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Endometriosis Association, Inc. Overview
The Endometriosis Association (EA) is an international, nonprofit organization founded in 1980 to provide education, support, and research to those with endo and their loved ones. Membership is $35 U.S./$52 Canadian per year for those with endo. Associate, family and gift memberships are also available. The EA produces educational literature including a bimonthly newsletter, brochures in 28 languages, educational videos(available in Spanish), audiotapes, CDs, and more. The EA also conducts and promotes research at the Vanderbilt University School of Medicine, and provides support to women and girls with the disease through local chapters and support groups, crisis call listeners, contact lists, a prescription drug discount program, correspondence networks, and more. A free informational packet including a catalog of materials and publications is available at 1-800-992-3636 (North America), or log onto the website at www.EndometriosisAssn.org.
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I would have given zero stars, but that is not allowed.
I called this place for some guidance after being diagnosed with endo. I asked to speak to the President and was told flat out that she doesn't talk to people. How can the head of an organization not talk to the public? Not even by a ...
I first came across the Endometriosis Association when I was diagnosed (belatedly, as so often happens) with endometriosis. I became a member and received the newsletter and publications, and right away I was impressed by the combination of “heart” and science in the EA—the commitment to ...
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I learned about the Endometriosis Association after I was diagnosed with this disease. This organization helped me so much and I learned accurate information in helping me deal with this disease. Just having someone understand what I was going through was very encouraging to me. After reading the...
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