{"id":27710,"date":"2015-03-12T18:23:38","date_gmt":"2015-03-12T22:23:38","guid":{"rendered":"https:\/\/nephcure.org\/bedford-mother-shares-her-story-at-rare-disease-day\/"},"modified":"2024-05-01T16:29:35","modified_gmt":"2024-05-01T20:29:35","slug":"madre-de-bedford-comparte-su-historia-en-el-dia-de-las-enfermedades-raras","status":"publish","type":"post","link":"https:\/\/nephcure.org\/es\/bedford-mother-shares-her-story-at-rare-disease-day\/","title":{"rendered":"Madre de Bedford comparte su historia en el D\u00eda de las Enfermedades Raras"},"content":{"rendered":"

El 23 de febrero de 2014, tambi\u00e9n conocido como D\u00eda de las Enfermedades Raras, Lisa Cimino, miembro de la familia NephCure y madre de Brianna, paciente de FSGS, comparti\u00f3 su historia y habl\u00f3 sobre c\u00f3mo es vivir con una enfermedad rara en la Casa del Estado en Boston. Lea su historia aqu\u00ed.\u00a0<\/a><\/p>","protected":false},"excerpt":{"rendered":"

El 23 de febrero de 2014, tambi\u00e9n conocido como D\u00eda de las Enfermedades Raras, Lisa Cimino, miembro de la familia NephCure y madre de Brianna, paciente de FSGS, comparti\u00f3 su historia y habl\u00f3 sobre... Leer m\u00e1s<\/a><\/p>","protected":false},"author":222,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"inline_featured_image":false,"footnotes":""},"categories":[354],"tags":[366,373,358],"disease-category":[],"resource-type":[260],"treatment-option":[],"hf_cat_post":[],"class_list":["post-27710","post","type-post","status-publish","format-standard","hentry","category-recent-news","tag-advocacy","tag-nephcure","tag-nephcure-kidney-international","resource-type-news"],"acf":[],"yoast_head":"\nBedford Mother Shares Her Story at Rare Disease Day - NephCure<\/title>\n<meta name=\"description\" content=\"On February 23, 2014, aka Rare Disease Day, Lisa Cimino - a member of the NephCure family and mother to FSGS patient Brianna - shared her story and talked - Read more about Bedford Mother Shares Her Story at Rare Disease Day on NephCure.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/nephcure.org\/es\/madre-de-bedford-comparte-su-historia-en-el-dia-de-las-enfermedades-raras\/\" \/>\n<meta property=\"og:locale\" content=\"es_MX\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Bedford Mother Shares Her Story at Rare Disease Day\" \/>\n<meta property=\"og:description\" content=\"On February 23, 2014, aka Rare Disease Day, Lisa Cimino - a member of the NephCure family and mother to FSGS patient Brianna - shared her story and talked - Read more about Bedford Mother Shares Her Story at Rare Disease Day on NephCure.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/nephcure.org\/es\/madre-de-bedford-comparte-su-historia-en-el-dia-de-las-enfermedades-raras\/\" \/>\n<meta property=\"og:site_name\" content=\"NephCure\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/nephcure\/\" \/>\n<meta property=\"article:published_time\" content=\"2015-03-12T22:23:38+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2024-05-01T20:29:35+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/nephcure.org\/wp-content\/uploads\/2024\/05\/Site-Image.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"1200\" \/>\n\t<meta property=\"og:image:height\" content=\"675\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"Lauren Eva\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:creator\" content=\"@nephcure\" \/>\n<meta name=\"twitter:site\" content=\"@nephcure\" \/>\n<meta name=\"twitter:label1\" content=\"Escrito por\" \/>\n\t<meta name=\"twitter:data1\" content=\"Lauren Eva\" \/>\n<!-- \/ Yoast SEO Premium plugin. -->","yoast_head_json":{"title":"Madre de Bedford comparte su historia en el D\u00eda de las Enfermedades Raras - NephCure","description":"El 23 de febrero de 2014, tambi\u00e9n conocido como D\u00eda de las Enfermedades Raras, Lisa Cimino, miembro de la familia NephCure y madre de Brianna, paciente de FSGS, comparti\u00f3 su historia y habl\u00f3. 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