lado123

**coffeelover** · 10-22-2009, 10:07 AM

I welcome you as well. I know that I too had not heard of this disease prior to my diagnosis. There are some here that are a wealth of information and some like me, still learning what I can as I struggle with the frustration of the ups and downs. But thankful for places like this forum and thankful to still be kicking and screaming.
Coffeelover

**moyan** · 03-11-2010, 07:35 AM

Hi Lado, nice to meet you.
I had the doc write down the name of the disease and when I asked he told me it was an inflammation of the bloodvessels. That was almost all I knew for 2 years. Found a little bit of info at J.Hopkins vaculitis, but only when I found this group facts fell into place.

**JanW** · 03-11-2010, 07:58 AM

Hi, Lado, and welcome. Ask any question here -- this is a wonderful and welcoming group and you will feel right at home. Since the symptoms of WG are so variable, you will find someone who has had almost every single one. When I was first diagnosed I spent a couple of days reading the forums, and then just jumped right in. Now I'm here nagging multiple times a day!