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The Endometriosis Foundation of America (EndoFound) strives to increase disease recognition, provide advocacy, facilitate expert surgical training, and fund landmark endometriosis research. Engaged in a robust campaign to inform both the medical community and the public, the EndoFound places particular emphasis on the critical importance of early diagnosis and effective intervention while simultaneously providing education to the next generation of medical professionals and their patients.

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EndoFound's Virtual Community

EndoFound's Virtual Community

There has never been a more important time to come together (virtually!) with your endo community and your support system, especially during…

Rep. Finkenauer Hailed Coast to Coast for Endometriosis Testimony

Rep. Finkenauer Hailed Coast to Coast for Endometriosis Testimony

Finkenauer went public with her story after reading statistics and stories from other women with the disease on the Endometriosis Foundation…

Iowa Congresswoman Shares Her Endo Story on U.S. House Floor

Iowa Congresswoman Shares Her Endo Story on U.S. House Floor

Few people outside of family and friends knew that Rep. Abby Finkenauer had been living much of her young life with endometriosis – until…

Coronavirus (COVID-19) Update for EndoFound's March Events

Coronavirus (COVID-19) Update for EndoFound's March Events

UPDATE (3/6/20) In response to the COVID-19 outbreak in the United States, the Foundation Board and the Chairs of the Conference have decided…

Cosmetics Entrepreneur Donates Profits to Fight Endo

Cosmetics Entrepreneur Donates Profits to Fight Endo

In the fall of 2018, just seven months after launching Karmela Cosmetics, founder Nechami Tenenbaum wanted to donate some of the proceeds of…

EndoMEtriosis: A Guide for Girls to Be Released  Worldwide on March 17, 2020

EndoMEtriosis: A Guide for Girls to Be Released Worldwide on March 17, 2020

Endometriosis takes an average of twelve years to diagnose. Twelve long years. That means most teenagers who have it suffer into at least their…

The Blossom Blog

2020 TCS New York City Marathon
Run, Rock, and Roll with The Endometriosis Foundation of America!

I want to get involved! Keep me updated on endometriosis news and events.

SEUD MEETING 2020

27-30 May 2020
Stockholm, Sweden


36th Annual Meeting of ESHRE

5 – 8 July 2020
Copenhagen, Denmark


Minimally Invasive Surgery Week / SLS Annual Meeting

26 – 29 August 2020
Honolulu, USA


All Events
EndoFound.org - Everyday Hero

How endometriosis disrupts women's lives: "Please just let me make it through today"

When Barden found out she had endometriosis, she said she was grateful to get a diagnosis. "In my gut, I knew," she said. "I said, 'once we figure out the underlying cause, I will get pregnant.'"


What Is Silent Endometriosis?

The lack of obvious symptoms can cloud diagnosis, lead to fertility problems.


Join the Movement - First-ever House Endometriosis Caucus

Join the Movement - First-ever House Endometriosis Caucus

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"I AM 1 IN 10" : PADMA LAKSHMI, LENA DUNHAM AND THEIR ENDOMETRIOSIS SISTERS DEMAND EARLY DIAGNOSIS IN INSPIRING VIDEO

One woman revealed she had 12 endometriosis-related surgeries to date

One in 10