Endometriosis Foundation of America: ‚ÄčAn Online Patient Community
The Endo Experience Through Dance: EndoGirl

Endo Girl, a short documentary dance film, portrays the endometriosis experience through dance. Directed and produced by Australian filmmaker Sophia Bender, the film tells the story of thirteen people who suffer from the disease. Their powerful words of pain and struggle are superimposed with metaphorical dance sequences that show the audience what an individual’s journey to diagnosis is like, as well as the effect the disease has on their day-to-day lives. Read Tara Mandarano’s review of the film, with an exclusive interview with Bender on her filming process, today—and watch the film here.

Learn More
Why I’m Fundraising to End Endo: Samantha By’s Endo Story
Endofound Shop

Before she was diagnosed, Samantha By didn’t experience the usual endometriosis symptoms. It wasn’t until she got pregnant and experienced excruciating back pain that her search for answers began. After an ectopic pregnancy caused by endometriosis lesions on her Fallopian tube, Samantha’s mission to advocate for endometriosis awareness began. Today, she’s hard at work fundraising for our June End Endo 5K and has already raised over $1,000!

Samantha’s Story
We’ve Surpassed Our Goal! And You Can Still Join the Effort
Endofound Shop

Team EndoFound has already surpassed their goal of raising $15,000 for the future of endometriosis care—and they’re still going! Do you want to make an impact? It’s not too late to join the team or you can donate to the team’s efforts here!

Sign Up Today
EndoTV: Tennis Champion Danielle Collins
Endofound Shop

This week on EndoTV, Diana Falzone speaks with American tennis champion, Danielle Collins, who shares the specific difficulty of managing endometriosis as a professional athlete. Danielle’s endometriosis was affecting her so much, she had to pull out of matches and tournaments.


Calling all June 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.

Follow the EndoFound on social media and be the first to hear about new research, program updates, or different ways to get involved. Our platforms provide a safe and supportive environment to connect people from around the world. Please visit our Facebook, Twitter, or Instagram and give us any feedback you may have by commenting on our posts or direct messaging us!

Endometriosis Foundation of America - 872 FIFTH AVENUE NEW YORK, NY 10065
Phone: +1 646.854.3309 - endofound.org

[Unsubscribe] to no longer receive emails from Endometriosis Foundation of America.
Change your email settings at [Manage Subscriptions].

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.