Friday, December 21, 2012

Treaty for the disabled falls short of ratification


WASHINGTON -- Senator John Kerry made an impassioned but ultimately futile plea for ratifying a treaty aimed at advancing the rights of the blind and disabled across the globe, urging Congress to do for the world what has already been accomplished in the United States to protect Americans with disabilities.
In the end, Kerry and other supporters fell five votes short of the 66 needed for ratification of the international pact known as the UN Convention on the Rights of Persons with Disabilities -- hailed by advocates as a human rights effort to transform how nations across the world treat those with long-term physical, mental and intellectual impairments, particularly children who face a future of bleakness because of their disabilities.
“We will keep fighting till we win for disabled, vets,” Kerry tweeted after the vote.
It was a clear disappointment for the senior senator from Massachusetts who pushed the bill as an extension of the work of the late Senator Edward Kennedy, a champion for expanding rights for the disabled and a co-sponsor of the landmark Americans With Disabilities Act, which served as a model for the treaty.
“This is not about politics, it is not about ideology,” Kerry said on the Senate floor before the vote. “It’s about people.”
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The treaty had already been approved by the European Union and 125 countries, including China and Russia.
Eight Republicans, including Senator Scott Brown of Massachusetts, and the Senate’s two independents joined Democrats in voting 61-38 in favor of ratification. The Constitution requires a two-thirds majority of the Senate for a treaty to be ratified.
Proponents argued that the treaty would help further advance rights for the disabled, including Americans already protected by the landmark anti-discrimination law but who, under the treaty, would benefit from barriers falling across the world.
The treaty was supported by President George W. Bush, who helped negotiate it and whose father, President George H. Bush, signed the ADA into law in 1990. The United States became a signatory to the treaty in 2009 under President Obama, a move signaling the country’s intent to ratify the agreement.
Former Senate Majority Leader Bob Dole, looking frail and requiring a wheelchair, returned to the chamber on Tuesday in a symbolic show of support for the treaty.
Senator John McCain, a Republican from Arizona and staunch supporter of the treaty, read from a letter written by Dole.
But McCain’s fellow Republican from Arizona, Senator Jon Kyl, helped defeat the bill.
“Just as with many treaties before this one, the CRPD would offer cover to regimes that have no intention of actually helping their citizens, while needlessly tying the hands of countries like the United States that have actually made great strides in this area,” Kyl said in a floor speech.
Kyl said the treaty would be toothless in forcing countries to adopt measures that would reduce the physical barriers that keep the disabled from having the same access to public facilities as able-bodied people.
Last week, former Senator Rick Santorum convened a news conference to take issue with wording in the treaty alluding to reproductive rights, which some conservatives take as code for abortion. Santorum and other opponents say the treaty risked the usurping of US sovereignty and the rights of parents with disabled children.
In a statement released by his office after the vote, Kerry called the vote one of the saddest in his 28 years in the Senate, “a wakeup call about a broken institution that’s letting down the American people.”
“Today the dysfunction hurt veterans and the disabled, and that’s unacceptable. This treaty was supported by every veterans group in America and Bob Dole made an inspiring and courageous personal journey back to the Senate to fight for it,” Kerry said.
Veterans, many maimed in combat, joined business groups, advocates for the disabled, and a few high-profile Republicans in attempting to change enough minds among a solid bloc of GOP members who thwarted passage of the bill because of concerns over abortion, US sovereignty, and timing.
“I could not sleep tonight if I were one of the senators who did not vote for this today,” said Steve Rothstein, president of the Perkins School for the Blind in Watertown, which is working in 67 countries to better the lives of the blind by building schools, training teachers, and advocating for civil rights of the sight-impaired. Some 4.5 million children worldwide, he said, don’t go to school because they are blind.
“It’s embarrassment for our country, which has been such a leader in disability rights,” Rothstein added. “Many counties don’t believe in the value of all human beings.”
Rhonda Neuhaus, who was born without legs, wept as the vote was tallied. “I’m angry, and I’m very sad,” said Neuhaus, who attended Brandeis University and is now a policy analyst at the Washington-based Disability Rights Education and Defense Fund.
“Today, the irrational and outrageous opposition of a bloc of Republican senators denied Senate ratification of the CRPD, betraying the US’s historic role as a global leader in fighting discrimination and opening doors of opportunity for people with disabilities,” said Wade Henderson, president of the Leadership Conference on Civil and Human Rights.

Paralympist Muffy Davis on dreams and being your very best


A ski accident changed Muffy Davis’ life, but it didn’t derail her Olympic dreams. She brought home three gold medals in the summer London Paralympics, and now she’s a role model for everyone to do their very best, as well as for those with disabilities — and with dreams. Those are lessons she wants to teach her daughter, Elle, 4, and the rest of the world. “Your body may be broken, but who you are is whole and shines — and to share that and give that inspiration and hope.”
Katherine Jones — Katherine Jones / Idaho Statesma

























She rolls her wheelchair into a room.
She says: “Instantly, the people who don’t know me, the first thing that comes across their minds is what I can’t do.
“And that’s what I’m trying to change.”
Muffy Davis reaches behind her wheelchair and pulls out a nondescript black pack. Nestled in the bag is a collection of medals: bronze, silver and gold. Each medal has a certain heft to it; none more so than the gold. Especially the gold. It has a certain — presence.
The medals don’t stay in the bag, nor do they reside in a safety deposit box. When she speaks to groups of schoolchildren, she brings them all along and passes them around, one at a time.
“I want people to wear them, to know what it feels like. … That’s the value for me … sharing (them), letting people feel the power of the medal.
“And then going and finding their own (dream).”
When Muffy was an 8-year-old skier in Sun Valley, she was already planning her Olympic future. And while the medals she now holds originate in that childhood determination, her path ended up being far different than what she imagined.
“I was an Olympic hopeful, but I am a Paralympic medalist. Who knows if I would have made it to the Olympics? I was a hopeful; it might not have happened. But I know what I am now: I am a Paralympic gold medalist.”
In her teens, Muffy was on the U.S. Development ski team, about to be named to the U.S. Ski Team (along with teammate Picabo Street). But that all changed when she was 16, on a curve at 50 mph, during a routine training run.
“You often wonder what you would have been, but I have a great life. I’ve done everything I’ve ever wanted to do — and more than I ever thought I would do.”
The first tree she hit crushed her spine. The second tree shattered her helmet. In the hospital, when doctors asked her to wiggle her toes, she couldn’t.
“I have been blessed that I never had to change my dreams or my goals because of my disability. ... Sports is a passion in my life. That was my first initial fear when I had my accident. … I learned that was an unfounded fear, and I can still do everything I love.”
Muffy, 39, is paralyzed from the middle of her ribs down. After the crash, she channeled her competitive energy into therapy. She laughs, remembering how she’d turn physical therapy into a race — like her three-minute “9-yard dash” in braces. Convinced she would walk again, initially, she declined the idea of adaptive skiing.
But then it snowed, and, frankly, she missed Baldy, Sun Valley’s ski mountain.
“On the mountain, I was free; on the mountain, I was whole. … (The mountain) became where my life changed — and I knew that someday it would become my freedom again. It was just figuring out how to get there.”
Muffy is an ambassador for Disabled Sports USA. Their motto is, “If I can do this, I can do anything.”
“That’s the way I feel sports have been for me. After my accident, getting back on the slopes was like, ‘Oh. I can still ski. Oh. Well then, I can go to school.’ It’s so empowering, using sports throughout life for what is possible, for what do you want to do. Don’t limit yourself.”
So Muffy skied again. “I had unfinished business,” she says now. In 1998, she took bronze at the Paralympic Winter Games in Nagano, Japan, riding a monoski. She won gold in the 2000 world championships, three silver medals in the 2002 Paralympic Winter Games in Salt Lake City, where she now lives, and then she retired.
“I thought I was done. The competition, the skiing — it couldn’t get any better. I competed in my home country, I got on the podium three times. I had a wonderful ski racing career, from able-bodied through adaptive.”
Always active, Muffy met the man who would become her husband on a rafting trip down the Grand Canyon. She and Jeff Burley, a recreation therapist for adaptive sports, were married in 2004, and in 2008, their daughter Elle was born. To keep in shape after her pregnancy, Muffy took up handcycling.
The sport is so new that when Muffy was injured 23 years ago, adaptive mountain bikes and handcycles didn’t exist. On her bike, Muffy lies on her back — an aerodynamic position — and pedals with her arms. She describes it as “a street luge with gears.”
“I love — love — riding. I love handcycling, almost more than skiing, which seems taboo (to say). I feel like I am the athlete I was before my accident. …
“Most of it is how hard can you crank, how hard can you get in that ‘pain cave.’ … I wouldn’t say I like the pain cave, but I like knowing I can push myself hard and push myself through that pain.
“I know (the pain) will end — dig deep. How hard can you dig, how long can you hurt? And that’s when you’re going to win.”
Driven athlete that she is, she set goals. She entered races, she went to a camp; on a whim, she competed in nationals — and won. The sport is so new that the field wasn’t deep, she says, but that win placed her on the U.S. World Championship team. In the world championships, Muffy got three silver medals.
“Once I knew I was competitive internationally, everything kind of changed.”
Going for the Paralympics again — competing on such an elite level — meant a serious, full-time commitment, a decision that, this time, affected more than her.
“You’ll never make the Paralympics or Olympics unless it’s a 100 percent commitment. And that means a sacrifice for everyone, the whole family. … So we went for it.
“It was a team. … That’s why we joke (that) I got three medals: one for me, one for Jeff, one for Elle.”
Three golds in London: in the handcycle time trial, road race and handcycle relay.
“I used to say ‘God made me to be a ski racer.’ Just this last year, I re-edited that. Now I say, ‘God made me to be a competitor.’ That’s where I am fully Muffy — when I’m in the starting gate or on that field to play, or pushing myself to be my best in athletics. That’s where I’m really me, 100 percent.”
(The full story continued in link below)

Read more here: http://www.idahostatesman.com/2012/10/21/2317891/light-lineywhat-are-your-dreams.html#wgt=rcntnews#storylink=cpy


Read more here: http://www.idahostatesman.com/2012/10/21/2317891/light-lineywhat-are-your-dreams.html#wgt=rcntnews#storylink=cpy

When Muffy was an 8-year-old skier in Sun Valley, she was already planning her Olympic future. And while the medals she now holds originate in that childhood determination, her path ended up being far different than what she imagined.
“I was an Olympic hopeful, but I am a Paralympic medalist. Who knows if I would have made it to the Olympics? I was a hopeful; it might not have happened. But I know what I am now: I am a Paralympic gold medalist.”
In her teens, Muffy was on the U.S. Development ski team, about to be named to the U.S. Ski Team (along with teammate Picabo Street). But that all changed when she was 16, on a curve at 50 mph, during a routine training run.
“You often wonder what you would have been, but I have a great life. I’ve done everything I’ve ever wanted to do — and more than I ever thought I would do.”
The first tree she hit crushed her spine. The second tree shattered her helmet. In the hospital, when doctors asked her to wiggle her toes, she couldn’t.
“I have been blessed that I never had to change my dreams or my goals because of my disability. ... Sports is a passion in my life. That was my first initial fear when I had my accident. … I learned that was an unfounded fear, and I can still do everything I love.”
Muffy, 39, is paralyzed from the middle of her ribs down. After the crash, she channeled her competitive energy into therapy. She laughs, remembering how she’d turn physical therapy into a race — like her three-minute “9-yard dash” in braces. Convinced she would walk again, initially, she declined the idea of adaptive skiing.
But then it snowed, and, frankly, she missed Baldy, Sun Valley’s ski mountain.
“On the mountain, I was free; on the mountain, I was whole. … (The mountain) became where my life changed — and I knew that someday it would become my freedom again. It was just figuring out how to get there.”
Muffy is an ambassador for Disabled Sports USA. Their motto is, “If I can do this, I can do anything.”
“That’s the way I feel sports have been for me. After my accident, getting back on the slopes was like, ‘Oh. I can still ski. Oh. Well then, I can go to school.’ It’s so empowering, using sports throughout life for what is possible, for what do you want to do. Don’t limit yourself.”
So Muffy skied again. “I had unfinished business,” she says now. In 1998, she took bronze at the Paralympic Winter Games in Nagano, Japan, riding a monoski. She won gold in the 2000 world championships, three silver medals in the 2002 Paralympic Winter Games in Salt Lake City, where she now lives, and then she retired.
“I thought I was done. The competition, the skiing — it couldn’t get any better. I competed in my home country, I got on the podium three times. I had a wonderful ski racing career, from able-bodied through adaptive.”
Always active, Muffy met the man who would become her husband on a rafting trip down the Grand Canyon. She and Jeff Burley, a recreation therapist for adaptive sports, were married in 2004, and in 2008, their daughter Elle was born. To keep in shape after her pregnancy, Muffy took up handcycling.
The sport is so new that when Muffy was injured 23 years ago, adaptive mountain bikes and handcycles didn’t exist. On her bike, Muffy lies on her back — an aerodynamic position — and pedals with her arms. She describes it as “a street luge with gears.”
“I love — love — riding. I love handcycling, almost more than skiing, which seems taboo (to say). I feel like I am the athlete I was before my accident. …
“Most of it is how hard can you crank, how hard can you get in that ‘pain cave.’ … I wouldn’t say I like the pain cave, but I like knowing I can push myself hard and push myself through that pain.
“I know (the pain) will end — dig deep. How hard can you dig, how long can you hurt? And that’s when you’re going to win.”
Driven athlete that she is, she set goals. She entered races, she went to a camp; on a whim, she competed in nationals — and won. The sport is so new that the field wasn’t deep, she says, but that win placed her on the U.S. World Championship team. In the world championships, Muffy got three silver medals.
“Once I knew I was competitive internationally, everything kind of changed.”
Going for the Paralympics again — competing on such an elite level — meant a serious, full-time commitment, a decision that, this time, affected more than her.
“You’ll never make the Paralympics or Olympics unless it’s a 100 percent commitment. And that means a sacrifice for everyone, the whole family. … So we went for it.
“It was a team. … That’s why we joke (that) I got three medals: one for me, one for Jeff, one for Elle.”
Three golds in London: in the handcycle time trial, road race and handcycle relay.
“I used to say ‘God made me to be a ski racer.’ Just this last year, I re-edited that. Now I say, ‘God made me to be a competitor.’ That’s where I am fully Muffy — when I’m in the starting gate or on that field to play, or pushing myself to be my best in athletics. That’s where I’m really me, 100 percent.”

Read more here: http://www.idahostatesman.com/2012/10/21/2317891/light-lineywhat-are-your-dreams.html#wgt=rcntnews#storylink=cpy
Read more here: http://www.idahostatesman.com/2012/10/21/2317891/light-lineywhat-are-your-dreams.html#wgt=rcntnews#storylink=cp
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Idaho Council on Developmental Disabilities

The Idaho Council on Developmental Disabilities is recruiting two new self-advocate members. We are looking for individuals with developmental disabilities who can bring a strong voice to the Council, understand the responsibilities of being a member, and know about the time commitment to prepare for and attend quarterly meetings. 
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Please go to the Council website at www.icdd.idaho.govfor more information about the Council and to download a Member application. All applicants must fill out the Council application and the Governor’s application. Completed applications should be sent to the Council office attention Tracy Warren.

Hoyer: Entitlement benefit cuts on the table in talks with GOP on 'fiscal cliff'


Entitlement cuts should remain on the table as party leaders seek to hash out an end-of-the-year budget deal, Rep. Steny Hoyer (D-Md.) said Tuesday.
A number of Democratic leaders — including Reps. Nancy Pelosi (Calif.), John Larson (Conn.) and Xavier Becerra (Calif.) — have said they would support some spending reductions in Medicare, but that cuts to direct benefits should not be a part of the negotiations. Along with Senate Majority Leader Harry Reid (D-Nev.), they also maintain that Social Security reform has no place at all in the "fiscal cliff" talks.
But Hoyer, the Democratic whip, warned that taking entitlement benefits off the table is a bad place to start the negotiations. Such entrenched positions are little different, he said, than the Republicans' refusal to consider hikes in tax rates — a central element of President Obama's deficit-reduction proposal.
Hoyer said GOP proposals to raise the Medicare eligibility age, make wealthier seniors pay higher Medicare rates and limit the cost-of-living increases for some federal programs are legitimate ones, even as he warned he might not support them.
“They clearly are on the table,” Hoyer said of the Medicare changes during his weekly press briefing in the Capitol. “They were on the table in the Boehner-Obama talks. They've been on the table for some period of time. That does not mean that I'd be prepared to adopt them now, but they're clearly, I think, on the table.”
Hoyer said the GOP's proposal to reduce the cost-of-living increases to certain federal programs – the so-called chained consumer price index (CPI) – should also be considered as part of the fiscal cliff talks.
“We have many Republicans say 'absolutely not' ... on [higher] rates or revenues,” he said. “There are Democrats on our side who say 'absolutely not' if they do A or they do B or they do C. … You've got to put everything on the table.”
CPI, a measure of inflation that attempts to gauge cost-of-living fluctuations, is used to index a number of government programs – including food stamps, federal pensions and determining tax brackets. But in the current deficit-reduction fight it's most often used in reference to Social Security payments.
Indeed, Senate Minority Leader Mitch McConnell (R-Ky.) last week urged that Social Security adopt the chained CPI formula.
“Those are the kinds of things that would get Republicans interested in new revenue,” McConnell told The Wall Street Journal.
Many Democrats have rejected the chained CPI for Social Security because it would reduce the cost-of-living increases under the popular seniors' program.
Hoyer's office said Tuesday that Hoyer's support for having chained CPI on the table was not a reference to Social Security, which they say he wants on “a separate track.” 



People With Disabilities, and Reaching the Federal Poverty Level.

SSI, People With Disabilities, and Reaching the Federal Poverty Level. Information Bulletin #366 (11/2012). Supplemental Security Income (SSI) is basically a federal program for people who are disabled (and older Americans). As of 2011, there were about 6.7 million people with disabilities who received SSI (another 1 million recipients were over 65). These people are the poorest of all the disabled people in the country. Most of them do not qualify for either Social Security or Medicare; some receive both SSI and Social Security, but combined only to the SSI level. Throughout the recent election campaign and well before that, there has been virtually no discussion, mention or let alone a moral outrage addressing a basic minimal, basic, livable support for people who struggle to survive on SSI. The current monthly federal SSI grant is $698 a month ($8,376 annually) for a single person and for a couple it’s $1,086 a month ($13,032 annually). SSI eligibility automatically triggers Medicaid eligibility. States have the option to provide a State Supplement to the federal SSI grant. Of the 6.7 million people with disabilities who somehow survive on SSI, only 1.6 million, who live in the community, receive a State Supplement. By and large, most States supplement SSI for persons who reside in personal care homes, Medicaid facilities, nursing homes, and other institutions – but not for people with disabilities who live independently in the community. The amount of institutional SSI State supplement is much higher than the SSI State supplement to live independently in the community. Hmmm. Sounds like another institutional bias, contrary to ADA’s “the most integrated setting” a la Olmstead. Let’s put the monthly federal SSI sums in some perspective. The federal poverty level is $10,890 for a single person and $14,710 for a couple, compared to the SSI federal $8,376 and $13,032 respectively. As inadequate as the federal poverty level is, it should be the bottom benchmark! For people with disabilities who must survive on SSI, they live on 75% of the federal poverty level for a single person and 83% of the FPL for a couple. This gap has been approximately the same for the last ten years. For those persons who reside in the community on SSI, to reach just the federal poverty level, the federal SSI grant (or a State supplement) would have to increase by $209 a month for a single person and $140 for a couple. Other than Alaska, no State provides that amount of a State Supplement for single persons with a disability who reside independently in the community. Only five States provide more than $140 a month for a couple. We all know how extremely difficult it is for a SSI recipient who is disabled to find a place to live that they can afford. The “2010 Priced Out” Report clearly demonstrated how the housing market overwhelmingly trumps the SSI grant. What advocates could do: 1. This is a federal issue. We do not believe any States will voluntarily increase their SSI State Supplements so people could afford to live healthy and safe lives independently in the community. 2. We need to make this a moral issue! It’s an outrage that the poorest disabled and elderly Americans are totally ignored and forgotten. 3. SSI cuts across all disability categories and the elderly. Therefore, increasing SSI is a great unifying and organizing issue. 4. Increasing the federal SSI amount even to the extremely inadequate federal poverty level is an economic stimulus on both a federal and State levels. People on SSI spend their entire grants just to survive, putting their entire grants into the economy. These are federal allocations well spent! 5. Where is the White House on this issue? Call the White House Domestic Policy, (202) 456-5594, and let them know. 6. Where are your U.S. Senators and House of Representatives who claim to represent and care about persons with disabilities and the elderly? Call them. Steve Gold, The Disability Odyssey continues Back issues of other Information Bulletins are available online at http://www.stevegoldada.com with a searchable Archive at this site divided into different subjects. Information Bulletins will also be posted on my blog located at http://stevegoldada.blogspot.com/ To contact Steve Gold directly, write to stevegoldada1@gmail.com or call 215-627-7100. Ext 227.

The Autism NOW Answer Series #1

Risk Management Consultation


Labor & Industries Risk Management Consultants can help you protect your employees and your profits.
What business risks do you face? How do you manage them? Do you know the connection between workplace safety and cost control? What would you do if one of your employees filed a workers’ comp claim?
Risk Managers can:
  • Show you why workplace safety makes good business sense.
  • Provide data and analysis specific to your business that shows how claims can affect the premiums you pay.
  • Discuss your “claim-free discount” and steps you can take to protect it.
  • Show you the cost/benefit of claim management strategies .
  • Identify return-to-work options and resources so you can return your injured employee to productive work sooner.
  • Review best practices in hiring strategies and procedures.

American Girl Dolls Embrace Differences and Disabilities


ht american doll hearing aid nt 121128 main American Girl Dolls Embrace Differences and Disabilities
I must admit, I find American Girl Dolls slightly unnerving. They are so eerily lifelike, and I know it’s a cliché, but the eyes really do follow you everywhere. My daughter has one, and we put it in the closet every night because mommy is a little crazy.
Despite these misgivings, it’s hard not to cheer for a doll company that goes out of its way to represent girls from all walks of life and every circumstance. The new Special Sparkle section in its  holiday catalog includes a miniature service dog in harness, a hearing aid and an allergy-free lunch kit.
“We have a long history of speaking to diversity and making girls feel good about themselves, and this is just another way we are expanding on the idea,” said American Girl Doll spokeswoman  Julie Parks.
Whereas many dolls from high-end companies resemble a stereotypical beauty unattainable for most little girls, American Girl has always seemed to strive for all-inclusiveness. The dolls come in a vast selection of skin tones, hair color and eye color, which can be mixed and matched so the doll resembles its owner. Now they can also be fitted with glasses, braces for the teeth, crutches or a wheel chair, and the company recently began to offer dolls without hair to represent those who have lost hair to cancer.
American Girl books and movies also do a good job of highlighting problems girls are likely to encounter in life. This year’s “Doll of the Year” McKenna is a talented gymnast who struggles with injuries and a learning disability. In the book and movie about her experiences, Jesse, her brainy friend and tutor, is confined to a wheel chair.
 Dr. Ari Brown, a developmental pediatrician in Austin, Texas, applauds American Girl’s mission of highlighting differences and a message of acceptance.
 ”I think it’s great American Girl tries to have dolls that have the same hodgepodge of traits and features you actually see in kids,” Brown said.
Brown said she also believes playing with a doll that uses a hearing aid,  requires a special diet or depends on a service dog can be an enriching experience for all girls, even if they themselves don’t have special needs.
“It can help kids learn to be more accepting of others who are different from them,” she said.
Perhaps because acceptance  for all is part of American Girl’s  mission, it has been more successful than other toy makers that have  attempted to make dolls with disabilities. Barbie’s wheelchair-bound friend, Share a Smile Becky, is a notable example. Even consumers who overlooked the condescending name couldn’t forgive the fact that Becky’s chair didn’t fit into the Barbie Dream House elevator.
Girl Power aside, all this diversity might have a limited reach. The price tag for a doll is $105, and from there the cash register never seems to stop ringing. The wheel chair costs $38, the hearing aid $9 and the allergy-free lunch bag $28.  Let’s not even mention the hair styling, ear piercing and tea parties.
Yet in spite of the steep cost of ownership, Parks said feedback has been overwhelmingly positive for the dolls in general and the new disability accessories in particular.
“Parents realize they are investing in something that builds strong character and helps every girl reach their full potential, no matter who they are or what they look like,” she said. “It’s all about engaging them in positive experiences and helping them fit in.”


Tuesday, November 20, 2012

Getting Your Federal Benefits by Check?


Don't Delay! Go Direct Today!

By March 1, 2013, everyone getting the following federal benefits by paper check is required to switch to electronic payments – direct deposit to a bank or credit union account or to the Direct Express® Debit MasterCard® card:
  • Social Security
  • Supplemental Security Income
  • Veterans Affairs
  • Railroad Retirement Board
  • Office of Personnel Management
  • Department of Labor (Black Lung)
Don't wait until time runs out. Learn more about this change. For additional information, visitwww.fms.treas.gov
Think electronic payments are at risk of cybercrime? Get the facts about electronic payments.

Want direct deposit?

It's fast and easy to get direct deposit of your benefits right into your checking or savings account.
GoDirect: Get Direct Deposit

You also can call (800) 333-1795 or visit your bank or credit union.

With direct deposit, the U.S. Treasury sends an electronic message to your bank or credit union crediting your account with the exact amount of your benefit. The difference is, your check isn’t printed or mailed.

If you don’t already have a bank account or you are not sure you can get a bank account, you might like to try a Treasury-sponsored ETA account. Learn more about an ETA account.

Prefer a prepaid debit card?

No bank account or credit check is required for theDirect Express® card, a Treasury-recommended prepaid debit card.
Prefer a prepaid debit card? DIRECT EXPRESS >® SIGN UP for the Direct Express ® card

You also can call toll-free (800) 333-1795 or contact the local office of the agency providing your federal benefits, such as the Social Security Administration or Department of Veterans Affairs.Learn more about the card’s fees and features. Have questions about how to use the card?  Learn more.

Medicare Extends Enrollment Period For Those Affected By Sandy


By Susan Jaffe
NOVEMBER 8TH, 2012, 1:18 PM
Medicare beneficiaries battered by Superstorm Sandy have one less problem to worry about: Federal officials have extended the Dec. 7 deadline to enroll in a private medical or drug plan for next year for those still coping with storm damage.
The Centers for Medicare & Medicaid Services “understands that many Medicare beneficiaries have been affected by this disaster and wants to ensure that all beneficiaries are able to compare their options and make enrollment choices for 2013,” Arrah Tabe-Bedward, acting director for the Medicare Enrollment and Appeals Group, wrote in a Nov. 7 letter to health insurance companies and State Health Insurance Assistance Programs.
Beneficiaries hit by the storm can still enroll after the midnight Dec. 7 deadline if they call Medicare’s 24-hour information line,1- 800-Medicare (1-800-633-4227).  Representatives will be able to review available plans and complete the enrollment process over the phone.
“We are committed to giving people with Medicare the information and the time they need to make important decisions about their coverage,” Medicare spokeswoman Isabella Leung said in an e-mail.  Medicare officials have not set a new deadline but have encouraged beneficiaries to make their decisions soon if possible.
Seniors currently in a plan will be automatically re-enrolled for next year in the same plan.
The extra time also applies to any beneficiaries who normally get help from family members or others to sort through dozens of plans but who have been unable to do so this year because they live in storm-ravaged areas.  Neither beneficiaries nor those who provide them assistance will be required to prove that they experienced storm damage.
“This is a really important recognition by CMS to accommodate Medicare enrollees affected by Hurricane Sandy,” said Leslie Fried, director for policy and programs at the National Council on Aging, a Washington, D.C., advocacy group.
In the aftermath of Hurricane Sandy, the Obama administration declared Connecticut, New Jersey, New York and Rhode Island as “major disaster areas,” according to the U.S. Federal Emergency Management Agency.  In addition, FEMA issued emergency declarations for parts of Delaware, the District of Columbia, Maryland, Massachusetts, New Hampshire, Pennsylvania, Virginia and West Virginia.
More than 4 million seniors in those states are enrolled in drugs-only plans and more than 2.8 million have Medicare Advantage policies, which includes medical and drug coverage.
Susan Jaffe can be reached at Jaffe.KHN@gmail.com
This post has been corrected.  Earlier versions mistakenly said coverage for those who do not enroll in a 2013 plan would expire at the end of the year. CMS says instead that seniors already in a plan will be automatically re-enrolled for next year in the same plan.

Just Launched!: 2012 Survey on Emergency Communications and People with Disabilities


While data collection is underway for the Survey of User Needs, the Wireless RERC's Consumer Research Team has also just launched a new survey on emergency communications.
Emergency communications generally include two main components: 1) contacting emergency response services (911 services) for help, and 2) receiving public emergency alerts for events like severe weather and other natural events, amber alerts for missing children, and other emergencies.
Some of you will remember that we conducted this survey once before, almost two years ago. Because the technology is changing so rapidly and new government rules are being implemented, we think it's the right time to conduct the survey again. The data will be of great interest to regulatory authorities and other professionals working to improve emergency response and disaster relief.
Consumers and industry colleagues, please feel free to distribute the link to the survey widely.  As an incentive for taking the survey, we will be giving away two $100 Amazon gift certificates to two lucky respondents.  Let your voice be heard!

LMI Launches New Program for College-enrolled Wounded Warriors


LMI announced the launch of the Wounded Warrior Fellowship Initiative, a new program for veterans with service-related disabilities who are now pursuing higher education. The program is designed to provide Wounded Warriors with skills they need for success in the civilian workforce and augment the abilities they gained during their military service.
“After reviewing our extensive support for veterans, we identified a gap in how Wounded Warriors are brought into the civilian workforce—veterans with service-related disabilities need exposure to critical skills that can help make their transition a successful one,” LMI President and CEO Nelson M. Ford said. “LMI proudly supports our nation’s Wounded Warriors and we hope this program, where our staff provides mentorship, direction, and work experience, can become a model for other organizations involved in this cause.”
The Wounded Warrior Fellowship Initiative is open to Wounded Warrior students who served post-September 11, 2001, and are now enrolled in accredited two- and four-year universities. The flexible program provides them with access to mentoring and workplace experience in public sector consulting, including data analysis, engineering, and information technology, as well as accounting, finance, human resources, security, and communications.
“Wounded Warriors have highly sought-after leadership abilities, interpersonal skills, and a passion to serve, all of which are critical to an organization like LMI,” said Lt. Gen. Rick Kelly, a veteran of the United States Marine Corps and the program’s senior advisor. “We are committed to helping them develop the unique skills required in a civilian business setting, and will provide a supportive, flexible environment that is attuned to their individual needs and in line with their professional goals. We just want them to be successful in their transition.”
The Wounded Warrior Fellowship Initiative is available at LMI’s McLean, Va., headquarters, along with LMI’s regional offices in San AntonioHuntsville, Ala., andSt. Louis.
For more information, visit www.lmi.org/wwfi.

About LMI

LMI is a government consulting firm committed to helping government leaders and managers reach decisions that make a difference. LMI draws on its 50 years of experience as a pioneer in logistics by applying an unmatched knowledge of people, processes, and assets to a variety of sectors, including defense, intelligence, healthcare, energy and environment, homeland security, and civil government. As a not-for-profit organization, LMI is a trusted advisor to the government—free from commercial or political bias and dedicated to the mission of advancing government management.

Accessible Technology On-line Webinar Series*


All Sessions are scheduled from 1:00-2:30 p.m. (90 minute sessions) Central Time Zone(CT). The program is available in the following formats:
  • Streaming Audio via Blackboard Collaborate webinar platform
  • Real-time Captioning via Blackboard Collaborate webinar platform
  • A telephone option is available by calling the toll number. NOTE: You will incur charges for telephone access based on your telephone provider.
All sessions will have a digital recording of the session archived on this site.

Continuing Education Credits/Certificates

A certificate of attendance is available upon request once actual attendance/participation is documented.

December 11, 2012 » Mobile Accessibility - The Status of Accessibility in Mobile Devices

David Dzumba, Chair of the Accessibility Working Group of the Mobile Manufacturer's Forum will take the lead in providing an insight into and perspective on the status of accessibility in mobile devices. David currently serves as the FCC Emergency Access Advisory Committee co-chair and is senior manager of Accessibility at Nokia.
 
Time:
1:00-2:30PM CT
Speaker:
Mobile Manufacturers' Forum
 

Digital tablets improve reading for people with vision disabilities


CHICAGO: People who have eye diseases that damage their central vision can regain the ability to read quickly and comfortably by using digital tablets, according to a recent study.
The research found that people with moderate vision disabilities could increase their reading speed by 15 words-per-minute, on average. Using a tablet with a back-lit screen resulted in the fastest reading speeds for all study participants, no matter what their level of visual acuity. The research is being presented today at the 116th Annual Meeting of the American Academy of Ophthalmology,jointly conducted this year with the Asia-Pacific Academy of Ophthalmology.
Loss of central vision affects millions of people who have eye diseases such as macular degeneration  or diabetic retinopathy, which damage the light-sensitive cells of the eye’s retina. The retina relays images to the optic nerve, which transmits them to the brain. When treatments such as eyeglasses, medications, or surgery are no longer effective, ophthalmologists – eye medical doctors and surgeons – help patients maximize their remaining sight by using low-vision aids. Before digital tablets came along, reading aids were limited to lighted magnifiers, which are cumbersome and inconvenient by comparison.
In the study, which was conducted at Robert Wood Johnson Medical School in New Jersey, researchers found that all of the 100 participants gained at least 42 words-per-minute (WPM) when using the iPad™ tablet on the 18-point font setting, compared with reading a print book or newspaper. A more modest gain of 12 WPM, on average, was achieved by all subjects when using the Kindle™ tablet set to 18-point font. Patients with the poorest vision – defined as 20/40 or worse in both eyes – showed the most improvement in speed when using an iPad or Kindle, compared with print.
The researchers believe the iPad’s back-illuminated screen is the key to the significantly improved reading speed achieved by patients with moderate vision disability. The vision factor involved is called contrast sensitivity, which means being able see an object as separate and distinct from its background and to discern shades of gray. Loss of contrast sensitivity is common in people with low vision. The high word/background contrast provided by a back-lit screen is a big plus for such patients. The original Kindle, which was used in this study, does not have a back-lit screen.
The study also assessed low vision patients’ comfort while reading and found that their preferred mode was linked to their degree of vision loss. People with the worst vision found the iPad most comfortable, while those with the best vision preferred print. This information will be useful to ophthalmologists in advising patients with various degrees of vision loss.
“Reading is a simple pleasure that we often take for granted until vision disability makes it difficult,” said Daniel Roth, M.D., an associate clinical professor at Robert Wood Johnson School of Medicine who led of the study. “Our findings show that at a relatively low cost, digital tablets can improve the lives of people with vision disabilities and help them reconnect with the larger world.”
The 116 Annual Meeting of the American Academy of Ophthalmology is in session November 10-13 at McCormick Place in Chicago. It is the world’s largest, most comprehensive ophthalmic education conference. More than 25,000 attendees and 500 companies gather each year to showcase the latest in ophthalmic education, research, clinical developments, technology, products and services. This year’s meeting is being held jointly with the Asia-Pacific Academy of Ophthalmology.
For more information, visit www.aao.org or  www.geteyesmart.org

HEALTH DISPARITIES RESEARCH AT THE INTERSECTION OF RACE, ETHNICITY, AND DISABILITY: A NATIONAL CONFERENCE


CONFERENCE PURPOSE

The conference is intended to bring together researchers, advocates, and policy makers in racial and ethnic disparities and disability-related disparities to:
  • Learn about barriers to health care and health promotion for people with disabilities in underserved racial and ethnic groups
  • Share your own work on health disparities at this intersection
  • Discuss priorities for future research and action

CONFERENCE ORGANIZERS

The conference is part of Project Intersect: Addressing Health Disparities at the Intersection of Race, Ethnicity, and Disability.  Project Intersect is based in the Institute on Development & Disability at Oregon Health & Science University.  Project partners include: ·        
  • Project Intersect Advisory Council – A national group of adults with disabilities and family members of adults with disabilities who are members of underserved racial and ethnic groups       
  • The National Center for Cultural Competence at Georgetown University   
  • The Department of Disability and Human Development at the University of Illinois – Chicago
  • USC UCEDD, University California and Childrens Hospital Los Angeles  
  • The Institute for Disability Studies at the University of Southern Mississippi 
  • Jana Peterson-Besse, MPH, PhD – Dr. Peterson-Besse is a researcher and teacher in public health, disability, health disparities, and social determinants of health


HOTEL INFORMATION

The conference will be held at the
Hyatt Regency Washington on Capital HillPlease check back once we open up the reservation process
 to ensure you get the conference rate for your stay. 

Check back soon for registration and additional conference details!

For questions please click here