Leah, a fellow Weggie, just posted this on Facebook, and I've been totally into it for the last 20 minutes. It's quite cool - both the slide show and the animation on what happens inside the blood vessels of a Weggie. I'll also put this link on the links section for easy access later.
http://www.ANCAVasculitis.com/index.php
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')
Finally I see the light!!! One year after being diagnosed I start to understand what actually is going on inside my body. I can't belive it took me so long to find out- lets call it denial.
ReplyDeleteI also rekommend info about ANCA vasculitis at: www.unckidneycenter.org/kidneyhealthlibrary
Thank you! Anna
I know. I feel like I learn something new every day. Thanks also for the link. Quite interesting. Hope all is good in your neck of the woods.
ReplyDeleteMarta