{"id":615,"date":"2015-04-29T08:06:42","date_gmt":"2015-04-29T13:06:42","guid":{"rendered":"https:\/\/restruct-lgmd-2021.pantheonsite.io\/?p=615"},"modified":"2015-04-29T08:06:42","modified_gmt":"2015-04-29T13:06:42","slug":"alicia","status":"publish","type":"post","link":"https:\/\/www.lgmd-info.org\/es\/individuals-with-lgmd-interviews\/2015\/04\/29\/alicia\/","title":{"rendered":"INDIVIDUO CON LGMD: Alicia"},"content":{"rendered":"<p>04\/29\/2015<\/p>\n<p><strong>Nombre:<\/strong>\u00a0 Alicia<\/p>\n<p><strong>Edad<\/strong>:  38 a\u00f1os<a href=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2015\/04\/LGMD2A-Alicia.png\"><img decoding=\"async\" class=\"lazyload  size-medium wp-image-616 alignright\" src=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27169%27%20viewBox%3D%270%200%20300%20169%27%3E%3Crect%20width%3D%27300%27%20height%3D%27169%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-orig-src=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2015\/04\/LGMD2A-Alicia-300x169.png\" alt=\"LGMD2A - Alicia\" width=\"300\" height=\"169\" \/><\/a><\/p>\n<p><strong>Pa\u00eds<\/strong>: Estados Unidos<\/p>\n<p><strong>Subtipo LGMD<\/strong>: LGMD2A \/ Calpainopat\u00eda<\/p>\n<p>&nbsp;<\/p>\n<p><strong>\u00bfA qu\u00e9 edad le diagnosticaron<\/strong>:<\/p>\n<p>Me lo diagnosticaron a los 35 a\u00f1os despu\u00e9s de a\u00f1os y a\u00f1os de diagn\u00f3sticos err\u00f3neos.<\/p>\n<p><strong>\u00bfCu\u00e1les fueron sus primeros s\u00edntomas?<\/strong>:<\/p>\n<p>Caminar y correr de puntillas y subir escaleras fueron los primeros s\u00edntomas.<\/p>\n<p><strong>\u00bfTiene otros familiares que padezcan LGMD?<\/strong><\/p>\n<p><strong>\u00bfCu\u00e1les crees que son los mayores retos de vivir con LGMD?<\/strong>:<\/p>\n<p>Uno de los mayores retos para m\u00ed ha sido encontrar m\u00e9dicos con formaci\u00f3n sobre la LGMD y los retos y s\u00edntomas que conlleva la enfermedad.  Muchos m\u00e9dicos no se tomaron en serio mis problemas (dolores musculares, p\u00e9rdida de fuerza, problemas para caminar\/escalar) o pensaron que ten\u00eda una enfermedad autoinmune antes de que encontrara un m\u00e9dico que finalmente me envi\u00f3 a la Cl\u00ednica Mayo. Despu\u00e9s de un EMG, an\u00e1lisis de sangre y una biopsia muscular finalmente me diagnosticaron, pero me llev\u00f3 muchos a\u00f1os y muchos m\u00e9dicos llegar a donde estoy.<\/p>\n<p><strong>\u00bfCu\u00e1l es su mayor logro?<\/strong>:<\/p>\n<p>Criar a dos hijas incre\u00edbles con mi marido de 14 a\u00f1os ha sido un logro y una bendici\u00f3n. Ense\u00f1arles a ser amables y a ser m\u00e1s emp\u00e1ticos con la gente, ya que nunca conocemos realmente las dificultades de los que nos rodean.<\/p>\n<p><strong>\u00bfC\u00f3mo le ha influido la LGMD para convertirse en la persona que es hoy? \u00a0<\/strong><\/p>\n<p>Me ha ense\u00f1ado a ser m\u00e1s amable, a escuchar m\u00e1s y a re\u00edr cada d\u00eda.  A veces lo \u00fanico que puedes hacer es re\u00edr.<\/p>\n<p><strong>\u00bfQu\u00e9 quiere que el mundo sepa sobre la LGMD?<\/strong>:<\/p>\n<p>Que actualmente no existen tratamientos ni cura para la LGMD y si tiene un familiar o incluso un amigo que haya sido diagnosticado, inf\u00f3rmese sobre la enfermedad.  Podr\u00eda significar mucho para alguien.<\/p>\n<p><strong>Si su LGMD pudiera \"curarse\" ma\u00f1ana, \u00bfqu\u00e9 ser\u00eda lo primero que desear\u00eda hacer?<\/strong>:<\/p>\n<p>\u00a1Baila toda la noche!<\/p>","protected":false},"excerpt":{"rendered":"<p>04\/29\/2015 Name:\u00a0 Alicia Age:\u00a0 38 yrs. old Country: United States [&hellip;]<\/p>","protected":false},"author":1,"featured_media":616,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[13,14],"tags":[12,15,16],"class_list":["post-615","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-individuals-with-lgmd-interviews","category-lgmd2a","tag-calpainopathy","tag-lgmd2a","tag-united-states"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>LGMD Spotlight Interview - Alicia<\/title>\n<meta name=\"description\" content=\"Alicia, who is diagnosed with Limb Girdle Muscular Dystrophy (LGMD), shares her experience in living with this progressive neuro-muscular disease.\" \/>\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.lgmd-info.org\/es\/individuals-with-lgmd-interviews\/2015\/04\/29\/alicia\/\" \/>\n<meta property=\"og:locale\" content=\"es_MX\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"LGMD Spotlight Interview - 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