FACEBOOK PAGE FOR UCTD

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!

http://www.facebook.com/pages/Support-Research-on-Undifferentiated-Connecti ve-Tissue-DiseaseDisorder/212133388907840

If the link doesn't work, just do a search for Support Research on Undifferentiated Connective Tissue Disorder/Disease

Thanks!!!

This discussion is closed to replies. We close all discussions after 90 days.

If there's something you'd like to discuss, click below to start a new discussion.

Things you can do

Discussion topics

Community leaders