I had this elsewhere and the link is now dead. So I went online and found it so that we all have access to this if we need to explain to a friend what our crazy disease is all about. I will also make a little booklet type thing so that we can print it out and understand better. I'll try and laymen-ize it. Wish me luck.
<iframe src="//www.slideshare.net/slideshow/embed_code/key/aCvWknCw06kxVM" width="595" height="485" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" style="border:1px solid #CCC; border-width:1px; margin-bottom:5px; max-width: 100%;" allowfullscreen> </iframe> <div style="margin-bottom:5px"> <strong> <a href="//www.slideshare.net/ameenrageh/granulomatosis-with-polyangiitis-wegeners-granulomatosis" title="granulomatosis with polyangiitis (Wegener’s granulomatosis) " target="_blank">granulomatosis with polyangiitis (Wegener’s granulomatosis) </a> </strong> from <strong><a href="https://www.slideshare.net/ameenrageh" target="_blank">Ameen Rageh</a></strong> </div>
Wegener's Granulomatosis. A rare auto-immune disease affecting 1 in 30,000 to 40,000 lucky winners. I'm one of those winners. Diagnosed in May 2010, life has changed dramatically in some cases for the worse and in some for the better. This is where I ramble on about my observations with this new friend called Wegener's - which makes me a Weggie (pronounced 'weg-ee')
