{"id":1542,"date":"2021-05-25T18:44:23","date_gmt":"2021-05-25T17:44:23","guid":{"rendered":"http:\/\/demainsansmucoviscidose.org\/?p=1542"},"modified":"2021-09-22T20:26:38","modified_gmt":"2021-09-22T19:26:38","slug":"temoignage-de-clelia-sur-le-site-internet-pemr-bfc-raconte-moi-ta-maladie-rare","status":"publish","type":"post","link":"https:\/\/demainsansmucoviscidose.org\/index.php\/2021\/05\/25\/temoignage-de-clelia-sur-le-site-internet-pemr-bfc-raconte-moi-ta-maladie-rare\/","title":{"rendered":"T\u00e9moignage de Cl\u00e9lia sur le site internet PEMR BFC \u00ab\u00a0raconte moi ta maladie rare\u00a0\u00bb"},"content":{"rendered":"<div dir=\"auto\">Cl\u00e9lia, marraine de notre association, t\u00e9moigne sur le site internet de la PEMR BFC (Plateforme d&rsquo;Expertise Maladies Rares) dans la rubrique \u00ab\u00a0raconte-moi ta maladie rare\u00a0\u00bb<\/div>\n<div dir=\"auto\"><strong><a class=\"oajrlxb2 g5ia77u1 qu0x051f esr5mh6w e9989ue4 r7d6kgcz rq0escxv nhd2j8a9 nc684nl6 p7hjln8o kvgmc6g5 cxmmr5t8 oygrvhab hcukyx3x jb3vyjys rz4wbd8a qt6c0cv9 a8nywdso i1ao9s8h esuyzwwr f1sip0of lzcic4wl py34i1dx gpro0wi8\" tabindex=\"0\" href=\"http:\/\/www.pemr-bfc.fr\/maladies-rares-et-vous\/raconte-moi-ta-maladie-rare\/?fbclid=IwAR261YzdcNS0lYXHWuIut3dRDQwjby_sc1_ujOX7oOioe9zgn3R6DJ0bvCQ\" target=\"_blank\" rel=\"nofollow noopener noreferrer\">http:\/\/www.pemr-bfc.fr\/malad&#8230;\/raconte-moi-ta-maladie-rare\/<\/a><\/strong><\/div>\n<div dir=\"auto\">\u00a0\u00a0<a href=\"http:\/\/demainsansmucoviscidose.org\/wp-content\/uploads\/2021\/05\/Site-PEMR-BFC1.jpg\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1540\" src=\"http:\/\/demainsansmucoviscidose.org\/wp-content\/uploads\/2021\/05\/Site-PEMR-BFC1-300x173.jpg\" alt=\"\" width=\"300\" height=\"173\" srcset=\"https:\/\/demainsansmucoviscidose.org\/wp-content\/uploads\/2021\/05\/Site-PEMR-BFC1-300x173.jpg 300w, https:\/\/demainsansmucoviscidose.org\/wp-content\/uploads\/2021\/05\/Site-PEMR-BFC1-768x444.jpg 768w, https:\/\/demainsansmucoviscidose.org\/wp-content\/uploads\/2021\/05\/Site-PEMR-BFC1-1024x592.jpg 1024w, https:\/\/demainsansmucoviscidose.org\/wp-content\/uploads\/2021\/05\/Site-PEMR-BFC1.jpg 1061w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><a href=\"http:\/\/demainsansmucoviscidose.org\/wp-content\/uploads\/2021\/05\/Site-PEMR-BFC2.jpg\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1541\" src=\"http:\/\/demainsansmucoviscidose.org\/wp-content\/uploads\/2021\/05\/Site-PEMR-BFC2-300x247.jpg\" alt=\"\" width=\"215\" height=\"177\" srcset=\"https:\/\/demainsansmucoviscidose.org\/wp-content\/uploads\/2021\/05\/Site-PEMR-BFC2-300x247.jpg 300w, https:\/\/demainsansmucoviscidose.org\/wp-content\/uploads\/2021\/05\/Site-PEMR-BFC2-768x632.jpg 768w, https:\/\/demainsansmucoviscidose.org\/wp-content\/uploads\/2021\/05\/Site-PEMR-BFC2.jpg 791w\" sizes=\"auto, (max-width: 215px) 100vw, 215px\" \/><\/a><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Cl\u00e9lia, marraine de notre association, t\u00e9moigne sur le site internet de la PEMR BFC (Plateforme d&rsquo;Expertise Maladies Rares) dans la rubrique \u00ab\u00a0raconte-moi ta maladie rare\u00a0\u00bb http:\/\/www.pemr-bfc.fr\/malad&#8230;\/raconte-moi-ta-maladie-rare\/ \u00a0\u00a0<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-1542","post","type-post","status-publish","format-standard","hentry","category-non-classe","item-wrap"],"_links":{"self":[{"href":"https:\/\/demainsansmucoviscidose.org\/index.php\/wp-json\/wp\/v2\/posts\/1542","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/demainsansmucoviscidose.org\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/demainsansmucoviscidose.org\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/demainsansmucoviscidose.org\/index.php\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/demainsansmucoviscidose.org\/index.php\/wp-json\/wp\/v2\/comments?post=1542"}],"version-history":[{"count":6,"href":"https:\/\/demainsansmucoviscidose.org\/index.php\/wp-json\/wp\/v2\/posts\/1542\/revisions"}],"predecessor-version":[{"id":1548,"href":"https:\/\/demainsansmucoviscidose.org\/index.php\/wp-json\/wp\/v2\/posts\/1542\/revisions\/1548"}],"wp:attachment":[{"href":"https:\/\/demainsansmucoviscidose.org\/index.php\/wp-json\/wp\/v2\/media?parent=1542"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/demainsansmucoviscidose.org\/index.php\/wp-json\/wp\/v2\/categories?post=1542"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/demainsansmucoviscidose.org\/index.php\/wp-json\/wp\/v2\/tags?post=1542"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}