Wegener’s Granulomatosis: Another Brave Face In The Crowd!
Posted Jul 21 2010 12:00am
After finishing my last article in my series about living with Churg Strauss for a second year, I went onto Facebook, and came across this post from Nicole Guerin, who has a video on YouTube focusing on
The video is here , and I’m glad that someone has the bravery to actually share their experience with others.
Nichole is going to be attending the Vasculitis Foundation’s Symposium in Long Branch California, coming up on July 31st and August 1st.
I am not going to be able to attend but I hope that if you are able to attend this event that you take the time to listen to what is discussed and are able to take away a better understanding of what it’s like to live with a vascular condition such as Wegener’s or Churg Strauss.
After finishing my last article in my series about living with Churg Strauss for a second year, I went onto Facebook, and came across this post from Nicole Guerin, who has a video on YouTube focusing on
The video is here , and I’m glad that someone has the bravery to actually share their experience with others.
Nichole is going to be attending the Vasculitis Foundation’s Symposium in Long Branch California, coming up on July 31st and August 1st.
I am not going to be able to attend but I hope that if you are able to attend this event that you take the time to listen to what is discussed and are able to take away a better understanding of what it’s like to live with a vascular condition such as Wegener’s or Churg Strauss.