1.0Welcome to Scottys Bloghttps://scottysblog.com/homeScotty Hawkeshttps://scottysblog.com/home/author/scotty-hawkes/rich600338<blockquote class="wp-embedded-content" data-secret="JtrLVHy5Jc"><a href="https://scottysblog.com/home/myeloma-infoday-london/">Myeloma Infoday London</a></blockquote><iframe sandbox="allow-scripts" security="restricted" src="https://scottysblog.com/home/myeloma-infoday-london/embed/#?secret=JtrLVHy5Jc" width="600" height="338" title="“Myeloma Infoday London” — Welcome to Scottys Blog" data-secret="JtrLVHy5Jc" 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://scottysblog.com/wp-includes/js/wp-embed.min.js </script> Hawksey & I went this Sat to the annual Myeloma Infoday, organised by Myeloma UK, the main charidee for my poxy disease. Was really well run and incredibly handy to be able to ask any medical question at all to a panel of experts – and actually get a reply (not quite what tends to happen with […]