February 26, 2012
I remember when I was finally diagnosed with Endometriosis. I had so many questions, but no one seemed to have the answers. I remember sitting in the waiting room of the doctors office and I picked up this yellow brochure for the Endometriosis Association. Later that day, I contacted them. It was life changing for me. Not only did I have a wealth of information and knowledge at my finger tips, but there were people who truly understood what I was going through by having this disease. As a member of the EA, you have access to the best information out there! The books, newsletters, healthcare provider list, programs and the ground breaking research are what truly make the difference. I have personally been involved for the past 5 years by serving on the board and I have seen first hand just how much goes on each and every day. I would encourage you to get involved by becoming a member or a donor. www.endometriosisassn.org
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