{"id":3156,"date":"2019-11-21T20:23:42","date_gmt":"2019-11-22T02:23:42","guid":{"rendered":"https:\/\/restruct-lgmd-2021.pantheonsite.io\/?p=3156"},"modified":"2019-11-21T20:23:42","modified_gmt":"2019-11-22T02:23:42","slug":"patrick","status":"publish","type":"post","link":"https:\/\/www.lgmd-info.org\/es\/individuals-with-lgmd-interviews\/2019\/11\/21\/patrick\/","title":{"rendered":"INDIVIDUO CON LGMD: Patrick"},"content":{"rendered":"<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%271024%27%20height%3D%27576%27%20viewBox%3D%270%200%201024%20576%27%3E%3Crect%20width%3D%271024%27%20height%3D%27576%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-orig-src=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2019\/11\/LGMD2E-Patrick-M-1024x576.png\" alt=\"\" class=\"lazyload wp-image-3157\"\/><\/figure>\n\n\n\n<h2 class=\"wp-block-heading\">LGMD \"ENTREVISTA EN PRIMER PLANO\"<\/h2>\n\n\n\n<p><strong>NOMBRE<\/strong>: Patrick&nbsp;&nbsp; <strong>EDAD<\/strong>:\n46 a\u00f1os<\/p>\n\n\n\n<p><strong>PA\u00cdS<\/strong>: EE.UU.<\/p>\n\n\n\n<p><strong>Subtipo LGMD<\/strong>:  LGMD 2E\/R4 B\u00e8ta-sarcoglycan-related<\/p>\n\n\n\n<p><strong>\u00bfA qu\u00e9 edad le\nle diagnosticaron<\/strong>:<\/p>\n\n\n\n<p>Ten\u00eda 12 a\u00f1os y corr\u00eda el a\u00f1o 1985. Al principio me diagnosticaron distrofia muscular de Becker.\nmuscular de Becker.<\/p>\n\n\n\n<p><strong>\u00bfCu\u00e1les fueron sus primeros s\u00edntomas?<\/strong>:\n<\/p>\n\n\n\n<p>Mis primeros s\u00edntomas fueron problemas para correr en clase de gimnasia, quedarme sin aliento al subir\nescaleras, caminar y correr de puntillas.<\/p>\n\n\n\n<p><strong>\u00bfTiene otros familiares\nfamiliares con LGMD: <\/strong><\/p>\n\n\n\n<p><strong>N<\/strong>o, soy la \u00fanica persona de mi familia con LGMD.<\/p>\n\n\n\n<p><strong>\u00bfCu\u00e1les cree que son los\nmayores retos de vivir con LGMD<\/strong>:<\/p>\n\n\n\n<p>Uno de los mayores retos es vivir sabiendo que esta enfermedad es\ncondici\u00f3n es progresiva y no saber cu\u00e1nto tiempo tendr\u00e9 funciones y\ncapacidades. Por eso aprovecho al m\u00e1ximo cada d\u00eda.<\/p>\n\n\n\n<p><strong>\u00bfCu\u00e1l es su mayor\nlogro<\/strong>:<\/p>\n\n\n\n<p>Tengo muchos. El principal de ellos es haber conocido a mi mujer Vanessa y haber criado a mis dos hijos.\nni\u00f1os, as\u00ed como ser un profesor de m\u00fasica a tiempo completo durante los \u00faltimos 25 a\u00f1os en una\nescuela media.<\/p>\n\n\n\n<p><strong>\u00bfC\u00f3mo te ha influido la LGMD\npara convertirte en la persona que eres hoy:<\/strong><\/p>\n\n\n\n<p>Me ha ense\u00f1ado que la vida es preciosa y que todos debemos tomarnos tiempo para respirar y buscar lo mejor en todas las personas y en todas nuestras relaciones.\nrespirar y buscar lo mejor en todas las personas y en todas nuestras relaciones. I\nHe aprendido a ser paciente y a no preocuparme por las cosas peque\u00f1as. Todos los problemas\nproblema puede solucionarse y mejorarse trabajando juntos.<\/p>\n\n\n\n<p><strong>\u00bfQu\u00e9 quiere que el mundo\nsepa sobre la LGMD<\/strong>:<\/p>\n\n\n\n<p>Que las personas con LGMD, y cualquier enfermedad cr\u00f3nica tienen d\u00edas buenos y malos, como\ncomo cualquier otra persona, y que llevamos vidas felices y plenas. Somos\npositivos y trabajamos duro.<\/p>\n\n\n\n<p><strong>Si su LGMD pudiera \"curarse\"\nma\u00f1ana, \u00bfqu\u00e9 ser\u00eda lo primero que querr\u00edas hacer<\/strong>:<\/p>\n\n\n\n<p>Soy percusionista y bater\u00eda de coraz\u00f3n. Con los a\u00f1os, he perdido casi toda la capacidad de tocar. Cuando me cure, me unir\u00e9 a una banda y tocar\u00e9 rock, \u00a1como hac\u00eda en mi juventud! Ja, ja. Paz a TODOS.<\/p>","protected":false},"excerpt":{"rendered":"<p>LGMD &#8220;SPOTLIGHT INTERVIEW&#8221; NAME: Patrick&nbsp;&nbsp; AGE: 46 yrs. old COUNTRY: [&hellip;]<\/p>","protected":false},"author":1,"featured_media":3157,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[13,62],"tags":[],"class_list":["post-3156","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-individuals-with-lgmd-interviews","category-lgmd2e"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>INDIVIDUAL WITH LGMD: Patrick - LGMD Awareness Foundation<\/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.lgmd-info.org\/es\/individuals-with-lgmd-interviews\/2019\/11\/21\/patrick\/\" \/>\n<meta property=\"og:locale\" content=\"es_MX\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"INDIVIDUAL WITH LGMD: Patrick - 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