Airlines now subject to Americans with Disabilities Act

January 28th, 2009

airplane

A monumental lawsuit between Northwest Airlines and five Detroit-area airline travelers with physical disabilities has brought attention to a crucial question: How does the Americans with Disabilities Act (ADA) protect air travelers with disabilities?
As the law is currently written, aircraft are excluded from the definition of “specified public transportation.” Past court cases have interpreted this to also mean that airport terminals are excluded from ADA coverage.

However, in this most recent case, U.S. District Judge George
Caram Steeh said in a 13-page opinion that this interpretation is
“inconsistent with the plain meaning of the statute.”
The Detroit-area residents filed suit against Northwest Airlines and Wayne County Airport Authority in Detroit (which was recently dropped as a defendant), claiming that the airline and airport failed to provide proper accommodations in a number of areas. Among several complaints, the plaintiffs said Northwest failed to provide boarding assistance in some cases, dropped passengers to the floor when assisting them improperly and damaged wheelchairs in the airline’s possession during flight.

Because aircraft are excluded from ADA coverage, airlines have been held to the standards of the Air Carriers Access Act (ACAA), which prohibits discrimination on the basis of disability in air travel and requires air carriers to accommodate the needs of passengers with disabilities. However, individuals are not allowed to file private claims under this law and must depend on the federal government for enforcement. Northwest argued the case should be dismissed because the ADA does not apply to airlines, and the ACAA does not allow individuals to file private claims.

Judge Steeh dismissed the plaintiffs’ claims under the ACAA, but ruled the ADA does apply to airport terminals and thus the case may continue. He said that although aircraft are covered by the ACAA, airports are covered by the ADA, which includes terminals operated by the airlines, such as Northwest Airline’s terminal at the Detroit airport. Therefore, Northwest’s terminal — and all airline terminals — must meet ADA guidelines.

“This interpretation is consistent with Congress’ intent to limit the ACAA’s reach to aircraft and the ADA’s reach to public spaces, such as terminals. In fact, to conclude otherwise would leave the door open for acts of discrimination that could not be remedied,” Judge Steeh said in his opinion. In the ADA language, “public accommodation” is defined to include entities affecting commerce such as “a terminal, depot, or other station used for specified public transportation.” And according to Judge Steeh, the Northwest Airlines terminal at the Detroit airport is considered a public accommodation, as it’s used for “bus, rail and other motorized transport along with its principal function as a center for transportation by aircraft.”

Peter Berg, project coordinator of technical assistance at Great Lakes ADA, said the ADA applies to airport facilities, which includes anything from the front door to the jet way. The ACAA requires airlines to assist travelers with disabilities, such as helping someone in a wheelchair board the plane safely and guiding someone who is visually impaired from the ticket counter
onto the airplane. These services are not limited to the airplanes
themselves, according to Berg; airlines are responsible for providing these services in the airport terminals. Thus, as they operate within their terminals, airlines are subject to the standards set forth by the ADA.

In an article in “The Detroit News,” Kristin Baur, a spokesperson for
Northwest, said the airline “is currently reviewing the ruling and evaluating its options regarding future actions.” Baur also said the airline continues to be committed to providing accessible air travel for all customers.

Visit the Federal Aviation Administration’s Web site at www.faa.gov to learn more about traveling rights for passengers with disabilities.

Disabled kids need exercise too

January 26th, 2009

kid-workout

NEW YORK — Children with chronic illnesses or disability can often benefit from the right exercise program, showing improved quality of life, greater aerobic capacity and better function, according to a report published this month.

But chronically ill or disabled children and teens who aren’t active can get out of shape and too fat, just like their peers who aren’t challenged by illness or disability, warns Dr. Patrick J. Morris of the University of Minnesota in Minneapolis.

Morris notes that children with cerebral palsy often have movement problems that make it difficult to walk, let alone exercise. But he points to a study in seven teens with the disease that showed three months of training improved their aerobic capacity and their ability to stand, walk, jump and run.

Physical activity is also beneficial to individuals with spinal cord injuries, Morris adds. And while the jury is still out on whether exercise can help people with cystic fibrosis get stronger and breathe more easily, he notes, the studies to date show no evidence that physical activity is harmful for these patients.

Even children with the bleeding disease hemophilia can engage in physical activity, according to Morris, if they choose a sport that’s appropriate for their fitness and coordination level.

Aerobic workouts can clearly help children with asthma get stronger and more fit, although the evidence is not as clear on whether training affects symptoms like breathlessness or the amount of medication a patient needs.

Exercise is also crucial for helping children with type 2 diabetes manage their illness, according to Morris, but a study out last year showed that adolescents found the hardest thing about following an exercise program was “lack of motivation.”

Just because exercise can benefit young people with disease “doesn’t mean it’s easier to get these kids to sign on to physical activity,” Morris concedes. To help motivate them, he suggests emphasizing “fun approaches with variety and freedom that are supported by peers, that have the option of family participation, and that foster success.”

Morris points to the offerings of Courage St. Croix, a rehab and resource center for disabled individuals near his home, as examples of activities that fit the bill: “power wheelchair soccer, hockey, softball or rugby; …handcycling, SCUBA, rock climbing, kayaking, downhill skiing, water skiing, golf, archery, and bicycling; … and yoga, tai chi and horseback riding.”

“Physical activity,” he concludes, “is a positive intervention for children growing up with the challenge of a chronic disease or disability. When physical activity becomes a lifestyle for these children, they’re supported on their way to becoming happier, healthier adults who are up to any challenge.”

Get to know the new political crew

January 22nd, 2009

 

american-flag

The campaign advertisements are gone, phone lines are no longer buzzing with endorsement calls and political debating has ceased. Many of us did our part to vote and participate in the election process. But, our work isn’t done.

With Barack Obama in the White House planning his next four years in office and countless legislators ready for action, now is the time to get

acquainted with your elected officials. Building personal relationships is key to influencing legislators and other officials who can impact the disability community with their public policy decisions.

It’s important to connect with not only new officials, but also with those who have been reelected. Reach out to your elected officials to introduce yourself and congratulate them on their win. Ask if they can meet with you to discuss issues affecting you and the disability community.

Or, send them a letter or e-mail to share issues of concern.

To learn more about Barack Obama, visit www.barackobama.com.

Local Events

January 22nd, 2009

Do you have an event in your area that you’d like to let others know about?  Maybe you know of a team or are on a team that would like to share their information, events & scores.  Simply click the link below that says “Comment” and let us know the who, what, when, where and all the other important stuff.  If it’s appropriate for the website we’ll post it and help you get the word out!

Groovability

January 22nd, 2009

 

WHO ARE WE

Groovability is a full 501c3 non profit organization founded on the need for alternative dance programs for the disabled in the Kansas City area. This organization exists to motivate people by providing the opportunity to free hidden dreams through learning and performing the arts.

Groovability is Kansas City Metro’s only performing arts organization of it’s kind. Our focus is on improving the quality of life to wheelchair users by::

1. Promoting dance and the arts to the general public
2. Improving the quality of life for all
3. Providing quality instruction
4. Raising awareness of the possibilities between the non-disabled and the disabled counities

Groovability will impact over 82,000 physically disabled individuals, making Kansas City a better place to live by removing barriers between the disabled and non-disabled communities.

OUR CLASSES

Groovability classes are currently held on Saturdays from 10:30 - 12:00.
We cover many different areas including:

1. Isolationary Movement
2. Balance
3. Dexterity
4. Syncronazation
5. Coupling
6. Connections
7. Chair Work
8. Posture

All participants are required to provide written consent from a Physician in order to participate in class.

Group Classes are $10

Private Lessons are $25

Contact Info:

Chris Pruitt, Executive Director 
816.719.6062
cpruitt@groovability.org
Joanne Fluke, Assistant Director
785.248.3023
jfluke@groovability.org
Donna Janes, Secretary 
913.558.1552
djanes@groovability.org

OR  Check out the website at   www.groovability.org

Power Soccer

January 22nd, 2009

As posted at:www.columbiatribune.com

OUR TOWN    Photo and story by NICK KING of the Tribune’s staff

Published Tuesday, September 30, 2008

 

Mark Ohrenberg sits in goal, with his nephew, Jarrett Pfeiffer, 10, on his lap while Tucker Johnsen, left, and Bev Earley try to score on him during a recent practice.

Mark Ohrenberg sits in goal as team members try to score on him. With his nephew Jarrett Pfeiffer, 10, on his lap, Mark, co-founder of the team and a coach/cheerleader, deflects a shot with his leg. He jokingly taunts the shooter, “No goal! No goal!” Everyone laughs.

From 2 to 4 p.m. every Sunday, members of the power soccer team Driving Force practice at Woodcrest Chapel in Columbia. Driving Force is part of the United States Power Soccer Association, where teams from across the country play power soccer, the first highly competitive sport in which people who use power wheelchairs can participate.

Players’ chairs are equipped with front bumpers that allow them to bump, push, pass and shoot a 13-inch soccer ball at a goal on either end of a basketball court during a four-on-four game. Mark, the youth and family coordinator for Services for Independent Living, and the agency’s executive director, Aimee Wehmeier, started the team after volunteer, MU doctoral student and current team member Romanda Walker brought the sport to their attention.

Ten practices and two months later, the team is on track and gearing up for its first game, tentatively planned for November against one of two St. Louis teams. Mark says the team could use more players; you have to be at least 8 years old and use an electric wheelchair. Also, Driving Force is in need of a regulation-size basketball court for practice as well as sponsors to help with costs, such as the $100-to-$400 chair bumpers, uniforms and the $60-to-$80 soccer balls.

“My main interest is to facilitate these opportunities,” Mark says. “We give people the opportunity to use their skills and their love of soccer to play soccer, to win against other teams, and to meet other people from around the country.”

If you are interested in joining or sponsoring the Driving Force power soccer team, contact Mark Ohrenberg at (573) 874-1646, ext. 216, or at mohrenberg@silcolumbia.org.

“Groovability” wheelchair dancers enjoy strutting their stuff

January 22nd, 2009

As posted at:  www.columbiamissourian.com

 

A Kansas City group of wheelchair ballroom dancers has performed at exhibitions across the state.

September 7, 2008 | 6:09 p.m. CDT

BY ERIC ADLER/THE KANSAS CITY STAR

KANSAS CITY - For JoAnne Fluke, it is all about the freedom … the movement … the feeling.

Oh, the feeling of ballroom dancing in a wheelchair. The cha-cha. The salsa. The “downright sexy rumba,” she said. Then there is the Viennese waltz. ”It makes me feel beautiful, elegant, like a lady,” Fluke said.

Ebullient and auburn-haired, the Ottawa, Kan., resident was born with a condition called caudal regression. Her legs, with no feeling, are tiny, the size of baby legs, webbed at the knees and all but nothing. They lie tucked beneath her so that when seated, her body looks like half a body, a torso in a chair.

But on the dance floor, when she hears the swell of the waltz, she’s lifted into the air by her teacher and able-bodied partner, Chris Pruitt, and swept into his arms. They dance face to face, body to body. Fluke’s right arm extends straight. Her back arches in elegant repose. Her head tilts regally.

“I don’t see my disability when I’m dancing,” Fluke said. “I see me.”

At 32, Fluke is spirited, bold, a former Miss Wheelchair Kansas, who from middle school through college at Baker University never shied away from the spotlight or had a single qualm about lowering herself from her chair to dance on her hands.  Loath to allow her disability to limit her, she tried out for the ABC program “The Bachelor” in 2002 when its producers came through Kansas City.

“You’re talking to a girl who, when she was 4 or 5 years old, wanted to be the first disabled Little Orphan Annie on Broadway,” she said.

Still, the idea that she would help create what, in the past 17 months, has become a small yet growing group of wheelchair ballroom dancers in Kansas City never occurred to her.  But it has happened nonetheless.  In the last year, Pruitt, Fluke and others formed a non-profit alternative dance organization called Groovability, as opposed to “disability.”

“I didn’t want to be the only one to have this opportunity,” Fluke said. “It’s too wonderful.”

Now, each Saturday, Fluke and maybe three or four friends roll their chairs out on the wood floor at Bella Studio in Westport’s Manor Square to practice in front of the wall-size mirror.  Tiny white Christmas lights hang from a low ceiling.

“We’re going to do some cha-cha today,” Pruitt, 31, said to the class on a recent Saturday.

To the dancers, it already seems like so much has happened since the whole thing began last year with a phone call and a lie.

“Do you teach wheelchair ballroom dancing?” Fluke asked Pruitt on the telephone back in March 2007.

Fluke and her 28-year-old friend, Tiffany Simpson, a speech pathologist from Kansas City, North, who has spina bifida - a birth defect resulting in an incomplete spinal cord - had been researching wheelchair ballroom dancing on the Internet. They work together as summer camp counselors in Excelsior Springs teaching children with spina bifida to dance.

On YouTube, they found dozens of videos of elegant women and men in wheelchairs: precise ballroom dancers in tuxedos and sparkling gowns, their hands clasped - one moving in the chair, the others standing - as crowds roared with applause during an international competition.

“Both of us were like, ‘I want to do this!’” Simpson said.

But when Fluke called several local dance studios last year to find a program, she came up empty. Then she called Pruitt, whose Bella Studio had just opened in June 2006 and had been struggling.  So when Fluke asked Pruitt about whether he held classes, he lied.

“Yes,” Pruitt told her, even though he had barely heard of wheelchair ballroom dancing.

“I had no clue,” he said.

He educated himself about how wheelchair ballroom dancing started in Sweden in the 1970s and has been huge in Europe ever since. On Oct. 24, dancers from scores of nations are expected to gather in Belarus’ capital, Minsk, for the International Paralympic Committee Dance Sport World Championships. In the United States, the sport is still growing, promoted by organizations such as the Wheelchair Dancesport USA Association and the American DanceWheels Foundation.  Early this year, the University of Delaware recognized the sport by starting what is thought to be the first class in wheelchair ballroom dancing at a major university.

Fluke arrived for her first class with Pruitt on April 1, 2007. Other women soon followed.

“I decided I was going to teach people the way I teach everybody,” said Pruitt..

Except there was a difference. To understand what was possible, to figure out what the body and chair could do together, Pruitt acquired a chair of his own. For four days, he lived as if he had a disability.

“I went to the bathroom from the wheelchair. I showered. I tied my legs together,” he said.”I’ll tell you, these women have taught me more about life than anyone, about how nothing can stop you. They have challenged me beyond my abilities, forcing me to come up with creative choreography: how to do this, how to do that.”

In the last year, the Groovability dancers have given exhibitions at local studios and able-bodied competitions from Nebraska to the St. Louis Star Ball. In early August, they joined some 600 able-bodied ballroom dancers at the Heart of America DanceSport Championships in Tiffany Springs.

In exhibitions, Fluke can leave her chair. But she knows that in real competition it’s not allowed. Wheelchair ballroom dancers must remain seated. The chair, although it can be spun or snapped or even tilted, must remain on at least one wheel at all times.

Back in class, Pruitt hopped in his chair and rolled to the front of the class.

“And we’re going to do crisscrosses and breaks with swivels today,” Pruitt told the group.

The five Groovability women lined up in a row behind him.

Along with Fluke and Simpson, there was Donna Janes, 57, of Lee’s Summit, who had polio as a child, then later took up wheelchair tennis and bowling.

“I truly believe that if you can move an eyelash, you can dance,” she said.

There was Jennifer Simmons, 49, of Independence. A paraplegic from childhood, Simmons is a dog trainer and horsewoman who found that wheelchair dancing brought her back out of a winter slump. Lorraine Cannistra, 39, of Lawrence, cried when she first saw Fluke and Janes dancing with Pruitt at an exhibition during the 2007 Miss Wheelchair Kansas pageant.

“It made me cry because it was beautiful,” she said. “It was graceful. Those are two words not often put together with wheelchairs. I knew in that moment I wanted to do it.”

Pruitt peppered the dancers with instructions, practicing quarter-turns, half-turns and full turns. Make sure the arms are down. Rotate at the waist, hips and shoulders. Engage the back. Don’t flail about. Keep the neck straight, keep the frame…

Cha-cha music, then samba, filled the studio. On this day, teenagers from Fluke’s church had come as stand-ins for able-bodied partners.

“You have to put emotion into it,” Pruitt told the group. “You have to feel it.”

The class continued for close to 90 minutes. At the end, the women were breathless. Each would later say that they know, in some ways, that people who see them dance often find them inspirational, breakers of stereotypes and the like.

Although it’s not a role any of the dancers disavow, every one of them also said it’s not why they do it.

“I get the opportunity to really express how I feel,” Fluke said. “It feels like it doesn’t matter that I have wheels instead of feet. It’s in the heart. It’s in the soul.”

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December 29th, 2008

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