{"id":29847,"date":"2011-01-02T07:08:42","date_gmt":"2011-01-02T05:08:42","guid":{"rendered":"http:\/\/www.turkishforum.com.tr\/en\/content\/?p=29847"},"modified":"2023-04-05T10:59:52","modified_gmt":"2023-04-05T07:59:52","slug":"nurturing-musical-dreams-in-a-wheelchair","status":"publish","type":"post","link":"https:\/\/www.turkishnews.com\/en\/content\/2011\/01\/02\/nurturing-musical-dreams-in-a-wheelchair\/","title":{"rendered":"Nurturing Musical Dreams in a Wheelchair"},"content":{"rendered":"<p>By JENNIFER MASCIA<\/p>\n<p>Published: January 1, 2011<\/p>\n<p>At the flip of some switches on his computer, Jason Celik\u2019s room fills with a melodic hip-hop beat. After a few bars, his older brother\u2019s sleepy, streetwise rhymes kick in, reminiscent of the young rapper Drake. Their father, Muzzafer, who is from Istanbul, stands in the background and proudly bobs his head, delighted by the strains of traditional Turkish music woven into the track.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter size-full wp-image-29849\" src=\"https:\/\/www.turkishnews.com\/en\/content\/wp-content\/uploads\/2011\/01\/celik-NEEDIEST.jpg\" alt=\"\" width=\"600\" height=\"347\" srcset=\"https:\/\/www.turkishnews.com\/en\/content\/wp-content\/uploads\/2011\/01\/celik-NEEDIEST.jpg 600w, https:\/\/www.turkishnews.com\/en\/content\/wp-content\/uploads\/2011\/01\/celik-NEEDIEST-300x174.jpg 300w\" sizes=\"auto, (max-width: 600px) 100vw, 600px\" \/><\/p>\n<p>\u201c \u2018Leylim Ley,\u2019 \u201d Mr. Celik said, identifying the song his son has sampled.<\/p>\n<p>Jason Celik\u2019s musical talents are all the more impressive given that he is able to move only his right hand and two fingers on his left. Now 21, he is paralyzed as a result of Duchenne muscular dystrophy, characterized by the progressive loss of muscle strength.<\/p>\n<p>When he was a toddler, his mother, Ann Marie, 48, recalled, \u201cI noticed he had a problem going up the stairs.\u201d By the time he was 7, he was in a wheelchair.<\/p>\n<p>Respiratory and cardiac problems are common with Duchenne, and when Jason Celik was 18, his respiratory muscles were so weak that he was intubated for six weeks and nearly died.<\/p>\n<p>\u201cSix weeks of fighting,\u201d Ms. Celik calls it, and during that time she clashed with insurance companies and doctors who wanted her son to have a tracheotomy tube permanently inserted.<\/p>\n<p>\u201cBy the grace of God, he\u2019s been O.K.,\u201d Ms. Celik said.<\/p>\n<p>His room, littered with medical devices, betrays how completely his life revolves around his illness. A cough-assist machine sucks phlegm from his lungs when his muscles are too weak. Without it, he would be plagued by bronchitis and pneumonia. He wears a brave smile, but he cannot scratch his own itches, use the bathroom without help, roll over in the middle of the night \u2014 his mother sleeps next to him so she can help with that \u2014 or haul himself into the shower. His musical collaborator and brother, Peter, 24, helps him to do that.<\/p>\n<p>\u201cBut as God as my witness, he never complains,\u201d Ms. Celik said as her husband nuzzled Jason\u2019s cheek.<\/p>\n<p>She added, however, \u201cJason is a man, and he wants to retain his dignity and have a shower.\u201d She described plans to install a rolling shower in one of the bathrooms.<\/p>\n<p>More drastic renovation was required before the Celiks could move into their four-bedroom house in Cedarhurst on Long Island. Doorways were widened for her son\u2019s wheelchair, and a sturdy wooden ramp was installed on one side of the house. It has been a vast improvement over the two-bedroom apartment the family shared in Elmont, which had holes in every wall from being hit by the wheelchair.<\/p>\n<p>The Celiks needed space, but it was not until they found a program called Partners in Dignity at FEGS Health and Human Services System that they imagined state funds could pay for their relocation and home renovations.<\/p>\n<p>At the agency, the Celiks learned of the Nursing Home Transition and Diversion Medicaid Waiver Program, which grants money to people with disabilities so they can alter their houses to accommodate their needs.<\/p>\n<p>Finding the house was difficult because landlords are often unwilling to accept the subsidy or to have their properties modified, especially since the state does not pay to have the work undone if the disabled tenant moves out, said Lori Hardoon, the director of Partners in Dignity.<\/p>\n<p>\u201cThank God for this grant, because, quite honestly, we never would have been able to move in here,\u201d said Ms. Celik, a 23-year veteran of the United States Postal Service.<\/p>\n<p>FEGS is a beneficiary of UJA-Federation of New York, one of the seven organizations supported by The New York Times Neediest Cases Fund. The fund contributed half the broker\u2019s fee, or $1,190.<\/p>\n<p>Ms. Celik home-schooled her son, who taught himself how to produce music with the help of computer programs.<\/p>\n<p>\u201cHe\u2019s a real go-getter,\u201d she said. More than anything, he wants a music internship. A framed print hanging above the futon in Peter\u2019s room, which doubles as a music studio, reads, \u201cFind your stage door and open it.\u201d<\/p>\n<p>\u201cPeople aren\u2019t very receptive,\u201d Ms. Celik said, gesturing to Jason in his wheelchair. \u201cBut they don\u2019t know just how much he can really do.\u201d<\/p>\n<p>Video: <\/p>\n<p>via <span class=\"removed_link\" title=\"http:\/\/www.nytimes.com\/2011\/01\/02\/nyregion\/02neediest.html?_r=1\">Nurturing Musical Dreams in a Wheelchair &#8211; Neediest Cases &#8211; NYTimes.com<\/span>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>By JENNIFER MASCIA Published: January 1, 2011 At the flip of some switches on his computer, Jason Celik\u2019s room fills with a melodic hip-hop beat. After a few bars, his older brother\u2019s sleepy, streetwise rhymes kick in, reminiscent of the young rapper Drake. Their father, Muzzafer, who is from Istanbul, stands in the background and [&hellip;]<\/p>\n","protected":false},"author":83,"featured_media":29849,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[34],"tags":[],"class_list":["post-29847","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-usa"],"_links":{"self":[{"href":"https:\/\/www.turkishnews.com\/en\/content\/wp-json\/wp\/v2\/posts\/29847","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.turkishnews.com\/en\/content\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.turkishnews.com\/en\/content\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.turkishnews.com\/en\/content\/wp-json\/wp\/v2\/users\/83"}],"replies":[{"embeddable":true,"href":"https:\/\/www.turkishnews.com\/en\/content\/wp-json\/wp\/v2\/comments?post=29847"}],"version-history":[{"count":0,"href":"https:\/\/www.turkishnews.com\/en\/content\/wp-json\/wp\/v2\/posts\/29847\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.turkishnews.com\/en\/content\/wp-json\/wp\/v2\/media\/29849"}],"wp:attachment":[{"href":"https:\/\/www.turkishnews.com\/en\/content\/wp-json\/wp\/v2\/media?parent=29847"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.turkishnews.com\/en\/content\/wp-json\/wp\/v2\/categories?post=29847"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.turkishnews.com\/en\/content\/wp-json\/wp\/v2\/tags?post=29847"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}