Hey all, have been reading your posts for a while...Andrew got me in finally. I was diagnosed this August, 2011 with what appears at this point to be a limited version of WG...mostly in my sinuses, some nerve damage (dropped foot), and all the irritating symptoms. If a friend and my wife hadn't seen that I was not doing well in early August, I may not be here today. I contracted pneumonia & possible Valley Fever (live near PHX)...after a lung biopsy, scaring my wife & children pretty badly, the hospital I was in sent my tests to Mayo Clinic as they could not be sure of what was going on in my lungs. The Mayo pathologist diagnosed WG. Now Mayo is treating me (prednisone & Methotrexate)...the clinic is the best, I am the luckiest. Has not been fun, am interested in sharing and learning more as this journey progresses...as much as I can. My best to all...am looking forward to meeting some of you in here.
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