{"id":5,"date":"2018-10-11T00:00:00","date_gmt":"2018-10-11T00:00:00","guid":{"rendered":"https:\/\/cota1.wpengine.com\/cotaforjensh\/our-story\/"},"modified":"2018-10-11T00:00:00","modified_gmt":"2018-10-11T00:00:00","slug":"our-story","status":"publish","type":"page","link":"https:\/\/cota.org\/cotaforjensh\/our-story\/","title":{"rendered":"Our Story"},"content":{"rendered":"<p>Jens was diagnosed with Cystic Fibrosis in 1984, at the age of 1. Jens&#8217;s health, due to Cystic Fibrosis, had been declining leading up to his transplant.&nbsp;Prior to his transplant in 2014, he spent over 4 hours a day doing breathing treatments, in addition to being hooked up to IV antibiotics for over 12 hours a day. His lung function was around 16%. At that point, he experienced his quality of life decline in such a way that he decided that it was time to pursue undergoing a double-lung transplant at the University of Pittsburgh Medical Center (<span data-scayt_word=\"UPMC\" data-scaytid=\"1\">UPMC<\/span>).<\/p>\n<p>On May 18, 2014, Jens received a double-lung transplant. He spent a year recovering in Pittsburgh, PA before moving to Durham, NC, where he currently resides.<\/p>\n<p>We hope that you will follow Jens&#8217;s amazing journey with us. Stay tuned to the Lungs 4 Jens&nbsp;<a href=\"http:\/\/www.facebook.com\/lungs4jens\" data-cke-saved-href=\"http:\/\/www.facebook.com\/lungs4jens\">Facebook page<\/a>&nbsp;and <a href=\"https:\/\/twitter.com\/Lungs4Jens\" data-cke-saved-href=\"https:\/\/twitter.com\/Lungs4Jens\">Twitter<\/a> for more updates!<\/p>\n<p>We are grateful to partner with the Children&#8217;s Organ Transplant Association (COTA), and organization that helps children and young adults who need a life-saving transplant by providing fundraising assistance and family support. COTA is the nation&rsquo;s only fundraising organization solely dedicated to raising life-saving dollars in honor of transplant-needy children and young adults. 100% of each contribution made to COTA in honor of our patients helps meet transplant-related expenses. COTA&rsquo;s services are free to our families, and gifts to COTA are tax deductible to the fullest extent of the law.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Jens was diagnosed with Cystic Fibrosis in 1984, at the age of 1. Jens&#8217;s health, due to Cystic Fibrosis, had been declining leading up to his transplant.&nbsp;Prior to his transplant in 2014, he spent over 4 hours a day doing breathing treatments, in addition to being hooked up to IV antibiotics for over 12 hours [&hellip;]<\/p>\n","protected":false},"author":0,"featured_media":6,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-5","page","type-page","status-publish","has-post-thumbnail","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/cota.org\/cotaforjensh\/wp-json\/wp\/v2\/pages\/5","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/cota.org\/cotaforjensh\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/cota.org\/cotaforjensh\/wp-json\/wp\/v2\/types\/page"}],"replies":[{"embeddable":true,"href":"https:\/\/cota.org\/cotaforjensh\/wp-json\/wp\/v2\/comments?post=5"}],"version-history":[{"count":0,"href":"https:\/\/cota.org\/cotaforjensh\/wp-json\/wp\/v2\/pages\/5\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/cota.org\/cotaforjensh\/wp-json\/wp\/v2\/media\/6"}],"wp:attachment":[{"href":"https:\/\/cota.org\/cotaforjensh\/wp-json\/wp\/v2\/media?parent=5"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}