{"version":"1.0","provider_name":"ALAN","provider_url":"https:\/\/alan.lu\/fr\/","title":"Rare Disease Day 2026 - ALAN","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"V2w9qFrpPQ\"><a href=\"https:\/\/alan.lu\/fr\/rare-disease-day-2026\/\">Rare Disease Day 2026<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/alan.lu\/fr\/rare-disease-day-2026\/embed\/#?secret=V2w9qFrpPQ\" width=\"600\" height=\"338\" title=\"\u00ab\u00a0Rare Disease Day 2026\u00a0\u00bb &#8212; ALAN\" data-secret=\"V2w9qFrpPQ\" 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\/2026\/02\/RDD-2026-banner-1300x930-1.png","thumbnail_width":1300,"thumbnail_height":930,"description":"Dans le cadre de la Journ\u00e9e internationale des Maladies Rares (Rare Disease Day), l\u2019association ALAN \u2013 Maladies Rares Luxembourg organise \u00ab Rare Voices \u00bb, une soir\u00e9e, accompagn\u00e9e d\u2019une campagne en ligne, visant \u00e0 donner voix et sc\u00e8ne aux personnes touch\u00e9es par une maladie rare. En outre, pour sensibiliser davantage le grand public et donner un signal fort de solidarit\u00e9, de multiples b\u00e2timents phares seront illumin\u00e9s dans les couleurs du Rare Disease Day pendant la derni\u00e8re semaine de f\u00e9vrier."}