1.0Sclérodermie Québechttps://sclerodermie.ca/en/sclerohttps://sclerodermie.ca/en/author/sclero/rich600338<blockquote class="wp-embedded-content" data-secret="uA6bsf9zdd"><a href="https://sclerodermie.ca/en/temoignages/dolores-story/">Dolorès Story</a></blockquote><iframe sandbox="allow-scripts" security="restricted" src="https://sclerodermie.ca/en/temoignages/dolores-story/embed/#?secret=uA6bsf9zdd" width="600" height="338" title="“Dolorès Story” — Sclérodermie Québec" data-secret="uA6bsf9zdd" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"></iframe><script> /*! This file is auto-generated */ !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); //# sourceURL=https://sclerodermie.ca/wp-includes/js/wp-embed.min.js </script> Dolorès Dupuis has had diffuse scleroderma for over 20 years. She has been actively involved for all that time within the scleroderma patients support community, to help people who, like her, have this incurable disease.  I remember, it was September 16, 1998. My doctor called me and told me to leave my office. The diagnosis […]https://sclerodermie.ca/wp-content/uploads/2014/12/A_SCLQ02_moisSclerodermie_siteWeb_bandeau-colonneCentre-temoignages_575x302.jpg