Ever feel like you're the ONLY PERSON who knows anything about UCTD? Do doctors/nurses even look at your strangely when you tell them your condition? Ever find it hard to put into words exactly what is going on with your body?
I have started a page in order to provide awareness about UCTD (I was diagnosed in 2007) and advocate for more research efforts to be focused on it. Please take the time to educate yourself about this condition and join my efforts in raising awareness!
If the link doesn't work, just do a search for Support Research on Undifferentiated Connective Tissue Disorder/Disease