{"id":9865,"date":"2024-03-24T07:58:56","date_gmt":"2024-03-24T07:58:56","guid":{"rendered":"https:\/\/sindromecharge.es\/index.php\/2024\/03\/24\/alvaro-villanueva-presidente-fundacion-ava\/"},"modified":"2024-03-24T07:58:56","modified_gmt":"2024-03-24T07:58:56","slug":"alvaro-villanueva-presidente-fundacion-ava","status":"publish","type":"post","link":"https:\/\/sindromecharge.es\/index.php\/2024\/03\/24\/alvaro-villanueva-presidente-fundacion-ava\/","title":{"rendered":"\u00c1lvaro Villanueva, presidente de Fundaci\u00f3n AVA: \u00abNuestro objetivo es atender a personas con una gran discapacidad, como mi hijo\u00bb"},"content":{"rendered":"<p>Leemos en Discapacidad la siguiente noticia que os reproducimos de forma \u00edntegra: <\/p>\n<div>\n<p>Su hijo fue la raz\u00f3n y la gran inspiraci\u00f3n que llev\u00f3 a <b>\u00c1lvaro Villanueva a crear la <a href=\"https:\/\/fundava.org\/\" target=\"_blank\" rel=\"nofollow noopener\">Fundaci\u00f3n AVA<\/a><\/b>, una organizaci\u00f3n sin \u00e1nimo de lucro que naci\u00f3 para apoyar a todas las personas con grandes necesidades de apoyo y sus familias. \u00c1lvaro, que as\u00ed se llama su hijo, tiene dos enfermedades raras de dif\u00edcil tratamiento, <b>esclerosis tuberosa y poliquistosis renal<\/b>. Al ver que no encontraba los recursos adecuados que necesitaban tanto \u00e9l como su familia, decidi\u00f3 crear estos recursos \u00e9l mismo. <\/p>\n<p>Tras siete a\u00f1os de trabajo incasable, AVA no deja de crecer, atiende a <b>m\u00e1s de 1.000 familias al a\u00f1o<\/b> en hospitales y apoya de manera intensiva a unas 70 con recursos como actividades deportivas y de ocio y respiro. Mientras, preparan el que, sin duda, ser\u00e1 su proyecto m\u00e1s importante hasta la fecha, Casa AVA, un centro residencial y de ocio con el que ayudar a todas las familias que lo necesiten.<\/p>\n<h1>Solo en Madrid hay 3.000 menores de edad con multidiscapacidad y, al margen de las enfermedades que tengan, tienen unas necesidades y tenemos que buscar soluciones<\/h1>\n<h1>Un hijo con problemas conductuales, que no entiende, que duerme mal y que tiene movimiento, requiere una atenci\u00f3n 24 horas, y esto acaba desgastando a la familia<\/h1>\n<h1>La vida de estos chavales vale la pena y pueden ser felices, y nosotros tenemos que luchar por darles esa felicidad<\/h1>\n<\/div>\n<p>Fuente: Discapacidad https:\/\/www.20minutos.es\/noticia\/5227518\/0\/alvaro-villanueva-presidente-fundacion-ava\/<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Su hijo fue la raz\u00f3n y la gran inspiraci\u00f3n que llev\u00f3 a \u00c1lvaro Villanueva a crear la Fundaci\u00f3n AVA, una organizaci\u00f3n sin \u00e1nimo de lucro que naci\u00f3 para&#8230;<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[8],"tags":[],"class_list":["post-9865","post","type-post","status-publish","format-standard","hentry","category-noticias"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - 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