May 19th, 2012
OVERLAND PARK, Kan.–(BUSINESS WIRE)–
Sprint (NYSE:S – News) today has made it easier for individuals with speech
disabilities to initiate calls using a wireless phone. Sprint’s newly
launched “My Wireless STS” service enables individuals with speech
disabilities to simply dial a short wireless code – *787 – to place an
operator-assisted call.
A Speech to Speech (STS) operator listens to the conversation and
repeats the words of the person with a speech disability to the other
party. STS users can instruct the STS operator to repeat every word
spoken or to simply repeat the words that are unclear. No special
equipment is needed.
STS users can access the *787 service from anywhere in the country 24
hours a day, 365 days per year – and at no charge to the user.
“We are very excited to announce *787 – a service that’s tailored to the
needs of STS users,” said Michael Ellis, Director, Sprint Relay. “We are
the first in the industry to bring this service to market, and we’re
pleased to have developed it in collaboration with speech disabled
communities across the country.”
Sprint also offers “My Email Set-up” for STS users with access to email.
“We know that some STS users may tire and speech may become more
difficult during long calls. Our new Email Set-Up makes it easier,”
Ellis said. “To reduce the amount of energy needed to provide calling
instructions, STS users can email that information directly to the STS
operator 2 to 24 hours prior to the call. This can include information
such as the number to be dialed, the name of the person being called,
any special instructions and subject of the call, or anything that makes
it easier for the STS user to complete the call.”
Sprint also recently announced the availability of dedicated customer
service for STS users. Sprint’s STS support staff provides one-on-one
assistance, training on the STS service and can assist STS users to
register their calling preferences. The new STS support toll-free number
is 1-877-787-1989.
More information about the enhanced STS features can be found at www.sprintsts.com
For its innovation and industry-leading customer service in the deaf,
hard of hearing and speech disabled communities, Sprint has been lauded
with third-party awards and endorsements. The Paisley Group National
Relay TTY Performance Index™ ranked Sprint Relay highest in customer
care and speed of service. Sprint Relay also earned ABILITY Magazine’s
Best Practices Award for its “spirit of inclusion” in the workplace and
in the consumer marketplace.”
Sprint now provides relay service to 32 states and the federal
government, to the country of New Zealand and the Commonwealth of Puerto
Rico. Sprint also provides Captioned Telephone “CapTel” services to 31
states and the federal government.
About Sprint Relay
Sprint is the largest and most technologically advanced TRS provider in
the nation with more than 20 years of experience in providing relay
services to persons who are deaf, hard of hearing, deaf-blind, or have a
speech disability to communicate with hearing persons on the phone.
Sprint’s experience in this field ensures Sprint Relay users receive
quality service regardless of the type of relay service they are using.
Sprint’s relay service is available 24 hours a day, 365 days a year,
with no restrictions on the number of calls placed or the length of
calls. For more information, visit www.sprintrelay.com.
About Sprint Nextel
Sprint Nextel offers a comprehensive range of wireless and wireline
communications services bringing the freedom of mobility to consumers,
businesses and government users. Sprint Nextel served more than 56
million customers at the end of the first quarter of 2012 and is widely
recognized for developing, engineering and deploying innovative
technologies, including the first wireless 4G service from a national
carrier in the United States; offering industry-leading mobile data
services, leading prepaid brands including Virgin Mobile USA, Boost
Mobile, and Assurance Wireless; instant national and international
push-to-talk capabilities; and a global Tier 1 Internet backbone. Newsweek
ranked Sprint No. 3 in its 2011 Green Rankings, listing it as one of
the nation’s greenest companies, the highest of any telecommunications
company. You can learn more and visit Sprint at www.sprint.com
or www.facebook.com/sprint
and www.twitter.com/sprint.
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May 19th, 2012
Seniors and people with disabilities are outraged that TransLink plans to eliminate the TaxiSaver program—a service that allows registered HandyDart users to receive a 50 per cent discount on taxi rides.
The program was introduced more than 20 years ago so that HandyDart users can use a taxi if a HandyDart is not readily available. However, it will be phased out starting in August, and the money saved will be re-invested to increase HandyDart services, said Heath McCain, Chair of the Access Transit Users’ Advisory Committee in a written statement.
TransLink estimates that the cost savings would allow the transit authority to fill an additional 19,900 HandyDart requests.
However, Jill Weiss, chair of the City of Vancouver’s Persons with Disabilities Advisory Committee, said eliminating TaxiSaver means seniors and those with disabilities will no longer be able to access same-day services.
“If you want to go somewhere on the same day, there are no rides available,” she said. “If you’re running a fever you can’t go to the doctor. If somebody invites you to dinner you can’t accept it. This takes away the small semblance of normalcy that we have to travel in the city and at least some independence and ability to get around.”
Laura Mackenrot, who is visually impaired, says she uses the TaxiSaver program when she is denied a ride from HandyDart. She says with the 50 per cent-discount gone, not only will she now have to watch her spending, her independence will also be taken away.
“The cost of having to take a taxi can add quite a lot to your expenses,” she said. “That just kind of tips it over the edge for a lot of people…I think they’ll just have to say no to friends and family and stay inside and be more home-bound, and I think that’s very disappointing.”
With files from CTV British Columbia’s Maria Weisgarber
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May 17th, 2012
County Council Chairman Butch Kirven, above, and other council members hear how the new interim director of the Greenville County Disabilities and Special Needs Board says he is working to correct problems there.
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May 17th, 2012
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May 15th, 2012
MONDAY, May 14 (HealthDay News) — Young adults with an autism
spectrum disorder are less likely to continue their education or get a job
after high school when compared to young adults with other disabilities,
new research indicates.
According to the study, only about 35 percent of young adults with
autism attended college and only 55 percent had a job during the first six
years after high school. Overall, they faced a greater than 50 percent
chance of being unemployed or not attending college when compared to those
with other disabilities, the researchers reported.
More than half of autistic young adults had no participation in either
work or education during the two years after leaving high school, and even
six years later more than one-third were without work or higher education,
the study found.
“Many families with children with autism describe leaving high school
as falling off a cliff because of the lack of services for adults with an
autism spectrum disorder,” said senior study author Paul Shattuck, an
assistant professor of social work at Washington University in St. Louis.
“So much of media attention focuses on children. It’s important for people
to realize autism does not disappear in adolescence. The majority of
lifespan is spent in adulthood.”
Part of the reason that young adults struggle after high school is that
a core feature of the disorder is difficulty knowing how to interpret
social interactions and handle a wide variety of social situations,
something that is a necessity in many jobs, experts say.
But researchers also note that more educational and job-related support
could help people with autism — including the wave of children recently
diagnosed — who will be aging over the next decade as they find their
place in society.
“We need to find ways to make room for adults with autism in our
communities and help them get connected to opportunities that people with
other forms of disabilities are participating in,” Shattuck said.
The study is published online May 14 and in the June print issue of
Pediatrics.
In it, researchers examined data from the National Longitudinal
Transition Study 2, a nine-year study of adolescents who were enrolled in
special education because of autism, learning disabilities, intellectual
disabilities or speech and language impairments.
Compared with youth in the three other disability categories, autistic
teens and young adults had significantly lower rates of employment and the
highest overall rates of no participation in any work or education.
For example, only 55 percent of young adults with autism had paid
employment, while 86 percent of those with a speech or language
impairment, 94 percent of those with a learning disability and 69 percent
of those with mental retardation did.
The education picture was a little brighter. About 35 percent of kids
with autism attended a two- or four-year college; 51 percent of those with
a speech or language delay did so, while 40 percent of those with a
learning disability and 18 percent of those with mental retardation
did.
For lower-income autistic teens and young adults, participation rates
were even lower.
An estimated one in 88 U.S. children has an autism spectrum disorder,
according to the latest figures from the U.S. Centers for Disease Control
and Prevention. About 50,000 youths with autism will turn 18 this year in
the United States.
Peter Bell, executive vice president of programs and services for
Autism Speaks and the father of a young adult with autism, said the
transition to adulthood can be particularly difficult for the families of
children with autism. During childhood, most services are centered in the
educational system and children are entitled to receive a public
education. In many states, special needs teens can continue to get some
services through the schools until around age 20 or 21.
After that, parents have to seek help from the social services system,
which is more fragmented and difficult to navigate. And yet, he added, the
report is not all bleak.
“I was pleasantly surprised that about 35 percent went on after leaving
high school to attend some form of college,” Bell said. “I was told 16
years ago when my son was diagnosed that there was very little chance he
would ever go to college. So the fact that over one-third of the autism
population goes on to some form of education after school should say to a
lot of parents, ‘You shouldn’t automatically assume your child is not
going to go to college’.”
His own 19-year-old son isn’t attending college, but he does work at
several jobs in their town, where he is a well-known and accepted part of
the community, Bell added.
More information
Autism Speaks has a toolkit to help teens with autism and their families
make the transition out of high school.
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May 15th, 2012
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Millions of dollars of funding has been allocated to help disabled people at home as part of the Government’s pre-budget spending.
This come the day after a Court of Appeal decision rejected a Ministry of Health policy that only non-related caregivers should be paid.
The disability sector will get $144 million over four years as part of the announcement.
That includes $58 million to boost the number of people using residential support services, and $55 million for home services that enable disabled people to live at home.
Kim Preston, who has three boys with special needs, told ONE News the boost in Government funding is a move in the right direction.
“It’s good to see that people are going to get the help they’re entitled to,” Preston told ONE News.
“More families need respite, just a little break. It is horrible to say you need a break from your children but some of these families do.”
Health Minister Tony Ryall said the funding will mean an extra 600 people will get help at home.
“That keeps them independent and living the sort of ordinary lives they want to,” Ryall said.
However, Labour leader David Shearer said: “Anything that is given here has to be cut from somewhere else. This is a zero budget, the Government has said that. We’re waiting to see now what other parts of the economy will be cut.”
This funding announcement comes the day after the Court of Appeal ruled parents of disabled children should be paid like other carers, a decision the Government says could cost taxpayers half a billion dollars.
But this new funding will not go towards that.
“We had planned this announcement quite some time before the Court of Appeal decision came out yesterday,” Ryall said.
But Shearer claims today’s decision “was a smokescreen to hide the fact the Government has a very poor record on disability issues.”
He said it is more than a coincidence the decision is being made today.
Ryall said the disability sector is the health vote’s biggest winner in next week’s Budget.
Politics News Video
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May 13th, 2012
Living with a disability has its tough times… but lots of lighter moments too. We interviewed people all over the country to hear their insights; these frank and funny conversations reveal the truth about disability and today we bring you the best moments from that series.
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May 13th, 2012
The number of children with complex disabilities is increasing and experts blame pre-term births and fetal alcohol syndrome as two key factors.Figures obtained by the Herald on Sunday revealed more than 60 per cent of schools…
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May 13th, 2012
Communication technique puts person before disability
Published 4:04pm Saturday, May 12, 2012
People with disabilities are — first and foremost — people who have individual abilities, interests and needs.
They are moms, dads, sons, daughters, sisters, brothers, friends, neighbors, coworkers, students and teachers. About 54 million Americans — one out of every five individuals — have a disability. Their contributions enrich our communities and society as they live, work and share their lives.
People with disabilities constitute our nation’s largest minority group, which is simultaneously the most inclusive and the most diverse. Everyone is represented: all genders, all ages, all religions, all socioeconomic levels and all ethnic backgrounds. The disability community is the only minority group that anyone can join at any time.
The language a society uses to refer to persons with disabilities shapes its beliefs and ideas about them. Words are powerful; Old, inaccurate, and inappropriate descriptors perpetuate negative stereotypes and attitudinal barriers. When we describe people by their labels of medical diagnoses, we devalue and disrespect them as individuals.
In contrast, using thoughtful terminology can foster positive attitudes about persons with disabilities. One of the major improvements in communicating with and about people with disabilities is “People-First Language.” People-First Language emphasizes the person, not the disability.
By placing the person first, the disability is no longer the primary, defining characteristic of an individual, but one of several aspects of the whole person. People-First Language is an objective way of acknowledging, communicating, and reporting on disabilities. It eliminates generalizations and stereotypes, by focusing on the person rather than the disability.
Disability is not the “problem.” For example, a person who wears glasses doesn’t say, “I have a problem seeing,” they say, “I wear/need glasses.” Similarly, a person who uses a wheelchair doesn’t say, “I have a problem walking,” they say, “I use/need a wheelchair.”
Our words and the meanings we attach to them create attitudes, drive social policies and laws, influence our feelings and decisions, and affect people’s daily lives and more. How we use them makes a difference. People First Language puts the person before the disability, and describes what a person has, not who a person is. Using a diagnosis as a defining characteristic reflects prejudice, and also robs the person of the opportunity to define him/herself.
Representation
Historically, people with disabilities have been regarded as individuals to be pitied, feared or ignored. They have been portrayed as helpless victims, repulsive adversaries, heroic individuals overcoming tragedy, and charity cases who must depend on others for their well-being and care. Media coverage frequently focused on heartwarming features and inspirational stories that reinforced stereotypes, patronized and underestimated individuals’ capabilities.
Much has changed lately. New laws, disability activism and expanded coverage of disability issues have altered public awareness and knowledge, eliminating the worst stereotypes and misrepresentations. Still, old attitudes, experiences and stereotypes die hard.
People with disabilities continue to seek accurate portrayals that present a respectful, positive view of individuals as active participants of society, in regular social, work and home environments. Additionally, people with disabilities are focusing attention on tough issues that affect quality of life, such as accessible transportation, housing, affordable health care, employment opportunities and discrimination.
By Jamey Helgeson The Arc of Mower County
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May 11th, 2012
A few months ago, some students at the College of Adaptive Arts would not even have pointed a toe or tapped a heel in front of someone.
On Saturday night, the Showboaters, all developmentally disabled adults, will appear on stage, performing the “Glee” version of “Lean On Me” and the Beach Boys’ “Be True To Your School,” for their annual Palooza fundraiser. At a rehearsal last week, they were in their element.
“The arts just ignite our kids,” said Linda Gonzales, who said her daughter Renee has blossomed at the college.
“To see these students grow is so amazing,” said Katie Zeisl, 23, who helps teach the Showboaters.
Student Trevor Lucken, 26, said his goal is to someday appear on “Dancing With The Stars.”
“I just love to dance,” he said.
The key word here is “goal.” The class at the fledgling college aims to help students such as Lucken dare to dream and to fulfill those aspirations.
Most educational services for disabled youths cease at age 22. The College of the Adaptive Arts hatched an idea so simple, it’s a wonder it has been elusive for so long. Using the arts, the college creates opportunities for continuous learning, achievement and progress for adults with developmental disabilities.
“We want to create lifelong collegiate experience through expression, exploration and friendship — delivering excellent services to adults of all disabilities,” said co-founder DeAnna Pursai.
Started in 2009 with
a handful of students, the college now has 75 students enrolled in 17 classes at two campuses in San Jose and one in Redwood City. Courses range from personal fitness and soccer to dance, puppetry and public speaking.
Both the Showboaters, who perform popular musical tunes, and the puppetry class take their shows to schools, senior citizen centers and other venues. A golf team, with clubs donated by a Roseville team, is in the works. An online health and fitness class meets via Skype every Wednesday.
The classes are free. While instructors are paid, Pursai and co-founder Pamela Lindsay they earn only a $300 monthly stipend.
The school is not accredited, but instructors are called professors and students work toward degrees. Pursai calls it “semantic validation,” to reinforce the notion of students attending college, becoming productive, contributing citizens.
“The way DeAnna and Pam work with our children — it’s their absolute belief in them that makes them feel valued,” said Jasmina Naleid, of Campbell. Her daughter, Maya, 21, has autism and Down syndrome. “I want her to continue learning,” Naleid said. “She lives for the days when she has the College of Adaptive Arts.”
Her daughter has made friends, socializes with classmates on Facebook and tours with a troupe, her mother said, that “brings lots of joy to people.”
“I like showboating,” said Kim Rains, 33, who during some performances also signs to interpret lyrics for the hearing-impaired.
Her mother, Candy Rains, of San Jose, like other parents was effusive about the classes. “My daughter is a born performer,” she said.
Both Kim Rains and Renee Gonzales joined the college’s Speaking with Confidence class on a field trip to a Toastmasters meeting at PayPal. “It was phenomenal,” Linda Gonzales said, because the students were treated like any other Toastmasters guest.
Extending those kinds of opportunities that others take for granted are part of the college’s mission.
Pursai, 40, had long been thinking of starting the college, spurred on by seeing how her younger sister Angel, who has Down syndrome, was treated.
“There’s a real disconnect between what so many adults are capable of contributing and the opportunities that are presented to them,” Pursai said.
A number of programs exist for adults with disabilities, but most focus on either living skills or recreation, like adult day care. The difference at the college is the idea of progress, that students are learning then refining skills and advancing to higher levels.
Across the country, programs like the college are popping up to broaden horizons for those with autism, cerebral palsy and other cognitive delays.
As with all nonprofits, the bottom line is a challenge. “We’re fundraising all the time,” said Lindsay, a professional actress who teaches theater at San Jose State. They’ve found sympathetic landlords in Randol School in San Jose, the Veteran’s Memorial Senior Center in Redwood City and Terry Peckham, co-founder of the Silver Creek Sportsplex in South San Jose.
Pursai and Lindsay’s goal is to create a full-fledged conservatory and to also serve high-functioning people with Asperger’s syndrome, those with physical disabilities, traumatic brain injury and hidden disabilities.
“Our biggest challenge is trying to find outside investors who believe in this new model,” Pursai said.
Eventually, she said, students will become professors and will run much of the school.
Student Kim Rains is enthusiastic. “My goal,” she said, “is to reach out to the other people and spread the word.”
Contact Sharon Noguchi at 408-271-3775. Follow her at Twitter.com/NoguchiOnK12.
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