1.0EndoActhttps://endoact.ca/fr/rich600338<blockquote class="wp-embedded-content" data-secret="J6FAW5IOQt"><a href="https://endoact.ca/fr/cait-2/">Cait</a></blockquote><iframe sandbox="allow-scripts" security="restricted" src="https://endoact.ca/fr/cait-2/embed/#?secret=J6FAW5IOQt" width="600" height="338" title="« Cait » — EndoAct" data-secret="J6FAW5IOQt" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"></iframe><script type="text/javascript"> /* <![CDATA[ */ /*! 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://endoact.ca/wp-includes/js/wp-embed.min.js /* ]]> */ </script> Endometriosis is something that I'm constantly having to plan around. I know that when I get my period I'll be bedridden, so I have to decline social events because of it, or constantly try to reschedule things. If I can't cancel or reschedule something, I make sure to take my pain relief with me, and set alarms on my phone to keep up with the doses. My symptoms are very difficult to deal with at school and work - I can't take days off, so I have to push through the pain.https://endoact.ca/wp-content/uploads/2021/01/20025-EndoAct-Instagram-Single_prf01.png12601260