Dear %Subscriber:CustomField1%,

Thank you for joining us for the Virtual Patient Conference! Curated by our Patient Advisory Committee, the conference included everything from patient stories to the latest in care from endometriosis experts. We hope you logged off feeling supported and armed with more information to help you live your best life with endo.

The panels and sessions from the conference will be available on our website on October 27th. We'll notify all conference registrants when it goes live. 

As always, it is you—the patient, the supporter, the endo advocate—who determines the future of endometriosis care. Your voice matters and impacts the taboos, stigmas, and misinformation that surrounds this disease. If you'd like to share your story, please visit this link.

In community,

Margaret Caspler Cianci
Executive Director, EndoFound

There are less than two weeks until the End Endo 5K on November 1st, 2020! Find your own course to walk, run, hike, bike, or even horseback ride to raise money for endometriosis advocacy, awareness, education, and research. Can’t participate this time? Encourage your friends and family to walk or run in your place! During our inaugural 5K in August, you raised over 30K—funds that will go directly towards research and education programs. Let’s make the same impact this November to work towards our goal: ending endo. 

Elle Hurley, endo advocate, patient, and writer, covered the Virtual Patience Conference over on the Blossom Blog, highlighting each session over the three-day weekend in depth. “Endometriosis can make us feel alone,” Elle writes, “like no one can understand our pain or empathize with what we go through. The Patient Conference is the tonic for those feelings of isolation. In a year marked by uncertainty and anxiety, this is the perfect time to tap into this community's resilience.” Read her coverage for Friday here, and Saturday and Sunday here!

Do you have a birthday coming up? Celebrate with EndoFound! Click here to set up your Facebook birthday fundraiser. From birthday fundraisers on Facebook to running 5Ks, you make it happen. With your help, we can continue working towards increasing endometriosis awareness, education, advocacy, and research. Thank you to everyone across the country who has fundraised in support of endometriosis.

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Remember that you have to login at smile.amazon in order to donate. You can also simply follow this link.

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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.