperson stated, “I’m not going to assume that it wasn’t, but we’re investigating that.” More recently Frontier has released a statement saying, “We’re sorry for the incident and are investigating its handling. In this situation we had a well-intentioned pilot who was seeking to do the right thing to ensure the safety and compliance of all involved.”

It is disturbing to see an airline not treating a person with a disability with the respect they deserve. It is extremely inconsistent for one pilot to deny a person with a disability where two others have no issues at all. It seems like the pilot in question might have had a power trip and instead of connecting with corporate to get a second opinion on the matter, he decided to call the cops. I am still having a hard time finding how John is a bigger safety issue than a child, especially when family is there to care for him. It is bad when one pilot can tarnish the image of an entire brand, but even worse for an airline to back up his actions.

I have posed questions to Frontier Airlines about their policies letting pilots remove passengers with disabilities and the inconsistencies with a captain’s ability to remove passengers. At the time of posting this, I have not heard back from them.
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ANOTHER SUCH REPORT, DIFFERENT PASSENGER:
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British Airways apologizes for turning away girl with Down syndrome

MSNBC : By Joy Jernigan, senior travel editor : June 16 2011

British Airways has apologized for refusing to issue a plane ticket to a girl who has Down syndrome.

Alice Saunders, 12, had planned to fly from London's Gatwick Airport to Glasgow, Scotland, to visit her aunt, the Daily Mail reports. Her mother, Heather Saunders, 49, called the airline to book a ticket and told the agent that her daughter has Down syndrome but is very independent and that she wanted her to travel as an unaccompanied minor.

Sauders said she was told by the customer service agent that "we don't take children with Down syndrome." When Saunders asked why, the agent responded: "Because we've had problems in the past."

Alice lives with her parents and three siblings in Littlehampton, West Sussex, and attends a mainstream school, reads at grade level and regularly travels with her church group.

Her mother told the newspaper that "I was very cross after speaking with British Airways.

"This is 2011. Most of the world has moved on in terms of their treatment of people with learning disabilities. People with Down syndrome go to mainstream school, college, they live independently, they hold down jobs, but, it would seem, cannot travel independently with British Airways."

A British Airways spokesperson on Thursday told msnbc.com that "we apologize unreservedly for the upset caused to Mrs. Saunders and her daughter. Our customer service agent made a mistake and we will ensure the matter is addressed."

It is not British Airways policy to deny travel to unaccompanied minors with Down syndrome, said an airline spokesperson. British Airways has announced a companywide disability awareness program and plans additional training for all customer service agents.

"We will be happy to accept Mrs. Saunders' daughter as an unaccompanied minor," the airline said in a statement. "We have offered Mrs. Saunders two return flight tickets in recognition of the distress caused."

Illinois institutions for developmentally disabled may be running out of time: report June 23, 2011

WREX : By Rebecca Klopf : June 23, 2011


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DIXON (WREX) - Parents of children with severe disabilities say if Illinois does not pay up, their kids could end up homeless. That's because funding is running out for state run institutions. An advocacy group for developmentally disabled people says without some sort of help, these homes could close as early as next week.

One mom tells 13 News without these institutions she worries about how her two adults sons will survive. Since they've already tried to live in more than a half dozen community facilities.

"Michael lived in a community placement but they could not handle is behaviors so they placed him in a psychiatric ward. And they drugged him so bad that he had to go through withdrawal, he almost died," Barbara Achino.

Barbara has two severely disabled adult sons, Michael and Bob. They both have fragile X syndrome and need constant care. The 38 and 41 year old men live at the state-run Jack Mabley Center in Dixon. Their condition puts them on a mental level of a 3 and 7 year old. The Illinois League of Advocates for the Developmentally Disabled (IL-ADD) Says without more funding from the state by July 1, the Mabley Center and 6 others like it could close. If that happens community facilities like Kreider Services, a community run non-profit center, might have to take them in.

"Kreider has about 230 people in residential beds throughout 26 group homes throughout northern Illinois. Of that number, probably 80 percent spent 6 months or more in state institutions," says Arlan McClain, CEO of Kreider Services, Inc.

McClain says his facility could handle extra patients, but not quickly. He would need addition state funding and time to build more homes and even then he's not sure if every should live a state facility.

"Michael beat himself enough to make himself blind. He will beat himself enough to make him die. I want to know who will take on that responsibility," says Achino.

The Human Services Department says it will make a decision about closing some state institutions by July 1st.

Thursday, June 23, 2011

Private hospitals are no place for people with learning disabilities: guardian.co.uk : June 22, 2011

report by David Brindle : The Guardian, Wednesday 22 June 2011

The sickening abuse at Winterbourne View hospital in Bristol, revealed by Panorama, shows why such private hospitals should no longer exist, say leading figures in learning disability sector

[photo: Calls are being made to end the placement of people with learning disabilities in private hospitals, such as Winterbourne View, above. Photograph: BBC/PA]

Three weeks on, the fallout continues from BBC Panorama's exposure of sickening abuse of people with learning disabilities at the Winterbourne View private hospital near Bristol. Already it –is clear that the programme will come to be seen as a key milestone on the long journey to a civilised system of care and support for this section of society.

On Wednesday, more than 80 leading figures in the learning disability sector lend their names to a letter to the prime minister demanding an end to the placement of people in such facilities. There is, the letter says, "no place for hospitals such as Winterbourne View" and seeking to improve them will not do. "The model is wrong and does not work."

Closing all NHS long-stay hospitals for learning-disabled people in England was a historic, if tortuous, achievement. But as Panorama has shown, some people are now sent to equivalent units run by private companies which, like Winterbourne View, masquerade as short-term assessment and treatment centres. There was nothing short-term about the placements in the programme, nor was there much evidence of assessment and treatment.

There was, however, plenty of evidence of the kind of physical and verbal abuse that was all too common in NHS units such as Orchard Hill in Sutton, south London, which was the last hospital of its kind to close, in 2009, after having itself been exposed two years earlier for a regime of physical and sexual abuse of people who lived there.

The link between Winterbourne View and Orchard Hill, and with an earlier NHS scandal in Cornwall, is made in today's letter to David Cameron. The learning from past inquiries "appears to have been forgotten", say the signatories, who include former government policy advisers Rob Greig and Jim Mansell, "in part because of the continual reorganisation of public services".

The letter calls for the phasing out over two years of placements in private hospitals, with commissioners of care "prevented" from making any future such arrangements. In the meantime, it says, inspectors should ensure a "dramatic" reduction in use of restraint techniques in the hospitals and an opening-up of their culture. All people placed in the hospitals should be guaranteed independent advocacy.

Forestalling the inevitable ministerial response that these are matters for local decision-making, the signatories say: "The underpinning issue is one of the overall service and system design – hence the need for government to take a lead."

Handily, powerful evidence has emerged this week to lend weight to the letter. Publishing an evaluation of how the last Orchard Hill residents have fared since they moved to live with support in the community, Sutton council says they are happier, fitter and enjoying far greater independence, dignity and control over their lives. Oh – and their care and support costs are almost a third less.

Bear in mind that these last 39 residents of Orchard Hill were considered the most dependent and challenging people placed there. One woman had a vocabulary of only 40 words. Today, she has command of one exceeding 1,400. The evaluation, carried out by the University of Chester, found "significant" improvement in the group's quality of life within just six months of leaving the hospital. Within 18 months, it had risen by a third.

"People are making the most remarkable progress, beyond all expectations," says Colin Stears, the council's executive member for adult social services. "Returning people to their local communities by making supported living a reality has restored the human rights of people with learning disabilities, many of whom have very complex needs."

Cameron, whose disabled son died two years ago, is said to have been distressed by the Panorama programme. He should need no further persuasion to stop the worst of old-style NHS institutional care, something we thought we had left behind, being replicated by the private sector at places like Winterbourne View.

• David Brindle is the Guardian's public services editor. He is a trustee of NDTi, a not-for-profit agency that works in the learning disability sector.

# For guardian.co.uk, please click headline or go to: http://www.guardian.co.uk/

For People With Disabilities In Two States, Opposite Fates : Illinois-very good : California.-very scary: June 23 2011

Dear Readers; Before you read the story below. I have done my best not to make comments on Ability Chicago posts. I have to break my own rule (again). The recent triumphant conclusion in Illinois of "Ligas vs Hamos" 'when the state agreed to part of a settlement that will effectively allow him and about 3,000 people with disabilities to move out of institutions and into community-based housing over the next six years. Ligas is scheduled to move out in the next two months.'

This is one of the most POSITIVE directions for people with disabilities for Illinois, to be part of, involved with, and experience the joys and at times disappointment of living your life with our general society. I am so proud of all the plaintiff's, the attorneys and organizations that put there hearts into this wonderful conclusion in Illinois

While the article below does explain the reasons why the city of
Los Angeles, California would have 'the city council vote almost unanimously to draft an ordinance that will essentially make it impossible for people who collect disability checks to live under the same roof in a single-family home –- that is, in a group home.'

I would hope a solution will be reached in LA, I am disappointed (disgusted) that in this country, based on civil rights and justice for all, the city of Los Angeles, California would take so many steps backwards for people with disabilities.

Please feel free to comment on my thoughts, and/or the below story.

Sincerely, Jim
----------------

For People With Disabilities In Two States, Opposite Fates
reported by AJ Barbosa and Saki Knafo : | Posted June 23, 2011

This story was reported in collaboration with our partners at Patch.com.

When people ask Stanley Ligas, a 43-year-old with Down syndrome, why he wanted to move into a group home after being more or less confined in a state institution for 14 years, he talked about the noise.

People were always "shouting, swearing," he said. Ligas shared the place with 95 other people, so it's easy to imagine that it got quite a bit louder than the typical household.

In any case, he got tired of it, and in 2005, he and eight other people with disabilities sued the state of Illinois for failing to comply with the Americans With Disabilities Act, which says that states must provide disability checks to people who qualify for them regardless of where they live. Illinois restricted its funding to people in institutions and whoever was lucky enough to make if off a 14-year waiting list.

People with disabilities who depend on government funding have more at stake than most in the decisions of lawmakers, and recent legal developments in two states have made this clear.

The first is the Illinois case, which came to a triumphant conclusion for Ligas on Wednesday when the state agreed to part of a settlement that will effectively allow him and about 3,000 people with disabilities to move out of institutions and into community-based housing over the next six years. Ligas is scheduled to move out in the next two months.

“I'm happy," he said. "I want to say goodbye to Sheltered Village."

[photo: On their way out of a federal courthouse where a landmark ruling gives people with developmental disabilities the freedom to move out of institutions and into a smaller places in the community, Stanley Ligas and David Cicarelli celebrate with Liga's sister, Gina Foster of St. Charles, and Cicarelli's father, Jim, of Arlington Heights: Mark Welsh | Staff Photographer]

The second is a proposed ordinance in California. If it passes, it will widely be seen by people with disabilities and their advocates as an enormous loss.

Earlier this month in Los Angeles, the city council voted almost unanimously to draft an ordinance that will essentially make it impossible for people who collect disability checks to live under the same roof in a single-family home –- that is, in a group home.

Neighbors often object to having group homes placed in their communities because they can bring violence, drugs and crime to neighborhoods. But everyone has to live somewhere, and if the final ordinance passes next week, many people with disabilities, mental illnesses and serious drug and alcohol addictions are expected to wind up living on the streets, or in seedy "residential" hotels. Or in noisy institutions.

Peggy Edwards, the executive director of the advocacy group United Homeless Healthcare Partners, said it was hard to track the number of people living in group homes in L.A., but she warned that if the ordinance goes through it could "significantly increase the homeless rate."

"People who are in violation of this ordinance could be evicted," she said. "There just isn't enough affordable housing, even if they could afford it."

One of those people is Daniel Orr, who lost his job as a handyman not long ago when he started using drugs again after six years of "clean time." The 47-year-old lost his home soon after that, and then he checked into a rehab center. Orr said it was either that or "skid row."

After the stint in rehab, things began getting better. For the past four months he's been living in a "Sunrise House" –- that's what the organization that runs it calls the group homes under its management. He takes 12-step classes in the house, and says its strict rules against drug and alcohol use have helped him stay sober. He said he'd like to take his time to decide when he's ready to return to "a regular life" and the challenges that go with it.

But as it turns out, California may end up making that decision for him. The proposed ordinance, which is now being drafted by a city official in preparation for a final vote by the council, says that everyone who lives under the same roof in a single-family home must be on the same lease. This will include people living in group homes.

This might not sound like a big deal, but here's the thing: In order to collect funding from the state, people with disabilities are required to maintain their own leases. Unless, of course, they live in a state institution –- like the one Stanley Ligas has lived in for 14 years.

Both the ordinance in L.A. and the settlement in Illinois are bound to affect a lot of people besides just Ligas and Orr.

In Illinois, J.J. Hanley, the mother of a son with autism and founder of a website on which people with disabilities post reviews of Chicago business, said she hoped the settlement would force the state to kick what she described as its "very bad addiction to institutions as places to warehouse people with disabilities." (Her own son has never been institutionalized -- she described him as high-functioning.)

Gail Schecter, the executive director of the Interfaith Housing Center, an organization that fights against housing discrimination in north Chicago, said the suit was "really about communities becoming integrated and not labeling people as 'others.'" She hopes that the settlement will help people with disabilities "become citizens of the community in the truest sense of the word."

With less than two months left before he leaves Sheltered Village, Ligas has been making plans: He wants to move into a neighborhood -- presumably a quiet one -- where he'll be close to sister. He plans to share a room with a fellow plaintiff with whom he became close friends.

Everyone who knows Ligas says he's ready for this. He holds down a job at Popeyes and manages his own finances.

But sadly, as Liga settles into a group home, Orr may be moving out of his. He believes that if the ordinance passes, he'll have two choices -- homelessness or a residential hotel -- and when it comes to living a sober life, he said, "those hotels are way worse than anything."

"There's prostitutes and crack in the courtyards and the hallways," he said. "That's not some place I want to go. I shouldn't have to go there.”

Illinois Disability Rights Advocates Say Budget Cuts Are "Drastic And Disproportionate" ; Progressive Illinois June 22nd, 2011

Progressive Illinois : by Aricka Flowers : June 22nd, 2011

Disability rights advocates are continuing to make their displeasure with the recently passed state budget known, this time by publicly releasing a letter sent to Governor Pat Quinn and Michelle Saddler, earlier this month.

In it, Rita Burke, president of the Illinois League of Advocates for the Developmentally Disabled (IL-ADD), warned that the state's eight developmental centers are being set up for failure, adding that by July 1 the facilities "will be so underfunded that decertification and loss of federal matching funds will certainly result."


Last month, the General Assembly passed the still-unsigned 2012 state budget, which will severely cut funding for the state's eight residential centers for Illinoisans with the most profound disabilities. Officials for IL-ADD say the 25 percent budget cut would amount to a loss of $80 million for the facilities located in Anna, Centralia, Dixon, Dwight, Jacksonville, Kankakee, Park Forest, and Waukegan.

In Burke's letter, she requested a meeting between Quinn and representatives from the eight facilities -- outlining the serious aftermath that could follow from the budget cuts. She also noted how the closure of just one State Operated Development Center (SODC) facility led to immense chaos and life-threatening adjustments for its residents:
------------------------------------------------------------------------
We understand that your proposed budget fully funded our Centers and this budget is not your doing. However, the decision of what to do with it is yours. We want you to understand how high the stakes are for our family members and need to know what you can do to save them.

We believe there is urgency in this request. By July 1, 2011, our Centers will be so underfunded that decertification and loss of federal matching funds will certainly result. Our Centers will not survive. Our family members cannot survive without them. Almost every SODC resident has come from failed community placements. The community cannot serve our loved ones’ extreme needs nor protect them from harm, can refuse to accept them, and can expel them, facts to which many family members can attest in their own anguished stories.

The closure of Howe Developmental Center took nearly a year and 70% of those residents moved to other SODCs. Despite a seemingly cautious pace and apparent care in the selection of the next placements, thirteen people died following transition from Howe, possibly related to the trauma of transition. This budget does not allow for a cautious pace nor movement to other SODCs. The community which is currently inadequate to support extremely high needs individuals is also cut in this budget and will become even more ill-equipped to fill a void left by SODC closures. Where will our loved ones go? What is their future—do they have one?

You must be aware that the advocates for SODC closures do not need that level of care and do not advocate for those who do. ... There are budget cuts that will not cost innocent lives. Cuts to our State Operated Developmental Centers are not among them.
-------------------------------------------------------------------------
Some Illinois families are taking matters into their own hands in order to ensure that their relative is in a place where they will get the care they need -- and in some cases that means abandoning the state altogether. A recent report in the Chicago Tribune highlighted this trend of migrating to states with perceivably better budgets for disability services, like Michigan and Wisconsin. Check out this video from the report of one Broadview, Illinois family's story detailing how life changed for them and their disabled daughter after having moved to Michigan:.

Kids with disabilities take the ride of their lives: Illinois : June 22, 2011

The State Journal-Register | Springfield, IL
By DEAN OLSEN : June 22, 2011

Maggie George of Springfield was riding a two-wheel bicycle Wednesday without training wheels, and her mother was ecstatic about her daughter’s accomplishment and reaction.

“I haven’t seen that big a smile in a long time, “ Donet George told 11-year-old Maggie. “Good job, sweetie."

Maggie, who has autism, is learning a new skill and gaining confidence during a camp operated by Lose the Training Wheels, a not-for-profit organization that works throughout the United States and Canada to help people with physical and intellectual disabilities learn to ride a bicycle.
“Riding a bike is a rite of passage for a lot of individuals, “ said Cory Bunner, 25, a physical-education teacher from Jacksonville and bicycle technician with the group. “We hope this skill will open up new avenues for our participants. It’s a great way for these kids to be successful."

Eighteen children and young adults are participating in a five-day camp that ends Friday in the iceless rink area at Springfield Park District’s Nelson Center. The Springfield camp, for which participants paid a $200 fee, is sponsored by the Land of Lincoln Down Syndrome Society and central Illinois chapter of the Autism Society of America.

Lose the Training Wheels, the brainchild of former University of Illinois mechanical engineering professor Richard Klein, uses special bicycles with rear-wheel roller systems developed by Klein that give participants stability and immediate feelings of success.

The roller is replaced with different versions over the five days so it more closely resembles a bicycle wheel as riders gain confidence and begin to master the balance, steering and coordination that has frustrated them and their parents in the past.

During once-a-day, 75-minute sessions, volunteers jog next to riders and use handles at the rear of the bikes to steady the participants while encouraging them.

At the end of the camps, 80 percent of campers can ride at least 75 feet without intervention, Bunner said, but the 12-year-old organization doesn’t have long-term data yet on how many people become independent bicycle riders.

Deana Koudelik said she and her husband, Tom, live in Pearland, Texas, and used a trip to visit relatives in Decatur as an opportunity for their son, Dale, to attend the camp.

Dale, 10, who has Asperger’s syndrome, wants to ride bikes with all the other children in his Texas neighborhood, Deana Koudelik said.

Dale smiled Wednesday as he rode a regular two-wheel bike for several dozen feet, totally on his own.

“I think he’s proud, “ his mother said.

Maggie George said the camp has helped to ease her fear of falling.

“I feel good," she said.

Kathy Mullen’s 16-year-old son, Spencer, who has Down syndrome, may not be an independent rider by the end of camp. But she said Spencer is making progress that she and her husband can build upon at their home in Girard and during future Lose the Training Wheels camps.

“He’s doing really good," she said, adding that riding a bike would allow Spencer to go on long bike rides with family members and take part in a lifelong physical activity for socialization, weight control and overall good health.

Becky Johnson, who is coordinating the camp on behalf of the Down syndrome society, said her 15-year-old daughter, Shelbie Nevill, took part in a Lose the Training Wheels camp three years ago. Shelbie, who has Down syndrome, now can ride on her own.

Johnson, a Springfield resident, said riding a bike can help people with disabilities change public attitudes by becoming more visible and showing the non-disabled population that they have abilities.

“It makes them look at our kids differently," she said.

On the Web: www.losethetrainingwheels.org

Copyright 2011 The State Journal-Register. Some rights reserved

Stress in the City: Brain Activity and Biology Behind Mood Disorders of Urbanites: ScienceDaily - June 22, 2011

Being born and raised in a major urban area is associated with greater lifetime risk for anxiety and mood disorders. Until now, the biology for these associations had not been described. A new international study, which involved Douglas Mental Health University Institute researcher Jens Pruessner, is the first to show that two distinct brain regions that regulate emotion and stress are affected by city living. These findings, published in Nature may lead to strategies that improve the quality of life for city dwellers.

"Previous findings have shown that the risk for anxiety disorders is 21 percent higher for people from the city, who also have a 39 percent increase for mood disorders," says co-author Jens Pruessner, a Douglas researcher. "In addition, the incidence for schizophrenia is almost doubled for individuals who are born and brought up in cities. These values are a cause for concern and determining the biology behind this is the first step to remedy the trend."

Distinct brain structures

Pruessner, with his colleagues from the Central Institute of Mental Health in Mannheim, looked at the brain activity of healthy volunteers from urban and rural areas. In a series of functional magnetic resonance experiments involving the Douglas' previously developed 'Montreal Imaging Stress Task',(MIST) protocol, they showed that city living was associated with greater stress responses in the amygdala, an area of the brain involved with emotional regulation and mood. In contrast, urban upbringing was found to be associated with activity in the cingulate cortex, a region involved in regulation of negative affect and stress.

"These findings suggest that different brain regions are sensitive to the experience of city living during different times across the lifespan," says Pruessner. "Future studies need to clarify the link between psychopathology and these affects in individuals with mental disorders.These findings contribute to our understanding of urban environmental risk for mental disorders and health in general. They further point to a new approach to interface social sciences, neurosciences and public policy to respond to the major health challenge of urbanization."

*Journal Reference:

1.Florian Lederbogen, Peter Kirsch, Leila Haddad, Fabian Streit, Heike Tost, Philipp Schuch, Stefan Wüst, Jens C. Pruessner, Marcella Rietschel, Michael Deuschle, Andreas Meyer-Lindenberg. City living and urban upbringing affect neural social stress processing in humans. Nature, 2011; 474 (7352): 498 DOI: 10.1038/nature10190

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

People With Disabilities Illinois Ride Free Program 2011 : RTA: CTA, METRA, PACE

June 2011 - To help people with disabilities maintain their independence, the RTA has partnered with the Illinois Department on Aging to offer the People with Disabilities Ride Free program. New legislation now provides free rides on fixed-route transit (regularly scheduled CTA, Metra, and Pace buses and trains) for any Illinois resident over the age of 16 who has been enrolled as a person with a disability in the Illinois Circuit Breaker program.

Individuals who are enrolled in the Circuit Breaker program with a disability must still apply for the RTA-issued “Circuit Permit” that will allow them to ride free on fixed-route transit in the RTA service region.

I am not enrolled in the Illinois Circuit Breaker program. Now what?
To ride free on RTA systems, you must first qualify and be enrolled in the Illinois Circuit Breaker program. This program is administered by the Illinois Department on Aging. As of January 1, the income levels for eligibility into the Circuit Breaker program has increased. The new income limit ranges from $27,610 to $45,657, depending on household size. Learn more about the Illinois Circuit Breaker program or call 1-800-252-8966 [TTY: 1-888-206-1327]. Information is also available at senior citizen centers, the Mayor’s Office on Disabilities in the City of Chicago, and Independent Living Centers.

I am enrolled in the Illinois Circuit Breaker program. How do I qualify for RTA’s People with Disabilities Ride Free program?
If you are already enrolled in the Illinois Circuit Breaker program, you can complete an application for an RTA-issued Circuit Breaker permit at any RTA Customer Service Center. The main center is located at 165 N. Jefferson in Chicago and there are over 200 registration centers located in Cook, DuPage, Kane, Lake, McHenry and Will counties.

At the registration center, you will be required to present a wallet-sized color photo of yourself that is approximately 1 1/2" square. Do not wear a hat, scarf or sunglasses in the photo. Some registration centers may charge up to $5 for taking your photo. The RTA’s Customer Service Center does not charge for this service. After verifying your eligibility with the Department on Aging, the RTA will issue a “Circuit Permit” within 3-4 weeks. This permit will allow you to ride free ride on fixed-route transit.

How do I use the RTA-issued Circuit Breaker permit?
On CTA and Pace buses, just insert the permit into the fare box or the turnstile for CTA trains. Metra riders will need to show their Circuit Permit to the conductor. Metra personnel may also request a second piece of government identification.

For any other questions regarding this program, please call 312-836-7000

# For RTA Website click headline or go to: http://rtachicago.com/

# For Illinois Department on Aging's Circuit Breaker program: http://www.cbrx.il.gov/

Wednesday, June 22, 2011

The 2011 Disability Mentoring Day National Launch : AAPD : Host - Chicago Mayor’s Office for People with Disabilities (MOPD) on October 14, 2011

American Association of People with Disabilities (AAPD) Disability Mentoring Day (DMD) Program is a national job-shadow and career exploration program designed to link students and jobseekers with disabilities to employers interested in hiring people with disabilities. AAPD coordinates DMD national through a network of more than 350 volunteer DMD Coordinators. DMD Coordinators are responsible for local DMD programs and share information about their programs on www.DisabilityMentor.net.

Disability Mentoring Day in Duluth, MN

(refresh if no video)

DMD is recognized nationally on the third Wednesday of every October, which is National Disability Employment Awareness Month. AAPD encourages our network of DMD Coordinators to center their local DMD activities around this date; however DMD activities can and do occur around the country on many different dates.

This year, on October 14, 2011, AAPD along with the City of Chicago Mayor’s Office for People with Disabilities (MOPD) will host the 2011 DMD National Launch in Chicago. The theme for the 2011 DMD National Launch is Transition to Independent Futures, focusing on the importance of education, employment, and independent living for people with disabilities. To find out when your local DMD program is happening, please visit www.DisabilityMentor.net.

The National Disability Mentoring Day Program began in 1999 with just 11 students with disabilities job shadowing in the White House under the Clinton administration. Now, DMD has grown to provide job-shadowing, career fairs and mentoring opportunities to more than 85,000 students and job seekers with disabilities in all 50 states, Puerto Rico, and the U.S. Virgin Islands. DMD is the nation’s largest job-shadowing program designed for people with disabilities, which allows career exploration to take place outside of the hiring context so that job seekers can meet and learn about employers committed to hiring from this diverse and untapped workforce.

In 2001, MOPD launched its first DMD Program with just 20 students in collaboration with the Office of Special Education and Supports in Chicago Public Schools. Since that time, the program has grown in size and scope. Now, DMD is the first prong of a year-long employment program designed to connect academic learning to employment. Each year, students with disabilities planning for life after high school take advantage of this event as a unique career building opportunity.

AAPD is excited to partner with MOPD for the national DMD 2011 launch to showcase Chicago’s outstanding model and success in furthering the employment of youth with disabilities.

Over 2,000 participating public and private employers hosted mentees at their places of employment, with many continuing the mentoring relationships for long-term periods.

# For more info from AAPD click headline or go to: http://www.aapd.com/site/c.pvI1IkNWJqE/b.5606851/k.CDB/Welcome_to_the_Disability_Mentoring_Program.htm

# City of Chicago Mayors Office for People with Disabilities (MOPD): http://www.cityofchicago.org/city/en/depts/mopd.html

The Art Institute of Chicago : Accessibility : 2011

The Art Institute of Chicago welcomes all visitors and affirms its commitment to making its programs and services accessible to everyone. The museum has a range of resources and programs designed specifically for adults and children with disabilities.

Access to the Museum :
Michigan Avenue Entrance
Ramp access is available at the Michigan Avenue entrance.


Millennium Park Lobby:
Drop offs are permitted. A traffic pullout is available from the eastbound lanes of Monroe Street. Ramp access is available at the Millennium Park entrance.

Parking:
Accessible parking is located in the following garages near the Art Institute:

•Millennium Park garage (enter at Columbus Drive and Monroe Street), with 8' clearance in some sections and an elevator at the exit
•East Monroe Street garage (enter at Columbus Drive and Monroe Street), with 6' 8" clearance and exit ramps at Monroe Street
•Grant Park North garage (enter at Michigan Avenue between Madison and Randolph), with 8' 3 " clearance for vans and an elevator at the exit
See additional parking information.


Inside the Museum:
Elevators are located throughout the museum with access to all floors. A limited number of wheelchairs and strollers are available for free on a first-come, first-served basis. Pay telephones have volume control and are lowered TDD/TYY- equipped phone is available in the Michigan Avenue lobby. Auditoria are equipped with designated wheelchair areas. Upon entry, please pick up a Museum Access Information Guide, also available in large type and braille.

Hearing-Assist Devices:
Fullerton Hall is equipped with hearing-assist devices. Pick one up in the Michigan Avenue checkroom.

Gallery Audio Guide:
A gallery guide is available for a self-guided tour of the Art Institute with a hand-held MP3 player. They can be purchased with a ticket at an admissions counter or at the audio tour counter in either the Michigan Avenue or Millenium Park lobby for $7 ($5 for members), and are free for visitors who are blind or with low vision and their escorts.

Audio tours for some special exhibitions may be available.

Pathfinder:
Explore the Museum using Pathfinder, our interactive floor plan. Discover and locate artworks on display as well as gallery panoramas, exhibitions, daily events, and visitor amenities.

Programs:
We suggest that all guests attend our daily public lectures. For information on topics and dates, ask for the weekly calendar at any information desk in the museum, call (312) 443-3680, or consult our online calendar.

Signed Interpretations:
As part of its commitment to accessibility for all audiences, the museum now offers American Sign Language interpretation for any of its scheduled gallery talks. Please call (312) 443-3682, TDD/TTY (312) 443-3680, or send an email to access@artic.edu two weeks in advance to schedule a signed interpretation.

Escorts for the Blind:
Visitors who are blind or have low vision may arrange for free guided tours of the museum by calling the Department of Museum Education from 9:00 to 5:00 weekdays at (312) 857-7641. The museum has a corps of volunteer escorts for visitors who are blind or have low vision. Please arrange for a tour one to two weeks in advance.

Exhibitions and Multimedia Programs:
The Touch Gallery is an exhibition of five portrait busts from the permanent collection that can be explored by sight and by touch. The exhibition is below the grand staircase and is accessible by using the elevator in the Michigan Avenue lobby. Labels are available in large-type print and Braille. The bronze and marble sculptures on display reflect cultures from around the world and provide an enriching experience for all audiences.

Located in the Ryan Education Center,The Curious Corner is a wheel chair-accessible station where families can learn about art through interactive stories and games.

Cleopatra: Multimedia Guide to the Art of the Ancient World is an online resource that provides educational videos with subtitles in English and Spanish.

New! TacTiles Kits:
The Art Institute is pleased to unveil a phenomenal and fresh approach to experiencing art for visitors who have low vision: "TacTiles." These kits consist of a series of masterpieces from the Art Institute's collection represented on hand-held tiles designed to be touched. The compositions and textures of the works of art are reproduced on the tiles, making these works legible through fingertips to visitors. Each TacTile fits into a slot in a specially designed carrying case, which also includes a color photograph, a large-type print description, and a braille description of each work.

Works of art represented include: Pierre Auguste Renoir's Two Sisters (On the Terrace), 1881 (pictured above); Trompe-L'Oeil Still Life with a Flower Garland and a Curtain by Ardriaen van der Spelt and Frans van Mieris, 1658; Joan Miró's Personages with Star, 1933; a Japanese screen by Tosa Mitsuoki, Flowering Cherry with Poem Slips, c. 1675; and the marvelous Aztec Coronation Stone of Motecuhzoma II, 1503.

The TacTiles are available free of charge in the Crown Family Educator Resource Center. Visitors may request a guided tour of the TacTiles with advanced notice. For more information, call (312) 857-7641.

TacTiles are made possible thanks to a generous grant from Buddy Mayer and the Rothschild Foundation.

TacTiles were developed by the Department of Museum Education of the Art Institute and Helen Maria Nugent, associate professor, School of the Art Institute of Chicago.

# Questions? Please call (312) 443-3600 or TDD/TTY 312-443-3890, 9:00 a.m.-5:00 p.m. weekdays.

# For webite click headline or go to: http://www.artic.edu/aic/visitor_info/access.html

Learning Disabilities Association of America 2012 Annual International Conference : February 22-25, 2012 in Chicago, IL

LDA 49th Annual International Conference
February 22-25, 2012
Chicago, IL

Plans are currently under way to offer high-quality presentations which will provide practical knowledge and research to help address problems in both children and adults with learning disabilities. We invite you to join us in February in Chicago for what promises to be another outstanding 4 days of the latest research and dialogue on learning disabilities, including specific workshops on Medical, Mental Health, Teacher Preparation, Public Policy, Adults, Assessment, Research and much, much more!

All events will take place at the Hilton Chicago – conveniently located on Michigan Avenue's Cultural Mile! Overlooking Grant Park, the Hilton is center to it all with museums, parks and shopping all within walking distance. A special group rate has been secured for LDA. Check back soon for further details!

Exhibitors, Advertisers & Sponsors – Become a part of our growing group of vendors and advertisers at the leading conference on learning disabilities. Join publishing companies, private schools, summer camp programs, software and educational product vendors. This is your best opportunity to reach educators and decision makers across the country. The full prospectus is available here. Contact us with any questions.

Who Should Attend this Conference: Adults with learning disabilities and attention deficit hyperactivity disorder, Parents of children with learning disabilities and attention deficit hyperactivity disorder, Teachers of special education and general education, Principals, Administrators, Counselors, Social Workers, Researchers, Medical and Mental Health Professionals, Education Policy Advocates and College Student Support Personnel.

What: The largest meeting on learning disabilities in the world, featuring over 200 workshops and exhibits.

Why You Should Attend: Discover the latest in LD research; learn effective teaching techniques and strategies; hear from leading experts in the LD field; network with colleagues and make new friends; learn about critical policy issues; earn graduate and/or continuing education credits (CEUs) and much more.

Visitors to Chicago will find magic in such sparkling attractions as Navy Pier – the Midwest’s top tourist destination – and its boardwalk, 150-foot Ferris wheel, boat and segway tours, and countless dining or shopping options. Millennium Park offers dazzling music, art, landscape design and architecture – including the mammoth stainless-steel Cloud Gate sculpture.

Chicago looks great from every angle, whether you’re exploring the city’s astonishing architecture during a guided tour (on foot or aboard a Chicago River boat, lakeshore cruise or sightseeing bus) or you’re enjoying the birds-eye view from the 103rd floor of Skydeck Chicago in the Willis Tower (formerly Sears Tower) and the 94th floor Hancock Observatory. The city’s 29 miles of lakefront paths are just one reason Chicago is one of the world’s most walkable and beautiful cities.

# For LDA website, click headline or go to: http://www.ldanatl.org/index.cfm

#For even more reasons to visit Chicago go to www.choosechicago.com.