{"version":"1.0","provider_name":"Fundaci\u00f3n Noelia","provider_url":"https:\/\/fundacionnoelia.org\/en\/","author_name":"admin","author_url":"https:\/\/fundacionnoelia.org\/en\/actualidad\/author\/admin_h6lwguow\/","title":"February 29, International Day of Rare Diseases - Fundaci\u00f3n Noelia","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"fUkzCUmvLl\"><a href=\"https:\/\/fundacionnoelia.org\/en\/actualidad\/february-29-international-day-of-rare-diseases\/\">February 29, International Day of Rare Diseases<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/fundacionnoelia.org\/en\/actualidad\/february-29-international-day-of-rare-diseases\/embed\/#?secret=fUkzCUmvLl\" width=\"600\" height=\"338\" title=\"&#8220;February 29, International Day of Rare Diseases&#8221; &#8212; Fundaci\u00f3n Noelia\" data-secret=\"fUkzCUmvLl\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script>\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/\/# sourceURL=https:\/\/fundacionnoelia.org\/wp-includes\/js\/wp-embed.min.js\n<\/script>\n","thumbnail_url":"https:\/\/fundacionnoelia.org\/wp-content\/uploads\/2024\/03\/noticia_29F.png","thumbnail_width":660,"thumbnail_height":420,"description":"On World Rare Disease Day, we raise our voices to shed light on collagen VI congenital muscular dystrophy and all rare medical conditions. At the Noelia Foundation we participate in different events to make the disease visible: II Conference on Minority Diseases, at the 12 de Octubre Hospital in Madrid. Maria, mother of a ColVI&hellip;"}