My Nonprofit Reviews

I was diagnosed with PSC in March 2012. My GI doc told me I had the disease, said there wasn't anything he could do to help me but he would try to follow up with me and sent me on my way. With a million questions in my mind, I searched the Internet and fount PSC Partners Seeking a Cure. My first post was answered in hours by two very knowledgable fellow PSCers who made me feel welcome and helped me feel not quite so lost in this new world. Without this organization I would still be floundering in acronyms, untruths and fear. I am still looking for a doctor but will have to travel to even find a hepatologist. As of now, I still haven't met anyone who knows of this disease or that has it so I am really looking forward to attending one of their conferences. PSC Partners is a daily stop for me in Facebook. I feel like I have a home there where everyone knows my disease. :) I can't imagine how I would feel if I hadn't found this organization. One of these days I will meet the faces behind the names and I know they will be instant friends.

More Feedback