{"id":3406,"date":"2017-12-05T07:35:57","date_gmt":"2017-12-05T07:35:57","guid":{"rendered":"https:\/\/sindromecharge.es\/index.php\/2017\/12\/05\/carta-a-jaime-mi-nino-de-oro\/"},"modified":"2017-12-05T07:35:57","modified_gmt":"2017-12-05T07:35:57","slug":"carta-a-jaime-mi-nino-de-oro","status":"publish","type":"post","link":"https:\/\/sindromecharge.es\/index.php\/2017\/12\/05\/carta-a-jaime-mi-nino-de-oro\/","title":{"rendered":"Carta a Jaime, mi ni\u00f1o de oro"},"content":{"rendered":"<p>Leemos en 20minutos la siguiente noticia que os reproducimos de forma \u00edntegra: <\/p>\n<p>@MADRERECIENTE<\/p>\n<ul>\n<li>Esta carta es una adaptaci\u00f3n del texto <a href=\"https:\/\/blogs.20minutos.es\/madrereciente\/2017\/12\/03\/hijo-11-anos-aun-no-me-ha-llamado-mama-discapacidadyrealidad\/\">Mi hijo tiene 11 a\u00f1os y a\u00fan no me ha llamado \u00abmam\u00e1\u00bb (pero no importa), <\/a>publicado el 3 de diciembre con motivo del D\u00eda de la Discapacidad.<\/li>\n<\/ul>\n<p><img loading=\"lazy\" decoding=\"async\" src=\"http:\/\/cdn.20m.es\/img2\/recortes\/2017\/12\/05\/594589-620-282.jpg?v=20171205083643\" width=\"620\" height=\"282\" alt=\"Jaime\" \/><\/p>\n<p>Jaime, mi ni\u00f1o de oro. <strong>Tienes once a\u00f1os y a\u00fan no me has llamado &#8216;mam\u00e1&#8217;.<\/strong> Puede que alg\u00fan d\u00eda llegues a hacerlo. Tal vez nunca. Tienes once a\u00f1os y autismo, y solo emites unas pocas aproximaciones voc\u00e1licas de aquello que m\u00e1s te importa conseguir: &#8216;Pa&#8217; por &#8216;pan&#8217;, &#8216;aua&#8217; por &#8216;agua&#8217;, &#8216;i&#8217; por &#8216;s\u00ed&#8217;, &#8216;o&#8217; por &#8216;no&#8217;&#8230;<\/p>\n<p>Para reclamar nuestra atenci\u00f3n vocalizas fuerte, as\u00ed que yo soy &#8216;aaaaa&#8217; o &#8216;eeeee&#8217;. Igual que tu padre, tus profesores o tus abuelos. Si no fuera por tu hermana peque\u00f1a, ser\u00eda una madre que nunca ha sido llamada como tal. <strong>Aunque no importa y te voy a contar el motivo.<\/strong><\/p>\n<p>Cuando hace dos domingos por la noche tu padre te trajo al aeropuerto,<strong> la sonrisa de felicidad pura que me regalaste<\/strong> al verme despu\u00e9s de cuatro d\u00edas lejos de casa fue el detonante de un instante de perfecta alegr\u00eda, de esos que hay que atesorar porque marcan la diferencia entre una vida gastada y una plena.<\/p>\n<p>No hablas, pero mi coraz\u00f3n canta cuando veo esa sonrisa. No existe otra igual. As\u00ed que no importa que no me llames &#8216;mam\u00e1&#8217;. <strong>He aprendido a distinguir lo esencial en lo que sustentarme y a evitar los anhelos in\u00fatiles que desgastan.<\/strong><\/p>\n<p><strong>S\u00ed que importa, en cambio, que est\u00e1s viviendo en un mundo pensado para los que hablamos sin problemas<\/strong>, para los que tenemos la fortuna de dominar esa magia que la ciencia a\u00fan no ha logrado desentra\u00f1ar del todo. Un mundo en el que el signado, los pictogramas y los textos adaptados a lectura f\u00e1cil no abundan; en el que poca gente es capaz de entender, por falta de paciencia, de conocimientos o de ambas cosas, a aquellos que se manejan con cuadernos de fotos o pictogramas, signos o dificultades en el lenguaje.<\/p>\n<p><strong>Un mundo que los que tenemos la suerte de hablar tenemos la obligaci\u00f3n moral de hacer m\u00e1s accesible<\/strong>, de convertir en un sitio inclusivo para todos aquellos que no pueden hacerlo, o que no pueden hacerlo igual de bien o con la misma facilidad.<\/p>\n<p>Un gran poder acarrea de la mano una gran responsabilidad.<\/p>\n<p><strong>Todo empieza por saber que son millones los que sois como t\u00fa<\/strong>, mi ni\u00f1o dorado, y que compart\u00eds espacio, sue\u00f1os, retos y alegr\u00eda con nosotros. No solemos ser conscientes de vuestra existencia si no tenemos a nadie con esas dificultades cerca, igual que no lo somos del milagro que es el lenguaje.<\/p>\n<p>Todo empieza adem\u00e1s por tomar conciencia de que en este mundo<strong> tambi\u00e9n hay millones que no pueden caminar, que no pueden ver que no pueden o\u00edr&#8230; o que lo <\/strong><strong>hacen con dificultad.<\/strong><\/p>\n<p>Todo comienza por saber que est\u00e1s ah\u00ed, con tu sonrisa<\/p>\n<p>Fuente: 20minutos <a href=\"http:\/\/www.20minutos.es\/opiniones\/carta-jaime-nino-dorado-3205273\/\" target=\"_blank\">Carta a Jaime, mi ni\u00f1o de oro<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Leemos en 20minutos la siguiente noticia que os reproducimos de forma \u00edntegra: @MADRERECIENTE Esta carta es una adaptaci\u00f3n del texto Mi hijo tiene 11 a\u00f1os y a\u00fan no me ha llamado \u00abmam\u00e1\u00bb (pero no importa), publicado el 3 de diciembre con motivo del D\u00eda de la Discapacidad. Jaime, mi ni\u00f1o de oro. Tienes once a\u00f1os [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[8],"tags":[31],"class_list":["post-3406","post","type-post","status-publish","format-standard","hentry","category-noticias","tag-discapacidad"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Carta a Jaime, mi ni\u00f1o de oro - Asociaci\u00f3n Espa\u00f1ola S\u00edndrome de Charge<\/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:\/\/sindromecharge.es\/index.php\/2017\/12\/05\/carta-a-jaime-mi-nino-de-oro\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Carta a Jaime, mi ni\u00f1o de oro - Asociaci\u00f3n Espa\u00f1ola S\u00edndrome de Charge\" \/>\n<meta property=\"og:description\" content=\"Leemos en 20minutos la siguiente noticia que os reproducimos de forma \u00edntegra: @MADRERECIENTE Esta carta es una adaptaci\u00f3n del texto Mi hijo tiene 11 a\u00f1os y a\u00fan no me ha llamado \u00abmam\u00e1\u00bb (pero no importa), publicado el 3 de diciembre con motivo del D\u00eda de la Discapacidad. 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