We’re honored to be a charity partner with New York Road Runners Club for the TCS New York City Marathon (this November 7th, 2021!), and we’re thrilled to introduce you to Team EndoFound! Hailing from Laramie, Wyoming to Roanoke, Virginia, these superstars are already hard at work training and fundraising for the future of endometriosis care. Get to know the team and why they’re running 26.2 miles for EndoFound.

In stunning and poignant writing, Leslie Harder tells the story of how being sick every day taught her so much about strength and resilience. “My twenties were no joke,” Leslie begins. “I basically got married three times, got cancer, lived in poverty, ended up without a home, and struggled needlessly with severe depression, anxiety, and undiagnosed adult ADHD. Somewhere in that whole mess, I was diagnosed with endometriosis."

In her documentary short, Blood & Guts: Exposing Endometriosis, Meg Allan Cole sheds light on how the medical community dismisses patients’ pain, which leads to a decade-long delay in diagnosis. Watch Diana Falzone’s exclusive interview with Meg on EndoTV today, where Meg discusses the need to improve access to endometriosis care and treatment.

Calling all August 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.

From bracelets and apparel to soothing heatable plushies and accessories, there is something for everyone in the EndoFound Shop—and, we have a special discount for Blossom subscribers! Snag 10% off with code blossomletter today.

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!

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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.