CALL FOR EXHIBITORS

Across the Lifespan Conference

CHULA VISTA RESORT

Wisconsin Dells, WI

December 3-4, 2015

Building on the great success of last years exciting co-conference, Wistech, Wisconsin AHEAD, WI Department of Health Services and the Stout Vocational Rehab Institute have again collaborated to provide a dynamic, affordable conference in December 2015.

Across the Lifespan Bringing the Best Together seeks exhibitors for this years conference. The Call for exhibitors opens up on March 16th!

Our attendees represent roles in the field of assistive technology, education, rehabilitation, community living, students, consumers and families. Your participation as an exhibitor ensures that the conference attendees will experience the latest technology, information and resources.

The conference will feature the following presentation topics:

• Assistive Technology
• Post-Secondary Disability Services
• Transition Services
• Employment Universal Design
• Special Education
• Independent living, recreation/leisure

The exhibition hall will be open to attendees on Thursday 12/3/15 from 8:00am- 6:00pm and Friday 12/4/15 from 8:00am-11:30am. We ask that exhibitors be set up and ready to go by 8:00am on December 3rd in order to participate in the Conference Welcome

Exhibitor Registration deadline is November 30th.

Click herefor more information.

This is an interesting article inDisability Scoop written by Shaun Heasley about questionable SSI payments. A report suggests that a questionable $5 billion was paid out in 2014.. This is believed to be due to errors in reporting income.

SSI Flagged For Billions In Improper Spending

By Shaun Heasley

A federal program designed to aid people with disabilities doled out billions of dollars in improper payments last year alone, government investigators say.

The Government Accountability Office estimates the Supplemental Security Income program paid out some $5 billion in questionable spending during the 2014 fiscal year.

The finding comes in areportfrom the investigative arm of Congress this week outlining nearly $125 billion in suspect expenditures last year across 22 different federal agencies.

SSI was one of a dozen programs highlighted for having over a billion dollars in improper payments. In addition, Medicaid and Medicare were also among the programs flagged for large spending errors.

Government investigators attributed the improper SSI payments at least in part to errors or omissions in reported income or resources by recipients of the means-tested program.

Sean Brune, a senior advisor at the Social Security Administration which administers SSI, told a U.S. Senate panel this week that despite the level of improper payments GAO found, the vast majority of benefits the agency administers are handled correctly.

Let me make clear that while we work diligently to correct and pursue them, improper payments do not equate with fraud. Improper payments can occur for a number of reasons, some of which are outside the control of the beneficiary or the agency, Brune said.

Source: http://www.disabilityscoop.com/2015/03/18/ssi-flagged-improper-spending/20143/

An article inDisability Scoopwritten by Michelle Diament about how Virginia became the first state to approve legislation related to the ABLE Act. Again, we haven't heard of action on it in Wisconsin yet, but hopefully soon we will.

ABLE Accounts Get Green Light In First State

By Michelle Diament

Three months after federal law established a new way for people with disabilities to save without jeopardizing their government benefits, the legislative hurdles are over in one state.

Virginia became the first state to approve legislation related to the Achieving a Better Life Experience, or ABLE, Act, when Gov. Terry McAuliffe signed a bill this week allowing for the new savings vehicle.

Under federal law, the ABLE Actallowspeople with disabilities to open special accounts where they can save up to $100,000 without risking eligibility for Social Security and other government programs. However, states must put regulations in place before financial institutions can begin offering the accounts.

In addition to Virginia, legislatures in West Virginia and Utah have sent ABLE bills to their governors. Whats more, legislation is under consideration in 29 other states and draft bills are in the works in another seven, according to Heather Sachs, director of state government affairs for the National Down Syndrome Society.

Sachs said there is special significance in the fact that Virginia was the first to approve the ABLE Act since the idea for the bill was born out of a kitchen-table conversation among a group of parents in the state.

So far weve seen a lot of legislative victories and we expect more as the weeks go by, Sachs said.

Even after legislation is approved, however, state governments and the financial industry are likely to need time to set up the new offerings before they are available to consumers and some states are further along than others in hammering out the behind-the-scenes details. Accordingly, advocates say, the first states to enact ABLE legislation may not be the first to offer accounts.

Sachs said she expects it will be at least late this year but more likely 2016 or 2017 before people with disabilities can begin opening ABLE accounts.

Currently, ABLE legislation is under consideration in Alabama, Arkansas, California, Connecticut, Florida, Hawaii, Illinois, Iowa, Kansas, Kentucky, Maryland, Massachusetts, Minnesota, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Dakota, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Vermont and Washington.

Source: http://www.disabilityscoop.com/2015/03/19/able-green-light-state/20145/

A great article in the Madison Magazinewritten by Maggie Ginsberg about how Madison is becoming more accessible and inclusive for people with disabilities. It's a bit long, but it does a good job of explaining that while lots of work still needs to be done, things are improving.

How do people with disabilities experience Madison?

Madison is becoming a more accessible and inclusive city, advocates say

By Maggie Ginsberg

Jane Earl is supposed to meet me at a west side coffee shop, but the brittle winter sky has broken into sleet, so its too dangerous and I have to come to her. Earl has muscular dystrophy and shes in a power scooter, which is usually not the first (or even the second or third) thing shell tell you about herself, because she never knows how it will color your perception of her, what assumptions youll make, what conclusions youll draw. Today she doesnt have a choice about disclosureI already know this pivotal thing about her; its why Im here. And it works out kind of perfectly anyway, because I can see, firsthand, just how inaccessible almost everything can be.

I plug the meter and jay-dart across the street to her downtown high-rise, pull the heavy front door against the usual vacuum and slide inside where its warm and dry. Ive already texted her that Im here, but now I press the buzzer and wait, probably three or four minutes, for her to make her way downstairs from the tenth floor. She motors up in an elegant burst of colorbright apple-green top, coral scarf wrapped around her slim neckand flashes me a dazzling smile. After decades of high-profile positions all over the country in both the corporate and nonprofit worlds, she knows by now how to make an entrance.

Earl shares a cozy, modest two-bedroom condo with her husband, former Wisconsin governor Tony Earl. She tells me they spent megabucks fixing it up with accommodations for her disability, but they have less control over the accessibility of the rest of the sixteen-floor, 174-unit building. Like her seemingly rock star parking space, for example, in the adjacent indoor garage. After the lengthy elevator ride upstairs but before heading down the long highway to Earls unit, we stop so she can show me her parking dilemma. Each floor of the building has a set of doors that lead directly out to the parking structure, and Earls got the handicapped stall right next to the doors on her floor. But it might as well be miles away.

This is classic, she says, in the ramp, next to her carnow retrofitted with a lift for her scooter so she can travel without assistanceas we contemplate getting back into the building. The door between the garage and the condo is not automated. Its a door like anystandard steel, very heavy, with a slim silver handle you pull to open. I see now what I wouldnt have seen before, even though Ive just walked right through it: its pretty much impossible for someone in a chair to open the door.

Earls got a system, though, one shes been forced to develop after a lot of trial and error: Using the controller on the right side of her chair, she drives up to where, if she positions the chair at precisely the right angle and leans her body forward, she can just reach the door handle with about an inch of clearance between the base of her chair and the foot of the door. Then, with several forwards and reverses, she uses the power of the chair to slowly pull the door open.

As I watch her navigate this aggravating ritualand Im not proud to admit thisI grow increasingly uncomfortable. Its taking everything in me to resist the urge to reach out, just grab the door, and yank it open for her. She finally manages to get the thing propped open just enough to wedge herself inside it, fashioning a doorstop out of her right leg, then gives one last quick pull, lets go and quickly motors forward. And I unclench, until I see our reward: a second non-accessible door. And so the excruciating process is repeated, this time in an even tighter space. (In the early days, while attempting to make it through this second door, Earl powered straight into the wall on the other side, resulting in smashed drywall, an expensive, out-of-pocket repair, and more than a little embarrassment and frustration.)

Technically, because of the elevator and the power doors at the front entrance (automated only for those who have a special key fob, for which Earl had to pay $50), this building is legally accessible. Although Jane is not the only tenant in a wheelchair or scooter, the condo association has understandably voted down the $44,000 it would cost to automate the parking garage doors on all sixteen floors (Jane says shed be satisfied with just one door, on any floor, which she conjectures would cost significantly less in return for immeasurably higher property value). Their solution is for Jane to take the elevator down to the front entrance, exit the front door, travel down the sidewalk and around to the parking garage entrance, drive her scooter all the way up the ramp to her floor, and retrieve her car from her parking spot next to the door. On most days, thats an inconvenience very few of us would tolerate. On icy days like today, its a dangerous risk she cant afford to take.

I am a strong-willed person. Im a confident person, says sixty-two-year-old Earl, who was diagnosed with this adult-onset, progressive disease in her mid-twenties, one week before her wedding to her first husband, when she went in for her marriage physical. Even as recently as four years ago, when she moved into Tonys condo, she did not yet need a scooter. And there still are daysand not very often, because I dont make a habit of feeling sorry for myselfbut there are days where the situation is so frustrating that it nearly brings me to tears.

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Earl has lived a lot of places, and admits Madison is actually pretty good in comparison. Our people are forward-thinking, kind, educated, well-meaning. Were sensitive to the virtues of diversity and inclusion. Our streets are relatively smooth, the crosswalks squawk clicks and warnings, the sidewalks have curb cutsalthough we forget this when it snows and we clear everything but them, making for treacherous, often impassable routes for people in wheelchairs as the rest of us tromp on, oblivious. We have a thick resource network of county and city agencies and private and grassroots advocacy groups delivering services and support to people with disabilities of all kinds. We have a public paratransit system, and flexible, progressive partnerships between school and local government for integrative classrooms and inclusive employment. We have entrepreneurs and innovators creating assistive technology. We have world-class healthcare, research and development facilities. And still, all over the city, every day, we have neighbors who cant even get through the door.

Both literally and figuratively, getting through that door is at the crux of most any conversation about disability rights. Universal access is a difficult thing to define, and the last thing anybody living with a disability wants is to be lumped in with everybody else. Earl happens to be one of the roughly four million Americans who will depend on a wheelchair or scooter for the rest of their days, but an estimated thirteen percent of us will temporarily use a wheelchair at some point in our lives, whether after injury or surgery, or the inevitable complications of just plain aging. Andthis is importantwhile people with conditions like muscular dystrophy, multiple sclerosis, cerebral palsy, ALS and spinal cord injuries may require wheelchairs and other accommodations, they certainly demand very different resources and support than those who have cognitive and developmental disabilities. And those two groups differ even further from those with visual or hearing impairments, or serious and persistent mental illness, or any number of other conditions on the long list of what constitutes disability. Were talking about a vast, broad, wildly diverse group of people here.

But for all the differences, there is a core common thread, according to the city of Madisons Jason Glozier: the othering effect. Its that thing that makes you different, sometimes isolated, maybe even invisible. And as painful and frustrating as that may be for people with disabilities, he says, its shortsighted to think theyre the only ones who suffer. What do the rest of us lose out on when we block or ignore the potential contributions of an entire segment of the population? When we, literally, dont let them in the door?

By losing that experience of people with disabilities, we lose the breadth of the experience of life, says Glozier, from his seat where weve met at a popular downtown coffee shop. The place is packed and, after wed zigzagged through the crowd and tightly clustered tables to snag a prime seat by the window, Glozier matter-of-factly points out how impossible that would have been, had either of us been in a chair. We dont think about the fact that stairs are a deterrent to people. We dont think about the fact that education isnt equal. We dont think about the fact that all these systems are designed to support people like you and me, and we keep designing systems just like that. But we all benefit from improvements that come from accommodating people with disability.

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Jason Glozier

Gloziers official title is disability rights and services program coordinator, housed in the citys Department of Civil Rights, which came about in 2006, after a somewhat controversial merger between Affirmative Action and Equal Opportunities. Up until now, the city has budgeted for these three services as separate entities, but the 2015 proposal indicates consolidation into a single Civil Rights entity to reflect the departments collaborative approach and broad mission to ensure the Citys employment and community activities are equitably undertaken. Maybe thats courting even more controversy, financially speaking. Or maybe its evidence of just how much Madison is expanding its views on what it means to be an accessible city for everyone.

On the surface, Gloziers job is to review all the city facilities, buildings and parks that go up in town, to make sure theyre adhering to accessibility laws, not just in letter, but in spirit. Its an important distinction, because he believes his real job is to ask us all to look at things a bit differently. Hes got an insiders perspective as a child of disability activist parents, ones who always foughtpeacefully, but very visiblyfor equity and integration for Gloziers brother, who has cerebral palsy. He knows from personal experience that just because a building like Earls appears to be accessible, it isnt, really, and that there are scenarios just like it unfolding all over the city. He knows there are very popular, very highly regarded restaurants in Madison that his friends in wheelchairs cant get inside, because buildings constructed before the Americans with Disabilities Act are not required to be accessible if doing so isnt readily achievable or costs an undue burden, according to the ADA. Or that a playgroundcritical to childhood development for all kidsmight actually inadvertently serve as yet another barrier. (Take that rubber chunk ground covering, for example. Accessible by legal standards and installed in parks across the country with the best of intentions, a little common sense tells us that its anything but easy to walk or wheel acrosshave you tried it lately?)

Its about building awareness capacity, because people arent aware of what theyre not aware of, says Glozier, and thats the thing: his peers already have these values of inclusion and diversity, its just that people simply dont understand disability until theyre affected by it. And even then, we tend to take an individualistic approachbut Glozier wants us to think as a community. He wants us to do more than the bare minimum (which is all that so many of our laws require) because our buildings and systems still exclude people unintentionally.

I could use the hammer of the law and say this is what you have to do, he says, but Ive found that building the bridge to what people value is the best way to start making some of this social change.

And its working. Glozier says hes been blown away by the many ways his peers have willingly gone above and beyond the letter of the law, from little improvements all over the city, to a brand-new, seven-thousand-square-foot, universally accessible playgroundthe first of its kind for city parksin the works for 2015 or 2016. Of course, funding is always an issue, but when basic things become commonplace, the cost is far less and the gains far greater. Glozier points to the citys most recent crown jewel, the Central Library, as an exquisite example of designing with accessibility in mind from the very start, so that you dont have to invest in expensive retrofits on existing buildings. Imagine what could happen, he says, if we built things the right waybuildings, systems, programs, housing, employment, education, social systems, everythingfrom the ground up? To do this, we all have to believe that were all in this together, that theres a very real benefit for all of us. Were not there yet, but Glozier is hopeful, particularly if we can start to look at people with disabilities as fully fledged citizens in a community empowered by their neighbors. His personal background makes it natural for him to see people with disabilities as entitled to this power, but thats not the way the rest of us are used to looking at things.

Its not the paradigm of disabilities that were framed with, says Glozier. Its most often the most disempowering thing that exists. And its usually framed in these aspects of pity and paternalism and fear.

Glozier also works on the citys Racial Equity and Social Justice Initiative, which brings us back to that collaboration idea within Civil Rights. Just as Madison has begun to come to grips with the way its been blatantly failing its people of colornot through outright racism, necessarily, but by privileged participation in systems that are inherently biasedso, too, can we start to see how we have rendered people with disabilities, at times, invisible. That same paradigm shift is necessary for people with disabilities, he says; it just hasnt fully happened yet. In some ways were miles ahead of where we were. In others, were breathtakingly behind, despite all these laws. Those with disabilities are the only people for whom its still legal to deny minimum wage, for example, which is nearly as unfathomable as not being able to get in a building. Nobody is inferring that race is a disability, thats utterly ridiculousbut the more subtle, multilayered, unintentional ways in which majority culture discriminates can be chillingly similar.

We ended the process of people of color going through the back door fifty years ago, says Glozier. Is that still a common practice that we have in the disability world? Absolutely.

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Part of the reason that some of this inclusion and integration stuff might still feel a little awkward is because its a relatively new concept. Up until thirty or forty years ago, when the deinstitutionalization movement started to unfold, we took care of people with disabilitiesparticularly developmental disabilitiesin segregated settings like group facilities and sheltered workshops. This idea of serving people in their homes, or in our schools, in our parks or in our workplaces, was sort of radical in your parents generation, possibly even in yours. The Americans with Disabilities Act, which not only prohibits discrimination based on disability but requires people and places to make reasonable accessibility accommodations, didnt even exist until 1990. And while a spate of other state and federal laws have been enacted to mandate and protect certain rights, of course you cant legislate shifts in perceptions or attitudes. You cant expect people to start seeing barriers for people with disabilities after lifetimes of not seeing people with disabilities at all.

Doug Hunt works for Dane County Human Services as the vocational services manager in the developmental disabilities unit, but he tells me his main job is to work on employment issues for adults with developmental disabilities. I ask him for a brief, local history and he tells me about Lou Brown, a UW professor in the Department of Rehabilitation Psychology and Special Education from 1969 to 2003, whom he credits as a pioneer in developing models that could prepare students with disabilities to integrate fully into society. He says parent advocates then led the charge to not only get support in schools for their kids, but to enlist the school district and Dane County in continuing that help into employment once they graduatedwhich brings us to today. He says there are more than eight hundred people with developmental disabilities working at around six hundred Dane County businesses as part of whats called Supported Employment. Between eighty-five and ninety-five percent of the forty to fifty young adults with developmental disabilities who graduate from Dane County high schools each year go on to community jobs.

Obviously this is good for people with developmental disabilities; it gives them access and opportunity, a chance at that same sense of identity and pride and satisfaction that we all get from a good days work. But this isnt nearly as simplistic as benevolence, and it goes even further than the aforementioned arguments for why we all need diversity; Hunt says there are good, solid business reasons for employing people with disabilities.

We find the people who are working in the community generally are very reliable, have really good attendance, are eager to work, and just by their presence in the workplace often add enthusiasm and a positive element, says Hunt. I think thats probably one of the eye-opening things for employers if they havent had much experience in the disability field, is how many unique strengths an individual with a disability can bring to the workplace.

The turnover rate for employees with disabilities is eight percent, as compared to forty-five percent for other workers. Furthermore, eighty-seven percent of customers say they would prefer to patronize businesses employing people with disabilitieswe look favorably upon companies for providing these opportunities and were more likely to spend our money there. It transitions people with developmental disabilities into tax contributors, and lets not forget that their families and friends need places to spend their money, too.

Those eight hundred people generate $3.6 million a year in wages, and virtually all of that money gets plowed back into the local Dane County economy, says Hunt of the $12 million Supported Employment program, funded with county, state and federal dollars. Because those are folks who live and work right here, either on their own with support or with their families.

Something thats especially cool about the way the county has chosen to find individualized employment for people with developmental disabilitiessomething maybe all of us could learn a little bit fromis how they match people to jobs. Most with these disabilities arent going to be able to meet all of the requirements of a standard job position posting, so it becomes important to figure out their individual skills and match those to a specific need.

Thats the very same thing that former restaurateur Nancy Christy accidentally made a living (and a reputation) doing when she and Andrea Craig opened Wilson Street Grill in 1987, in a spot known as the black hole because three previous restaurants in that space had failed. The partners never set out to make a statement when they determined that one third of their staff would be people with disabilities. They certainly never expected the national media attention, or the awards and accolades. For Christy, it just felt right. Bringing together people who cared about other people and loved what they didwhether that was creating a gourmet dish from scratch or simply sweeping the floorwas the way she wanted to spend her time.

What started out as this kind of idiosyncratic desire to pull my interest in people and my interest in food together ended up as a picture that benefited everybody, says Christy. Benefited our business, our employees, our turnover, our everything. And that was such a surprise.

Much as Hunt described, Christy, rather than hiring to fit a job description, hired people, pinpointed their skills and passions and gave them those responsibilities. Not only would that particular task be performed really, really well, but sometimes people who were initially perceived as having very limited capacity blossomed under the unique conditions. Take Roger Touchette, who came to the Grill from the Yahara House, a Journey Mental Healthfacilitated, national clubhouse model that supports people with severe and persistent mental illness to secure employment. In the beginning, Touchettes only job was to weigh the dough and press it into a bread pan. At first he required daily assistance, but six months later, he was doing it on his own. And, eventually, he was doing all kinds of things.

Touchette crushed, cut and roasted all the tomatoes. He picked and prepared all of the herbs. He was coming in early and staying late. He was working on holidays when the restaurant was closed (The manager came in so that Roger could work because he just couldnt stand not coming in, says Christy.) He stayed for years, as did so many of his coworkers, with or without disabilities, in an industry traditionally fraught with high turnover. Even more surprising, many employees would open up about their own profound struggles, because they felt safe and supported in an environment where we all have abilities and disabilities, bottom line. Christy spent far less time hiring, interviewing, and training new people because the existing people stayedand they brought their friends and their families, and they celebrated their birthdays and they toasted their anniversaries, and the Grill had a really solid, really successful, fifteen-year run.

It wasnt a utopia, by any means. Running a business this way took time, money and patience, but it had rewards that border on rare for a lot of us in our careers. It provided Christy a quality of life that comes only when youre truly living in synchronicity with your values, and so shes clear that shes the one who really benefited. And although she was not a trained disability person and the Grill closed for good more than ten years ago now, shes still held in high regard by the disability community for creating and cultivating an integrated workforce model that worked. What she did was considered innovative back then, but Christy says todays business climate is perfectly positioned to do the same thing. So many companies are already prioritizing sustainability and diversity, they just arent necessarily thinking about integrating people with disabilities as a key part of that.

People can understand sustainability that its good for the wholebut they havent been able to quite see hiring as part of that sustainable concept, says Christy. Biodiversity, and I think diversity in general, it enriches everything. It comes with its own set of issues, but the payoffs, I think, are worth it.

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Building bridges: At LOV-Dane, Amanda Bell (right)
helps connect members like Daniel Ellis (left) to passion projects.

Amanda Bell is living in sync with her values, too. Just about nine years ago now, after ten years as a special ed teacher at West High and Sherman Middle schools, Bell took a job at a Dane Countyfunded, UW Waisman Centeraffiliated project called LOV-Dane, or Living Our Visions. Her job (and LOV-Dane itself) started out as a proposed solution to the waiting list problemessentially, a growing number of families waiting for county funding and resources once their kids with disabilities left high school. That number of kids transitioning into the community has risen at a rate of between twenty and fifty a year, while annual budget cuts have restricted (or shrunk) the pool of money that supports them. Its a complex issue, no doubt, but Bell was charged with addressing only one piece of it: if the money isnt there but the need forand, more importantly, the county-recognized value ofcommunity inclusion still is, what do we do with families on the waiting list in the meantime?

Theres a growing number of folks within the developmental disability system who might have a little bit of support to work but who dont have enough support to move out or to necessarily get the full life that they want, says Bell. You can have a good inclusive life and be part of school clubs and part of regular ed classes and have those relationships, and then you leave school. And while Dane does a great job supporting people to be employed, that still is not the same kind of life that school offers. That is a big transition for people.

So Bell set out to help families work outside the system to create their own personalized solutions. She dove in at the grassroots level, inviting herself over to peoples homes for coffee, listening hard and looking for common threads. Right away, it was clear that these families were often isolated from each other but wanted the same things. They wanted connection. They wanted to contribute to and participate in their communities. They wanted the same thing we all want: quality of life. But they needed help.

And so we started with eight people in a living room saying, what could we do together that we cant do by ourselves, says Bell. And now were about 130 families.

Those families are no longer limited to those living with developmental disabilitiesanyone with a disability who needs that connection and support is welcome (Youre a member if you say youre a member) and all LOV-Dane programs are family designed, family run. Bell and her teams job is to find the issue and pull people together, to not only draw on the community connections theyve developed over the years, but to support families in exploring their own networksa neighbor whos a property manager, say, or an uncle whos an electrician, or a former employer whos an artist. As she puts it, her job isnt to deliver services, its to help get people in a room and move what they want to do forward.

LOV-Dane has a lot of irons in the firesupport groups, outings, voting drives, employment opportunities, housing solutionsbut the longest ongoing project is probably Bridge Builder. Several member families pooled their money to hire a person to act on their behalf on the ground, to facilitate relationships between them and other people out there in the community. Families created the concept, wrote the job descriptions, developed the budget and eventually hired two full-time Bridge Builders. The project goal is to help people with disabilities find their passions and contribute to the community in a way that benefits everyone.

LOV-Dane member Daniel Ellis, for example, wanted to try woodworkingand now a guy named Tom Liebl hangs out with him once a month, having coffee and building Little Free Libraries and bat houses to put up around town. Steven Clerico wanted to join a faith community but has the sort of disability where he needs physical support all the time, and thats expensive; the Bridge Builder joined Clerico at his new church until its members built a natural relationship with him and organically took over helping him get there every Sunday. Or take Jon Glenberg, a guy who dreamed of joining a travel circle in Madison, basically a group of people who could get together to talk about the trips theyve taken. When Glenberg couldnt find one, he created his own.

Whats lovely is Jon got to be the instigator and actually develop something that is an asset and a gift to Madison long term, because it was his passion, says Bell. At LOV-Dane, were really committed that its not token inclusion. Its reciprocal inclusion. We really believe that theres something more that can happen if both the person and their family and the community groups get a little bit of nurture to see it.

When it became increasingly clear that many people with developmental disabilities had no idea what their passions were, because theyd never really been asked or had the opportunity to explore such a question, LOV-Dane came up with this idea called Samplers. They connected with UW Wheelhouse (formerly Mini Courses) and Lussier Community Education Center to bring in groups of members and let them try different classes. True to Bells philosophy, it wasnt only LOV-Dane members who benefited from the collaboration.

The Wheelhouse staff figured out that actually having connections to these young people with disabilities was fabulous and they wanted more of it, says Bell. Now we get to work with them to figure out what the barriers are to having these people be able to join the regular Wheelhouse classes. How do we work through it so that in fact people can get connected.

Of course LOV-Dane families, like all families with disabilities, still very much need the resources and support of taxpayer-funded systems. Of course, Bell and others are worried about the increasing strain on a local government that gets it, but cant necessarily sustain the current model forever. In working from the ground up, shes run right up against systemic barriers, ones that require systemic solutionslike transportation, for instanceand she knows she couldnt do so much of what she does without the system. But shell continue to mobilize at the grassroots level because that, she believes, is a fundamental part of the long-term solution for all of us.

LOV-Danes theory is, build really good stuff, because if you build good stuff, says Bell, any system change is less likely to take it apart.

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You might have noticed that weve sort of transitionedideally, expandedthis conversation to people with develop-mental disabilities. And perhaps it bears repeating now that we get it: people with developmental disabilities have very different needs and challenges than those who primarily struggle getting their wheelchairs in and out of buildings or events. Thats because this is not some brazen attempt to cover all things accessible for all of Madison; its to look for the core similarities, like Gloziers othering effect. Glozier, Bell, Hunt, Christy, theyre all saying essentially the same thing: awareness changes everything. And when we become more aware, this stuff just makes good sense. There are very basic things that too many of us are still taking for granted that are still denied to so many people with disabilities, and there are equally basic ways were all denied the experience of living among people with disabilities of all kinds. Barriers dont just deny basic rights to some of us; they eliminate the critical normalizing effect that mainstreaming has on the rest of us.

I think the corrective for me is to remind myself to look for capacity, rather than to look for dysfunction or disability or difference, says Howard Mandeville, who retired last year as executive director of Movin Out Madison. How can we support people where there are gaps in capacity, and really see people in terms of what they can contribute, what they can do, the value and merit that they bring to their existence.
And ours. Movin Out is a nonprofit that provides housing solutions to people with disabilities, not only to provide the tools to access four walls and a roof, but to help create a sense of home. And a critical part of that is building a life in a neighborhood, in a community, with all of us, for all of us. Home represents safety, warmth, nourishment, connection, identity, independence, stability. Everybody knows theres no place like home.

So when you think about all the stuff that we load into what home is, no wonder its an important thing for any of us, says Mandeville. And then its all the more bewildering that for vulnerable peoplepeople vulnerable because of their disabilitieswe would erode or erase the opportunity for people to actually have that kind of calm.

So, over the past fifteen or so years, Movin Out has collected a portfolio of propertiessingle-family homes, duplexes, condos, essentially existing housing in existing neighborhoodsthat theyve purchased, fixed up and rehabbed for accessibility.

Mandeville knows that deinstitutionalization is not the same thing as fully integrating people with disabilities into our communities. Its one thing to retrofit old homes with accommodations or create new buildings from the ground up with universal accessibility in mind, quite another to foster integrated neighborhoods where people of all abilities have regular, day-to-day interactions with one another.

What weve seen over a couple hundred years of separating people with disabilities from their communities and their families, concentrating them in one place, it isnt what people want and weve learned it isnt good for people, says Mandeville. It emphasizes the vulnerability associated with disability, because if theyre seen as so different than the rest of us that they need to be served in these special settings, isolated from the normal flow of the community, thats stigmatizing. And it creates consequences for people that are worse than the attributes of their disability.

Its in this spirit that Movin Out is embarking on what could be characterized as its most ambitious project to date: Dempsey Place, a partnership with Stone House Development in the Royster Crossing project on Cottage Grove Road, one bolstered by city and state affordable housing tax credits and private financing. While Royster Crossing will provide a mix of retail and hundreds of housing units, Dempsey Place will include seventy one-, two- and three-bedroom rentals, about a quarter of which will have enhanced accessibility features (roll-in showers, wider doorways, barrier-free floor plans) and an equally important feature of accessibility: affordable rent for people with permanent disabilities (along with military veterans and those needing workforce housing). Theres the added bonus of the surrounding redeveloped neighborhood providing employment opportunities and services for people with disabilities literally in their own backyard, and theres something more, too: visible inclusion, integration, a sort of normalizing and mainstreaming by design. And thats a big deal.

What were doing is creating a context for people with disabilities not to be concentrated with just other people with disabilities, but more integrated into a natural community. Theres this intention to create a more diverse, more welcome community for all kinds of people, says Mandeville. So its another way of creating opportunities for people to have an identity, other than just a disability. They have an identity as a neighbor, and as a tenant or a homeowner. And [they] are a part of whats going on where they live.

Im walking into another coffee shop to meet another person in a wheelchair and, like Jane Earl, Brett Masbruch would rather disclose that information to you on his own terms. But it just doesnt work that way when youve got cerebral palsy, or any other significant disability. We see the condition first, the person second. Besides, so many times when hes disclosed his disability, doors have shuthowever gentlyin his face.

This time its an unseasonably warm day and so the weather isnt an issue, but transportation is, he tells me, from the table hes snagged right by the door. Hes been here fifteen minutes already and hell probably be here fifteen minutes after I leave, because he has to schedule such a wide window with Madison Metros paratransit system. He also, as an east sider, has to be careful about where we meet; parts of his neighborhood fall into Monona, and thats not technically Madison, and Metro Plus services only within the city limits. On the one hand, he feels grateful to have the resource. On the other, it can be wildly unpredictable. And it always serves as yet another reminder of something the rest of us take for granted that is completely out of his control.
My passion for accessibility really started after I lost my first job, says the forty-two-year-old Madison native, who is a clinical substance abuse counselor with a masters degree in mental health counseling. Im realizing that all the places that I would want to work at arent accessible.

Masbruch has gotten to know ADA law by default and hes more familiar than hed like to be with many of the apparent loopholesbuildings with only two floors arent required to have an elevator; you dont have to install accessibility modifications if you can prove financial hardship or if your building is a certain ageand he also measures accessibility in two parts: can he get in the building, and can he do his job once hes inside? Its usually this second part that doesnt work out, because these are the kinds of issues most of us still arent seeing. Can he reach the overhead cabinet? Can he get to the copy machine? Can his chair make the tight corner into his office? Most of all, to take it a step further, if any of his or his colleagues patients have disabilities, can they access these mental health services?

Masbruch and I have a long conversation on this day. We talk about his passions and his challenges. We talk about the balance hes always trying to strike between coming across like the accessibility police and leaving each job or space or friendship a little bit more accessible than he found it. We talk more about transportation, and snow removal, how he doesnt even try to be a part of iconic Madison experiences like Brat Fest or the farmers market. About the assumptions people make, about the way hes so often patronized or condescended to, because his body is bound to a chair but his brain is as sharp and average as yours. We talk about how hes a member of the Recovery Coalition of Dane County because he wants to work from the inside to make his entire field more accessible to addicts and alcoholics with disabilities, because its a large market with an unmet need. About how hed love to serve as a consultant in general for people who are designing buildings and systems, to help them see what theyre not yet seeing, from his chair.

I know Ill never get all of his concerns down in these pages. I know Ill never even begin to scrape the surface of this complex topic at all, or effectively describe the budget concerns from all sides, or tell about all the different boards and agencies, businesses and groups doing really important work in this community. But I ask him anyway, because its the same thing I ask everybody, on every story like this I write: youve got five minutes in an elevator with all of Madison. What do you most want people to know?

He takes a while to think it over, and I imagine him sifting through the long laundry list of critical legal and practical issues facing people with disabilities. I imagine him weighing each one carefully, prioritizing what hed most like you to hear, if given just one chance. And Im so surprised when he finally says what he says.

Just, he says, before pausing again for a few more seconds, just know were out there.

Reinventing the wheel

The wide-open field of assistive technology is ripe for revolution

On a Roll: Rowheels is poised to transform the wheelchair industry by offering wheels that a user pulls rather than pushes.

Serial entrepreneur Rimas Buinevicius spent only ten weeks of his life in awheelchair, but it changed everything. The former Sonic Foundry CEO and co-founder of the Madcelerator early-stage business incubator slipped while sailing in 2011, suffering a spiral fracture on his leg. After only three days in a standard, medical-grade wheelchair, he was fed up with shoulder pain and the difficulty of pushing. And as a guy whod built a career based on thinking outside the box, he just knew there had to be a better way.

Four years, a partnership with quadriplegic NASA inventor and scientist Salim Nasser, a 2012 Governors Business Plan grand prize and a new Madison business later, Rowheels is poised to potentially break the $2 billion wheelchair market wide open with its brilliant, seemingly basic innovation: Why push when you can pull?

When you look at a rowboat, its not called a push boat; its called a rowboat for a reason. And thats because its just easier on your body, says Buinevicius of the wheels that easily attach to most any standard manual wheelchair on the market, allowing its users to pull instead of push. Rowing actively engages eight of nine upper-body muscles; pushing, on the other hand, engages only two, often leading to chronic pain and repetitive stress injuries, and the sort of hunched-over posture common to long-term wheelchair users. Rowheels is in the beginning phases of production here in Madison (using many Wisconsin manufacturers, including Madisons Saris Cycling Group for the rim, tire, tubes and spokes), while the marketing team is out introducing it to the health care industry around the country at places like trade shows and hospital and medical centers in-service trainings.

Ive had in-service sessions where literally the nurses were crying, says Buinevicius. Its really rewarding, because you get into these in-services where the people really know what were doing because theyve been treating this forever, and thats where I think people really get blown away by it. And it hasnt even hit the market en masse yet.

Buinevicius never set out to make anybody cry, or even make anybodys life easierhe just saw a gaping need and an entrepreneurial opportunity. Thats kind of how it went for Jay Martin, too, a UWMadison engineering professor who, in 1999, experienced the worst: his sixteen-year-old son, Liam, suffered a cervical spinal injury in a diving accident that left him paralyzed from the chest down. As an engineer, with a brain calibrated to see problems and solve them, in those dark months in the hospital after his sons accident, Martin saw problems everywhere he looked.

It was so eye-opening to me that I no longer could work on anything else, says Martin, who dragged a then-rare, uber-expensive, shipped-from-Switzerland low air loss mattress into Liams hospital room on a Sundaybecause you can do anything in a hospital on a Sundayto ward off pressure ulcers, the deadly condition that killed Christopher Reeve. (He says the hospital has since switched to these mattresses, although he takes no credit for it).

Martin then left the competitive field of combustion for assistive technology and co-founded the UW-CREATe lab, or the Center for Rehabilitation Engineering and Assistive Technology, where his students went on to design innovations like the Funicular, a platform that uses a chain hoist and rollers to drive wheelchairs up stairs. And in 2013 he left UW to start his own design firm, with chief business development officer Jim Guither, and chief operations officer Liamwho not only managed to graduate high school with his class after his accident, but went on to earn a UWMadison bachelors degree.

Inspired innovation: Jay Martin (left) rigged his hangar so it can lift son Liam (center) up to his plane. The space also serves as a lab for Martin Product Design, where James Guither (right) also works.

One of the most promising products in the one-hundred-plus Martin Product Design portfolio is a sort-of garden-hose-reel device that solves the problem of piles of jumbled hospital cords. Because while working in combustion, particularly as it relates to advancements in auto technology, Martin had to find slivers of subtle, highly specialized problems to solve if he wanted to make any kind of difference. But when I looked at the field of assistive technology, there was nobody. And there were so many problems. I mean, to find a good problem, all you had to do was walk out the door and there it was, he says. And when I say walk out the door, theres almost no building in Madison that has the door buttons in the right place.

Just as Buinevicius is clear that Rowheels is about innovation and Liam is clear he doesnt want to be some sort of inspirational wheelchair poster boy, Martin insists that hes doing what he loves and that hes found a field where the skys the limit. Guither points out Liams $200 water bottle, one hes had to modify and the only one like it available on the market in a country where the rest of us puzzle between hundreds of styles, colors and materials, and breaks it down in capitalist terms: Theres a tremendous unmet market need here, says Guither, before turning the conversation in a more philosophical direction. We know we can do so much better.

Like so many other components of Universal Design, Martins user-centered innovations are not only good business, theyre better for everyone. That hospital cord device, for example, has real implications for patient care professionals, for one, but also for actual garden hoses. The hands-free devices so many of us use in our cars started with assistive technology. That perennial wedding registry item, the Cuisinart food processor, was invented to accommodate people with physical limitations. When were pushing our babies in strollers down the sidewalk, were shocked when we cant find a curb cut. When we press the elevator button over here and the doors open way down there, weve got time to wander in and get settledthat pause was designed to accommodate people with disabilities. Just like the door buttons Martin mentioned, those squares we palm-slap to open doors when were carrying groceries or backpacks or kids. Were benefiting all day long from assistive technology, even as the multitude of remaining problems stay invisible to us. And the potential for economic growth and groundbreaking innovation in the field of assistive technology is staggeringly big.

Its funny because in my former life, if you work in combustion youre associated with automobiles, and our automobiles are amazing devices right now. If they dont work perfectly, everybodys totally upset, says Martin. In the world of disability, its so different. If it works at all, youre happy.

Access Ability

Two local groups help enhance quality of life for people with disabilities

Before chaperoning the 2001 middle school skiing field trip that left her spinal cord completely severed, Monica Kamal didnt think a whole lot about accessibility or adaptive recreation. She had some awareness, sure, but not the brutally inescapable kind that comes only when its you, waking up to your new normal, in a city that has become utterly unrecognizableand inaccessibleovernight. Kamal had never really thought about how easy it was to hike a state park trail or slip a kayak into smooth, cool waters, or even hop in the car and run to parent-teacher conferences. Today, she thinks of little else.

Because its Madison, you think its this place of strong resources, says Kamal, who has since founded Madison Spinal Cord Injury & Issues, or Madison SCI, an all-inclusive, nonprofit awareness, information and support group for people with disabilities. And it has strong resources for children with disabilities, but if youre over eighteen and under fifty-five, there are hardly any resources there for you.

Today, Madison SCI, celebrating its tenth anniversary, strives to be one of those resources. What started as a support group, after Kamal couldnt find one to join herself, has evolved into a chapter of the United Spinal Association with seventy to eighty local membersand not just people with spinal cord injuries.

Anyone who has mobility impairments is welcome, including those with conditions such as multiple sclerosis and cerebral palsy andperhaps most notablyable-bodied family members. Thats a big reason Madison SCI existsto help people with disabilities engage in the same activities and opportunities their loved ones enjoy.

The group facilitates meet-ups at the Memorial Union and Concerts on the Square, hosts monthly topic meetings featuring visits from groups like the UWWhitewater basketball team and Madison Curling Club and organizes adaptive cycling and kayaking outings with the help of student volunteers from the University of Wisconsin Physical Therapy program.

We just want people out in the community and showing what is possible, says Tina McFadden, Madison SCI treasurer and member coordinator. Because it is scary when youre first injured and you dont think you can do anything. You have two lives, your life before and your life after. By joining Madison SCI, I feel like my life is a lot fuller.
McFadden was struck by a boat while waterskiing on Lake Waubesa, causing a T12 spinal cord injury that left some feeling in her toes and slight muscle movement in her legs.

It was 1990, practically lifetimes ago in the disability rights movement. There were no curb cuts, no adaptive kayak outings. The Americans with Disabilities Act had just passed. McFadden was an active and social bank teller just starting a real estate career who loved to go dancing with her girlfriends. She was twenty-five years old.

There was no support, there was just nothing, says McFadden, who exercised five to six hours a day in the months and years after her accident to regain what movement she could. Today she can pull herself to standing.

I was at the hospital for three and a half months and I cried when I left, because at least there, its a structure. You get up, you get therapy, you have art class, you have people to talk to. You come home, theres nothing. So its very scary.

Before joining Madison SCI, McFadden had no other friends in wheelchairs. She didnt know about the Adapted Fitness program at the UW Natatorium she frequents today, and, despite her healthy and active lifestyle, had never tried hand biking or kayaking or any of the other adaptive recreational hobbies she and her able-bodied partner (Rick, her boyfriend since 1987, before her accident) now regularly do together.

We want Madison to be as accessible as possible for people to do as much as they want, says McFadden. Were just trying to show that youre only as limited as you think you are. So if you want to try to do something, there is a way of doing it.

One of the groups key goals is to acquire adaptive equipment for free use by its members, because such equipment can be highly cost prohibitive (an adaptive hand bicycle, for example, runs $3,000 to 4,000). Just this year, Madison SCI received a $4,293 grant from the Christopher & Dana Reeve Foundation to purchase an adaptive tandem kayak, allowing for an able-bodied person and a person with mobility issues to get out on the water together.

Kamal was especially touched by an able-bodied member who, after an adaptive kayak outing with his sister who has multiple sclerosis, said it was the first time he saw her not as a wheelchair user, but just as his sister.

So that was pretty special, says Kamal, who also co-founded Access Ability Wisconsin to help people with disabilities access the states rich natural resources through activities such as adaptive hunting and fishing. The Dane County group just raised enough funds to acquire its first all-terrain wheelchair.

What Id like Wisconsinites to know is that there are opportunities that are naturally given to people that everybody wants to do, whether theyre a wheelchair user or not, says Kamal. And so be thankful about the gifts and opportunities youre given. And if youre able to help others get out and experience that, that decreases depression, increases opportunities and, because of that, helps their health and our health care system.

Source:http://www.channel3000.com/madison-magazine/home-lifestyle/How-do-people-with-disabilities-experience-Madison/31867206

Connect|Share|Learn|http://sdnetworkwi.org/

Share your picture from Disability Advocacy Day!

Over 700 people attended this years Disability Advocacy Day at the Capitol. Wed love to see photos you took from the event. Weve set up a photo album, so you canshare your photoson the Network!

Keep Informed on the Budget Proposal!

With new information coming out almost daily, weve been working hard to keep theBudget Proposal pageup to date. Keep up to date with thelatest informationabout how the budget proposal would affect people with disabilities.

There have been a couple of different discussions started about the budget. April started adiscussionabout her concern over how the budget would affect her sons life. Bubba shared aletterabout his opinion regarding the budget that he has sent to several different newspapers. We have also started adiscussionhighlighting several points discussed during the Coffee Break we had with Lynn Breedlove on March 3^rd. We strongly encourage you to get involved in these discussions or start your own.

The Results Are In!

According to the last poll, approximately 90% of members feel worried and/or angry about the budget proposal. About 6% of members dont know enough about the proposed changes and/or feel it doesnt affect them, and less than 3% of members feel the changes will be good. Now, we want to know what you are doing about the proposed budget. Take our newone-minute poll.

It Only Takes "Five"

Take five minutes to check out what's happening on the Self-Determination Network:

• Join the discussion: An interesting new concept has surfaced on the Internet. Websites and apps are being created where people can rate places based on accessibility. What do you think of the idea? What are the pros and cons?
• Comparison: Mark posted a great comparison of how self-direction differs between Family Care and IRIS.
• Stacys Journal: This month Stacy shares about her journey to independent living.

• Get Involved: The Living a Self-Determined Conference is looking for exhibitors and sponsors for 2015.
• Learn: This is an interesting article about how the FCC has put together a disability advisory committee to provide expertise and recommendations on communications and video programming issues.
• Be Inspired: Read this inspiring story about an UW-Oshkosh alum who doesnt let his disability stop him from living his dream!
• Assistive Technology Survey: Take this survey about assistive technology.
• Read: The National Council on Disabilities released Home and Community-Based Services: Creating Systems for Success at Home, at Work and in the Community.
• Disabilities Act Complaint Form: Complaint forms are now available electronically.
• Rental Assistance: An article about how some states, including Wisconsin, will receive money to help people with disabilities access community-basedhousing.
• Gaming Accessibility: This is an interesting article about how the gaming industry is trying to be more accessible.
• ABLE Act: An article about how states are moving forward with the ABLE Act.
• Post news or start a discussion: It's easy to do and a great way to share information and network with others!

New Members

Stop by to welcomeournewest members

• Shes aparentwho is interested in staying on top of all of the long-term care issues.
• Hes aparentwho wants to reach out to the disability community.
• Shes amotherwhos looking for resources to better advocate for her daughter.
• Self-determination is a core value for thisperson.
• Thismotheris on the board for HearthStone of Wisconsin.
• Thisparentof four has two daughters in IRIS.
• This person is aWork Incentives Benefits Specialist.
• She wants to help withdisability advocacy.
• This person doesnt let her disability stop her fromhelping others.
• Shes anadvocatefor her sister.
• Thisparentwants to learn more ways to advocate for her child.
• She directs asupported employment program.
• Shes aguardianfor an adult with special needs.
• Hes anadvocatefor his brother.
• Thisparentis very concerned about the budget proposal.
• He has been along term care providerfor 12 years.
• Thismotheris interested in self-determination.
• Shes a mother and she alsoworks with people with disabilities.
• Thisfatherhas a son who uses IRIS.
• Shes an advocate whohas worked in the field for 35 years.
• This father is anadvocatefor his son.
• Thismotherwants to be heard.
• This person enjoyslearning about issues important to people with disabilities.
• Shes aProvider Service Managerfor Family Care.
• Hes theCommunity Supported Living Program Managerwith Lutheran Social Services.
• Hes beeninvolved in self-directionfor many years.
• Shes aformer teacherwho has strong opinions about the proposed budget.
• Thismomwants to keep informed about changes that would hurt self-determination.
• This dad is aRegional Athletic Directorfor Special Olympics.
• This mother of three is anadvocatefor Disability Rights Wisconsin.

Do you know someone who should join the Self-Determination Network? Spread the word and invite friends, families and other interested folks!

Upcoming Events

Here's a sample ofupcoming eventslisted on the Self-Determination Network:

• WI FACETS Spring Self-Advocacy Workshop: Employment Panel: March 24^th, 6pm to 8pm, WI FACETS, Milwaukee WI
• WI FACETS Spring Self-Advocacy Workshop: Healthy Relationships: April 14^th, 6pm to 8pm, WI FACETS, Milwaukee WI
• WI FACETS Spring Self-Advocacy Workshop: Self-Advocate Spotlight: April 28^th, 6pm to 8pm, WI FACETS, Milwaukee WI
• Circles of Life Conference 2015; April 30^thto May 1^st, Holiday Inn Convention Center, Stevens Point WI
• The National ADA Symposium: May 10^thto 13^th, National Center for Civil & Human Rights, Atlanta GA
• ADA Free Pontoon Boat Rides on Madison lakes: June 14^thto August 16^th, Tenney Park, Madison WI
• ADA Legacy Bus Tour: June 25^th, 11am to 4pm, State Capitol, Madison WI
• State-wide Institute on Best Practices in Inclusive Education 2015:July 27^thto 29^th, Westwood Conference Center, Wausau WI
• 3rd Annual Disability Pride Festival: July 25^th, 12pm to 5pm, Brittingham Park, Madison WI
• Self-Determination Conference: November 9^thto 11^th, Kalahari Resort, Wisconsin Dells WI

Post your eventon the Self-Determination Network and it can be included in future Network News emails to members! Questions? Suggestions? ContactStacy Ellingen.

The Self-Determination Network is powered by In Control Wisconsin and supported financially by ourmembersandSponsors. We couldn't keep this Network going with you! Find out how you can help support the Network.

An interesting article inDisability Scoopwritten by Michelle Diament about how many states are taking steps to move forward on the ABLE Act. Likely due to all of the budget stuff, there hasn't been much action taken in Wisconsin yet (that we know of), but it's interesting to read what other states have done so far.

States Moving Forward On ABLE Accounts

By Michelle Diament

Just months after federal lawmakers created a way for people with disabilities to save without risking their government benefits, most states are working to make the new accounts available.

The Achieving a Better Life Experience, or ABLE, Act, which wassignedlate last year by President Barack Obama, paves the way for people with disabilities to open special accounts where they can save up to $100,000 without jeopardizing eligibility for Social Security and other government programs.

Before the accounts can become available, however, states must put regulations in place.

To date, lawmakers in more than half of states have taken steps to create the new savings vehicles, advocates say.

This week, legislatures in West Virginia and Utah sent ABLE bills to their governors for approval. Legislation is also before the governor in Virginia.

Whats more, active bills are under consideration in legislatures in 29 states and draft bills are in the works in an additional seven, according to Heather Sachs, director of state government affairs for the National Down Syndrome Society.

We are very, very pleasantly surprised at how quickly states are moving on this, Sachs said.

Despite the momentum across much of the country, however, lawmakers in some states have opted to wait on ABLE legislation until after federal officials issue regulations on the new accounts, a move expected by the end of the summer.

This week, the Internal Revenue Service and the U.S. Department of Treasury sought to urge those states along, with a notice assuring lawmakers that a transition period will be incorporated in any guidance to account for circumstances in which state rules do not fully comply with federal requirements.

The Treasury Department and the IRS do not want the lack of guidance to discourage states from enacting their enabling legislation and creating their ABLE programs, which could delay the ability of the families of disabled individuals or others to begin to fund ABLE accounts for those disabled individuals, the agencies said.

Even in states where legislation is enacted, Sachs said she expects it will be at least late this year, but more likely 2016 or 2017 before people with disabilities can open ABLE accounts. Thats because the process is highly state specific and will involve significant behind-the-scenes work for governments and the banking industry, she said.

To aid in that process, disability advocates are also at work on a National ABLE Resource Center, designed to serve as an information clearinghouse on the new accounts for families, government officials, financial professionals and other stakeholders. More than a dozen advocacy groups are collaborating on the center, which is being spearheaded by the National Disability Institute and is expected to launch in July.

Source:http://www.disabilityscoop.com/2015/03/13/states-moving-forward-able/20131/

It was May 2009. I had just graduated from UW-Whitewater. As our van pulled out of Whitewater for the final time, I was overcome with emotion. UW-Whitewater gave me so much more than just a degree. It made me become so much more independent and self-confident. I proved to myself and others that if given the right supports, I could live independently. Like many college graduates, I moved back in with my parents.

When I moved back to Fond du Lac, I thought finding a care agency and an apartment would not be that difficult. I couldnt have been more wrong! It was a nightmare. Finding cares was not an easy task--especially in Fond du Lac! Before I could even really look for apartments, I had to get cares lined up first because I could not live on my own without assistance. For various reasons, agencies could not staff my shifts. In the year and a half I was at my parents, we tried two different agencies, and the most we ever got covered was two shifts per day (I need four care shifts per daygetup, lunch, dinner, and bed). This was unbelievably frustrating.

In summer 2010, I began researching different living options on the internet. I came across Cerebral Palsy of Mideast Wisconsins Independent Living website. My mom and I came to tour an apartment late that August. Its in Oshkosh--about 20 minutes away from Fondy. I admit, I was skeptical because I am not particularly fond of the idea of segregating people with disabilities. However, when I saw the setup of the Willo Apartments, I was very impressed! The Willos are actually three long buildings, with four apartments in each one. All of the apartments have two bedrooms. Some have two clients in them, but most have one person with a disability living there. The units are so accessible and, although all the residents have disabilities, its nothing like a group home. After we toured, I knew this was where I wanted to be.

Its very unique as Cerebral Palsy of Mideast Wisconsin is a care agency. Residents of the Willos arent required to use their agency, but they can if they choose to. For me, this was key. Although, I could have hired my own workers because Im in IRIS, at the time, my family and I felt more comfortable going through an agency.

Its subsidized housing, so, of course, there was a wait list. Fortunately, one became available in December 2010, and I was next on the list. Some renovations needed to be done to the unit and cares needed to be setup, so I moved in in February 2011. After such a frustrating year and a half in Fond du Lac, I was thrilled to be on my own again.

Living here for over four years now, Im still pretty pleased most of the time. I have the independence I need. The fact that Im only about a half hour from my parents has been greatespecially since I had some serious health issues in the recent years. I love my apartment. However, Im not sure its my forever home. Although, I love my neighbors, at times I feel pretty segregated. I think Id like to be in a little bigger city that has more to offer. I dont plan to move anytime in the near future, but maybe someday. Once all this budget stuff gets settled, I plan to reevaluate my living situation from a few different angles and possibly make some changes. Well see what happens.

Living independently is so important to me. In my opinion, everyone should be able to choose where they live and who they live with. What are your thoughts on this?

The views expressed here are strictly those of the author and do not necessarily reflect those of InControl Wisconsin, the Network or any of our sponsors.

An interesting article in theHuffington Postwritten by Damon Beres about how PlayStation is making gaming more accessible for people with disabilities. It explains some of the accessibility features it's adding.

PlayStation May Soon Transform Gaming For People With Disabilities

By Damon Beres

The PlayStation 4 may be poised to make gaming more accessible for people with disabilities.

An upcomingfirmware updatecouldadd new featurescatering to people with visual, auditory or other impairments. Twitter user Ahsan Rasheed (@IsAParrot) posted photos of a friend's beta version of the 2.50 firmware patch, including one that shows alist of new PS4 settingslike text-to-speech, color inversion, text enlargement, closed captions and button reassignment, among others.

Here's the photo of the accessibility feature list:

A spokesperson for Sony Computer Entertainment America told The Huffington Post that the next PS4 update "will be released soon," but would not confirm whether these accessibility features will be included.

Rasheed, who told HuffPost he's a former medical student active on game industry forums likeNeoGAF, has beenwrongabout a gaming rumors before, which he admitted to. But he's also beenright.

An additional source who was familiar with the update but unauthorized to reveal details told HuffPost that the added features are the real deal.

Accessibility features in PS4 would be huge for the gaming community according to Steven Spohn, chief operations officer atTheAbleGamers Foundation, a nonprofit that works to eliminate barriers and help individuals with disabilities to enjoy gaming.

"We're talking millions of people who are suddenly going to have an easier time playing games," said Spohn.

Button assignments in particular, he said, would be a major addition to PS4. This feature would allow individuals to customize which controller buttons do what before jumping into a game. People with muscular diseases or disorders who have trouble pressing the "trigger" button, for example, could map it instead to the more accessible "triangle" button on the front of the controller, according to Spohn.

A big part of AbleGamers' work, Spohn said, is creating custom controllers or configurations for gamers who can't use the default device that comes with a system. Spohn tends to recommend the Xbox One for gamers with disabilities because it allows customized third-party controllers. These controllers, however, can cost hundreds of dollars.

What's more, the Xbox One doesn't offer built-in accessibility options like the ones that might be coming to PS4.

"This is a game-changer," Spohn said of the potential PS4 update. "Unless Xbox catches up now and does the same thing, we're going to have to change what we recommend to people."

Representatives for Xbox did not immediately respond to a request for comment.

Of course, this potential PS4 update isn't a cure-all. Certain games present challenges regardless of how the controls are set up -- multiple buttons might need to be pressed in a specific way while moving a joystick, for example -- and players who can't move their fingers far enough to reach each button would still benefit from the ability to use a custom third-party controller, whichSony does not allowon the PlayStation 4.

Still, it's a start.

Source: http://www.huffingtonpost.com/2015/03/11/playstation-4-accessibility-update_n_6842544.html

Washington, DC The National Council on Disability (NCD), an independent federal agency, in a cooperative agreement with the National Association of State Directors of Developmental Disabilities Services (NASDDDS), released Home and Community-Based Services: Creating Systems for Success at Home, at Work and in the Community online Tuesday, February 24, 2015.

The new report offers a number of recommendations for federal and state entities from a thorough review of the legal and regulatory home and community-based services framework outlined by the Americans with Disabilities Act and the new Home & Community-Based Services (HCBS) regulations. The bearing of setting size and configuration on the quality of supports and services received by people with intellectual and developmental disabilities and individuals with mental health disabilities in home and community-based arrangements is the focus of the findings.

The legal mandate shifting service delivery for people with disabilities away from institutions to home and community settings is unequivocal, said Joan Durocher, NCDs Director of Policy. Yet, transitioning from institutional to more individualized, person-centered settings integrating people with disabilities into the community continues to challenge policymakers, providers, and stakeholders alike. Ensuring that the size of, and type of, supports and services for people with disabilities are aligned with best practices is essential. Home and Community-Based Services: Creating Systems for Success at Home, at Work and in the Community details factors that can make a crucial difference between meaningful integration or segregation in the delivery of HCBS.

Key Findings:

--States have been offered federal financial incentives to shift away from institutional services and towards HCBS; --Many states continue to deliver services through HCBS funding authorities that are not meaningfully integrated into their communities and do not meet the new federal standards; --HCBS systems should provide clear incentives to providers to deliver residential, day and employment services within small or individual settings scattered throughout the community; --Under the new rule, states will need to shift funding away from settings currently funded as HCBS that are institutional in nature; and --Stakeholders, including state legislators and policy makers current need information about setting type and size for informed decisions and guidance impacting people with disabilities.

To read the full report, visit NCD online at:http://www.ncd.gov/publications/2015/02242015

Information above taken from the Great Lakes ADA Center listserv

The Department of Justice has announced that individuals wishing to file ADA complaints with the Department will be able to fill out the form and submit it completely electronically. Filers will also immediately receive a "reference number" that can be used whenever contacting the Department about that complaint. The new electronic form is available at:http://www.ada.gov/complaint/

EffectiveMarch 15, 2015DOJ will no longer accept email complaints. However, complaints will still be accepted by U.S. mail. Contact the Department's ADA Information Line at1-800-514-0301(V);1-800-514-0383(TTY) to receive a paper complaint form by mail.

Above information taken from the Great Lakes ADA Center listserv.