I was diagnosed with UC a couple of years ago and have been working through all the information to see what may work and what might not to control the symptoms. I want to share some recent information with the group in hopes that it can help someone else.
As I am am sitting in the hospital room, on which is day 3, of this depressing, terrifying and humbling experience, I debated on even writing a post; especially since my husband is the writer in the family. The thing is that this disease is isolating. I just happened to be web searching about UC; which is all you can do when you are stuck inside; when I came across this site. I found it to be comforting to know that people have and are experiencing the same stuff as me.