FULLERTON, Calif. (AP) — In the nearly two decades since his son descended into madness, Ron Thomas has worried every day that the schizophrenic 37-year-old would die of exposure or illness on the streets. He never imagined the end would come in a violent confrontation with police.
The death last month was the end of a trajectory that began when Kelly Thomas was in his early 20s and started showing the first signs of what would later be diagnosed as schizophrenia: he shuttled between addresses, preferred to sleep on the floor and stopped showering.
In treatment, Thomas did well and was able to hold down a job — but when he stopped taking his pills, he disappeared onto the streets. He racked up an array of charges, from public urination to assault with a deadly weapon, and alarmed his parents with his bizarre behavior.
"My daughter and I have talked for years that we'd get the call that something had happened to him, whether it was from organ failure because he's not drinking enough fluids or the elements or maybe gang activity," said his father, Ron Thomas.
Last month, he was sitting on a bench at the Fullerton Transportation Center, a hub for buses and commuter trains where homeless people congregate, when six police officers arrived to investigate reports of a man burglarizing cars nearby. Police said he ran when they tried to search his backpack and that he resisted arrest.
The incident was captured by a bystander with a cell phone, and bus surveillance tape released Monday showed agitated witnesses describing how officers beat Thomas and used a stun gun on him repeatedly as he cried out for his father.
On the cell phone video, a man can be heard screaming over a fast, clicking sound that those on the tape identify as a stun gun being deployed.
Thomas was taken off life support five days after the July 5 altercation. His father said Wednesday he was stunned when he learned police officers caused his son's severe head and neck injuries.
"When I arrived at the hospital to see him, I honestly thought that gang bangers had got a hold of him like the cowards sometimes do and just beat him with a baseball bat in the face," he said. "Immediately my thoughts were to get with Fullerton police ... and I didn't learn until a certain amount of hours later the truth. That put me in absolute shock."
A police spokesman, Sgt. Andrew Goodrich, said the case was an isolated incident.
"We have a good department full of good individuals," he said. "We've made more than half-a-million law enforcement contacts over the past 4.5 years ... This is the only instance of this kind that's happened."
Goodrich said officers receive training on how to deal with the mentally ill and the homeless. But an attorney representing the department, Michael D. Schwartz, said that "public perception of officers' trying to control a combative, resistive suspect rarely conform to those officers' training, experiences, and what those officers were experiencing at the time or reality."
The revelations have caused growing outrage in this quiet college town. More than 70 people spoke at the City Council meeting Wednesday, and a city councilwoman called for the resignation of the police chief. Thomas' father and others were planning a protest outside the police station this weekend, the second in as many weeks.
"My son needs a voice," he said. "Now, the people have become Kelly's voice and, yeah, I'm leading the charge."
Kelly Thomas was an outgoing child who loved to play the guitar, participated in Boy Scouts and Cub Scouts and aspired to be a wildland firefighter, said his father, who raised him alone after he and Thomas' mother divorced.
After his diagnosis, he went to a live-in facility that provided meals and monitored his medication, his father said. Thomas was able to hold down a job at a gas station and then a printing facility and even started to train with the California Department of Forestry and Protection.
But each time he began to improve, he stopped his medications and wound up back on the streets, moving between Yorba Linda, Placentia, Fullerton and Cypress — all places where he had once lived or had family and friends. One of the hardest parts of his death has been hearing their son described as homeless, the father said.
"That's the heartbreaking part for all of us. We all have ideas of what we'd like our kids to be like and to do in life. With Kelly, we didn't get to realize that and it constantly broke our heart," his father said. "Kelly wasn't homeless at all, he had so many homes, but he wanted to be a drifter and he did."
Life on the streets led to criminal charges.
He pleaded guilty to assault with a deadly weapon other than a firearm in 1995 and since 2004 has had a string of arrests for a host of lesser crimes including public urination, trespassing, battery, unlawful camping, petty theft and vandalism. He racked up traffic violations for jaywalking and failing to obey traffic signals.
His mother sought a restraining order against him in December 2010 after he refused to leave her front porch, took off his clothes and urinated by the front door, according to court papers. In the same court papers, his mother alleged that Thomas grabbed her by the throat when they shared an apartment, although it was unclear when the incident occurred.
The family said they sought the order to try to get him into treatment as his behavior spiraled out of control.
On the day of the beating, bystanders said Thomas was approached by two officers and ran from them. Bus surveillance video showed witnesses talking about the confrontation to the driver of a bus that pulled up minutes later.
In the grainy, black-and-white video, a woman who appears upset says: "The cops are kicking this poor guy over there. ... He's almost halfway dead."
A male witness says the man, identified as Thomas, was sitting on a bench when he was approached by two officers and ran from them. The man says police used a stun gun on Thomas six times.
"They caught him, pound his face, pound his face against the curb ... and they beat him up," the man said. "They beat him up, and then all the cops came and they hogtied him, and he was like, 'Please God! Please Dad!'"
The police department has turned over the investigation to the district attorney's office and placed on paid administrative leave six officers involved in the beating. The FBI also launched a probe into whether the officers violated Thomas' civil rights in the incident.
People with untreated mental illness make up about one-third of the nation's 600,000 homeless, said Kristina Ragosta, legislative and policy counsel for the Treatment Advocacy Center.
More needs to be done by police departments to train officers in how to recognize symptoms and deal with people with mental illness, said Elaine Deck, the senior program manager at the International Association of Chiefs of Police.
Sometimes, an untrained officer can make a situation worse, she said.
"Handcuffing them may escalate the behavior where the officer may think they are trying to calm the person," Deck said. "They may not know that this may actually escalate a response."
___
By GILLIAN FLACCUS - Associated Press | AP
Associated Press writers Amy Taxin in Tustin and Thomas Watkins in Los Angeles contributed to this report.
..
Disability News Service, Resources, Diversity, Americans with Disabilities Act; Local and National.
Disability News Service, Resources, Diversity, Americans with Disabilities Act; Local and National.
Thursday, August 4, 2011
USA TechGuide: a webguide to wheelchairs, mobility scooters, and assistive technology: read and submit reviews
A program of United Spinal Association
USA TechGuide is a webguide to wheelchairs, mobility scooters, and assistive technology choices. You can read and submit wheelchair reviews, mobility scooter reviews, wheelchair cushion reviews, standing device reviews, and search The TechGuide for all types of assistive equipment.
Read reviews by product users. Take the time to submit a review. Your review will help others make the right choice.
Find assistive technology, home medical equipment, adaptive recreational products and services.
# For USA TechGuide, visit: http://www.usatechguide.org/
USA TechGuide is a webguide to wheelchairs, mobility scooters, and assistive technology choices. You can read and submit wheelchair reviews, mobility scooter reviews, wheelchair cushion reviews, standing device reviews, and search The TechGuide for all types of assistive equipment.
Read reviews by product users. Take the time to submit a review. Your review will help others make the right choice.
Find assistive technology, home medical equipment, adaptive recreational products and services.
# For USA TechGuide, visit: http://www.usatechguide.org/
Illinois; Will County Hosts Paratransit Update : Event coincided with anniversary of Americans with Disabilities Act 2011
Tuesday, July 26th marked the 21st anniversary of the Americans with Disabilities Act (ADA) and Will County recognized this landmark anniversary as efforts continued to expand paratransit services throughout Will County. Local township officials and social service agencies gathered to hear and update on efforts Will County is making to improve transit options.
Nick Palmer, chief of staff to Will County Executive Larry Walsh, led a Will County paratransit update meeting with local elected officials and community groups at Governors State University in University Park.
In attendance were Joe Voccia, program manager of the Regional Transportation Authority (RTA), Bob Howard, Washington Township supervisor and Will County Board member, representatives from Crete, Monee, Will and Rich Townships and leaders from various Will County social services organizations.
“Transportation options are a critical piece of our resident’s quality of life,” Walsh said. “My administration has continued to bring stakeholders from across Will County together to determine the best way we can all work together to improve and expand transit services throughout Will County. In such tough economic times, we must all be working together to maximize efficiencies while still maintaining levels of service.”
The focus of the Tuesday’s meeting was to review the 2010 Coordinated Paratransit Study and update the stakeholders on a new RTA grant that Will County is pursing to fund a Mobility Manager and operational funding for paratransit and dial-a-ride services in the six townships in Eastern Will County. RTA grants are being pursued by the county to hire a Mobility Manager and operational support, both efforts seek to improve cooperation among existing paratransit providers and improve access for underserved areas. A Paratransit Coordinating Council will be established by the executive’s office to continue to advise on future improvements in Will County transit efforts.
“Will County is fortunate to have a number of transit systems that are working well,” Palmer said. “However, we know that there remain gaps in services and a growing need for disabled residents, seniors, and others for trips for medical treatment and employment. We are continuing to seek partners who can help us address these unmet needs.”
Palmer expressed confidence in the program's future, acknowledging support from the RTA and the Will County Board. He emphasized the need for commitment and collaboration among local governments, service agencies and funding partners to pursue expanded transportation to provide seniors and disabled individuals in Will County more freedom to become more active consumers.
Will County remains one of the fastest growing counties in Illinois by total population numbers. The recent 2010 Census put Will County’s population at 677,560 with projections of a population in excess of 1.2 million by 2030. This growth signals the need for greater transportation options to meet this growing demand for services.
Additional information on the 2010 Will County Coordinated Paratransit study can be found on the county’s website at www.willcountyillinois.com.
For more information on the Americans with Disabilities Act, visit these websites: www.ada.org, the Great Lakes ADA Center at www.adagreatlakes.org, and the American Association of People with Disabilities at www.aapd.com.
# As posted at the Patch Network
Nick Palmer, chief of staff to Will County Executive Larry Walsh, led a Will County paratransit update meeting with local elected officials and community groups at Governors State University in University Park.
In attendance were Joe Voccia, program manager of the Regional Transportation Authority (RTA), Bob Howard, Washington Township supervisor and Will County Board member, representatives from Crete, Monee, Will and Rich Townships and leaders from various Will County social services organizations.
“Transportation options are a critical piece of our resident’s quality of life,” Walsh said. “My administration has continued to bring stakeholders from across Will County together to determine the best way we can all work together to improve and expand transit services throughout Will County. In such tough economic times, we must all be working together to maximize efficiencies while still maintaining levels of service.”
The focus of the Tuesday’s meeting was to review the 2010 Coordinated Paratransit Study and update the stakeholders on a new RTA grant that Will County is pursing to fund a Mobility Manager and operational funding for paratransit and dial-a-ride services in the six townships in Eastern Will County. RTA grants are being pursued by the county to hire a Mobility Manager and operational support, both efforts seek to improve cooperation among existing paratransit providers and improve access for underserved areas. A Paratransit Coordinating Council will be established by the executive’s office to continue to advise on future improvements in Will County transit efforts.
“Will County is fortunate to have a number of transit systems that are working well,” Palmer said. “However, we know that there remain gaps in services and a growing need for disabled residents, seniors, and others for trips for medical treatment and employment. We are continuing to seek partners who can help us address these unmet needs.”
Palmer expressed confidence in the program's future, acknowledging support from the RTA and the Will County Board. He emphasized the need for commitment and collaboration among local governments, service agencies and funding partners to pursue expanded transportation to provide seniors and disabled individuals in Will County more freedom to become more active consumers.
Will County remains one of the fastest growing counties in Illinois by total population numbers. The recent 2010 Census put Will County’s population at 677,560 with projections of a population in excess of 1.2 million by 2030. This growth signals the need for greater transportation options to meet this growing demand for services.
Additional information on the 2010 Will County Coordinated Paratransit study can be found on the county’s website at www.willcountyillinois.com.
For more information on the Americans with Disabilities Act, visit these websites: www.ada.org, the Great Lakes ADA Center at www.adagreatlakes.org, and the American Association of People with Disabilities at www.aapd.com.
# As posted at the Patch Network
Managing Your Symptoms in MS: Tremors, Seizures, and Loss of Balance - Video from National MS Society
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From: NationalMSSociety | Jan 27, 2010
MS Learn Online is the National MS Society's online educational webcast series. This video features Michael Kaufman, MD, who discusses how to treat tremors, seizures, and loss of balance in multiple sclerosis.
# For the National MS Society, visit: http://www.nationalmssociety.org/index.aspx
Wednesday, August 3, 2011
60% of adults in Illinois are registered organ & tissue donors: Register today and make a difference for someone in the future : 2011
Donate Life Illinois is a coalition of agencies responsible for organ, tissue, eye, blood and marrow donation, as well as donor education and registration in Illinois. It is one of 45 regional coalitions and 50 national businesses or associations making up Donate Life America, a not-for-profit alliance that serves as a national voice and inspires all people to save and enhance lives through organ, eye and tissue donation.
Donate Life Illinois member organizations include:
American Liver Foundation-Illinois
Biological Resource Center of Illinois
Gift of Hope Organ & Tissue Donor Network
Heartland Lions Eye Bank
Illinois Eye-Bank
Illinois Secretary of State Organ/Tissue Donor Program
LifeSource
Mid-America Transplant Services
Musculoskeletal Transplant Foundation
National Kidney Foundation of Illinois
National Marrow Donor Program
The coalition provides numerous programs and “Donate Life” outreach through its member organizations. To contact us, call 888/307-DON8 (3668)
[photo: Illinois Secretary of State Jesse White & transplant recipient Micaela Prunty]
"One of the most generous acts a person can make is to register as an organ/tissue donor. This simple decision can have a tremendous impact on many lives.
Register today and make a difference for someone in the future.
Then join us in this important effort. Encouraging your friends and relatives to join you as a registered donor and help save lives."
- Jesse White,
Illinois Secretary of State
About Illinois Campaign:
“I am. Are you?” is a campaign to increase the number of Illinois residents who joined the state’s organ/tissue donor registry. The campaign is part of a national effort through Donate Life America to increase the number of Americans who have taken action to become donors in their states to 100 million.
In Illinois, a 2006 statewide poll revealed that 87% of Illinois residents know that registering to be an organ, eye and tissue donor is the “right thing to do.” Yet, 40% of Illinoisans have not registered.
It’s important that everyone who supports becoming a donor takes a few minutes to register this important decision. In January 2006, Illinois law changed and a new donor registry was launched. By joining the First-Person Consent Registry, you will ensure that your decision to donate will be honored.
Commit your decision to help save lives by joining the First-Person Consent Registry here. Remember, you must be at least age 18 years old.
To contact us about the campaign, call us at 888/307-DON8.
# For more information or to register visit Donate Life Illinois at: https://www.donatelifeillinois.org/donatelife/registration.aspx
Donate Life Illinois member organizations include:
American Liver Foundation-Illinois
Biological Resource Center of Illinois
Gift of Hope Organ & Tissue Donor Network
Heartland Lions Eye Bank
Illinois Eye-Bank
Illinois Secretary of State Organ/Tissue Donor Program
LifeSource
Mid-America Transplant Services
Musculoskeletal Transplant Foundation
National Kidney Foundation of Illinois
National Marrow Donor Program
The coalition provides numerous programs and “Donate Life” outreach through its member organizations. To contact us, call 888/307-DON8 (3668)
[photo: Illinois Secretary of State Jesse White & transplant recipient Micaela Prunty]
"One of the most generous acts a person can make is to register as an organ/tissue donor. This simple decision can have a tremendous impact on many lives.
Register today and make a difference for someone in the future.
Then join us in this important effort. Encouraging your friends and relatives to join you as a registered donor and help save lives."
- Jesse White,
Illinois Secretary of State
About Illinois Campaign:
“I am. Are you?” is a campaign to increase the number of Illinois residents who joined the state’s organ/tissue donor registry. The campaign is part of a national effort through Donate Life America to increase the number of Americans who have taken action to become donors in their states to 100 million.
In Illinois, a 2006 statewide poll revealed that 87% of Illinois residents know that registering to be an organ, eye and tissue donor is the “right thing to do.” Yet, 40% of Illinoisans have not registered.
It’s important that everyone who supports becoming a donor takes a few minutes to register this important decision. In January 2006, Illinois law changed and a new donor registry was launched. By joining the First-Person Consent Registry, you will ensure that your decision to donate will be honored.
Commit your decision to help save lives by joining the First-Person Consent Registry here. Remember, you must be at least age 18 years old.
To contact us about the campaign, call us at 888/307-DON8.
# For more information or to register visit Donate Life Illinois at: https://www.donatelifeillinois.org/donatelife/registration.aspx
Aurea Picasso, Former Hanover Township, Illinois Welfare Director Sentenced to Six Years in Prison: article Aug 03 2011
Hanover Township, Ill. - Aurea Picasso, the former welfare director of northwest suburban Hanover Township pleaded guilty Wednesday to stealing more than $193,110 in funds for dental work, car insurance, cell phones and her daughter’s ‘Sweet 16’ birthday party.
Picasso, 45, formerly of Aurora, pled guilty to one count of theft of government funds over $100,000 and sentenced to six years in prison during a court appearance on Wednesday, according to a release from the Cook County State’s Attorney’s office.
Picasso served as welfare director for Hanover Township from 2003 until 2009, the release said. The department was responsible for providing welfare checks to the needy and also ran a food pantry.
Picasso had access to the township’s checkbooks as well as an additional checking account provided by the Salvation Army for emergency situations, the release said. She allegedly wrote $124,560 in checks from these accounts to pay for dental work, car insurance, cell phones, and expenses for her daughter’s ‘Sweet 16’ birthday party.
She is also accused of enrolling family, friends, and others for welfare benefits, forging their signatures and depositing the $68,550 worth of funds in her bank account, the release said.
In 2009, when a new administration took over, officials became suspicious that funds had been diverted and contacted the state’s attorney’s office, the release said.
Picasso is alleged to have stolen $193,110 in township funds, the release said.
In October 2010, Picasso was arrested a day before she was scheduled to be released on parole from Dwight Correctional Facility where she has been serving a prison sentence for an unrelated identity theft case.
# Sun-Times Media Wire; Published : Wednesday, 03 Aug 2011
Picasso, 45, formerly of Aurora, pled guilty to one count of theft of government funds over $100,000 and sentenced to six years in prison during a court appearance on Wednesday, according to a release from the Cook County State’s Attorney’s office.
Picasso served as welfare director for Hanover Township from 2003 until 2009, the release said. The department was responsible for providing welfare checks to the needy and also ran a food pantry.
Picasso had access to the township’s checkbooks as well as an additional checking account provided by the Salvation Army for emergency situations, the release said. She allegedly wrote $124,560 in checks from these accounts to pay for dental work, car insurance, cell phones, and expenses for her daughter’s ‘Sweet 16’ birthday party.
She is also accused of enrolling family, friends, and others for welfare benefits, forging their signatures and depositing the $68,550 worth of funds in her bank account, the release said.
In 2009, when a new administration took over, officials became suspicious that funds had been diverted and contacted the state’s attorney’s office, the release said.
Picasso is alleged to have stolen $193,110 in township funds, the release said.
In October 2010, Picasso was arrested a day before she was scheduled to be released on parole from Dwight Correctional Facility where she has been serving a prison sentence for an unrelated identity theft case.
# Sun-Times Media Wire; Published : Wednesday, 03 Aug 2011
Visually Impaired Law student takes home a win in her own federal case: article & video report : August 2, 2011
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Burlington, Vermont - August 2, 2011
A Vermont Law School student is entering her final year, but she has already won one decision in Federal Court. Deanna Jones, 44, hopes to practice disability law in the future, but this case could play a huge role in whether or not that happens.
Jones has been studying for her ethics exam, required of every law student in the country, for the better part of the summer. Thanks to a federal judge's ruling, she will be able to take it the way she wants. A dream of hers since childhood.
She said, "People used to say with that mouth of yours you need to be a lawyer."
Jones is legally blind, and has been since she was five. Later in life, she was also diagnosed with an auditory learning disability which means she needs to have text so she can read along when someone is reading to her for her to fully comprehend.
"Kurzweil reads to me and Zoom Text gives me the ability to zoom in if I really need to look at a word," she explained.
She says these computer programs which enlarge the font to size 72, highlight words in different colors and read the text aloud are the reason she has made it this far in law school.
Jones explained, "Using these in combination has been the gold ticket."
She wants to use these programs to navigate her required ethics exam in just a few days, but the National Conference of Bar Examiners denied her request arguing that is not necessary. So Jones made a federal case about it.
Jones' lawyer, Emily Joselson, said, "We had to ask the court to issue a preliminary injunction which is an unusual measure asking the court to order a party to do something in a relatively short period of time."
The bar examiners had agreed to let Jones have someone read her the test, but in court argued against letting her use the computer program, saying it could help someone, "place a thumb drive in the laptop and copy the test."
That it has already accommodated visually impaired test takers by "no longer using a human voice on it's audio CD finding a synthetic voice preferable."
And that it's just too expensive saying the company would incur costs of $300,000 a year based on their estimation of 60 requests annually.
Jones' lawyers argued not only does she need these programs, but according to the American with Disabilities Act using them is her legal right.
"How you could gain any advantage from that is really beyond me," Jones said.
Judge Christina Reiss granted Deanna's injunction allowing her to take the test this Friday with the computer, saying that her arguments are reasonable. But Jones' lawyers say the fight is not over yet, and that the battle could continue for years if the NCBE does not back down.
# As repoted by Molly Smith - WCAX News
COMMONLY ASKED QUESTIONS ABOUT CHILD CARE CENTERS AND THE AMERICANS WITH DISABILITIES ACT: USDJ ADA Home Page
U.S. Department of Justice
Civil Rights Division
Disability Rights Section
COMMONLY ASKED QUESTIONS ABOUT CHILD CARE CENTERS AND THE AMERICANS WITH DISABILITIES ACT
Coverage
1. Q: Does the Americans with Disabilities Act -- or "ADA" -- apply to child care centers?
A: Yes. Privately-run child care centers -- like other public accommodations such as private schools, recreation centers, restaurants, hotels, movie theaters, and banks -- must comply with title III of the ADA. Child care services provided by government agencies, such as Head Start, summer programs, and extended school day programs, must comply with title II of the ADA. Both titles apply to a child care center's interactions with the children, parents, guardians, and potential customers that it serves.
A child care center's employment practices are covered by other parts of the ADA and are not addressed here. For more information about the ADA and employment practices, please call the Equal Employment Opportunity Commission (see question 30).
2. Q: Which child care centers are covered by title III?
A: Almost all child care providers, regardless of size or number of employees, must comply with title III of the ADA. Even small, home-based centers that may not have to follow some State laws are covered by title III.
The exception is child care centers that are actually run by religious entities such as churches, mosques, or synagogues. Activities controlled by religious organizations are not covered by title III.
Private child care centers that are operating on the premises of a religious organization, however, are generally not exempt from title III. Where such areas are leased by a child care program not controlled or operated by the religious organization, title III applies to the child care program but not the religious organization. For example, if a private child care program is operated out of a church, pays rent to the church, and has no other connection to the church, the program has to comply with title III but the church does not.
General Information
3. Q: What are the basic requirements of title III?
A: The ADA requires that child care providers not discriminate against persons with disabilities on the basis of disability, that is, that they provide children and parents with disabilities with an equal opportunity to participate in the child care center's programs and services. Specifically:
Centers cannot exclude children with disabilities from their programs unless their presence would pose a direct threat to the health or safety of others or require a fundamental alteration of the program.
Centers have to make reasonable modifications to their policies and practices to integrate children, parents, and guardians with disabilities into their programs unless doing so would constitute a fundamental alteration.
Centers must provide appropriate auxiliary aids and services needed for effective communication with children or adults with disabilities, when doing so would not constitute an undue burden.
Centers must generally make their facilities accessible to persons with disabilities. Existing facilities are subject to the readily achievable standard for barrier removal, while newly constructed facilities and any altered portions of existing facilities must be fully accessible.
4. Q: How do I decide whether a child with a disability belongs in my program?
A: Child care centers cannot just assume that a child's disabilities are too severe for the child to be integrated successfully into the center's child care program. The center must make an individualized assessment about whether it can meet the particular needs of the child without fundamentally altering its program. In making this assessment, the caregiver must not react to unfounded preconceptions or stereotypes about what children with disabilities can or cannot do, or how much assistance they may require. Instead, the caregiver should talk to the parents or guardians and any other professionals (such as educators or health care professionals) who work with the child in other contexts. Providers are often surprised at how simple it is to include children with disabilities in their mainstream programs.
Child care centers that are accepting new children are not required to accept children who would pose a direct threat (see question 8) or whose presence or necessary care would fundamentally alter the nature of the child care program.
5. Q: My insurance company says it will raise our rates if we accept children with disabilities. Do I still have to admit them into my program?
A: Yes. Higher insurance rates are not a valid reason for excluding children with disabilities from a child care program. The extra cost should be treated as overhead and divided equally among all paying customers.
6. Q: Our center is full and we have a waiting list. Do we have to accept children with disabilities ahead of others?
A: No. Title III does not require providers to take children with disabilities out of turn.
7. Q: Our center specializes in "group child care." Can we reject a child just because she needs individualized attention?
A: No. Most children will need individualized attention occasionally. If a child who needs one-to-one attention due to a disability can be integrated without fundamentally altering a child care program, the child cannot be excluded solely because the child needs one-to-one care.
For instance, if a child with Down Syndrome and significant mental retardation applies for admission and needs one-to-one care to benefit from a child care program, and a personal assistant will be provided at no cost to the child care center (usually by the parents or though a government program), the child cannot be excluded from the program solely because of the need for one-to-one care. Any modifications necessary to integrate such a child must be made if they are reasonable and would not fundamentally alter the program. This is not to suggest that all children with Down Syndrome need one-to-one care or must be accompanied by a personal assistant in order to be successfully integrated into a mainstream child care program. As in other cases, an individualized assessment is required. But the ADA generally does not require centers to hire additional staff or provide constant one-to-one supervision of a particular child with a disability.
8. Q: What about children whose presence is dangerous to others? Do we have to take them, too?
A: No. Children who pose a direct threat -- a substantial risk of serious harm to the health and safety of others -- do not have to be admitted into a program. The determination that a child poses a direct threat may not be based on generalizations or stereotypes about the effects of a particular disability; it must be based on an individualized assessment that considers the particular activity and the actual abilities and disabilities of the individual.
In order to find out whether a child has a medical condition that poses a significant health threat to others, child care providers may ask all applicants whether a child has any diseases that are communicable through the types of incidental contact expected to occur in child care settings. Providers may also inquire about specific conditions, such as active infectious tuberculosis, that in fact pose a direct threat.
9. Q: One of the children in my center hits and bites other children. His parents are now saying that I can't expel him because his bad behavior is due to a disability. What can I do?
A: The first thing the provider should do is try to work with the parents to see if there are reasonable ways of curbing the child's bad behavior. He may need extra naps, "time out," or changes in his diet or medication. If reasonable efforts have been made and the child continues to bite and hit children or staff, he may be expelled from the program even if he has a disability. The ADA does not require providers to take any action that would pose a direct threat -- a substantial risk of serious harm -- to the health or safety of others. Centers should not make assumptions, however, about how a child with a disability is likely to behave based on their past experiences with other children with disabilities. Each situation must be considered individually.
10. Q: One of the children in my center has parents who are deaf. I need to have a long discussion with them about their child's behavior and development. Do I have to provide a sign language interpreter for the meeting?
A: It depends. Child care centers must provide effective communication to the customers they serve, including parents and guardians with disabilities, unless doing so poses an undue burden. The person with a disability should be consulted about what types of auxiliary aids and services will be necessary in a particular context, given the complexity, duration, and nature of the communication, as well as the person's communication skills and history. Different types of auxiliary aids and services may be required for lengthy parent-teacher conferences than will normally be required for the types of incidental day-to-day communication that take place when children are dropped off or picked up from child care. As with other actions required by the ADA, providers cannot impose the cost of a qualified sign language interpreter or other auxiliary aid or service on the parent or guardian.
A particular auxiliary aid or service is not required by title III if it would pose an undue burden, that is, a significant difficulty or expense, relative to the center or parent company's resources.
11. Q: We have a "no pets" policy. Do I have to allow a child with a disability to bring a service animal, such as a seeing eye dog?
A: Yes. A service animal is not a pet. The ADA requires you to modify your "no pets" policy to allow the use of a service animal by a person with a disability. This does not mean that you must abandon your "no pets" policy altogether, but simply that you must make an exception to your general rule for service animals.
12. Q: If an older child has delayed speech or developmental disabilities, can we place that child in the infant or toddler room?
A: Generally, no. Under most circumstances, children with disabilities must be placed in their age-appropriate classroom, unless the parents or guardians agree otherwise.
13. Q: Can I charge the parents for special services provided to a child with a disability, provided that the charges are reasonable?
A: It depends. If the service is required by the ADA, you cannot impose a surcharge for it. It is only if you go beyond what is required by law that you can charge for those services. For instance, if a child requires complicated medical procedures that can only be done by licensed medical personnel, and the center does not normally have such personnel on staff, the center would not be required to provide the medical services under the ADA. If the center chooses to go beyond its legal obligation and provide the services, it may charge the parents or guardians accordingly. On the other hand, if a center is asked to do simple procedures that are required by the ADA -- such as finger-prick blood glucose tests for children with diabetes (see question 20) -- it cannot charge the parents extra for those services. To help offset the costs of actions or services that are required by the ADA, including but not limited to architectural barrier removal, providing sign language interpreters, or purchasing adaptive equipment, some tax credits and deductions may be available (see question 24).
Personal Services
14. Q: Our center has a policy that we will not give medication to any child. Can I refuse to give medication to a child with a disability?
A: No. In some circumstances, it may be necessary to give medication to a child with a disability in order to make a program accessible to that child. While some state laws may differ, generally speaking, as long as reasonable care is used in following the doctors' and parents' or guardians written instructions about administering medication, centers should not be held liable for any resulting problems. Providers, parents, and guardians are urged to consult professionals in their state whenever liability questions arise.
15. Q: We diaper young children, but we have a policy that we will not accept children more than three years of age who need diapering. Can we reject children older than three who need diapering because of a disability?
A: Generally, no. Centers that provide personal services such as diapering or toileting assistance for young children must reasonably modify their policies and provide diapering services for older children who need it due to a disability. Generally speaking, centers that diaper infants should diaper older children with disabilities when they would not have to leave other children unattended to do so.
Centers must also provide diapering services to young children with disabilities who may need it more often than others their age.
Some children will need assistance in transferring to and from the toilet because of mobility or coordination problems. Centers should not consider this type of assistance to be a "personal service."
16. Q: We do not normally diaper children of any age who are not toilet trained. Do we still have to help older children who need diapering or toileting assistance due to a disability?
A: It depends. To determine when it is a reasonable modification to provide diapering for an older child who needs diapering because of a disability and a center does not normally provide diapering, the center should consider factors including, but not limited to, (1) whether other non-disabled children are young enough to need intermittent toileting assistance when, for instance, they have accidents; (2) whether providing toileting assistance or diapering on a regular basis would require a child care provider to leave other children unattended; and (3) whether the center would have to purchase diapering tables or other equipment.
If the program never provides toileting assistance to any child, however, then such a personal service would not be required for a child with a disability. Please keep in mind that even in these circumstances, the child could not be excluded from the program because he or she was not toilet trained if the center can make other arrangements, such as having a parent or personal assistant come and do the diapering.
Issues Regarding Specific Disabilities
17. Q: Can we exclude children with HIV or AIDS from our program to protect other children and employees?
A: No. Centers cannot exclude a child solely because he has HIV or AIDS. According to the vast weight of scientific authority, HIV/AIDS cannot be easily transmitted during the types of incidental contact that take place in child care centers. Children with HIV or AIDS generally can be safely integrated into all activities of a child care program. Universal precautions, such as wearing latex gloves, should be used whenever caregivers come into contact with children's blood or bodily fluids, such as when they are cleansing and bandaging playground wounds. This applies to the care of all children, whether or not they are known to have disabilities.
18. Q: Must we admit children with mental retardation and include them in all center activities?
A: Centers cannot generally exclude a child just because he or she has mental retardation. The center must take reasonable steps to integrate that child into every activity provided to others. If other children are included in group sings or on playground expeditions, children with disabilities should be included as well. Segregating children with disabilities is not acceptable under the ADA.
19. Q: What about children who have severe, sometimes life-threatening allergies to bee stings or certain foods? Do we have to take them?
A: Generally, yes. Children cannot be excluded on the sole basis that they have been identified as having severe allergies to bee stings or certain foods. A center needs to be prepared to take appropriate steps in the event of an allergic reaction, such as administering a medicine called "epinephrine" that will be provided in advance by the child's parents or guardians.
The Department of Justice's settlement agreement with La Petite Academy addresses this issue and others (see question 26).
20. Q: What about children with diabetes? Do we have to admit them to our program? If we do, do we have to test their blood sugar levels?
A: Generally, yes. Children with diabetes can usually be integrated into a child care program without fundamentally altering it, so they should not be excluded from the program on the basis of their diabetes. Providers should obtain written authorization from the child's parents or guardians and physician and follow their directions for simple diabetes-related care. In most instances, they will authorize the provider to monitor the child's blood sugar -- or "blood glucose" -- levels before lunch and whenever the child appears to be having certain easy-to-recognize symptoms of a low blood sugar incident. While the process may seem uncomfortable or even frightening to those unfamiliar with it, monitoring a child's blood sugar is easy to do with minimal training and takes only a minute or two. Once the caregiver has the blood sugar level, he or she must take whatever simple actions have been recommended by the child's parents or guardians and doctor, such as giving the child some fruit juice if the child's blood sugar level is low. The child's parents or guardians are responsible for providing all appropriate testing equipment, training, and special food necessary for the child.
The Department of Justice's settlement agreements with KinderCare and La Petite Academy address this issue and others (see question 26).
21. Q: Do we have to help children take off and put on their leg braces and provide similar types of assistance to children with mobility impairments?
A: Generally, yes. Some children with mobility impairments may need assistance in taking off and putting on leg or foot braces during the child care day. As long as doing so would not be so time consuming that other children would have to be left unattended, or so complicated that it can only done by licensed health care professionals, it would be a reasonable modification to provide such assistance.
The Department of Justice's settlement agreement with the Sunshine Child Center of Gillett, Wisconsin, addresses this issue and others (see question 26).
Making the Child Care Facility Accessible
22. Q: How do I make my child care center's building, playground, and parking lot accessible to people with disabilities?
A: Even if you do not have any disabled people in your program now, you have an ongoing obligation to remove barriers to access for people with disabilities. Existing privately-run child care centers must remove those architectural barriers that limit the participation of children with disabilities (or parents, guardians, or prospective customers with disabilities) if removing the barriers is readily achievable, that is, if the barrier removal can be easily accomplished and can be carried out without much difficulty or expense. Installing offset hinges to widen a door opening, installing grab bars in toilet stalls, or rearranging tables, chairs, and other furniture are all examples of barrier removal that might be undertaken to allow a child in a wheelchair to participate in a child care program. Centers run by government agencies must insure that their programs are accessible unless making changes imposes an undue burden; these changes will sometimes include changes to the facilities.
23. Q: We are going to build a new facility. What architectural standards do we have to follow to make sure that our facility is accessible to people with disabilities?
A: Newly constructed privately-run child care centers -- those designed and constructed for first occupancy after January 26, 1993 -- must be readily accessible to and usable by individuals with disabilities. This means that they must be built in strict compliance with the ADA Standards for Accessible Design. New centers run by government agencies must meet either the ADA Standards or the Uniform Federal Accessibility Standards.
Tax Provisions
24. Q: Are there tax credits or deductions available to help offset the costs associated with complying with the ADA?
A: To assist businesses in complying with the ADA, Section 44 of the IRS Code allows a tax credit for small businesses and Section 190 of the IRS Code allows a tax deduction for all businesses.
The tax credit is available to businesses that have total revenues of $1,000,000 or less in the previous tax year or 30 or fewer full-time employees. This credit can cover 50% of the eligible access expenditures in a year up to $10,250 (maximum credit of $5,000). The tax credit can be used to offset the cost of complying with the ADA, including, but not limited to, undertaking barrier removal and alterations to improve accessibility; provide sign language interpreters; and for purchasing certain adaptive equipment.
The tax deduction is available to all businesses with a maximum deduction of $15,000 per year. The tax deduction can be claimed for expenses incurred in barrier removal and alterations.
To order documents about the tax credit and tax deduction provisions, contact the Department of Justice's ADA Information Line (see question 30).
The Department of Justice's Enforcement Efforts
25. Q: What is the Department of Justice's enforcement philosophy regarding title III of the ADA?
A: Whenever the Department receives a complaint or is asked to join an on-going lawsuit, it first investigates the allegations and tries to resolve them through informal or formal settlements. The vast majority of complaints are resolved voluntarily through these efforts. If voluntary compliance is not forthcoming, the Department may have to litigate and seek injunctive relief, damages for aggrieved individuals, and civil penalties.
26. Q: Has the United States entered into any settlement agreements involving child care centers?
A: The Department has resolved three matters through formal settlement agreements with the Sunshine Child Center, KinderCare Learning Centers, and La Petite Academy.
In the first agreement, Sunshine Child Center in Gillett, Wisconsin, agreed to: (1) provide diapering services to children who, because of their disabilities, require diapering more often or at a later age than nondisabled children; (2) put on and remove the complainant's leg braces as necessary; (3) ensure that the complainant is not unnecessarily segregated from her age-appropriate classroom; (4) engage in readily achievable barrier removal to its existing facility; and (5) design and construct its new facility (planned independently of the Department's investigation) in a manner that is accessible to persons with disabilities.
In 1996, the Department of Justice entered into a settlement agreement with KinderCare Learning Centers -- the largest chain of child care centers in the country -- under which KinderCare agreed to provide appropriate care for children with diabetes, including providing finger-prick blood glucose tests. In 1997, La Petite Academy -- the second-largest chain -- agreed to follow the same procedures.
In its 1997 settlement agreement with the Department of Justice, La Petite Academy also agreed to keep epinephrine on hand to administer to children who have severe and possibly life-threatening allergy attacks due to exposure to certain foods or bee stings and to make changes to some of its programs so that children with cerebral palsy can participate.
The settlement agreements and their attachments, including a waiver of liability form and parent and physician authorization form, can be obtained by calling the Department's ADA Information Line or through the Internet (see question 30). Child care centers and parents or guardians should consult a lawyer in their home state to determine whether any changes need to be made before the documents are used.
27. Q: Has the Department of Justice ever sued a child care center for ADA violations?
A: Yes. On June 30, 1997, the United States filed lawsuits against three child care providers for refusing to enroll a four-year-old child because he has HIV. See United States v. Happy Time Day Care Center, (W.D. Wisc.); United States v. Kiddie Ranch, (W.D. Wisc.); and United States v. ABC Nursery, Inc. (W.D. Wisc.).
28. Q: Does the United States ever participate in lawsuits brought by private citizens?
A: Yes. The Department sometimes participates in private suits either by intervention or as amicus curiae -- "friend of the court." One suit in which the United States participated was brought by a disability rights group against KinderCare Learning Centers. The United States supported the plaintiff's position that KinderCare had to make its program accessible to a boy with multiple disabilities including mental retardation. The litigation resulted in KinderCare's agreement to develop a model policy to allow the child to attend one of its centers with a state-funded personal assistant.
Additional Resources
29. Q: Are there any reference books or video tapes that might help me further understand the obligations of child care providers under title III?
A: Through a grant from the Department of Justice, The Arc published All Kids Count: Child Care and the ADA, which addresses the ADA's obligations of child care providers. Copies are available for a nominal fee by calling The Arc's National Headquarters in Arlington, Texas:
800-433-5255 (voice)
800-855-1155 (TDD)
Under a grant provided by the Department of Justice, Eastern Washington University (EWU) produced eight 5-7 minute videotapes and eight accompanying booklets on the ADA and child care providers. The videos cover different ADA issues related to child care and can be purchased as a set or individually by contacting the EWU at:
509-623-4246 (voice)
TDD: use relay service
30. Q: I still have some general questions about the ADA. Where can I get more information?
A: The Department of Justice operates an ADA Information Line. Information Specialists are available to answer general and technical questions during business hours on the weekdays. The Information Line also provides 24-hour automated service for ordering ADA materials and an automated fax back system that delivers technical assistance materials to fax machines or modems.
800-514-0301 (voice)
800-514-0383 (TDD)
The ADA Home Page, which is updated frequently, contains the Department of Justice's regulations and technical assistance materials, as well as press releases on ADA cases and other issues. Several settlement agreements with child care centers are also available on the Home Page.
www.usdoj.gov/crt/ada/adahom1.htm
The Department of Justice also operates an ADA Electronic Bulletin Board, on which a wide variety of information and documents are available.
202-514-6193 (by computer modem)
There are ten regional Disability and Business Technical Assistance Centers, or DBTAC's, that are funded by the Department of Education to provide technical assistance under the ADA. One toll-free number connects to the center in your region.
800-949-4232 (voice & TDD)
The Access Board offers technical assistance on the ADA Accessibility Guidelines.
800-872-2253 (voice)
800-993-2822 (TDD)
Electronic Bulletin Board
202-272-5448
The Equal Employment Opportunity Commission, or EEOC, offers technical assistance on the ADA provisions for employment which apply to businesses with 15 or more employees.
Employment questions
800-669-4000 (voice)
800-669-6820 (TDD)
Employment documents
800-669-3362 (voice)
800-800-3302 (TDD)
If you have further questions about child care centers or other requirements of the ADA, you may call the U.S. Department of Justice's toll-free ADA Information Line at: 800-514-0301 (voice) or 800-514-0383 (TDD).
Note: Reproduction of this document is encouraged.
# For more ADA information, check for updates please visit: http://www.ada.gov/
Civil Rights Division
Disability Rights Section
COMMONLY ASKED QUESTIONS ABOUT CHILD CARE CENTERS AND THE AMERICANS WITH DISABILITIES ACT
Coverage
1. Q: Does the Americans with Disabilities Act -- or "ADA" -- apply to child care centers?
A: Yes. Privately-run child care centers -- like other public accommodations such as private schools, recreation centers, restaurants, hotels, movie theaters, and banks -- must comply with title III of the ADA. Child care services provided by government agencies, such as Head Start, summer programs, and extended school day programs, must comply with title II of the ADA. Both titles apply to a child care center's interactions with the children, parents, guardians, and potential customers that it serves.
A child care center's employment practices are covered by other parts of the ADA and are not addressed here. For more information about the ADA and employment practices, please call the Equal Employment Opportunity Commission (see question 30).
2. Q: Which child care centers are covered by title III?
A: Almost all child care providers, regardless of size or number of employees, must comply with title III of the ADA. Even small, home-based centers that may not have to follow some State laws are covered by title III.
The exception is child care centers that are actually run by religious entities such as churches, mosques, or synagogues. Activities controlled by religious organizations are not covered by title III.
Private child care centers that are operating on the premises of a religious organization, however, are generally not exempt from title III. Where such areas are leased by a child care program not controlled or operated by the religious organization, title III applies to the child care program but not the religious organization. For example, if a private child care program is operated out of a church, pays rent to the church, and has no other connection to the church, the program has to comply with title III but the church does not.
General Information
3. Q: What are the basic requirements of title III?
A: The ADA requires that child care providers not discriminate against persons with disabilities on the basis of disability, that is, that they provide children and parents with disabilities with an equal opportunity to participate in the child care center's programs and services. Specifically:
Centers cannot exclude children with disabilities from their programs unless their presence would pose a direct threat to the health or safety of others or require a fundamental alteration of the program.
Centers have to make reasonable modifications to their policies and practices to integrate children, parents, and guardians with disabilities into their programs unless doing so would constitute a fundamental alteration.
Centers must provide appropriate auxiliary aids and services needed for effective communication with children or adults with disabilities, when doing so would not constitute an undue burden.
Centers must generally make their facilities accessible to persons with disabilities. Existing facilities are subject to the readily achievable standard for barrier removal, while newly constructed facilities and any altered portions of existing facilities must be fully accessible.
4. Q: How do I decide whether a child with a disability belongs in my program?
A: Child care centers cannot just assume that a child's disabilities are too severe for the child to be integrated successfully into the center's child care program. The center must make an individualized assessment about whether it can meet the particular needs of the child without fundamentally altering its program. In making this assessment, the caregiver must not react to unfounded preconceptions or stereotypes about what children with disabilities can or cannot do, or how much assistance they may require. Instead, the caregiver should talk to the parents or guardians and any other professionals (such as educators or health care professionals) who work with the child in other contexts. Providers are often surprised at how simple it is to include children with disabilities in their mainstream programs.
Child care centers that are accepting new children are not required to accept children who would pose a direct threat (see question 8) or whose presence or necessary care would fundamentally alter the nature of the child care program.
5. Q: My insurance company says it will raise our rates if we accept children with disabilities. Do I still have to admit them into my program?
A: Yes. Higher insurance rates are not a valid reason for excluding children with disabilities from a child care program. The extra cost should be treated as overhead and divided equally among all paying customers.
6. Q: Our center is full and we have a waiting list. Do we have to accept children with disabilities ahead of others?
A: No. Title III does not require providers to take children with disabilities out of turn.
7. Q: Our center specializes in "group child care." Can we reject a child just because she needs individualized attention?
A: No. Most children will need individualized attention occasionally. If a child who needs one-to-one attention due to a disability can be integrated without fundamentally altering a child care program, the child cannot be excluded solely because the child needs one-to-one care.
For instance, if a child with Down Syndrome and significant mental retardation applies for admission and needs one-to-one care to benefit from a child care program, and a personal assistant will be provided at no cost to the child care center (usually by the parents or though a government program), the child cannot be excluded from the program solely because of the need for one-to-one care. Any modifications necessary to integrate such a child must be made if they are reasonable and would not fundamentally alter the program. This is not to suggest that all children with Down Syndrome need one-to-one care or must be accompanied by a personal assistant in order to be successfully integrated into a mainstream child care program. As in other cases, an individualized assessment is required. But the ADA generally does not require centers to hire additional staff or provide constant one-to-one supervision of a particular child with a disability.
8. Q: What about children whose presence is dangerous to others? Do we have to take them, too?
A: No. Children who pose a direct threat -- a substantial risk of serious harm to the health and safety of others -- do not have to be admitted into a program. The determination that a child poses a direct threat may not be based on generalizations or stereotypes about the effects of a particular disability; it must be based on an individualized assessment that considers the particular activity and the actual abilities and disabilities of the individual.
In order to find out whether a child has a medical condition that poses a significant health threat to others, child care providers may ask all applicants whether a child has any diseases that are communicable through the types of incidental contact expected to occur in child care settings. Providers may also inquire about specific conditions, such as active infectious tuberculosis, that in fact pose a direct threat.
9. Q: One of the children in my center hits and bites other children. His parents are now saying that I can't expel him because his bad behavior is due to a disability. What can I do?
A: The first thing the provider should do is try to work with the parents to see if there are reasonable ways of curbing the child's bad behavior. He may need extra naps, "time out," or changes in his diet or medication. If reasonable efforts have been made and the child continues to bite and hit children or staff, he may be expelled from the program even if he has a disability. The ADA does not require providers to take any action that would pose a direct threat -- a substantial risk of serious harm -- to the health or safety of others. Centers should not make assumptions, however, about how a child with a disability is likely to behave based on their past experiences with other children with disabilities. Each situation must be considered individually.
10. Q: One of the children in my center has parents who are deaf. I need to have a long discussion with them about their child's behavior and development. Do I have to provide a sign language interpreter for the meeting?
A: It depends. Child care centers must provide effective communication to the customers they serve, including parents and guardians with disabilities, unless doing so poses an undue burden. The person with a disability should be consulted about what types of auxiliary aids and services will be necessary in a particular context, given the complexity, duration, and nature of the communication, as well as the person's communication skills and history. Different types of auxiliary aids and services may be required for lengthy parent-teacher conferences than will normally be required for the types of incidental day-to-day communication that take place when children are dropped off or picked up from child care. As with other actions required by the ADA, providers cannot impose the cost of a qualified sign language interpreter or other auxiliary aid or service on the parent or guardian.
A particular auxiliary aid or service is not required by title III if it would pose an undue burden, that is, a significant difficulty or expense, relative to the center or parent company's resources.
11. Q: We have a "no pets" policy. Do I have to allow a child with a disability to bring a service animal, such as a seeing eye dog?
A: Yes. A service animal is not a pet. The ADA requires you to modify your "no pets" policy to allow the use of a service animal by a person with a disability. This does not mean that you must abandon your "no pets" policy altogether, but simply that you must make an exception to your general rule for service animals.
12. Q: If an older child has delayed speech or developmental disabilities, can we place that child in the infant or toddler room?
A: Generally, no. Under most circumstances, children with disabilities must be placed in their age-appropriate classroom, unless the parents or guardians agree otherwise.
13. Q: Can I charge the parents for special services provided to a child with a disability, provided that the charges are reasonable?
A: It depends. If the service is required by the ADA, you cannot impose a surcharge for it. It is only if you go beyond what is required by law that you can charge for those services. For instance, if a child requires complicated medical procedures that can only be done by licensed medical personnel, and the center does not normally have such personnel on staff, the center would not be required to provide the medical services under the ADA. If the center chooses to go beyond its legal obligation and provide the services, it may charge the parents or guardians accordingly. On the other hand, if a center is asked to do simple procedures that are required by the ADA -- such as finger-prick blood glucose tests for children with diabetes (see question 20) -- it cannot charge the parents extra for those services. To help offset the costs of actions or services that are required by the ADA, including but not limited to architectural barrier removal, providing sign language interpreters, or purchasing adaptive equipment, some tax credits and deductions may be available (see question 24).
Personal Services
14. Q: Our center has a policy that we will not give medication to any child. Can I refuse to give medication to a child with a disability?
A: No. In some circumstances, it may be necessary to give medication to a child with a disability in order to make a program accessible to that child. While some state laws may differ, generally speaking, as long as reasonable care is used in following the doctors' and parents' or guardians written instructions about administering medication, centers should not be held liable for any resulting problems. Providers, parents, and guardians are urged to consult professionals in their state whenever liability questions arise.
15. Q: We diaper young children, but we have a policy that we will not accept children more than three years of age who need diapering. Can we reject children older than three who need diapering because of a disability?
A: Generally, no. Centers that provide personal services such as diapering or toileting assistance for young children must reasonably modify their policies and provide diapering services for older children who need it due to a disability. Generally speaking, centers that diaper infants should diaper older children with disabilities when they would not have to leave other children unattended to do so.
Centers must also provide diapering services to young children with disabilities who may need it more often than others their age.
Some children will need assistance in transferring to and from the toilet because of mobility or coordination problems. Centers should not consider this type of assistance to be a "personal service."
16. Q: We do not normally diaper children of any age who are not toilet trained. Do we still have to help older children who need diapering or toileting assistance due to a disability?
A: It depends. To determine when it is a reasonable modification to provide diapering for an older child who needs diapering because of a disability and a center does not normally provide diapering, the center should consider factors including, but not limited to, (1) whether other non-disabled children are young enough to need intermittent toileting assistance when, for instance, they have accidents; (2) whether providing toileting assistance or diapering on a regular basis would require a child care provider to leave other children unattended; and (3) whether the center would have to purchase diapering tables or other equipment.
If the program never provides toileting assistance to any child, however, then such a personal service would not be required for a child with a disability. Please keep in mind that even in these circumstances, the child could not be excluded from the program because he or she was not toilet trained if the center can make other arrangements, such as having a parent or personal assistant come and do the diapering.
Issues Regarding Specific Disabilities
17. Q: Can we exclude children with HIV or AIDS from our program to protect other children and employees?
A: No. Centers cannot exclude a child solely because he has HIV or AIDS. According to the vast weight of scientific authority, HIV/AIDS cannot be easily transmitted during the types of incidental contact that take place in child care centers. Children with HIV or AIDS generally can be safely integrated into all activities of a child care program. Universal precautions, such as wearing latex gloves, should be used whenever caregivers come into contact with children's blood or bodily fluids, such as when they are cleansing and bandaging playground wounds. This applies to the care of all children, whether or not they are known to have disabilities.
18. Q: Must we admit children with mental retardation and include them in all center activities?
A: Centers cannot generally exclude a child just because he or she has mental retardation. The center must take reasonable steps to integrate that child into every activity provided to others. If other children are included in group sings or on playground expeditions, children with disabilities should be included as well. Segregating children with disabilities is not acceptable under the ADA.
19. Q: What about children who have severe, sometimes life-threatening allergies to bee stings or certain foods? Do we have to take them?
A: Generally, yes. Children cannot be excluded on the sole basis that they have been identified as having severe allergies to bee stings or certain foods. A center needs to be prepared to take appropriate steps in the event of an allergic reaction, such as administering a medicine called "epinephrine" that will be provided in advance by the child's parents or guardians.
The Department of Justice's settlement agreement with La Petite Academy addresses this issue and others (see question 26).
20. Q: What about children with diabetes? Do we have to admit them to our program? If we do, do we have to test their blood sugar levels?
A: Generally, yes. Children with diabetes can usually be integrated into a child care program without fundamentally altering it, so they should not be excluded from the program on the basis of their diabetes. Providers should obtain written authorization from the child's parents or guardians and physician and follow their directions for simple diabetes-related care. In most instances, they will authorize the provider to monitor the child's blood sugar -- or "blood glucose" -- levels before lunch and whenever the child appears to be having certain easy-to-recognize symptoms of a low blood sugar incident. While the process may seem uncomfortable or even frightening to those unfamiliar with it, monitoring a child's blood sugar is easy to do with minimal training and takes only a minute or two. Once the caregiver has the blood sugar level, he or she must take whatever simple actions have been recommended by the child's parents or guardians and doctor, such as giving the child some fruit juice if the child's blood sugar level is low. The child's parents or guardians are responsible for providing all appropriate testing equipment, training, and special food necessary for the child.
The Department of Justice's settlement agreements with KinderCare and La Petite Academy address this issue and others (see question 26).
21. Q: Do we have to help children take off and put on their leg braces and provide similar types of assistance to children with mobility impairments?
A: Generally, yes. Some children with mobility impairments may need assistance in taking off and putting on leg or foot braces during the child care day. As long as doing so would not be so time consuming that other children would have to be left unattended, or so complicated that it can only done by licensed health care professionals, it would be a reasonable modification to provide such assistance.
The Department of Justice's settlement agreement with the Sunshine Child Center of Gillett, Wisconsin, addresses this issue and others (see question 26).
Making the Child Care Facility Accessible
22. Q: How do I make my child care center's building, playground, and parking lot accessible to people with disabilities?
A: Even if you do not have any disabled people in your program now, you have an ongoing obligation to remove barriers to access for people with disabilities. Existing privately-run child care centers must remove those architectural barriers that limit the participation of children with disabilities (or parents, guardians, or prospective customers with disabilities) if removing the barriers is readily achievable, that is, if the barrier removal can be easily accomplished and can be carried out without much difficulty or expense. Installing offset hinges to widen a door opening, installing grab bars in toilet stalls, or rearranging tables, chairs, and other furniture are all examples of barrier removal that might be undertaken to allow a child in a wheelchair to participate in a child care program. Centers run by government agencies must insure that their programs are accessible unless making changes imposes an undue burden; these changes will sometimes include changes to the facilities.
23. Q: We are going to build a new facility. What architectural standards do we have to follow to make sure that our facility is accessible to people with disabilities?
A: Newly constructed privately-run child care centers -- those designed and constructed for first occupancy after January 26, 1993 -- must be readily accessible to and usable by individuals with disabilities. This means that they must be built in strict compliance with the ADA Standards for Accessible Design. New centers run by government agencies must meet either the ADA Standards or the Uniform Federal Accessibility Standards.
Tax Provisions
24. Q: Are there tax credits or deductions available to help offset the costs associated with complying with the ADA?
A: To assist businesses in complying with the ADA, Section 44 of the IRS Code allows a tax credit for small businesses and Section 190 of the IRS Code allows a tax deduction for all businesses.
The tax credit is available to businesses that have total revenues of $1,000,000 or less in the previous tax year or 30 or fewer full-time employees. This credit can cover 50% of the eligible access expenditures in a year up to $10,250 (maximum credit of $5,000). The tax credit can be used to offset the cost of complying with the ADA, including, but not limited to, undertaking barrier removal and alterations to improve accessibility; provide sign language interpreters; and for purchasing certain adaptive equipment.
The tax deduction is available to all businesses with a maximum deduction of $15,000 per year. The tax deduction can be claimed for expenses incurred in barrier removal and alterations.
To order documents about the tax credit and tax deduction provisions, contact the Department of Justice's ADA Information Line (see question 30).
The Department of Justice's Enforcement Efforts
25. Q: What is the Department of Justice's enforcement philosophy regarding title III of the ADA?
A: Whenever the Department receives a complaint or is asked to join an on-going lawsuit, it first investigates the allegations and tries to resolve them through informal or formal settlements. The vast majority of complaints are resolved voluntarily through these efforts. If voluntary compliance is not forthcoming, the Department may have to litigate and seek injunctive relief, damages for aggrieved individuals, and civil penalties.
26. Q: Has the United States entered into any settlement agreements involving child care centers?
A: The Department has resolved three matters through formal settlement agreements with the Sunshine Child Center, KinderCare Learning Centers, and La Petite Academy.
In the first agreement, Sunshine Child Center in Gillett, Wisconsin, agreed to: (1) provide diapering services to children who, because of their disabilities, require diapering more often or at a later age than nondisabled children; (2) put on and remove the complainant's leg braces as necessary; (3) ensure that the complainant is not unnecessarily segregated from her age-appropriate classroom; (4) engage in readily achievable barrier removal to its existing facility; and (5) design and construct its new facility (planned independently of the Department's investigation) in a manner that is accessible to persons with disabilities.
In 1996, the Department of Justice entered into a settlement agreement with KinderCare Learning Centers -- the largest chain of child care centers in the country -- under which KinderCare agreed to provide appropriate care for children with diabetes, including providing finger-prick blood glucose tests. In 1997, La Petite Academy -- the second-largest chain -- agreed to follow the same procedures.
In its 1997 settlement agreement with the Department of Justice, La Petite Academy also agreed to keep epinephrine on hand to administer to children who have severe and possibly life-threatening allergy attacks due to exposure to certain foods or bee stings and to make changes to some of its programs so that children with cerebral palsy can participate.
The settlement agreements and their attachments, including a waiver of liability form and parent and physician authorization form, can be obtained by calling the Department's ADA Information Line or through the Internet (see question 30). Child care centers and parents or guardians should consult a lawyer in their home state to determine whether any changes need to be made before the documents are used.
27. Q: Has the Department of Justice ever sued a child care center for ADA violations?
A: Yes. On June 30, 1997, the United States filed lawsuits against three child care providers for refusing to enroll a four-year-old child because he has HIV. See United States v. Happy Time Day Care Center, (W.D. Wisc.); United States v. Kiddie Ranch, (W.D. Wisc.); and United States v. ABC Nursery, Inc. (W.D. Wisc.).
28. Q: Does the United States ever participate in lawsuits brought by private citizens?
A: Yes. The Department sometimes participates in private suits either by intervention or as amicus curiae -- "friend of the court." One suit in which the United States participated was brought by a disability rights group against KinderCare Learning Centers. The United States supported the plaintiff's position that KinderCare had to make its program accessible to a boy with multiple disabilities including mental retardation. The litigation resulted in KinderCare's agreement to develop a model policy to allow the child to attend one of its centers with a state-funded personal assistant.
Additional Resources
29. Q: Are there any reference books or video tapes that might help me further understand the obligations of child care providers under title III?
A: Through a grant from the Department of Justice, The Arc published All Kids Count: Child Care and the ADA, which addresses the ADA's obligations of child care providers. Copies are available for a nominal fee by calling The Arc's National Headquarters in Arlington, Texas:
800-433-5255 (voice)
800-855-1155 (TDD)
Under a grant provided by the Department of Justice, Eastern Washington University (EWU) produced eight 5-7 minute videotapes and eight accompanying booklets on the ADA and child care providers. The videos cover different ADA issues related to child care and can be purchased as a set or individually by contacting the EWU at:
509-623-4246 (voice)
TDD: use relay service
30. Q: I still have some general questions about the ADA. Where can I get more information?
A: The Department of Justice operates an ADA Information Line. Information Specialists are available to answer general and technical questions during business hours on the weekdays. The Information Line also provides 24-hour automated service for ordering ADA materials and an automated fax back system that delivers technical assistance materials to fax machines or modems.
800-514-0301 (voice)
800-514-0383 (TDD)
The ADA Home Page, which is updated frequently, contains the Department of Justice's regulations and technical assistance materials, as well as press releases on ADA cases and other issues. Several settlement agreements with child care centers are also available on the Home Page.
www.usdoj.gov/crt/ada/adahom1.htm
The Department of Justice also operates an ADA Electronic Bulletin Board, on which a wide variety of information and documents are available.
202-514-6193 (by computer modem)
There are ten regional Disability and Business Technical Assistance Centers, or DBTAC's, that are funded by the Department of Education to provide technical assistance under the ADA. One toll-free number connects to the center in your region.
800-949-4232 (voice & TDD)
The Access Board offers technical assistance on the ADA Accessibility Guidelines.
800-872-2253 (voice)
800-993-2822 (TDD)
Electronic Bulletin Board
202-272-5448
The Equal Employment Opportunity Commission, or EEOC, offers technical assistance on the ADA provisions for employment which apply to businesses with 15 or more employees.
Employment questions
800-669-4000 (voice)
800-669-6820 (TDD)
Employment documents
800-669-3362 (voice)
800-800-3302 (TDD)
If you have further questions about child care centers or other requirements of the ADA, you may call the U.S. Department of Justice's toll-free ADA Information Line at: 800-514-0301 (voice) or 800-514-0383 (TDD).
Note: Reproduction of this document is encouraged.
# For more ADA information, check for updates please visit: http://www.ada.gov/
How can I make my garden accessible? : answers from Paralyzed Veterans of America
Question: Before my accident, I was an avid gardener, and I spent many happy hours on my knees cultivating my flowers and vegetables. Now that I am in a wheelchair, I cannot reach down to tend Mother Earth, and my wheels bog down in the soft earth. I love to watch my garden grow, but I want to get my hands dirty and enjoy gardening again. How can I make my garden accessible?
Answer: Raised planting beds are on old cottage garden tradition that can be adapted to make your garden accessible. Raised beds for flowers and vegetables have been traditionally used to overcome soil problems such as heavy clay and poor drainage. This is especially true in climates with cool wet springs that delay spring planting until the soil has warmed and dried sufficiently. Soil in raised beds is improved with the addition of manure, compost, sand, and now vermiculite or perlite to make the soil more fertile and friable. Paths between the raised beds are typically paved with brick or flagstone on a sand base to eliminate mud, provide drainage, and to absorb solar heat, warming the planting beds for earlier spring planting.
To adapt this gardening tradition to make your garden wheelchair accessible, you will need to raise the height of the planting beds to be within your reach range. At a minimum the soil height should be 9” above the path. A soil planting bed height of 12” to 15” will be easier for you to cultivate. If you raise the soil height in the planting beds any higher, flowers and vegetables may grow beyond your upper side reach height limit of 48”. Raised planting beds should be narrow enough for you to reach from either side of the bed. A maximum width of 20” for 9” high beds and a maximum width of 24” for 12 to 15” high beds is recommended.
You can make the raised planting beds as long as you want, but you will need convenient access to both sides. For maximum sun exposure the length of the beds should have an east-west orientation. To maximize the planting surface area, you will want to keep the path width between the planting beds a minimum width of 36”. Include a turn around space at the ends of paths between your raised planting beds. A 60” x 60” T-shaped maneuvering space will fit into 36” wide paths. U turns around the narrow ends of your raised planting beds will require a 42” path width, with 48” clearance at the ends of planting beds. For wheelchair passage, paths should be paved. Brick, flagstone or even concrete pavers can be tight set on a sand base so that rain and supplemental watering can soak into your garden. Impervious paving such as concrete, asphalt or mortared brick paths will waste water that would otherwise benefit your garden.
For potting, sorting bulbs, and other garden tasks you will need some accessible flat working surfaces. Ideally, the surfaces should be designed so that you can work with both hands in front of you. Low benches can be incorporated into the ends of your planting beds and also serve as handy places for a basket, watering can, or hand tool. With adequate toe clearance (9” high minimum) you will need 42” clear in front of a low bench for a frontal approach in your wheelchair.
Traditional cottage gardens often use raised planting beds as cold frames for early spring and late fall gardening under glazed window sash. The accessible raised planting beds can be easily adapted as accessible cold frames by fitting them with removable hinged pairs of window sash. They can open to either end and be accessed from either north or south sides of the raised planting beds. The raised planting beds will not only enable you to get your green thumbs into the earth from your wheelchair, but many of your flowers and vegetables will be growing at an ideal level for you to enjoy the scents and sights of a well-tended garden.
# For Paralyzed Veterans of America website CLICK HERE
Answer: Raised planting beds are on old cottage garden tradition that can be adapted to make your garden accessible. Raised beds for flowers and vegetables have been traditionally used to overcome soil problems such as heavy clay and poor drainage. This is especially true in climates with cool wet springs that delay spring planting until the soil has warmed and dried sufficiently. Soil in raised beds is improved with the addition of manure, compost, sand, and now vermiculite or perlite to make the soil more fertile and friable. Paths between the raised beds are typically paved with brick or flagstone on a sand base to eliminate mud, provide drainage, and to absorb solar heat, warming the planting beds for earlier spring planting.
To adapt this gardening tradition to make your garden wheelchair accessible, you will need to raise the height of the planting beds to be within your reach range. At a minimum the soil height should be 9” above the path. A soil planting bed height of 12” to 15” will be easier for you to cultivate. If you raise the soil height in the planting beds any higher, flowers and vegetables may grow beyond your upper side reach height limit of 48”. Raised planting beds should be narrow enough for you to reach from either side of the bed. A maximum width of 20” for 9” high beds and a maximum width of 24” for 12 to 15” high beds is recommended.
You can make the raised planting beds as long as you want, but you will need convenient access to both sides. For maximum sun exposure the length of the beds should have an east-west orientation. To maximize the planting surface area, you will want to keep the path width between the planting beds a minimum width of 36”. Include a turn around space at the ends of paths between your raised planting beds. A 60” x 60” T-shaped maneuvering space will fit into 36” wide paths. U turns around the narrow ends of your raised planting beds will require a 42” path width, with 48” clearance at the ends of planting beds. For wheelchair passage, paths should be paved. Brick, flagstone or even concrete pavers can be tight set on a sand base so that rain and supplemental watering can soak into your garden. Impervious paving such as concrete, asphalt or mortared brick paths will waste water that would otherwise benefit your garden.
For potting, sorting bulbs, and other garden tasks you will need some accessible flat working surfaces. Ideally, the surfaces should be designed so that you can work with both hands in front of you. Low benches can be incorporated into the ends of your planting beds and also serve as handy places for a basket, watering can, or hand tool. With adequate toe clearance (9” high minimum) you will need 42” clear in front of a low bench for a frontal approach in your wheelchair.
Traditional cottage gardens often use raised planting beds as cold frames for early spring and late fall gardening under glazed window sash. The accessible raised planting beds can be easily adapted as accessible cold frames by fitting them with removable hinged pairs of window sash. They can open to either end and be accessed from either north or south sides of the raised planting beds. The raised planting beds will not only enable you to get your green thumbs into the earth from your wheelchair, but many of your flowers and vegetables will be growing at an ideal level for you to enjoy the scents and sights of a well-tended garden.
# For Paralyzed Veterans of America website CLICK HERE
Public Art on Chicago Transit Authority (CTA) - video, accessibility info : July 2011
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Public Art on CTA - July 2011 - Connections - From: CTAConnections | July 22, 2011
The CTA is home to an impressive collection of art -- including mosaics, sculptures and paintings. More than 50 pieces of art are exhibited at over 40 CTA stations.
Many of the pieces are a result of the Arts in Transit Program, which is funded by the Federal Transit Administration and coordinated locally through the City of Chicago's Department of Tourism and Culture. A number of other pieces were created through the CTA's Adopt-A-Station program and through partnerships with organizations such as the Chicago Public Art Group. Visit http://www.transitchicago.com/art/
# For CTA Accessibility information, click headline or visit: http://www.transitchicago.com/accessibility/
Tuesday, August 2, 2011
Preserving Medicare's Promise : opinion Barbara Franklin IARP Aug 2011
The following is an op-ed by , president of the Illinois Alliance for Retired Americans.
This year Medicare turns 46, an occasion that gives good cause to celebrate a program that is one of our nation’s greatest accomplishments. Medicare has saved countless lives, providing coverage to millions of older Americans and people with disabilities who without the program would not have access to high-quality, affordable health care. Indeed, it is this fact that first inspired the passage of Medicare.
The Medicare population is often misunderstood. Most do not live in lush retirement communities. In fact, half of the Medicare population lives on incomes of $22,000 or less. Many rely on Social Security as their major source—in some cases their sole source—of income. And yet, while people with Medicare live on less income, they pay more for their care because their need for health care coverage is great. In 2006, nearly half of all non-institutionalized Medicare beneficiaries had three or more chronic conditions, almost one-third had a cognitive or mental impairment, and over one-fourth reported being in fair or poor health or having a limitation in activities of daily living. As a result, people with Medicare already spend on average 15 percent of their incomes on health care, three times more than the non-Medicare population.
This is why we must fight to protect to the program. Many proposals under consideration, such as increasing cost-sharing, redesigning the benefit, raising the Medicare eligibility age, and limiting Medigap coverage, save the government money by shifting costs to beneficiaries and decreasing access to care. However, none of these proposals addresses the underlying cause of growing costs in Medicare: growing costs in the health care sector overall. For this reason, we must adopt policies like those included in the Affordable Care Act (ACA), which attempt to address the root of health care inflation by promoting prevention, care coordination and changes in provider payment incentives to reward the quality, rather than the quantity, of care provided. Other policies that address the high cost the government pays for drugs under the Medicare prescription drug benefit, such as allowing Medicare to negotiate drug prices or rebate plans for drugs used by low-income Medicare beneficiaries, would also help to achieve savings without passing the buck to older Americans, people with disabilities and their families.
By including these policies in a balanced approach that includes increases in revenue through the elimination of tax cuts and loopholes for the wealthiest Americans and corporations, we can avert deep cuts to Medicare that would result in permanent and detrimental changes to the program. Most of all, we can preserve the promise we made as a nation back in 1965—that we all have a right to access high-quality, affordable health care, and to live with dignity regardless of age or disability.
Barbara Franklin is president of the Illinois Alliance for Retired Americans.
This year Medicare turns 46, an occasion that gives good cause to celebrate a program that is one of our nation’s greatest accomplishments. Medicare has saved countless lives, providing coverage to millions of older Americans and people with disabilities who without the program would not have access to high-quality, affordable health care. Indeed, it is this fact that first inspired the passage of Medicare.
The Medicare population is often misunderstood. Most do not live in lush retirement communities. In fact, half of the Medicare population lives on incomes of $22,000 or less. Many rely on Social Security as their major source—in some cases their sole source—of income. And yet, while people with Medicare live on less income, they pay more for their care because their need for health care coverage is great. In 2006, nearly half of all non-institutionalized Medicare beneficiaries had three or more chronic conditions, almost one-third had a cognitive or mental impairment, and over one-fourth reported being in fair or poor health or having a limitation in activities of daily living. As a result, people with Medicare already spend on average 15 percent of their incomes on health care, three times more than the non-Medicare population.
This is why we must fight to protect to the program. Many proposals under consideration, such as increasing cost-sharing, redesigning the benefit, raising the Medicare eligibility age, and limiting Medigap coverage, save the government money by shifting costs to beneficiaries and decreasing access to care. However, none of these proposals addresses the underlying cause of growing costs in Medicare: growing costs in the health care sector overall. For this reason, we must adopt policies like those included in the Affordable Care Act (ACA), which attempt to address the root of health care inflation by promoting prevention, care coordination and changes in provider payment incentives to reward the quality, rather than the quantity, of care provided. Other policies that address the high cost the government pays for drugs under the Medicare prescription drug benefit, such as allowing Medicare to negotiate drug prices or rebate plans for drugs used by low-income Medicare beneficiaries, would also help to achieve savings without passing the buck to older Americans, people with disabilities and their families.
By including these policies in a balanced approach that includes increases in revenue through the elimination of tax cuts and loopholes for the wealthiest Americans and corporations, we can avert deep cuts to Medicare that would result in permanent and detrimental changes to the program. Most of all, we can preserve the promise we made as a nation back in 1965—that we all have a right to access high-quality, affordable health care, and to live with dignity regardless of age or disability.
Barbara Franklin is president of the Illinois Alliance for Retired Americans.
EEOC Sues Illinois Temp Agency For Disability Discrimination : PRESS RELEASE 7-28-11
PRESS RELEASE
7-28-11
EEOC Sues Illinois Temp Agency For Disability Discrimination
Federal Agency Says JES Personnel / Genie Temporary Service Fired Employee Because of His Epilepsy
CHICAGO – JES Personnel Consultants, Inc., doing business as Genie Temporary Service, violated federal disability discrimination law by refusing to allow an employee to return to work because of his epilepsy, the U.S. Equal Employment Opportunity Commission (EEOC) charged in a lawsuit it filed today. Genie is a temporary service agency with an office in LaSalle, Ill., that supplies employees to various client employers.
John Rowe, director of the EEOC’s Chicago District, said that the agency’s pre-suit investigation indicated that Genie had placed the employee with Clover Technologies Group, LLC, where he unpacked and sorted ink cartridges. After he had a brief epileptic seizure on his first day of work, according to Rowe, Clover allowed him to work the rest of the day, but asked him to provide a note from his doctor authorizing him to return to work after that. The EEOC said that the employee provided the note to Genie the next day, and Genie neither advised him that the note was inadequate nor forwarded the note to Clover, but the employee was not permitted to return and was effectively terminated.
Such alleged conduct violates the Americans With Disabilities Act (ADA), which prohibits disability discrimination in employment. The EEOC filed suit after first attempting to reach a pre-litigation settlement through its conciliation process. The case, EEOC v. JES Personnel Consultants, Inc. d/b/a Genie Temporary Serivce, Civil Action No. 11 CV 5117, was filed today in U.S. District Court for the Northern District of Illinois, Eastern Division and has been assigned to U.S. District Judge Rebecca R. Pallmeyer. The government’s litigation effort will be led by EEOC Trial Attorney Gordon Waldron and Supervisory Trial Attorney Gregory Gochanour.
“Temp agencies and other employment agencies play an important role as gatekeepers to employment opportunities throughout our economy,” said John Hendrickson, the EEOC’s regional attorney in Chicago. “They have an obligation under federal law to give fair consideration to qualified people with disabilities when making placement decisions.”
The EEOC Chicago District Office is responsible for processing charges of discrimination, administrative enforcement, and the conduct of agency litigation in Illinois, Wisconsin, Minnesota, Iowa, and North and South Dakota, with Area Offices in Milwaukee and Minneapolis.
The EEOC is responsible for enforcing federal laws prohibiting employment discrimination. Further information about the EEOC is available on its web site at www.eeoc.gov.
7-28-11
EEOC Sues Illinois Temp Agency For Disability Discrimination
Federal Agency Says JES Personnel / Genie Temporary Service Fired Employee Because of His Epilepsy
CHICAGO – JES Personnel Consultants, Inc., doing business as Genie Temporary Service, violated federal disability discrimination law by refusing to allow an employee to return to work because of his epilepsy, the U.S. Equal Employment Opportunity Commission (EEOC) charged in a lawsuit it filed today. Genie is a temporary service agency with an office in LaSalle, Ill., that supplies employees to various client employers.
John Rowe, director of the EEOC’s Chicago District, said that the agency’s pre-suit investigation indicated that Genie had placed the employee with Clover Technologies Group, LLC, where he unpacked and sorted ink cartridges. After he had a brief epileptic seizure on his first day of work, according to Rowe, Clover allowed him to work the rest of the day, but asked him to provide a note from his doctor authorizing him to return to work after that. The EEOC said that the employee provided the note to Genie the next day, and Genie neither advised him that the note was inadequate nor forwarded the note to Clover, but the employee was not permitted to return and was effectively terminated.
Such alleged conduct violates the Americans With Disabilities Act (ADA), which prohibits disability discrimination in employment. The EEOC filed suit after first attempting to reach a pre-litigation settlement through its conciliation process. The case, EEOC v. JES Personnel Consultants, Inc. d/b/a Genie Temporary Serivce, Civil Action No. 11 CV 5117, was filed today in U.S. District Court for the Northern District of Illinois, Eastern Division and has been assigned to U.S. District Judge Rebecca R. Pallmeyer. The government’s litigation effort will be led by EEOC Trial Attorney Gordon Waldron and Supervisory Trial Attorney Gregory Gochanour.
“Temp agencies and other employment agencies play an important role as gatekeepers to employment opportunities throughout our economy,” said John Hendrickson, the EEOC’s regional attorney in Chicago. “They have an obligation under federal law to give fair consideration to qualified people with disabilities when making placement decisions.”
The EEOC Chicago District Office is responsible for processing charges of discrimination, administrative enforcement, and the conduct of agency litigation in Illinois, Wisconsin, Minnesota, Iowa, and North and South Dakota, with Area Offices in Milwaukee and Minneapolis.
The EEOC is responsible for enforcing federal laws prohibiting employment discrimination. Further information about the EEOC is available on its web site at www.eeoc.gov.
Access Living Organization Video - 2011 - empowering people with disabilities in Chicago & the Nation!
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Uploaded by AccessLiving on Jun 27, 2011
Access Living's Organization video, produced in 2011. The video documents Access Living history, and presents an overview of the organization's current work to empower people with disabilities in Chicago and around the country to live independently.
# For Access Living click headline or visit: http://www.accessliving.org/
Arthritis Foundation: Illinois Jingle Bell Run/Walk 2011, info
What is Jingle Bell Run/Walk
Jingle Bell Run/Walk is a fun and festive way to kick off the holidays with family, friends and coworkers. Form a team, raise funds and organize your very own holiday-themed costumes. Then tie jingle bells to your shoelaces, and complete a 5 kilometer route.
Be there with bells on!
Get in the spirit this holiday season at the Arthritis Foundation’s Jingle Bell Run/Walk for Arthritis®. Be one of the thousands of runners and walkers who hit the nation’s pavements, pathways and parks this winter to fight arthritis, the nation’s most common cause of disability.
Event Locations
Jingle Bell Run/Walk - Normal, IL
November 13, 2011
10:00 am - 3:00 pm
Register Online
Heartland Community College
1500 West Raab Road
Normal, IL 61761
Join us on Facebook
Jingle Bell Run/Walk - Springfield, IL
November 19, 2011
9:00 am - 12:00 pm
Register Online
Lincoln Land Community College
5250 Shepherd Road
Springfield, IL 62794
Join us on Facebook
Jingle Bell Run/Walk - Rockford, IL
November 19, 2011
7:00 am - 12:00 pm
Register Online
Rockford Memorial Hospital -- campus & neighborhood
2400 N. Rockton Avenue
Rockford, IL 61103
Join us on Facebook
Jingle Bell Run/Walk - Quincy, IL
December 3, 2011
9:00 am
Register Online
Quincy Mall
3347 Quincy Mall
Quincy, IL 62301
Join us on Facebook
Jingle Bell Run/Walk - Peoria, IL
December 3, 2011
8:00 am - 1:00 pm
Register Online
RiverPlex Recreation & Wellness Center
600 NE Water St
Peoria, IL 61603
Join us on Facebook
Jingle Bell Run/Walk - Peru, IL
December 3, 2011
8:30 am
Register Online
Baker Lake
1345 Chartres St.
LaSalle, IL 61301
Join us on Facebook
Jingle Bell Run/Walk - Freeport, IL
December 3, 2011
7:00 am - 12:00 pm
Register Online
Family YMCA of Northwest Illinois at Highland Community College
2998 Pearl City Road
Freeport, IL 61103
Join us on Facebook
Jingle Bell Run/Walk - Ina, IL
December 3, 2011
9:00 am - 12:00 pm
Register Online
Rend Lake College
468 Ken Gray Parkway
Ina, IL 62846
Join us on Facebook
2011 Jingle Bell Run/Walk - Alton, IL
December 3, 2011
Registration at 7am, Race starts at 8am
Gordon F. Moore Park
4550 College Ave. 62002
Register Online
Jingle Bell Run/Walk - Champaign, IL
December 4, 2011
12:00 pm - 4:00 pm
Register Online
Centennial Park
Bound by Kirby Ave., Crescent Dr., John St., & Kenwood Rd
Champaign, IL 61821
Join us on Facebook
Jingle Bell Run/Walk - Kankakee, IL
December 11, 2011
9:00 am - 11:30 am
Register Online
Shapiro Developmental Center
100 East Jeffery St
Kankakee, IL 60901
Join us on Facebook
Jingle Bell Run/Walk - Chicago, IL
December 17, 2011
9:00 am - 12:00 pm
Register Online
Peggy Notebaert Nature Museum
2430 North Cannon Drive
Chicago, IL 60614
Join us on Facebook
# For the Arthritis Foundation Illinois Jingle Bell Run/Walk visit: http://www.arthritis.org/chapters/illinois/jbr.php
Jingle Bell Run/Walk is a fun and festive way to kick off the holidays with family, friends and coworkers. Form a team, raise funds and organize your very own holiday-themed costumes. Then tie jingle bells to your shoelaces, and complete a 5 kilometer route.
Be there with bells on!
Get in the spirit this holiday season at the Arthritis Foundation’s Jingle Bell Run/Walk for Arthritis®. Be one of the thousands of runners and walkers who hit the nation’s pavements, pathways and parks this winter to fight arthritis, the nation’s most common cause of disability.
Event Locations
Jingle Bell Run/Walk - Normal, IL
November 13, 2011
10:00 am - 3:00 pm
Register Online
Heartland Community College
1500 West Raab Road
Normal, IL 61761
Join us on Facebook
Jingle Bell Run/Walk - Springfield, IL
November 19, 2011
9:00 am - 12:00 pm
Register Online
Lincoln Land Community College
5250 Shepherd Road
Springfield, IL 62794
Join us on Facebook
Jingle Bell Run/Walk - Rockford, IL
November 19, 2011
7:00 am - 12:00 pm
Register Online
Rockford Memorial Hospital -- campus & neighborhood
2400 N. Rockton Avenue
Rockford, IL 61103
Join us on Facebook
Jingle Bell Run/Walk - Quincy, IL
December 3, 2011
9:00 am
Register Online
Quincy Mall
3347 Quincy Mall
Quincy, IL 62301
Join us on Facebook
Jingle Bell Run/Walk - Peoria, IL
December 3, 2011
8:00 am - 1:00 pm
Register Online
RiverPlex Recreation & Wellness Center
600 NE Water St
Peoria, IL 61603
Join us on Facebook
Jingle Bell Run/Walk - Peru, IL
December 3, 2011
8:30 am
Register Online
Baker Lake
1345 Chartres St.
LaSalle, IL 61301
Join us on Facebook
Jingle Bell Run/Walk - Freeport, IL
December 3, 2011
7:00 am - 12:00 pm
Register Online
Family YMCA of Northwest Illinois at Highland Community College
2998 Pearl City Road
Freeport, IL 61103
Join us on Facebook
Jingle Bell Run/Walk - Ina, IL
December 3, 2011
9:00 am - 12:00 pm
Register Online
Rend Lake College
468 Ken Gray Parkway
Ina, IL 62846
Join us on Facebook
2011 Jingle Bell Run/Walk - Alton, IL
December 3, 2011
Registration at 7am, Race starts at 8am
Gordon F. Moore Park
4550 College Ave. 62002
Register Online
Jingle Bell Run/Walk - Champaign, IL
December 4, 2011
12:00 pm - 4:00 pm
Register Online
Centennial Park
Bound by Kirby Ave., Crescent Dr., John St., & Kenwood Rd
Champaign, IL 61821
Join us on Facebook
Jingle Bell Run/Walk - Kankakee, IL
December 11, 2011
9:00 am - 11:30 am
Register Online
Shapiro Developmental Center
100 East Jeffery St
Kankakee, IL 60901
Join us on Facebook
Jingle Bell Run/Walk - Chicago, IL
December 17, 2011
9:00 am - 12:00 pm
Register Online
Peggy Notebaert Nature Museum
2430 North Cannon Drive
Chicago, IL 60614
Join us on Facebook
# For the Arthritis Foundation Illinois Jingle Bell Run/Walk visit: http://www.arthritis.org/chapters/illinois/jbr.php
If Federal aid cut to States, they may hit borrow button : article Aug 01 2011
States may go their own way in adopting fiscal policies and turn to more borrowing if Congress on Monday enacts a last-minute compromise plan raising the federal debt ceiling.
Across the nation, local officials -- who spent the last month fretting that the United States would default for the first time -- now fear the debt-cap bill will cut the federal deficit by yanking billions of dollars of aid from them.
The resulting cuts in all levels of government spending could further crimp consumers' lifestyles, make poverty worse and threaten public safety. Also at stake are job-creating government contracts for healthcare and defense companies, and possibly heightened risks for public pension investments.
Tom Cochran, executive director of the U.S. Conference of Mayors, said the federal cuts in the debt-ceiling agreement "mean fewer cops, fewer firefighters and less money for job- creation projects, housing and elderly care."
To make up for the federal cuts, he called on Congress to close tax loopholes for corporations and individuals.
Philip Fischer, a managing principal at eBooleant Consulting, LLC, said in a report: "The federal, state and local governments cannot justify the reduction in the standard of living that must occur to reduce a trillion-dollar federal deficit without a crisis."
Saying the deficit crisis will continue, he added, "Severe cutbacks in all federal programs seem inevitable."
Fischer said states might boost long-term debt to replace lost federal aid.
"To maintain their own fiscal integrity, the states will need to assert more autonomy," he said.
THE DANGERS OF DEPENDENCY
Some states, for instance, have sued to block the Obama administration's healthcare law, while others have sought waivers from Medicaid program requirements.
"The degree of dependence on the federal government now becomes a state credit issue and rainy day funds a critical tool," Fischer said.
Four states depend on federal aid for more than 40 percent of their spending: Arkansas, Illinois, Missouri and North Carolina, according to a report by RBC Capital Markets.
Eighteen states get over 30 percent of their spending from taxpayers around the country -- Florida, Georgia, Idaho, Indiana, Louisiana, Maine, Michigan, Mississippi, Montana, Nevada, New Mexico, New York, Ohio, Pennsylvania, South Carolina, South Dakota, Tennessee and Texas.
Still, John Miller, chief investment officer of Nuveen Asset Management, told CNBC that states in the category of "above 30 percent" might be able to absorb a 5 percent across-the-board cut in federal aid spread out over 10 years, which might work out to only 1.5 percent of all the revenue a state gets.
To New York state Comptroller Thomas DiNapoli, who runs the $146 billion state pension fund, the struggle to raise the federal debt ceiling has inflicted "collateral damage" by raising doubts about the U.S. government's AAA credit rating.
As Florida and Texas demonstrate, the deficit deal's impact could spread to many industries that are vital local employers. The Texas Health Care Association said the prospect of even more Medicare cuts "places seniors and caregiver jobs in an extremely perilous position."
South Florida, home to Miami and Fort Lauderdale, has at least $400 million at risk this year in the anticipated $2.4 trillion of budget cuts agreed by Washington leaders, according to an analysis by the Miami Herald newspaper.
"Pentagon spending -- a top target of the plan if Congress can't agree to other cuts -- looms large in the region," The Miami Herald said, adding that two local companies each year sell $50 million of armored vehicles and vests to the U.S. military.
Los Angeles Mayor Antonio Villaraigosa, who is also the president of the U.S. Conference of Mayors, urged Congress to now address the "sky-high unemployment rates that persist across the country."
Connecticut was one of 24 states that lost payroll jobs in June, state Comptroller Kevin Lembo said, predicting that at the current rate of job growth, it will take more than a decade for the state to win back the more than 100,000 jobs lost due to the recession.
# As posted NEW YORK (Reuters) Aug 01 2011
(Reporting by Joan Gralla; Additional reporting by Karen Pierog in Chicago, Michael Connor in Miami and Lisa Lambert in Washington; Editing by Jan Paschal)
Across the nation, local officials -- who spent the last month fretting that the United States would default for the first time -- now fear the debt-cap bill will cut the federal deficit by yanking billions of dollars of aid from them.
The resulting cuts in all levels of government spending could further crimp consumers' lifestyles, make poverty worse and threaten public safety. Also at stake are job-creating government contracts for healthcare and defense companies, and possibly heightened risks for public pension investments.
Tom Cochran, executive director of the U.S. Conference of Mayors, said the federal cuts in the debt-ceiling agreement "mean fewer cops, fewer firefighters and less money for job- creation projects, housing and elderly care."
To make up for the federal cuts, he called on Congress to close tax loopholes for corporations and individuals.
Philip Fischer, a managing principal at eBooleant Consulting, LLC, said in a report: "The federal, state and local governments cannot justify the reduction in the standard of living that must occur to reduce a trillion-dollar federal deficit without a crisis."
Saying the deficit crisis will continue, he added, "Severe cutbacks in all federal programs seem inevitable."
Fischer said states might boost long-term debt to replace lost federal aid.
"To maintain their own fiscal integrity, the states will need to assert more autonomy," he said.
THE DANGERS OF DEPENDENCY
Some states, for instance, have sued to block the Obama administration's healthcare law, while others have sought waivers from Medicaid program requirements.
"The degree of dependence on the federal government now becomes a state credit issue and rainy day funds a critical tool," Fischer said.
Four states depend on federal aid for more than 40 percent of their spending: Arkansas, Illinois, Missouri and North Carolina, according to a report by RBC Capital Markets.
Eighteen states get over 30 percent of their spending from taxpayers around the country -- Florida, Georgia, Idaho, Indiana, Louisiana, Maine, Michigan, Mississippi, Montana, Nevada, New Mexico, New York, Ohio, Pennsylvania, South Carolina, South Dakota, Tennessee and Texas.
Still, John Miller, chief investment officer of Nuveen Asset Management, told CNBC that states in the category of "above 30 percent" might be able to absorb a 5 percent across-the-board cut in federal aid spread out over 10 years, which might work out to only 1.5 percent of all the revenue a state gets.
To New York state Comptroller Thomas DiNapoli, who runs the $146 billion state pension fund, the struggle to raise the federal debt ceiling has inflicted "collateral damage" by raising doubts about the U.S. government's AAA credit rating.
As Florida and Texas demonstrate, the deficit deal's impact could spread to many industries that are vital local employers. The Texas Health Care Association said the prospect of even more Medicare cuts "places seniors and caregiver jobs in an extremely perilous position."
South Florida, home to Miami and Fort Lauderdale, has at least $400 million at risk this year in the anticipated $2.4 trillion of budget cuts agreed by Washington leaders, according to an analysis by the Miami Herald newspaper.
"Pentagon spending -- a top target of the plan if Congress can't agree to other cuts -- looms large in the region," The Miami Herald said, adding that two local companies each year sell $50 million of armored vehicles and vests to the U.S. military.
Los Angeles Mayor Antonio Villaraigosa, who is also the president of the U.S. Conference of Mayors, urged Congress to now address the "sky-high unemployment rates that persist across the country."
Connecticut was one of 24 states that lost payroll jobs in June, state Comptroller Kevin Lembo said, predicting that at the current rate of job growth, it will take more than a decade for the state to win back the more than 100,000 jobs lost due to the recession.
# As posted NEW YORK (Reuters) Aug 01 2011
(Reporting by Joan Gralla; Additional reporting by Karen Pierog in Chicago, Michael Connor in Miami and Lisa Lambert in Washington; Editing by Jan Paschal)
Top Five Reasons to Join The Social Challenge! A campaign That target's "R" word users and raise awareness.
The top five reasons to join The Social Challenge!
5. You're interested in making a change, but you don't know how to do it.
Look no further than www.thesocialchallenge.org, where you can be the change without ever leaving your computer!
4. You're bored with the usual internet hangouts and looking for a cool new site.
Have you swung by The Social Challenge lately? It's sleek, cool, and just try to take your eyes off of the sliding 'R' word feed -- we dare you!
3. You've been burned by words before.
You know that words can hurt, and the careless use of the 'R' word is particularly painful for those in the community. By taking The Social Challenge you can issue gentle, anonymous reminders to others to choose their words more carefully.
2. There are 200,000 people with developmental disabilities in Illinois.
That number may include you, your cherished loved ones, dear friends, neighbors or classmates. If you don't register for yourself, register for them!
And... drumroll please....
1. You want to challenge yourself, challenge others, and join us in creating a community rooted in equality!

# THE STATS:
20,654 actions since March 2011
1,352 registrants
942 Facebook Likes
431 apologies from Twitter users
As if you needed any other reasons! Come one, come all to www.thesocialchallenge.org! or click headline...
5. You're interested in making a change, but you don't know how to do it.
Look no further than www.thesocialchallenge.org, where you can be the change without ever leaving your computer!
4. You're bored with the usual internet hangouts and looking for a cool new site.
Have you swung by The Social Challenge lately? It's sleek, cool, and just try to take your eyes off of the sliding 'R' word feed -- we dare you!
3. You've been burned by words before.
You know that words can hurt, and the careless use of the 'R' word is particularly painful for those in the community. By taking The Social Challenge you can issue gentle, anonymous reminders to others to choose their words more carefully.
2. There are 200,000 people with developmental disabilities in Illinois.
That number may include you, your cherished loved ones, dear friends, neighbors or classmates. If you don't register for yourself, register for them!
And... drumroll please....
1. You want to challenge yourself, challenge others, and join us in creating a community rooted in equality!
# THE STATS:
20,654 actions since March 2011
1,352 registrants
942 Facebook Likes
431 apologies from Twitter users
As if you needed any other reasons! Come one, come all to www.thesocialchallenge.org! or click headline...
Monday, August 1, 2011
Autism Forum: Parents Talk About Their Children's Options : Residents flock to Highland Park, IL for discussion about disability Aug 1 2011
Fort Sheridan resident Latonya Harris is the mother of an 11 year-old girl with cognitive impairment. Relatively new to the area, she has been frustrated in finding resources to help her daughter.
In hopes of gaining useful information, Harris attended the resource fair and forum on autism and developmental disabilities last week at the Highland Park Country Club.
State Rep. Karen May (D-Highland Park) sponsored the event, and introduced a series of panel discussions by describing her goals:
“My mission is for children with developmental disabilities to lead a normal life, for them not to be isolated, to have a home and not just a bed," she said.
May described how she wanted a forum where officials from townships, libraries, schools and park districts could gather with other organizations and parents so they could get creative in finding solutions to support families who are often overwhelmed.
Creative ideas overcome hurdles
Chris Kennedy, an attorney and father of a child with autism and epilepsy, opened the discussion with a grim overview of the services provided by the state government. He described a system based on outdated thinking that devotes more resources to institutions rather than the community settings or home-based services, which are generally seen as being more effective.
According to Kennedy, Illinois ranks 47th in per capita spending on persons with developmental disabilities in their homes and communities.
That set the stage for the remaining panels, which focused on what individuals can do to help their disabled children. A panel on housing, for instance, described solutions that family members created on their own.
Margaret Tanenberg, a director at the Center for Independent Futures in Evanston, recounted how two mothers formed a not-for-profit organization that helped families create supported-living alternatives so that their adult children can live more independently.
Self-started programs were also highlighted in a discussion on employment for the developmentally disabled.
Jacob Metrick described how a discussion about a dearth of employment opportunities for his sister with autism led to the creation of the Perk Center Café at the Park Center in Glenview. The cafe serves breakfast, lunch and snacks, but, more importantly, provides job skills and work opportunities for people with developmental disabilities.
Brenda Weitzberg spoke about how her son with Asperger’s syndrome was unable to find meaningful employment despite having a four-year college degree. Her son’s case was not unusual, she said, as 85 percent to 90 percent of people on the autism spectrum are unemployed or underemployed.
Weitzberg said she and her husband had set about to do something about it. They found that individuals with high-functioning autism have skills that are perfect for software testing: attention to detail, ability to focus, love of computers.
The couple created a company in Highland Park that provides software-testing services. Aspiritech now employs 10 people on the autism spectrum, enabling them to have work that is commensurate with their skills.
Government-funded programs were also discussed. Joanell Voigt of Community Alternatives Unlimited described how her not-for-profit agency helps advocate for families to receive funding from the Illinois government.
Teri Steinberg described a project called the Illinois Association of Microboards and Cooperatives (IAMC). The agency gives direction on how individuals can create a microboard, a not-for-profit association that benefits only one person.
Under the microboard approach, the person who is supported, and his or her family and friends, make up the board of directors. This enables a person with a disability to lead the life they want to live with the support of family, friends, community and public resources.
The panel discussions were preceded by a resource fair, featuring more than 20 organizations that provide a wide variety of services for the developmentally disabled.
Reaction
Afterward, May said she was “very pleased with the participation of the panel” but added that she was “disappointed that more elected officials did not come.”
But for Harris, the mother looking for help for her daughter, the evening was a complete success.
“I have been trying to get this information for years. Now I have a good start on what I can do," she said. "This forum was awesome."
## As posted at Patch.com, article By Yuji Fukunaga; Aug 01 2011
In hopes of gaining useful information, Harris attended the resource fair and forum on autism and developmental disabilities last week at the Highland Park Country Club.
State Rep. Karen May (D-Highland Park) sponsored the event, and introduced a series of panel discussions by describing her goals:
“My mission is for children with developmental disabilities to lead a normal life, for them not to be isolated, to have a home and not just a bed," she said.
May described how she wanted a forum where officials from townships, libraries, schools and park districts could gather with other organizations and parents so they could get creative in finding solutions to support families who are often overwhelmed.
Creative ideas overcome hurdles
Chris Kennedy, an attorney and father of a child with autism and epilepsy, opened the discussion with a grim overview of the services provided by the state government. He described a system based on outdated thinking that devotes more resources to institutions rather than the community settings or home-based services, which are generally seen as being more effective.
According to Kennedy, Illinois ranks 47th in per capita spending on persons with developmental disabilities in their homes and communities.
That set the stage for the remaining panels, which focused on what individuals can do to help their disabled children. A panel on housing, for instance, described solutions that family members created on their own.
Margaret Tanenberg, a director at the Center for Independent Futures in Evanston, recounted how two mothers formed a not-for-profit organization that helped families create supported-living alternatives so that their adult children can live more independently.
Self-started programs were also highlighted in a discussion on employment for the developmentally disabled.
Jacob Metrick described how a discussion about a dearth of employment opportunities for his sister with autism led to the creation of the Perk Center Café at the Park Center in Glenview. The cafe serves breakfast, lunch and snacks, but, more importantly, provides job skills and work opportunities for people with developmental disabilities.
Brenda Weitzberg spoke about how her son with Asperger’s syndrome was unable to find meaningful employment despite having a four-year college degree. Her son’s case was not unusual, she said, as 85 percent to 90 percent of people on the autism spectrum are unemployed or underemployed.
Weitzberg said she and her husband had set about to do something about it. They found that individuals with high-functioning autism have skills that are perfect for software testing: attention to detail, ability to focus, love of computers.
The couple created a company in Highland Park that provides software-testing services. Aspiritech now employs 10 people on the autism spectrum, enabling them to have work that is commensurate with their skills.
Government-funded programs were also discussed. Joanell Voigt of Community Alternatives Unlimited described how her not-for-profit agency helps advocate for families to receive funding from the Illinois government.
Teri Steinberg described a project called the Illinois Association of Microboards and Cooperatives (IAMC). The agency gives direction on how individuals can create a microboard, a not-for-profit association that benefits only one person.
Under the microboard approach, the person who is supported, and his or her family and friends, make up the board of directors. This enables a person with a disability to lead the life they want to live with the support of family, friends, community and public resources.
The panel discussions were preceded by a resource fair, featuring more than 20 organizations that provide a wide variety of services for the developmentally disabled.
Reaction
Afterward, May said she was “very pleased with the participation of the panel” but added that she was “disappointed that more elected officials did not come.”
But for Harris, the mother looking for help for her daughter, the evening was a complete success.
“I have been trying to get this information for years. Now I have a good start on what I can do," she said. "This forum was awesome."
## As posted at Patch.com, article By Yuji Fukunaga; Aug 01 2011
Time to Wheelchair Bungee Jump! "Our biggest limitations in life aren't physical, but mental." Brad's Story
Well I suppose I should tell you why I decided to fly across the country, then leave the country, all so someone could harness me up and throw me off a 160 foot bridge. Three years ago I woke up after being in a car accident. After they told me I had a c-5 burst fracture, broke all the ribs on my right side, fractured pelvis, lacerated lungs, and that maybe in six months I could breathe on my own again it gets you thinking.
Of course I have lots of physical goals, and I have been so fortunate to meet all of them so far. With amazing support from my family and help from amazing therapists I've been able to regain my independence and walk with a walker. I even walked a 5k in Louisville for Team Reeve which was an amazing feeling to accomplish that. (Really proud of that one had to throw that in there. Don't tell anyone I was sore for two weeks after haha.) But this has nothing to do with walking, but living a life without limitations
Anyone with a SCI realizes pretty quickly it's not just the physical aspect that's hard to deal with but the mental aspects as well. I always wanted to travel, see the world and experience different cultures and places.
Well it's been 3 years since my injury and I decided it's time to do that. I always wanted to bungee jump. Unfortunately I had trouble finding a place to do that till I found this place in Whistler, Canada. So I decided it's time for me to take my first trip on my own. I contacted my friend in Portland, Oregon and told him I was going to fly out and see him for a few days, and oh yeah, we're going to go jump off a bridge in Canada. He thought I was crazy, but the thought of seeing me thrown off a bridge got the better of him and he was game. What are friends for right!
I should mention this was my first time flying, ever. I was so nervous the night before I barely slept. Wondering what it would be like, would all my stuff make it, am I really flying all the way across the country by myself for the first time. Nothing like some fear to let you know you're alive.
So the next day I hopped on a plane from Ohio to Oregon with a layover in Texas. Flying was an experience, and overall a good one. Some planes I could walk onto, grabbing seat to seat to walk down the skinny aisle ways, and some I used the aisle chair. I kept an open mind and a positive attitude, and I've learned as long as you do that people are receptive and helpful so I had a good experience flying. I even had a couple flights bumped up to first class for free! I'm sure that didn't hurt my experience at all haha. Even the wheelchair escorts between flights to different terminals were great. Basically I was on five airplanes in seven days. If you're going to do something do it right I guess.
So at the end my stay in Oregon we flew to Vancouver, I rented a car, and took the drive into Whistler. I must say B.C. was one of the most beautiful places I have ever seen. When we got to Whistler and we're driving down this back road to the bridge, I remember feeling a sense of accomplishment that I was there.
I hadn't made the jump yet, but just having made the trip, following through on something, it was a good feeling driving up to that bridge. Then I saw the bridge and thought what was I thinking!
There is a dirt road that takes you almost all the way up to the top. The rest of the way I hopped in my chair and needed just a little help to get onto the bridge. So there they harness you like anyone else, then attach the wheelchair to you. After the guy harnessing me looks at me and says, "I hope that works, eh" my confidence was at an all-time high haha. Seriously though he told me he gets some people in chairs out there every year so I wasn't worried. Sort of, I mean I am getting thrown off a bridge.
So the time comes and it's my turn, I wheel myself over to the edge of the railing. The railing is about 4 feet high so you can't really see over it. Then they asked me if I was ready and began to pick up my wheelchair.
In the span of about half a second I'm up and on the railing and looking over this bridge and at the rushing water 160 feet below me. At that moment of realization that you're staring over the edge of a 160 foot bridge, you are already plummeting in a free fall towards the river.
It is such a rush and before you know it the bungee cord catches you and hurls you back in the air and you do it again. When you stop bouncing they lower a rope down, you attach it to your harness and they raise you back up. This is the point where I breathed a sigh of relief that I didn't have to tell all my therapists I hurt myself because I jumped off a bridge haha.
The next day we drove back to Vancouver, my buddy flew back to Oregon and I flew back home to Ohio. I was exhausted, happy to be home, and felt very accomplished. This was a great trip for me and the start of many more to come.
That first time doing anything is always the most special. Whether it's your first time driving again, first class, first time anything. It's hard to explain that "first" feeling but I know a lot of you reading this understand what I'm talking about. And if you don't it's about time you discovered it.
Our biggest limitations in life aren't physical, but mental. I know I let go of some limitations at the bottom of that bridge in Canada, and I know bungee jumping isn't everyone's cup of tea, but whatever it is I encourage you to go for it.
And if you're crazy like me, well, now you know a great place to get thrown off a bridge
[refresh if no video]
Uploaded on YouTube by burns2133 on Jun 27, 2011
# Article as posted at The Christopher and Dana Reeve Foundation website - for more info visit:
http://www.reevefoundation.org/
Of course I have lots of physical goals, and I have been so fortunate to meet all of them so far. With amazing support from my family and help from amazing therapists I've been able to regain my independence and walk with a walker. I even walked a 5k in Louisville for Team Reeve which was an amazing feeling to accomplish that. (Really proud of that one had to throw that in there. Don't tell anyone I was sore for two weeks after haha.) But this has nothing to do with walking, but living a life without limitations
Anyone with a SCI realizes pretty quickly it's not just the physical aspect that's hard to deal with but the mental aspects as well. I always wanted to travel, see the world and experience different cultures and places.
Well it's been 3 years since my injury and I decided it's time to do that. I always wanted to bungee jump. Unfortunately I had trouble finding a place to do that till I found this place in Whistler, Canada. So I decided it's time for me to take my first trip on my own. I contacted my friend in Portland, Oregon and told him I was going to fly out and see him for a few days, and oh yeah, we're going to go jump off a bridge in Canada. He thought I was crazy, but the thought of seeing me thrown off a bridge got the better of him and he was game. What are friends for right!
I should mention this was my first time flying, ever. I was so nervous the night before I barely slept. Wondering what it would be like, would all my stuff make it, am I really flying all the way across the country by myself for the first time. Nothing like some fear to let you know you're alive.
So the next day I hopped on a plane from Ohio to Oregon with a layover in Texas. Flying was an experience, and overall a good one. Some planes I could walk onto, grabbing seat to seat to walk down the skinny aisle ways, and some I used the aisle chair. I kept an open mind and a positive attitude, and I've learned as long as you do that people are receptive and helpful so I had a good experience flying. I even had a couple flights bumped up to first class for free! I'm sure that didn't hurt my experience at all haha. Even the wheelchair escorts between flights to different terminals were great. Basically I was on five airplanes in seven days. If you're going to do something do it right I guess.
So at the end my stay in Oregon we flew to Vancouver, I rented a car, and took the drive into Whistler. I must say B.C. was one of the most beautiful places I have ever seen. When we got to Whistler and we're driving down this back road to the bridge, I remember feeling a sense of accomplishment that I was there.
I hadn't made the jump yet, but just having made the trip, following through on something, it was a good feeling driving up to that bridge. Then I saw the bridge and thought what was I thinking!
There is a dirt road that takes you almost all the way up to the top. The rest of the way I hopped in my chair and needed just a little help to get onto the bridge. So there they harness you like anyone else, then attach the wheelchair to you. After the guy harnessing me looks at me and says, "I hope that works, eh" my confidence was at an all-time high haha. Seriously though he told me he gets some people in chairs out there every year so I wasn't worried. Sort of, I mean I am getting thrown off a bridge.
So the time comes and it's my turn, I wheel myself over to the edge of the railing. The railing is about 4 feet high so you can't really see over it. Then they asked me if I was ready and began to pick up my wheelchair.
In the span of about half a second I'm up and on the railing and looking over this bridge and at the rushing water 160 feet below me. At that moment of realization that you're staring over the edge of a 160 foot bridge, you are already plummeting in a free fall towards the river.
It is such a rush and before you know it the bungee cord catches you and hurls you back in the air and you do it again. When you stop bouncing they lower a rope down, you attach it to your harness and they raise you back up. This is the point where I breathed a sigh of relief that I didn't have to tell all my therapists I hurt myself because I jumped off a bridge haha.
The next day we drove back to Vancouver, my buddy flew back to Oregon and I flew back home to Ohio. I was exhausted, happy to be home, and felt very accomplished. This was a great trip for me and the start of many more to come.
That first time doing anything is always the most special. Whether it's your first time driving again, first class, first time anything. It's hard to explain that "first" feeling but I know a lot of you reading this understand what I'm talking about. And if you don't it's about time you discovered it.
Our biggest limitations in life aren't physical, but mental. I know I let go of some limitations at the bottom of that bridge in Canada, and I know bungee jumping isn't everyone's cup of tea, but whatever it is I encourage you to go for it.
And if you're crazy like me, well, now you know a great place to get thrown off a bridge
[refresh if no video]
Uploaded on YouTube by burns2133 on Jun 27, 2011
# Article as posted at The Christopher and Dana Reeve Foundation website - for more info visit:
http://www.reevefoundation.org/
Disability Etiquette :Guide to interacting with people with different disabilities
Disability Etiquette
People with disabilities are entitled to the same courtesies you would extend to anyone, including personal privacy. If you find it inappropriate to ask people about their sex lives, or their complexions, or their incomes, extend the courtesy to people with disabilities.
- If you don't make a habit of leaning or hanging on people, don't lean or hang on someone's wheelchair. Wheelchairs are an extension of personal space.
- When you offer to assist someone with a vision impairment, allow the person to take your arm. This will help you to guide, rather than propel or lead, the person.
- Treat adults as adults. Call a person by his or her first name only when you extend this familiarity to everyone present. Don't patronize people who use wheelchairs by patting them on the head. Reserve this sign of affection for children.
In conversation...
- When talking with someone who has a disability, speak directly to him or her, rather than through a companion who may be along.
- Relax. Don't be embarrassed if you happen to use common expressions, such as "See you later" or "I've got to run", that seem to relate to the person's disability.
- To get the attention of a person who has a hearing disability, tap the person on the shoulder or wave your hand. Look directly at the person and speak clearly, slowly and expressively to establish if the person can read your lips. Not everyone with hearing impairments can lip-read. Those who do will rely on facial expressions and other body language to help understand. Show consideration by facing a light source and keeping your hands and food away from your mouth when speaking. Keep mustaches well-trimmed. Shouting won't help, but written notes will.
- When talking with a person in a wheelchair for more than a few minutes, place yourself at the wheelchair user's eye level to spare both of you a stiff neck.
- When greeting a person with a severe loss of vision, always identify yourself and others who may be with you. Say, for example, "On my right is Andy Clark". When conversing in a group, remember to say the name of the person to whom you are speaking to give vocal cue. Speak in a normal tone of voice, indicate when you move from one place to another, and let it be known when the conversation is at an end.
- Give whole, unhurried attention when you're talking to a person who has difficulty speaking. Keep your manner encouraging rather than correcting, and be patient rather than speak for the person. When necessary, ask questions that require short answers or a nod or shake of the head. Never pretend to understand if you are having difficulty doing so. Repeat what you understand. The person's reaction will guide you to understanding.
Common courtesies...
- If you would like to help someone with a disability, ask if he or she needs it before you act, and listen to any instructions the person may want to give.
- When giving directions to a person in a wheelchair, consider distance, weather conditions and physical obstacles such as stairs, curbs and steep hills.
- When directing a person with a visual impairment, use specifics such as "left a hundred feet" or "right two yards".
- Be considerate of the extra time it might take a person with a disability to get things done or said. Let the person set the pace in walking and talking.
- When planning events involving persons with disabilities, consider their needs ahead of time. If an insurmountable barrier exists, let them know about it prior to the event.
Easter Seals provides exceptional services, education, outreach, and advocacy so that people living with autism and other disabilities can live, learn, work and play in our communities.
26,000 face loss of aid for prescriptions ; State of Illinois July 2011
BLOOMINGTON, IL — Fewer older adults and people with disabilities will be eligible for pharmaceutical assistance under the Illinois Cares Rx program — effective Sept. 1 — as a result of a cut in the recently approved state budget.
About 26,000, or 15 percent, of 175,000 current enrollees statewide may no longer be eligible for the program because of changes in income eligibility guidelines, said Mike O’Donnell, executive director of the Bloomington-based East Central Illinois Area Agency on Aging. In 16 counties covered by the area agency, 24,321 people are enrolled in Illinois Cares Rx and that includes 2,306 people in McLean County, O’Donnell said Wednesday.
Illinois Department on Aging, which administers the program, will send letters explaining changes to enrollees, he said.
The state budget, for the fiscal year that began July 1, funds Illinois Cares Rx at 50 percent of last year’s $107 million. The program is for low- to moderate-income people age 65 and older and people 64 and younger with a disability.
Because of the state cut, income limits have been lowered from $27,610 to $21,780 for a single-person household; from $36,635 to $29,420 for a two-person household; and from $45,657 to $37,060 for a three-person-or-more household. People who earn more than that may no longer be eligible for assistance.
For those still eligible, Illinois Cares Rx will continue to pay Medicare Part D premiums and deductibles. However, co-pays would increase from $2.50 to $5 for generic drugs, from $6.30 to $15 for preferred brand name drugs, and from $15 to $20 for non-preferred brand name drugs, O’Donnell said. The co-pay for specialty drugs would remain $15.
After the total cost of drugs (paid by enrollee and the plan) reaches $2,840, enrollees will pay 25 percent of the cost of each prescription, in addition to co-pays. Now, enrollees pay 20 percent after $2,830, O’Donnell said.
Changes have no effect on the Illinois Circuit Breaker property tax relief program, which continues using current income eligibility guidelines, O’Donnell said.
O’Donnell and Kathryn Johnson, assistant director of PATH (Providing Access To Help) Senior Services, recommended that enrollees determine whether their income has changed. If they are no longer eligible, PATH Senior Outreach workers can help enrollees in McLean, Livingston and DeWitt counties evaluate their coverage and advise them on other possible plans, Johnson said.
Help is available
For Illinois Cares Rx enrollees with questions about upcoming changes, help is available from:
• Health Benefits Hotline at 800-226-0768 and Senior HelpLine at 800-252-8966
• Senior Health Insurance Program (SHIP) at 800-548-9034
• www.illinoiscaresrx.com and www.cbrx.il.gov
• County outreach sites, including PATH in McLean, Livingston and DeWitt counties at 309-827-4005 or 211.
SOURCES: Illinois Department of Healthcare and Family Services, Kathryn Johnson, Mike O’Donnell
## AS posted by pantagraph.com,report; By Paul Swiech July 6, 2011
Read more: http://www.pantagraph.com/news/local/government-and-politics/e59f6588-a839-11e0-9e4b-001cc4c002e0.html#ixzz1Tme4c5jn
About 26,000, or 15 percent, of 175,000 current enrollees statewide may no longer be eligible for the program because of changes in income eligibility guidelines, said Mike O’Donnell, executive director of the Bloomington-based East Central Illinois Area Agency on Aging. In 16 counties covered by the area agency, 24,321 people are enrolled in Illinois Cares Rx and that includes 2,306 people in McLean County, O’Donnell said Wednesday.
Illinois Department on Aging, which administers the program, will send letters explaining changes to enrollees, he said.
The state budget, for the fiscal year that began July 1, funds Illinois Cares Rx at 50 percent of last year’s $107 million. The program is for low- to moderate-income people age 65 and older and people 64 and younger with a disability.
Because of the state cut, income limits have been lowered from $27,610 to $21,780 for a single-person household; from $36,635 to $29,420 for a two-person household; and from $45,657 to $37,060 for a three-person-or-more household. People who earn more than that may no longer be eligible for assistance.
For those still eligible, Illinois Cares Rx will continue to pay Medicare Part D premiums and deductibles. However, co-pays would increase from $2.50 to $5 for generic drugs, from $6.30 to $15 for preferred brand name drugs, and from $15 to $20 for non-preferred brand name drugs, O’Donnell said. The co-pay for specialty drugs would remain $15.
After the total cost of drugs (paid by enrollee and the plan) reaches $2,840, enrollees will pay 25 percent of the cost of each prescription, in addition to co-pays. Now, enrollees pay 20 percent after $2,830, O’Donnell said.
Changes have no effect on the Illinois Circuit Breaker property tax relief program, which continues using current income eligibility guidelines, O’Donnell said.
O’Donnell and Kathryn Johnson, assistant director of PATH (Providing Access To Help) Senior Services, recommended that enrollees determine whether their income has changed. If they are no longer eligible, PATH Senior Outreach workers can help enrollees in McLean, Livingston and DeWitt counties evaluate their coverage and advise them on other possible plans, Johnson said.
Help is available
For Illinois Cares Rx enrollees with questions about upcoming changes, help is available from:
• Health Benefits Hotline at 800-226-0768 and Senior HelpLine at 800-252-8966
• Senior Health Insurance Program (SHIP) at 800-548-9034
• www.illinoiscaresrx.com and www.cbrx.il.gov
• County outreach sites, including PATH in McLean, Livingston and DeWitt counties at 309-827-4005 or 211.
SOURCES: Illinois Department of Healthcare and Family Services, Kathryn Johnson, Mike O’Donnell
## AS posted by pantagraph.com,report; By Paul Swiech July 6, 2011
Read more: http://www.pantagraph.com/news/local/government-and-politics/e59f6588-a839-11e0-9e4b-001cc4c002e0.html#ixzz1Tme4c5jn
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