What club do I belong to? What's lurking?
Autoimmune disease "club" for certain. "Your complicated" is what I've been told—"smoldering" and "atypical presentation" when discussing Granulomatosis with Polyangiitis (Wegener's). Possibly Central Nervous System (CNS) vasculitis. "We should consider treatment."
Rituxan
Likely, my next step. If inclined, please share your experiences. The doctors say they've had great success. My mother's nickname for me was "worry wort"; at age 57, and my mother long gone, I still carry the mantle of worry. Some things you just can't change
The World's Rarest Colors (goo.gl/images/bV6BPs)
Maybe not freaks. The forums here have been life changing. Without all the wonderful "colors" I would be lost. The information shared—whether it be on topic or not—has kept me going. Lots of dark days. The color all of you have provided has helped lift me out of the dark. Thank you.
With gratitude,
Canygirl61
P.S. I wish I was as gifted and witty a writer as mamici1
Hubby now given continuing Prednisolone but what else does he need please?
How are you actually feeling?
How was you diagnosed? My bloods are normal , I don’t feel normal and the doctors seem baffled. 
Am I stressing for no reason or does this seem like unfair treatment and a valid reason to be upset?
Hubby secured referral to Man Roy Inf but to a dermatologist?
