{"id":14819,"date":"2020-10-30T06:56:57","date_gmt":"2020-10-29T18:56:57","guid":{"rendered":"https:\/\/spence-chapin.org\/?p=14819"},"modified":"2020-11-05T06:58:25","modified_gmt":"2020-11-04T18:58:25","slug":"keagan-una-historia-del-programa-de-adopcion-para-necesidades-especiales","status":"publish","type":"post","link":"https:\/\/spence-chapin.org\/es\/keagan-a-special-needs-adoption-program-story\/","title":{"rendered":"Keagan: una historia del programa de adopci\u00f3n para necesidades especiales"},"content":{"rendered":"<div class=\"wp-block-image\"><figure class=\"alignright size-large\"><img fetchpriority=\"high\" decoding=\"async\" width=\"198\" height=\"258\" src=\"https:\/\/spence-chapin.org\/wp-content\/uploads\/2020\/10\/Keagan.png\" alt=\"Keagan\" class=\"wp-image-14820\"\/><\/figure><\/div>\n\n\n\n<p>En febrero de 2017, Spence-Chapin recibi\u00f3 una llamada telef\u00f3nica sobre un beb\u00e9 que naci\u00f3 con un nevo gigante. M\u00e1s del 50% de la piel del beb\u00e9 estaba cubierto de nevus, una marca de nacimiento parecida a un lunar que cubr\u00eda una parte importante de su pecho y brazos. Sus padres no ten\u00edan los recursos econ\u00f3micos para cuidar a un ni\u00f1o con necesidades m\u00e9dicas importantes y sab\u00edan que le resultar\u00eda dif\u00edcil ser aceptado dentro de su comunidad.<\/p>\n\n\n\n<p>Spence-Chapin brind\u00f3 a la familia biol\u00f3gica asesoramiento continuo y servicios de apoyo mientras elaboraban un plan de adopci\u00f3n.  Mientras estaba en la unidad de cuidados intensivos neonatales, Keagan experiment\u00f3 una convulsi\u00f3n subcl\u00ednica, se le realiz\u00f3 una resonancia magn\u00e9tica y se le diagnostic\u00f3 melanosis neurocut\u00e1nea, una afecci\u00f3n grave en la que las c\u00e9lulas nevus est\u00e1n presentes en el cerebro, lo que potencialmente causa convulsiones y presi\u00f3n adicionales. Keagan fue trasladado a un centro pedi\u00e1trico para recibir atenci\u00f3n y seguimiento adicionales. Mientras Keagan estaba siendo atendido en el centro de salud pedi\u00e1trico, Spence-Chapin identific\u00f3 una familia adoptiva.<\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"alignleft size-large\"><img decoding=\"async\" width=\"270\" height=\"360\" src=\"https:\/\/spence-chapin.org\/wp-content\/uploads\/2020\/10\/Keagan3.png\" alt=\"Keagan3\" class=\"wp-image-14821\" srcset=\"https:\/\/spence-chapin.org\/wp-content\/uploads\/2020\/10\/Keagan3.png 270w, https:\/\/spence-chapin.org\/wp-content\/uploads\/2020\/10\/Keagan3-225x300.png 225w\" sizes=\"(max-width: 270px) 100vw, 270px\" \/><\/figure><\/div>\n\n\n\n<p>La madre adoptiva de Keagan ten\u00eda experiencia con necesidades especiales, tuvo dos hijos mayores adoptados y, lo mejor de todo, se enamor\u00f3 a primera vista al ver la foto de Keagan. R\u00e1pidamente identific\u00f3 al experto en Nevus en su \u00e1rea y se conect\u00f3 con grupos de apoyo en l\u00ednea. El d\u00eda de la colocaci\u00f3n, la madre adoptiva de Keagan lleg\u00f3 al hospital para recibir el alta, donde se reuni\u00f3 directamente con todo su equipo m\u00e9dico. Ella ya hab\u00eda comprado ropa apta para Nevus para Keagan para asegurarse de que estuviera c\u00f3modo porque las \u00e1reas cubiertas por nevus no tienen gl\u00e1ndulas sudor\u00edparas t\u00edpicas. La madre biol\u00f3gica de Keagan se acerc\u00f3 a Spence-Chapin despu\u00e9s de la colocaci\u00f3n para decirle que siente \u201cpaz\u201d al saber que Keagan est\u00e1 en buenas manos.<\/p>\n\n\n\n<p>Spence-Chapin contin\u00faa recibiendo actualizaciones de la madre adoptiva de Keagan. En 2020, le hizo saber a Spence-Chapin que Keagan era el modelo de una conferencia internacional de Nevus. Tambi\u00e9n ha aparecido en la revista People. Camina y habla y le encanta andar en kayak, nadar y meterse en todo.  Adora a su hermano y a su hermana y ellos a \u00e9l. Keagan usa un aud\u00edfono, lo que le ha ayudado enormemente a aprender nuevas palabras, y ha sido dado de alta de fisioterapia y terapia ocupacional. No ha tenido m\u00e1s problemas debido al nevo en su cerebro, pero contin\u00faa recibiendo resonancias magn\u00e9ticas de rutina.<\/p>\n\n\n\n<p>En un correo electr\u00f3nico a Spence-Chapin, su madre escribi\u00f3: <\/p>\n\n\n\n<figure class=\"wp-block-pullquote\"><blockquote><p>\u201cEs un ni\u00f1o incre\u00edblemente inteligente; asombra a todos los que lo conocen, incluidos los m\u00e9dicos. Si a eso le sumamos su ingenio y encanto, es bastante irresistible... Lo amo, lo adoro y siempre estar\u00e9 agradecida por haberlo dejado con nosotros\u201d.<\/p><\/blockquote><\/figure>\n\n\n\n<p class=\"has-normal-font-size\"><em>Esta historia es parte de nuestra serie de historias del Programa de Adopci\u00f3n para Necesidades Especiales, que conmemora los 25 a\u00f1os de nuestro Programa de Adopci\u00f3n para Necesidades Especiales. Celebramos estas historias y m\u00e1s durante todo el mes de noviembre para el Mes Nacional de la Adopci\u00f3n. Si desea apoyar programas para ni\u00f1os y familias como nuestro Programa de Adopci\u00f3n para Necesidades Especiales, visite&nbsp;<strong><a rel=\"noreferrer noopener\" href=\"https:\/\/spence-chapin.org\/es\/donar\/\" target=\"_blank\">www.spence-chapin.org\/donate<\/a>&nbsp;<\/strong>o comun\u00edquese con nuestra Oficina de Desarrollo al 212-360-0263. \u00a1Gracias!<\/em><\/p>","protected":false},"excerpt":{"rendered":"<p>In February 2017, Spence-Chapin received a phone call regarding a baby boy born with Giant Nevus. Over 50% of the baby\u2019s skin was covered with nevus, a \u00a0mole-like birthmark \u00a0covering a significant portion of his chest and arms. His parents did not have the financial resources to care for a child with significant medical needs, [&hellip;]<\/p>\n","protected":false},"author":7,"featured_media":14822,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"give_campaign_id":0,"footnotes":""},"categories":[1],"tags":[],"class_list":["post-14819","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Keagan: A Special Needs Adoption Program Story - Spence-Chapin<\/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:\/\/spence-chapin.org\/es\/keagan-una-historia-del-programa-de-adopcion-para-necesidades-especiales\/\" \/>\n<meta property=\"og:locale\" content=\"es_MX\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Keagan: A Special Needs Adoption Program Story - Spence-Chapin\" \/>\n<meta property=\"og:description\" content=\"In February 2017, Spence-Chapin received a phone call regarding a baby boy born with Giant Nevus. 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His parents did not have the financial resources to care for a child with significant medical needs, [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/spence-chapin.org\/es\/keagan-una-historia-del-programa-de-adopcion-para-necesidades-especiales\/\" \/>\n<meta property=\"og:site_name\" content=\"Spence-Chapin\" \/>\n<meta property=\"article:published_time\" content=\"2020-10-29T18:56:57+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2020-11-04T18:58:25+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/spence-chapin.org\/wp-content\/uploads\/2020\/10\/Keagan2.png\" \/>\n\t<meta property=\"og:image:width\" content=\"262\" \/>\n\t<meta property=\"og:image:height\" content=\"352\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"Erin Brown\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Escrito por\" \/>\n\t<meta name=\"twitter:data1\" content=\"Erin Brown\" \/>\n\t<meta name=\"twitter:label2\" content=\"Tiempo de lectura\" \/>\n\t<meta name=\"twitter:data2\" content=\"2 minutos\" \/>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Keagan: una historia del programa de adopci\u00f3n para necesidades especiales - Spence-Chapin","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/spence-chapin.org\/es\/keagan-una-historia-del-programa-de-adopcion-para-necesidades-especiales\/","og_locale":"es_MX","og_type":"article","og_title":"Keagan: A Special Needs Adoption Program Story - Spence-Chapin","og_description":"In February 2017, Spence-Chapin received a phone call regarding a baby boy born with Giant Nevus. 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