The Endometriosis Foundation of America 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.
The TCS 50th Anniversary NYC Marathon marathon is scheduled for November 7th, 2021, and we hope you'll be able to run for endometriosis awareness and advocacy. We know these are extremely uncertain times, so we ask that you please only fill out this form if you are certain about your interest and can commit to fundraise the minimum amount for charities of $3,000 per entry!
Abby Finkenauer, former Congresswoman for Iowa, made national headlines when she courageously shared her struggle with endometriosis on the House floor to announce the historic House Endometriosis Caucus in March 2020. During her term, Finkenauer…
“It can’t be endometriosis,” the gynecologist said, her voice steady and certain, to the mother of the 15-year-old girl. Her mom had asked if her daughter could have endometriosis, and the gynecologist had answered…
The End Endo 5K is back this June! Find your own course to walk, run, hike, bike, or even roller-skate to shine the spotlight on this disease and raise funds to change the course of endometriosis.
In January of this year, my roommate, Siobhan, walked into our apartment and found me on the floor. I was completely immobile, alternating between periods of screaming and an inability to speak due to pain. She encouraged me to go to the hospital,…
This June, find your own course to walk, run, hike, or bike to shine the spotlight on endometriosis and raise funds to change the course of the disease. Individuals with endometriosis need your help now to promote awareness, fund landmark…
I got my first period when I was 15-years-old and once I turned 19 I began to have horrible periods—I’m talking legs going numb and tingling, extremely heavy periods, dizziness, and painful cramps. I did not understand what was…
NEW YORK (April 6, 2021) – Today, the Endometriosis Foundation of America (EndoFound) announced actor and producer Corinne Foxx as their newest ambassador. Foxx, 27, was diagnosed with endometriosis about five years ago. She recently…
Olivia Culpo is a model, an actress, and a businesswoman who (pre-pandemic) is usually found jetting off to a new location to tackle her latest project. She’s also an ambassador for the Endometriosis Foundation of America. But a year…
Connecting Patients with Science: Highlights from the International Patient Conference Did you miss this year’s International Patient Conference? Covering fertility, the importance of early intervention, alternative treatments, and so…
International Patient Conference 2021 The Path Towards A Cure: Connecting Patients with Science Dearne Richards:Hi, my name's Dearne Richards and I live in Sydney, Australia. I'm 36 years old, and I have stage four endometriosis as well as…
Judy Joo
Moderator: Diana Falzone Speakers Tamer Seckin, MD Dan Martin, MD
