{"id":2994,"date":"2020-05-27T19:29:33","date_gmt":"2020-05-27T19:29:33","guid":{"rendered":"http:\/\/alianzapacientes.org\/?p=2994"},"modified":"2020-05-27T19:29:33","modified_gmt":"2020-05-27T19:29:33","slug":"treacher-collins-dia-campana-y-cine","status":"publish","type":"post","link":"https:\/\/www.marianakirby.com\/alapa\/2020\/05\/27\/treacher-collins-dia-campana-y-cine\/","title":{"rendered":"Treacher Collins: d\u00eda, campa\u00f1a y cine"},"content":{"rendered":"<p>No es un d\u00eda m\u00e1s para las personas con el <strong>S\u00edndrome de Treacher Collins<\/strong>. Tampoco para sus familiares y amigos. En este d\u00eda lideran una lucha que no tiene fronteras: lograr que el <strong>28 de mayo<\/strong> sea reconocido como el <strong>D\u00eda Mundial del S\u00edndrome de Treacher Collins<\/strong>. La iniciativa cuenta con el apoyo de organizaciones de Espa\u00f1a, M\u00e9xico, Costa Rica y la Argentina. Apuestan a visibilizar a esta <strong>enfermedad poco frecuente<\/strong> a trav\u00e9s de una campa\u00f1a viral en las redes sociales.<\/p>\n<p>Pero primero, debemos saber de qu\u00e9 hablamos cuando decimos S\u00edndrome de Treacher Collins. Tal vez algunos tendr\u00e1n alguna idea por la pel\u00edcula <strong>Wonder<\/strong>.<\/p>\n<p><a href=\"https:\/\/www.orpha.net\/consor\/cgi-bin\/index.php?lng=ES\" target=\"_blank\" rel=\"noopener noreferrer\">Orphanet<\/a>, p\u00e1gina de cabecera a la hora de buscar informaci\u00f3n sobre enfermedades poco frecuentes, lo define como un trastorno cong\u00e9nito del desarrollo craneofacial caracterizado por una displasia otomandibular sim\u00e9trica bilateral sin anomal\u00edas de las extremidades, asociado a diversas anomal\u00edas de cabeza y cuello.<\/p>\n<p>En la <strong>Argentina<\/strong> no existe un registro de cu\u00e1ntas personas hay con este s\u00edndrome pero desde <a href=\"https:\/\/www.facebook.com\/sindrometreacherArgentina\/\" target=\"_blank\" rel=\"noopener noreferrer\"><strong>Amigos S\u00edndrome Treacher Collins Argentina<\/strong><\/a> afirmaron que tienen contacto con entre 60 y 70 familias de todo el pa\u00eds.<\/p>\n<p>&nbsp;<\/p>\n<figure id=\"attachment_2997\" aria-describedby=\"caption-attachment-2997\" style=\"width: 347px\" class=\"wp-caption aligncenter\"><img fetchpriority=\"high\" decoding=\"async\" class=\"wp-image-2997\" src=\"http:\/\/alianzapacientes.org\/wp-content\/uploads\/2020\/05\/Treacher-foto-300x194.jpg\" alt=\"Foto de pacientes con el S\u00edndrome de Treacher Collins\" width=\"347\" height=\"224\" srcset=\"https:\/\/www.marianakirby.com\/alapa\/wp-content\/uploads\/2020\/05\/Treacher-foto-300x194.jpg 300w, https:\/\/www.marianakirby.com\/alapa\/wp-content\/uploads\/2020\/05\/Treacher-foto-768x498.jpg 768w, https:\/\/www.marianakirby.com\/alapa\/wp-content\/uploads\/2020\/05\/Treacher-foto.jpg 833w\" sizes=\"(max-width: 347px) 100vw, 347px\" \/><figcaption id=\"caption-attachment-2997\" class=\"wp-caption-text\">Foto de Amigos S\u00edndrome Treacher Collins Argentina<\/figcaption><\/figure>\n<p>&nbsp;<\/p>\n<h3><span style=\"color: #800080;\"><strong>\u00a1Fuera estereotipos!<\/strong><\/span><\/h3>\n<p>Como dec\u00edamos previamente, organizaciones y grupos de pacientes de diferentes pa\u00edses han convenido trabajar para que el 28 de mayo sea reconocido como el <strong>D\u00eda Mundial del S\u00edndrome de Treacher Collins<\/strong>.<\/p>\n<p>Para este d\u00eda han propuesto una campa\u00f1a a trav\u00e9s de las redes sociales cuyo objetivo es visibilizar a esta enfermedad poco frecuente mostrando una foto junto a un paciente con este s\u00edndrome. La misma debe ser acompa\u00f1ada con el siguiente texto:<\/p>\n<p>&nbsp;<\/p>\n<blockquote>\n<h4 style=\"text-align: center;\"><span style=\"color: #000000;\"><em><strong>#28-M #DiaTreacherCollins <\/strong><\/em><\/span><\/h4>\n<h4 style=\"text-align: center;\"><span style=\"color: #000000;\"><em><strong>\u00a1Fuera estereotipos! En el mundo cabemos todos<\/strong><\/em><\/span><\/h4>\n<\/blockquote>\n<p>&nbsp;<\/p>\n<h3><span style=\"color: #800080;\"><strong>Treacher Collins en la Argentina<\/strong><\/span><\/h3>\n<p>En nuestro pa\u00eds se puede obtener m\u00e1s informaci\u00f3n sobre la patolog\u00eda siguiendo la p\u00e1gina <a href=\"https:\/\/www.facebook.com\/sindrometreacherArgentina\/\" target=\"_blank\" rel=\"noopener noreferrer\">Amigos S\u00edndrome Treacher Collins Argentina<\/a>.<\/p>\n<p>Este grupo present\u00f3 hace m\u00e1s de cuatro a\u00f1os un proyecto para lograr la declaraci\u00f3n del <strong>D\u00eda Nacional del S\u00edndrome de Treacher Collins<\/strong>. El proyecto no lleg\u00f3 a tratarse en plenario en la C\u00e1mara de Diputados ya que la diputada que lo impulsaba, cumpli\u00f3 con su mandato y el proyecto se cay\u00f3. El a\u00f1o pasado lo intentaron nuevamente pero con el contexto actual, no hubo avances.<\/p>\n<p>&nbsp;<\/p>\n<figure id=\"attachment_2999\" aria-describedby=\"caption-attachment-2999\" style=\"width: 347px\" class=\"wp-caption aligncenter\"><img decoding=\"async\" class=\"wp-image-2999\" src=\"http:\/\/alianzapacientes.org\/wp-content\/uploads\/2020\/05\/treacher-wonder-300x150.jpg\" alt=\"Flyer de difusi\u00f3n de la pel\u00edcula Wonder.\" width=\"347\" height=\"174\" srcset=\"https:\/\/www.marianakirby.com\/alapa\/wp-content\/uploads\/2020\/05\/treacher-wonder-300x150.jpg 300w, https:\/\/www.marianakirby.com\/alapa\/wp-content\/uploads\/2020\/05\/treacher-wonder-768x384.jpg 768w, https:\/\/www.marianakirby.com\/alapa\/wp-content\/uploads\/2020\/05\/treacher-wonder.jpg 800w\" sizes=\"(max-width: 347px) 100vw, 347px\" \/><figcaption id=\"caption-attachment-2999\" class=\"wp-caption-text\">Flyer de difusi\u00f3n de la pel\u00edcula Wonder.<\/figcaption><\/figure>\n<p>&nbsp;<\/p>\n<h3><span style=\"color: #800080;\"><strong>La pel\u00edcula Wonder y su efecto<\/strong><\/span><\/h3>\n<p>A fines de 2017 fue estrenada la pel\u00edcula Wonder, basada en el libro de Raquel Palacio, que cont\u00f3 con la actuaci\u00f3n de Julia Roberts, Owen Wilson y Jacob Tremblay.<\/p>\n<p>Refleja la historia de un ni\u00f1o de 10 a\u00f1os que tiene S\u00edndrome de Treacher Collins y que, luego de varias operaciones y de ser educado en su casa, ingresa al colegio en el quinto grado.<\/p>\n<p>La pel\u00edcula muestra lo que viven a diario las personas con esta patolog\u00eda pero tambi\u00e9n, todo lo que pueden lograr.<\/p>\n<p>M\u00e1s all\u00e1 del gusto personal o no por la pel\u00edcula, la misma logr\u00f3 que se sepa m\u00e1s sobre la patolog\u00eda. Despu\u00e9s de su emisi\u00f3n, en la Argentina los casos identificados por <a href=\"https:\/\/www.facebook.com\/sindrometreacherArgentina\/\" target=\"_blank\" rel=\"noopener noreferrer\">Amigos S\u00edndrome Treacher Collins Argentina<\/a> pasaron de 40 a 70.<\/p>\n<p>&nbsp;<\/p>\n<p><iframe title=\"Wonder - Trailer espa\u00f1ol (HD)\" width=\"800\" height=\"450\" src=\"https:\/\/www.youtube.com\/embed\/S6AXHRx_0xk?feature=oembed\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture; web-share\" referrerpolicy=\"strict-origin-when-cross-origin\" allowfullscreen><\/iframe><\/p>\n","protected":false},"excerpt":{"rendered":"<p>No es un d\u00eda m\u00e1s para las personas con el S\u00edndrome de Treacher Collins. Tampoco para sus familiares y amigos. En este d\u00eda lideran una lucha que no tiene fronteras: lograr que el 28 de mayo sea reconocido como el D\u00eda Mundial del S\u00edndrome de Treacher Collins. La iniciativa cuenta con el apoyo de organizaciones [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":2996,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_joinchat":[],"footnotes":""},"categories":[7],"tags":[],"class_list":["post-2994","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-enfermedades-poco-frecuentes"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Treacher Collins: d\u00eda, campa\u00f1a y cine - Alianza Argentina de Pacientes - ALAPA<\/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:\/\/www.marianakirby.com\/alapa\/2020\/05\/27\/treacher-collins-dia-campana-y-cine\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Treacher Collins: d\u00eda, campa\u00f1a y cine - Alianza Argentina de Pacientes - ALAPA\" \/>\n<meta property=\"og:description\" content=\"No es un d\u00eda m\u00e1s para las personas con el S\u00edndrome de Treacher Collins. Tampoco para sus familiares y amigos. En este d\u00eda lideran una lucha que no tiene fronteras: lograr que el 28 de mayo sea reconocido como el D\u00eda Mundial del S\u00edndrome de Treacher Collins. 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