Endometriosis Foundation of America: An Online Patient Community
The Endometriosis Events of 2022

Our annual Medical Conference, Patient Day, and Blossom Ball are officially booked for 2022. Throughout the past year, we still came together virtuallly to bring you Patient Day and Medicial Conference. Now, we're excited to announce our plans to come together in person—including for Blossom Ball, our major fundraising event of the year!

Alaia Baldwin Aronow Opens Up About Endo
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On the latest EndoTV episode, EndoFound Ambassador Alaia Baldwin Aronow shares her deeply personal journey coping with endometriosis during her pregnancy and postpartum with Diana Falzone. 

Live Q&A with Dr. Dan Martin on Managing and Treating Endo
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Have questions about managing and treating endometriosis? Join endometriosis specialist Dr. Dan Martin, our Scientific and Medical Director, on July 20, 2021, for a live webinar hosted by MyEndometriosisTeams on all aspects of living with endometriosis.

Register Today
Join EndoFound’s Staff & Make a Difference
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We’re seeking a highly skilled, experienced and results-oriented development professional for the role of Director of Development! This newly created position will provide strategic leadership in building relationships, identifying, cultivating and soliciting individuals, corporations and foundations to grow unrestricted support for EndoFound, while promoting opportunities for targeted funding for select programs and initiatives.

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Calling all July birthdays! Donate your birthday to improve the future of endometriosis care. Click here to set up your Facebook birthday fundraiser. Every $10 will provide critical endometriosis education materials for one student and their family, reducing delays in diagnosis. Plus, if your birthday fundraiser raises $200 or more we'll provide a special gift for you: $15 towards any purchase in the Endo Shop.

Share Your Endo Story!
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This year we’ve already published 14 endometriosis stories from our community. Each endo story is as unique as a fingerprint and helps tackle the silence surrounding the disease—a silence that contributes to misdiagnoses and improper treatment. What's your story? Share yours today and join the movement in speaking your truth on our path towards a cure.

Share Your Endo Story
Raise Endo Awareness this Summer
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Raise awareness all summer long in our brand-new tie-dye baseball cap and simple warrior tee—perfect for the beach, pool, or picnic. Wearing your awareness can not only make you feel empowered but also spread the word about the disease!

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Disclaimer: The information contained on the Endometriosis Foundation of America ("EndoFound") web site and social media is provided for your general information only. EndoFound does not give medical advice or engage in the practice of medicine. The EndoFound under no circumstances recommends particular treatment for specific individuals and in all cases recommends that you consult your physician or local treatment center before pursuing any course of treatment.

References to any entity, product, service, or source of information not related to the EndoFound in this site should not be considered an endorsement, either direct or implied, by the Endometriosis Foundation of America. The EndoFound does not recommend or endorse any specific tests, products, procedures, opinions or other information that may be provided on any linked web sites. The linked web sites may contain text, graphics, images or information that you find offensive. EndoFound has no control over and accepts no responsibility for such materials.

We hope that you find endofound.org useful in providing information and in helping you make your own health care decisions.