{"id":14,"date":"2024-09-27T18:14:56","date_gmt":"2024-09-27T18:14:56","guid":{"rendered":"https:\/\/cota1.wpengine.com\/cloningsite\/?page_id=14"},"modified":"2025-07-28T19:03:57","modified_gmt":"2025-07-28T19:03:57","slug":"our-story","status":"publish","type":"page","link":"https:\/\/cota.org\/cotafordeclansheart\/our-story\/","title":{"rendered":"Our Story"},"content":{"rendered":"\n<p>Our son Declan was diagnosed with hypertrophic cardiomyopathy, a genetic heart condition, as an infant.&nbsp; The disease progressed over the years to the point where he needed open-heart surgery in the summer of 2025, when he was 6 years old.&nbsp; We traveled to the Mayo Clinic in Minnesota from our home in Los Angeles for his surgery, which was on July 2<sup>nd<\/sup>, expecting to stay for two weeks.&nbsp; The surgery itself went well, but there were complications in the hours following, resulting in a total of 4 surgeries in the first week.&nbsp; He is now confined to the hospital on an ECMO (life support) machine to support his heart while he awaits a heart transplant here in Minnesota, so far from our home.<\/p>\n\n\n\n<p>We are working with the Children&#8217;s Organ Transplant Association (COTA) to raise funds for current and future transplant-related expenses in honor of Declan and children like him.&nbsp;&nbsp;<\/p>\n\n\n\n<p>COTA helps children and young adults who need a life-saving transplant by providing fundraising assistance and family support. COTA is the nation\u2019s 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\u2019s services are free to our families, and gifts to COTA are tax deductible to the fullest extent of the law.<\/p>\n\n\n\n<p>Thank you from the bottom of our hearts,<\/p>\n\n\n\n<p>Ryan and Kelly Quiller<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Our son Declan was diagnosed with hypertrophic cardiomyopathy, a genetic heart condition, as an infant.&nbsp; The disease progressed over the years to the point where he needed open-heart surgery in the summer of 2025, when he was 6 years old.&nbsp; We traveled to the Mayo Clinic in Minnesota from our home in Los Angeles for [&hellip;]<\/p>\n","protected":false},"author":5,"featured_media":83,"parent":0,"menu_order":0,"comment_status":"open","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-14","page","type-page","status-publish","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v26.6 (Yoast SEO v26.6) - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Our Story - COTA for Declan&#039;s Heart<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/cota.org\/cotafordeclansheart\/our-story\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Our Story\" \/>\n<meta property=\"og:description\" content=\"Our son Declan was diagnosed with hypertrophic cardiomyopathy, a genetic heart condition, as an infant.&nbsp; 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