{"id":92306,"date":"2016-04-13T15:15:34","date_gmt":"2016-04-13T19:15:34","guid":{"rendered":"\/news\/?p=92306"},"modified":"2016-05-13T15:48:09","modified_gmt":"2016-05-13T19:48:09","slug":"voice-contestant-spreads-awareness-children-special-needs","status":"publish","type":"post","link":"https:\/\/archive.liveaction.org\/news\/voice-contestant-spreads-awareness-children-special-needs\/","title":{"rendered":"&#8216;The Voice&#8217; contestant&#8217;s son with special needs &#8216;grateful to be alive&#8217;"},"content":{"rendered":"<div style=\"margin-top: 0px; margin-bottom: 0px;\" class=\"sharethis-inline-share-buttons\" ><\/div><p>When Nick Hagelin stepped onto the stage to audition for <em>The Voice<\/em>, he had a big fan backstage in his young son Bash. Bash, along with his mom Christina, joined Hagelin on stage after the audition and it was immediately visible that Bash has special needs. Hagelin explained that doctors told them Bash might never be able to walk, but there he was, walking out onto the stage to show support for his dad.<\/p>\n<p><!--more--><\/p>\n<p>At just nine days old Bash was diagnosed with Arthrogryposis Multiplex Congenita (AMC), a condition in which joints are permanently fixed in a bent or straightened position. Some children born with this condition do not survive, including one baby boy who was born just hours apart from Bash in the same hospital and delivered by the same midwife. That baby\u2019s spin was bent and locked in a C shape and he was unable to breathe. In Bash\u2019s case, his elbows were locked straight, and his hands locked in a bent position. His knees and feet were also affected. Doctors said that he may never be able to take care of himself, but his parents were determined to help their son become independent in any way they could.<\/p>\n<p><iframe loading=\"lazy\" style=\"border: none; overflow: hidden;\" src=\"https:\/\/www.facebook.com\/plugins\/post.php?href=https%3A%2F%2Fwww.facebook.com%2FNickHagelinOfficial%2Fposts%2F10153949325864663%3A0&amp;width=500\" width=\"500\" height=\"715\" frameborder=\"0\" scrolling=\"no\"><\/iframe>\u201cHard work has always been a part of this boy\u2019s life and it\u2019s his perseverance and winning attitude in the face of adversity that make him such a remarkable individual. [\u2026] It\u2019s never about what you can\u2019t do and always about what you can do,\u201d Hagelin says in <a href=\"http:\/\/www.bashdimpleton.com\/\">a video about Bash<\/a>. His family chronicles Bash\u2019s challenges and achievements in order to raise awareness for AMC and help other families discover therapies to help their children.<\/p>\n<p><iframe loading=\"lazy\" src=\"https:\/\/player.vimeo.com\/video\/42240952\" width=\"500\" height=\"281\" frameborder=\"0\" allowfullscreen=\"allowfullscreen\"><\/iframe><\/p>\n<p><a href=\"https:\/\/vimeo.com\/42240952\">See Bash Go: An Inspirational Story<\/a> from <a href=\"https:\/\/vimeo.com\/seebashgo\">Bash Dimpleton<\/a> on <a href=\"https:\/\/vimeo.com\">Vimeo<\/a>.<\/p>\n<p>Hagelin describes his son as \u201cfull of wonderment and bliss with a big appetite for life.\u201d He says that Bash \u201cgreets each day with a smile, grateful to be alive.\u201d<\/p>\n<p>Bash\u2019s devoted family has used every therapy available to them to help Bash, and that plan eventually paid off. When Bash was one and a half, he was finally able to move around on his own by rolling, scooting, riding his toys, and using a specialized device that allowed him to walk with assistance. His parents worked tirelessly to help him stand up and flex his arms. Then on Easter Sunday at two years old, he took his first independent steps, which Hagelin called a \u201cmiracle.\u201d<\/p>\n<div id=\"attachment_92308\" style=\"width: 484px\" class=\"wp-caption aligncenter\"><img aria-describedby=\"caption-attachment-92308\" decoding=\"async\" loading=\"lazy\" class=\"wp-image-92308 size-large\" src=\"https:\/\/www.liveactionnews.org\/wp-content\/uploads\/2016\/04\/bash-560x700.jpg\" alt=\"Nick and Bash Hagelin via Facebook\" width=\"474\" height=\"593\" srcset=\"https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/04\/bash-560x700.jpg 560w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/04\/bash-240x300.jpg 240w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/04\/bash-768x959.jpg 768w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/04\/bash.jpg 1080w\" sizes=\"(max-width: 474px) 100vw, 474px\" \/><p id=\"caption-attachment-92308\" class=\"wp-caption-text\">Nick and Bash Hagelin via Facebook<\/p><\/div>\n<p>Without elbows that bend, it has always been extremely difficult, and one would think even impossible, for Bash to feed himself, but this boy doesn\u2019t quit. Even after so many attempts that end with the fork on the floor, he keeps going and keeps smiling. At age two, Bash became eligible for surgery on his elbows that his parents hoped would finally allow him to overcome this challenge.<\/p>\n<p>\u201cI want to feed myself,\u201d he says as his parents prepare him for his surgery by having him perform \u201csurgery\u201d on a Buzz Lightyear toy. And he would. That surgery was successful, and his elbows now have a 90 degree bend allowing him to feed himself consistently. He still has a lot of work to do to strengthen his muscles which are weak and underused, but his family recently learned about a device called Magic Arms that can help him gain even more mobility.<\/p>\n<div class=\"video-container\"><iframe loading=\"lazy\" width=\"1000\" height=\"563\" src=\"https:\/\/www.youtube.com\/embed\/oC5vNuZe61M?feature=oembed\" frameborder=\"0\" allowfullscreen><\/iframe><\/div>\n<p>Most of his treatments have not been covered by insurance, so the Hagelins have had to rely on donations, but Bash, now age four, has a huge network of support which has grown even larger thanks to his father\u2019s appearances on The Voice. Bash is showing the world that children with special needs and different abilities live beautiful lives. He has a contagiously happy spirit, a hilarious sense of humor, a dimpled smile, and a very bright future.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>When Nick Hagelin stepped onto the stage to audition for The Voice, he had a big fan backstage in his young son Bash. Bash, along with his mom Christina, joined Hagelin on stage after the audition and it was immediately visible that Bash has special needs. Hagelin explained that doctors told them Bash might never [&hellip;]<\/p>\n","protected":false},"author":62,"featured_media":92415,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false},"categories":[4],"tags":[1966,8350,8349,8347,8348],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v20.7 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>The Voice contestant&#039;s son with special needs &quot;grateful to be alive&quot;<\/title>\n<meta name=\"description\" content=\"&quot;Hard work has always been a part of this boy\u2019s life and it\u2019s his perserverance and winning attitude... that make him such a remarkable individual.&quot;\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/archive.liveaction.org\/news\/voice-contestant-spreads-awareness-children-special-needs\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"The Voice contestant&#039;s son with special needs &quot;grateful to be alive&quot;\" \/>\n<meta property=\"og:description\" content=\"&quot;Hard work has always been a part of this boy\u2019s life and it\u2019s his perserverance and winning attitude... that make him such a remarkable individual.&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/archive.liveaction.org\/news\/voice-contestant-spreads-awareness-children-special-needs\/\" \/>\n<meta property=\"og:site_name\" content=\"Live Action News\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/liveaction\" \/>\n<meta property=\"article:published_time\" content=\"2016-04-13T19:15:34+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2016-05-13T19:48:09+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/04\/bash-2-1.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"672\" \/>\n\t<meta property=\"og:image:height\" content=\"359\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"Nancy Flanders\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:creator\" content=\"@liveaction\" \/>\n<meta name=\"twitter:site\" content=\"@liveaction\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Nancy Flanders\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"3 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\/\/archive.liveaction.org\/news\/voice-contestant-spreads-awareness-children-special-needs\/#article\",\"isPartOf\":{\"@id\":\"https:\/\/archive.liveaction.org\/news\/voice-contestant-spreads-awareness-children-special-needs\/\"},\"author\":{\"name\":\"Nancy Flanders\",\"@id\":\"https:\/\/archive.liveaction.org\/news\/#\/schema\/person\/d61ca3dd1aacf12635bdf71d75c328ef\"},\"headline\":\"&#8216;The Voice&#8217; 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