{"version":"1.0","provider_name":"ALAN","provider_url":"https:\/\/alan.lu\/fr\/","title":"Rare Disease Day 2024 - ALAN","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"muel6aRaPH\"><a href=\"https:\/\/alan.lu\/fr\/news-rare-disease-day-2024\/\">Rare Disease Day 2024<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/alan.lu\/fr\/news-rare-disease-day-2024\/embed\/#?secret=muel6aRaPH\" width=\"600\" height=\"338\" title=\"\u00ab\u00a0Rare Disease Day 2024\u00a0\u00bb &#8212; ALAN\" data-secret=\"muel6aRaPH\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script type=\"text\/javascript\">\n\/* <![CDATA[ *\/\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:\/\/alan.lu\/wp-includes\/js\/wp-embed.min.js\n\/* ]]> *\/\n<\/script>\n","thumbnail_url":"https:\/\/alan.lu\/wp-content\/uploads\/2024\/01\/Rare-Disease-Day-2024-website-banner-1300x930-1.jpg","thumbnail_width":1300,"thumbnail_height":930,"description":"Le 29 f\u00e9vrier 2024 nous c\u00e9l\u00e9brons le 17e Rare Disease Day (Journ\u00e9e Internationale des Maladies Rares), une journ\u00e9e d\u00e9di\u00e9e \u00e0 sensibiliser le grand public sur les maladies rares et leur impact sur la vie des personnes concern\u00e9es, dont approximativement 30.000 personnes au Luxembourg. Sous l\u2019\u00e9gide d\u2019EURORDIS, l\u2019alliance internationale regroupant plus de 1000 associations de patients atteints d\u2019une maladie rare, des milliers de personnes s\u2019engagent chaque ann\u00e9e le dernier jour de f\u00e9vrier pour lancer des actions et des \u00e9v\u00e9nements de sensibilisation dans plus de 100 pays diff\u00e9rents."}