{"id":30065,"date":"2021-05-24T15:58:21","date_gmt":"2021-05-24T14:58:21","guid":{"rendered":"https:\/\/worldmsday.org\/?p=30065"},"modified":"2021-05-27T12:38:28","modified_gmt":"2021-05-27T11:38:28","slug":"historias-de-ms-connections","status":"publish","type":"post","link":"https:\/\/worldmsday.org\/es\/historias-de-ms-connections\/","title":{"rendered":"Historias de MS Connections"},"content":{"rendered":"<div class=\"wysiwyg__content--skinny\">\n<p>\u00bfC\u00f3mo describir\u00edas la vida con EM? \u00bfCu\u00e1les son los mayores desaf\u00edos y por qui\u00e9nes est\u00e1s agradecido? Respuestas de personas con EM en T\u00fanez, Macedonia, Colombia y mucho m\u00e1s.<\/p>\n<\/div>\n\n<div class=\"wysiwyg__content--skinny\">\n<p>\u00abEso no me impide seguir adelante y hacer mi mejor esfuerzo\u00bb.<\/p>\n<\/div>\n\n\n<figure class=\"wp-block-embed is-type-video is-provider-youtube wp-block-embed-youtube wp-embed-aspect-16-9 wp-has-aspect-ratio\"><div class=\"wp-block-embed__wrapper\">\n<iframe loading=\"lazy\" title=\"Rania&#039;s #MSConnections story\" width=\"1200\" height=\"675\" src=\"https:\/\/www.youtube.com\/embed\/QVKx1gkinBA?feature=oembed\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture\" allowfullscreen><\/iframe>\n<\/div><\/figure>\n\n\n<div class=\"wysiwyg__content--skinny\">\n<p>A Rania le diagnosticaron EM en T\u00fanez hace 11 a\u00f1os. Los s\u00edntomas de EM a veces interrumpen el tiempo de calidad que pasa con sus hijas, pero eso no ha impedido a Rania vivir al m\u00e1ximo. \u00a1Gracias por compartir tu fuerza y felicidad con nosotros, Rania! <\/p>\n<\/div>\n\n<div class=\"wysiwyg__content--skinny\">\n<p>Agradecemos a <a href=\"http:\/\/www.atsep.tn\/arabe\/index.html\">ATSEP<\/a> (Association Tunisienne des Malades de la Scl\u00e9rose en Plaque) por comunicarnos con Rania. <\/p>\n<\/div>\n\n<div class=\"wysiwyg__content--skinny\">\n<p>\u00abCuando una persona de la familia tiene EM, toda la familia vive con EM\u00bb.<\/p>\n<\/div>\n\n\n<figure class=\"wp-block-embed is-type-video is-provider-youtube wp-block-embed-youtube wp-embed-aspect-16-9 wp-has-aspect-ratio\"><div class=\"wp-block-embed__wrapper\">\n<iframe loading=\"lazy\" title=\"Aleksandar&#039;s #MSConnections story\" width=\"1200\" height=\"675\" src=\"https:\/\/www.youtube.com\/embed\/x9k3fMz30L0?feature=oembed\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture\" allowfullscreen><\/iframe>\n<\/div><\/figure>\n\n\n<div class=\"wysiwyg__content--skinny\">\n<p>Aleksandar conoce el impacto que la EM puede tener en la vida familiar. Tanto \u00e9l como su madre viven con EM en Macedonia. Han salido adelante gracias a la fuerza y al apoyo de su familia. \u00a1Gracias a todas las familias que apoyan a sus seres queridos con EM en todo el mundo! <\/p>\n<\/div>\n\n<div class=\"wysiwyg__content--skinny\">\n<p>A big thank you to the <a href=\"https:\/\/msmakedonija.eu.org\">\u041d\u0430\u0446\u0438\u043e\u043d\u0430\u043b\u043d\u043e \u0437\u0434\u0440\u0443\u0436\u0435\u043d\u0438\u0435 \u0437\u0430 \u041c\u0421<\/a> (the National Association for MS in Macedonia) for putting us in touch with Aleksandar.<\/p>\n<\/div>\n\n<div class=\"wysiwyg__content--skinny\">\n<p>\u00abLa vida sigue, no se detiene, y la EM tampoco me detendr\u00e1\u00bb.<\/p>\n<\/div>\n\n\n<figure class=\"wp-block-embed is-type-video is-provider-youtube wp-block-embed-youtube wp-embed-aspect-16-9 wp-has-aspect-ratio\"><div class=\"wp-block-embed__wrapper\">\n<iframe loading=\"lazy\" title=\"Mar\u00eda Teresa&#039;s #MSConnections story\" width=\"1200\" height=\"675\" src=\"https:\/\/www.youtube.com\/embed\/zctIprbH868?feature=oembed\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture\" allowfullscreen><\/iframe>\n<\/div><\/figure>\n\n\n<div class=\"wysiwyg__content--skinny\">\n<p>Mar\u00eda Teresa, de Colombia, comparte sus mayores desaf\u00edos y consejos para vivir con EM. \u00a1No te pierdas estas palabras para implementar en tu vida! Nos encantan estos hermosos consejos para tener una vida equilibrada y seguir conectados y optimistas.<\/p>\n<\/div>\n\n<div class=\"wysiwyg__content--skinny\">\n<p><br>Gracias a la <a href=\"https:\/\/www.alcem.org.ar\">Asociaci\u00f3n para la Lucha contra la Esclerosis M\u00faltiple<\/a> por conectarnos con Mar\u00eda Teresa. <\/p>\n<\/div>\n\n<div class=\"wysiwyg__content--skinny\">\n<p>\u00abEso me ayuda a afrontar la incertidumbre que siento\u00bb.<\/p>\n<\/div>\n\n\n<figure class=\"wp-block-embed is-type-video is-provider-youtube wp-block-embed-youtube wp-embed-aspect-16-9 wp-has-aspect-ratio\"><div class=\"wp-block-embed__wrapper\">\n<iframe loading=\"lazy\" title=\"David&#039;s #MSConnections story\" width=\"1200\" height=\"675\" src=\"https:\/\/www.youtube.com\/embed\/AGPZ38Ho0Vk?feature=oembed\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture\" allowfullscreen><\/iframe>\n<\/div><\/figure>\n\n\n<div class=\"wysiwyg__content--skinny\">\n<p>Te presentamos a David, un investigador de EM que vive con la enfermedad. Mira esta entrevista para descubrir por qu\u00e9 David sigue siendo optimista, a pesar de vivir con s\u00edntomas imprevisibles. <\/p>\n<\/div>\n\n<div class=\"wysiwyg__content--skinny\">\n<p>Gracias a David y a <a href=\"https:\/\/msra.org.au\">MS Research Australia<\/a> por su extraordinaria investigaci\u00f3n sobre EM.<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>\u00bfC\u00f3mo describir\u00edas la vida con EM? \u00bfCu\u00e1les son los mayores desaf\u00edos y por qui\u00e9nes est\u00e1s agradecido? Respuestas de personas con EM en T\u00fanez, Macedonia, Colombia y mucho m\u00e1s. \u00abEso no me impide seguir adelante y hacer mi mejor esfuerzo\u00bb. A Rania le diagnosticaron EM en T\u00fanez hace 11 a\u00f1os. Los s\u00edntomas de EM a veces [&hellip;]<\/p>\n","protected":false},"author":43,"featured_media":30036,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[],"tags":[],"class_list":["post-30065","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Historias de MS Connections - D\u00eda Mundial de la EM<\/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:\/\/worldmsday.org\/es\/historias-de-ms-connections\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Historias de MS Connections - D\u00eda Mundial de la EM\" \/>\n<meta property=\"og:description\" content=\"\u00bfC\u00f3mo describir\u00edas la vida con EM? \u00bfCu\u00e1les son los mayores desaf\u00edos y por qui\u00e9nes est\u00e1s agradecido? Respuestas de personas con EM en T\u00fanez, Macedonia, Colombia y mucho m\u00e1s. \u00abEso no me impide seguir adelante y hacer mi mejor esfuerzo\u00bb. A Rania le diagnosticaron EM en T\u00fanez hace 11 a\u00f1os. 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