The Endometriosis Association: A Legacy of Firsts
Endometriosis Patient Group Leaders meet in Berlin, Germany (Spring 2015).
From left: Jacqueline Veit, Associazione Italiana Endometriosi; Femke Jansen, Endometriosis Association Belgium; Karin Grundler, Endometriosis Association Sweden; Bianca DeBie, Endometriose Stichting, Netherlands; Mary Lou Ballweg, Endometriosis Association
(International Headquarters in Milwaukee, WI USA). Also participating: Daniella,
Endometriosis Association UK.
DONATE on GIVING TUESDAY!
The Endometriosis Association is the recognized authority
a life-altering hormone and immune
system disease affecting millions worldwide.
The most common symptom of endometriosis is pelvic pain that may have a monthly pattern, may or may not be consistent, and may interfere with activities of daily living. Learn more...
The ultimate goal of the Endometriosis Association is to find a cure and prevention for endometriosis while at the same time providing education, support, and research to those affected. We are an international nonprofit organization that provides information about endometriosis in numerous languages. Free brochures . . .
Suffering with endometriosis can be lonely—it seems like no one understands.
For 35 years we’ve extended a helping hand to those experiencing endo pain and we’re here to help you. See how. . . .
Let’s get one step closer to finding a cure. Click here for info.
CLICK HERE to read additional messages from our friends and colleagues
New! Teen DVD and More
Watch Now: "Teens Speak Out On Endometriosis." Our award-winning DVD, “Teens Speak Out,” is made for presenting to a group of teens. Let us know if you are interested in presenting this to a group. NOW AVAILABLE for Ordering