{"id":5486,"date":"2020-09-16T21:54:44","date_gmt":"2020-09-17T01:54:44","guid":{"rendered":"https:\/\/desis.osu.edu\/seniorthesis\/?p=5486"},"modified":"2020-09-16T21:54:46","modified_gmt":"2020-09-17T01:54:46","slug":"giving-people-with-severe-disabilities-the-tools-to-create-art","status":"publish","type":"post","link":"https:\/\/desis.osu.edu\/seniorthesis\/index.php\/2020\/09\/16\/giving-people-with-severe-disabilities-the-tools-to-create-art\/","title":{"rendered":"Giving People With Severe Disabilities the Tools to Create Art"},"content":{"rendered":"\n<p>People with severe disabilities are learning to express themselves through art, thanks to the passion of Tim Lefens, named a&nbsp;<em>Robert Wood Johnson Foundation Community Health Leader<\/em>&nbsp;in 1998.<\/p>\n\n\n\n<p><strong>The problem.&nbsp;<\/strong>People with severe physical disabilities often feel that the essence of who they are is trapped inside their bodies. And they are often infantilized, treated as if they have little to offer. How can people who cannot walk or talk and have limited use of their hands experience the joy of creating their own art?<\/p>\n\n\n\n<p><strong>Finding his passion in the Big Apple.&nbsp;<\/strong>From the time he was able to hold a paintbrush, Tim Lefens was making art. Recognizing his gift, his parents sometimes invited little Tim to draw a picture to entertain their friends at dinner parties.<\/p>\n\n\n\n<p>When Lefens was in first grade, the family relocated from Michigan to Belle Mead, N.J.\u2014a fortuitous move, Lefens says, because it was just a bus ride to the art museums of Manhattan. His favorite, the Museum of Modern Art, was right next to the office where his father worked as a civil engineer.<\/p>\n\n\n\n<p>By the time he was in high school, Lefens wanted to do nothing else but draw and paint\u2014much to the displeasure of the teachers whose classes he ignored. He poured over art books filled with the works of Manet, Cezanne and Picasso. \u201cTheir quest to push their paintings to the frontier of art read to me like a story of adventure,\u201d he wrote in his book&nbsp;<em>Flying Colors: The Story of a Remarkable Group of Artists and the Transcendent Power of Art<\/em>. \u201cIn time, I pictured painting that would go even further; painting that would connect more directly with the flash of raw energy I experienced being alive.\u201d<\/p>\n\n\n\n<p><strong>Pushing the limits of art.&nbsp;<\/strong>Lefens needed a guide into the realm of abstract art. He found one in a friend\u2019s father \u2014painter Roy Lichtenstein who chauffeured the boys to the beach in the summer and invited Lefens into his studio in Southampton, Long Island, N.Y.<\/p>\n\n\n\n<p>Lefens went to art school in Utah, where the works of purely abstract painters like Jackson Pollock and Willem de Kooning introduced him to \u201ca visual language I could use to go directly to the life I sensed inside,\u201d Lefens writes in&nbsp;<em>Flying Colors.&nbsp;<\/em>He transferred to Virginia Commonwealth University in Richmond, which had an art program sympathetic to abstraction. After earning his bachelor\u2019s degree in 1977, he trained at the Mason Gross School of the Arts in New Jersey.<\/p>\n\n\n\n<p><strong>The light is going out.&nbsp;<\/strong>By the early 1980s, Lefens work had been shown in New York art galleries and caught the attention of influential art critics. Lefens recalls this time as a swirl of loft parties in lower Manhattan, surfing Tres Palmas in Puerto Rico, and trips to arts venues in Italy.<\/p>\n\n\n\n<p>Then in 1988, Lefens began noticing changes in his vision and soon heard the news no visual artist should hear. \u201cYou have retinitis pigmentosa,\u201d the doctor told him. \u201cYou have two years, five at the outside, of usable vision left.\u201d<\/p>\n\n\n\n<p>Three consecutive specialists made wisecracks to the effect of, \u201cWell, it\u2019s a good thing you\u2019re an abstract painter because you don\u2019t need your eyes.\u201d<\/p>\n\n\n\n<p>\u201cI vowed I would never put myself in the hands of an eye doctor who was not also an artist,\u201d Lefens says.<\/p>\n\n\n\n<p>He eventually found an ophthalmologist who was also a sculptor. In his office, Lefens showed him reproductions of his paintings. The doctor looked carefully at each image, looked up at Lefens and said, \u201cI\u2019d like you to come to the school where I am teaching. They\u2019re starting an art program. I\u2019d like you to show slides of your work to my students.\u201d<\/p>\n\n\n\n<p><strong>\u201cI saw something in their eyes.\u201d&nbsp;<\/strong>The main campus of the Matheny Medical and Educational Center in Peapack, N.J., is home to 101 children and adults with medically complex developmental disabilities. Most have cerebral palsy, and some have spina bifida and a wide range of other uncommon, but devastating conditions, as well as vision and hearing deficits, seizure disorders, and cognitive disabilities.<\/p>\n\n\n\n<p>Showing his art at Matheny was a turning point for Lefens. \u201cI could see by looking in their eyes how much they were still there, 100 percent,\u201d he says. \u201cThey were really intense, but they were being spoken to as if they were infants, and it was really upsetting to me.<\/p>\n\n\n\n<p>\u201cThere is something wrong here,\u201d he recalls thinking. \u201cThey are being mistaken for being idiots. What if they could use a different language? Maybe painting, which I believe in so much, could be their way out. But how can you paint if you can\u2019t move?\u201d<\/p>\n\n\n\n<p><strong>Lassoing the power of technology.&nbsp;<\/strong>Lefens\u2019 first answer to that question was to secure a large canvas on the floor, slather paint on it and cover it with plastic. Then he invited those in motorized wheelchairs to drive across it, using the power and weight of the chair like a big paintbrush to leave a mark. \u201cThe paintings were awesome from day one,\u201d Lefens says. \u201cThey were \u2018in there,\u2019 just as I suspected.\u201d<\/p>\n\n\n\n<p>But this method excluded those who did not have power wheelchairs, and even those who did eventually wanted more of a challenge. Lefens decided to experiment with light. He bought a target laser at a local gun store and attached it to an old welder\u2019s helmet, with the plastic visor removed.<\/p>\n\n\n\n<p>Wearing the device, students were able to indicate their choices of color, texture, size, and brush type and to trace where they wanted the paint to go. Lefens trained able-bodied trackers, studio assistants who applied the paint exactly where the artists pointed the light on the canvas. Lefens likens the process to an architect directing builders. \u201cThe person is really choosing and the result has meaning,\u201d he says.<\/p>\n\n\n\n<p>Soon his eight students were painting large abstracts expressing the raw emotion that had so long been trapped inside. \u201cThe paintings look like feeling, real feeling,\u201d Lefens says. He could see the painters \u201ccross the line from stasis\u2014nothing is happening, they are getting cleaned up by staff, they are being fed, being wheeled on the bus\u2014to being \u2018the boss,\u2019 and everything is their vision.\u201d<\/p>\n\n\n\n<p><strong>Launching a new venture.&nbsp;<\/strong>Lefens\u2019 and his students dreamed of an art opening in New York. As a step toward that goal, Lefens organized a show at the School of Visual Arts at Rutgers University, in New Brunswick, N.J., which drew art lovers and donors. Soon after, \u201cCBS Evening News\u201d featured the art program on an \u201cEye on America\u201d segment.<\/p>\n\n\n\n<p>The national attention was a public relations boon for the Matheny School, but when Lefens broached the idea of taking his technologies to people with disabilities around the country, the school\u2019s president balked. A doctor friend took Lefens aside and said, \u201cYou could do this yourself.\u201d Lefens replied, \u201cI am a painter, not a business man. I\u2019m terrified. It sounds right, but how can I do it?\u201d<\/p>\n\n\n\n<p>But he pressed forward with help from friends, setting up a nonprofit corporation called&nbsp;<a href=\"https:\/\/www.google.com\/search?q=Tim+Lefens,+A.R.T.&amp;tbm=isch&amp;tbo=u&amp;source=univ&amp;sa=X&amp;ei=LWcBUuGrCYWs4AO_5YDIDA&amp;ved=0CEUQsAQ&amp;biw=1364&amp;bih=622\">A.R.T.<\/a>, for Artistic Realization Technologies, in 1995. Roy Lichenstein sent the first $5,000, and then the second. Lefens hired an assistant, then bought a computer\u2014\u201cbecause all businesses have computers,\u201d he says\u2014and a program that enabled him to use it with his failing sight.<\/p>\n\n\n\n<p>Then came that long-hoped-for gallery opening in New York, where the entire show of student paintings sold out. A seven-foot abstract called \u201cA Bear,\u201d painted by a man named J.R., sold to a Disney executive in California. \u201cJ.R.\u2019s mother was told at his birth to let him go, to put him in the system, and not to follow up,\u201d Lefens says. \u201cHe would be incapable of anything, period. He would just be a heartache \u2026 . That is a long way away from being incapable.\u201d<\/p>\n\n\n\n<p><strong>Becoming an&nbsp;<em>RWJF Community Health Leader<\/em>.&nbsp;<\/strong>When Lefens was awarded the&nbsp;<em>Community Health Leader<\/em>&nbsp;grant in 1998, A.R.T. had little more than its breakthrough technology, a small studio in Princeton, N.J., a couple of office staff and some volunteer trackers. \u201cWe absolutely took off with the RWJF grant,\u201d he says. \u201cIt was a game changer.\u201d<\/p>\n\n\n\n<p>With the grant, Lefens was able to reach out to numerous organizations that served people with profound disabilities\u2014from large ones, like Easter Seals and United Cerebral Palsy, to public schools systems, to the small, private institutions that are tucked away around the country.<\/p>\n\n\n\n<p>Being a Community Health Leader provided him much more than money, Lefens says. \u201cThey [<em>Community Health Leader<\/em>&nbsp;program staff] were heavy duty guides,\u201d he says. \u201cI could go to them and say, \u2018I\u2019m trying to do this. What do we do?\u2019 It was a very active connection\u2014two times a week talking to them for years.\u201d<\/p>\n\n\n\n<p>In the early 2000s, Lefens, at that point legally blind, used Window Eyes, a computer program for the visually impaired, to write&nbsp;<em>Flying Colors,<\/em>&nbsp;about his journey to create A.R.T. It was published by Beacon Press and named the best nonfiction book of 2002 by&nbsp;<em>Reader\u2019s Digest<\/em>.<\/p>\n\n\n\n<p><strong>Looking ahead.&nbsp;<\/strong>Blessed with a restless mind, Lefens has created other technologies that enable people with disabilities to create sculptures, art photography, and music. But in a poor economy, most organizations can\u2019t afford the systems, he says. His simple laser system for painting, largely unchanged since its creation, remains the core of A.R.T.\u2019s model.<\/p>\n\n\n\n<p>As of 2013, A.R.T. had 27 programs up and running in 11 states. Funders in addition to RWJF include Kessler Foundation, Christopher and Dana Reeve Foundation, the National Endowment for the Arts, and Princeton University.<\/p>\n\n\n\n<p>A.R.T. has worked with children as young as three up through people in their 40s. Lefens would also like to reach elderly people and returning veterans with traumatic brain injuries and lost limbs, but he has yet not been able to find an opening into the Veterans Administration system.<\/p>\n\n\n\n<p>\u201cIf they would let us in, we would bring our wagon and set up the studio, and work with some of these guys who\u2019ve got a really bad deal,\u201d Lefens says. \u201cOur thing is not a pity party. It is complete self-control. It is empowering. It is not like \u2018Oh, I\u2019m going to hold your hand and you make a valentine.\u2019 If you have a dark vision, you can make that happen in a painting.\u201d<\/p>\n\n\n\n<p><strong>RWJF Perspective:&nbsp;<\/strong>RWJF recognized the first 10 Community Health Leaders in 1993. They are unsung and inspiring individuals who work in their communities\u2014often among the most disenfranchised populations\u2014to address some of the nation\u2019s most intractable health care problems. The formal recognition of these&nbsp;<em>Robert Wood Johnson Foundation Community Health Leaders<\/em>&nbsp;and their programs often launches them to greater levels of influence and extends their reach to serve more vulnerable populations. For more information on the program see&nbsp;<a href=\"https:\/\/www.rwjf.org\/content\/rwjf\/en\/library\/research\/2011\/10\/robert-wood-johnson-foundation-community-health-leaders.html\">Program Results Report<\/a>.<\/p>\n\n\n\n<p>Under the&nbsp;<em>RWJF Community Health Leaders&nbsp;<\/em>award, each year RWJF has provided a $125,000 award to 10 individuals and their organizations ($105,000 supports a project at their organization and $20,000 goes directly to the leader for personal development). RWJF also connects the&nbsp;<em>RWJF Community Health Leaders<\/em>&nbsp;with each other so they can continue their work with the support and experience of their peers and previous award winners.<\/p>\n\n\n\n<p>\u201cCommunity Health Leaders are characterized by three specific traits\u2014they are courageous, they are creative, and they are committed,\u201d says National Program Director Janice Ford Griffin. \u201cThe Foundation recognizes the tremendous resource of experience among the leaders and we look forward to mining that resource as we consider future initiatives.\u201d<\/p>\n\n\n\n<p>\u201cThrough the&nbsp;<em>Robert Wood Johnson Foundation Community Health Leaders<\/em>&nbsp;award, we at the Foundation have the opportunity to recognize innovative and courageous local leaders behind ground-breaking efforts in communities across the United States,\u201d said Sallie George, MPH, program officer at RWJF. \u201cThese individuals remind us that one person can have a powerful impact on health and health care within their communities.\u201d<\/p>\n\n\n\n<p>The last round of leaders was chosen in the fall of 2012.<\/p>\n\n\n\n<p><strong>Overview<\/strong><\/p>\n\n\n\n<p>An artist who began to lose his sight decided that he wanted to help disabled people find a way to still create art. Instead of treating them as helpless and incompetent, he gave them back the power to make decisions and express themselves in a way they could not do before. He created interesting systems, such as large floor paintings and a laser to display their decisions, that allowed very disabled people the control to make something amazing. The art that came out of this is really inspiring, and it reinforces the idea that disabled people must be viewed as equal to everyone else. They have so much inside that they have not been given an avenue to express. We as designers must provide that for them, so that we can learn even more from them.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>People with severe disabilities are learning to express themselves through art, thanks to the passion of Tim Lefens, named a&nbsp;Robert Wood Johnson Foundation Community Health Leader&nbsp;in 1998. The problem.&nbsp;People with severe physical disabilities often feel that the essence of who they are is trapped inside their bodies. And they are often infantilized, treated as if [&hellip;]<\/p>\n","protected":false},"author":32,"featured_media":5487,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[21],"tags":[],"class_list":{"0":"post-5486","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-arts"},"_links":{"self":[{"href":"https:\/\/desis.osu.edu\/seniorthesis\/index.php\/wp-json\/wp\/v2\/posts\/5486","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/desis.osu.edu\/seniorthesis\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/desis.osu.edu\/seniorthesis\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/desis.osu.edu\/seniorthesis\/index.php\/wp-json\/wp\/v2\/users\/32"}],"replies":[{"embeddable":true,"href":"https:\/\/desis.osu.edu\/seniorthesis\/index.php\/wp-json\/wp\/v2\/comments?post=5486"}],"version-history":[{"count":1,"href":"https:\/\/desis.osu.edu\/seniorthesis\/index.php\/wp-json\/wp\/v2\/posts\/5486\/revisions"}],"predecessor-version":[{"id":5489,"href":"https:\/\/desis.osu.edu\/seniorthesis\/index.php\/wp-json\/wp\/v2\/posts\/5486\/revisions\/5489"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/desis.osu.edu\/seniorthesis\/index.php\/wp-json\/wp\/v2\/media\/5487"}],"wp:attachment":[{"href":"https:\/\/desis.osu.edu\/seniorthesis\/index.php\/wp-json\/wp\/v2\/media?parent=5486"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/desis.osu.edu\/seniorthesis\/index.php\/wp-json\/wp\/v2\/categories?post=5486"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/desis.osu.edu\/seniorthesis\/index.php\/wp-json\/wp\/v2\/tags?post=5486"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}