EndoFound's online magazine.
Sam explains that from being misgendered in doctors appointments to tapping into a support network online, gendered language has meant they’ve felt excluded and alienated in their mission to get an…
New show “Ask the Doctors” launches on EndoTV hosted by Diana Falzone
EndoFound and MyHealthTeams partner to bring community, conversation and content to the 1 in 10 women living with endometriosis
From California to Maine, we had over 350 Team EndoFound members coming together to end endo across the map. Our participants ranged from patients to friends, family members, and partners.
In the United States, the National Institutes of Health (NIH) didn’t require medical research to include women until 1993. The Guardian outlined that people excused this omission by arguing that women’s…
When I first watched Endo Girl, a short documentary dance film, I felt like I was watching my own story reflected on the screen. Directed and produced by Australian filmmaker Sophia Bender, Endo Girl…
In one survey that specifically addressed trust in health care providers, many respondents expressed frustration with a lack of medical knowledge of endometriosis and the breadth of its clinical manifestations,…
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…
What does it mean when the actual endo is gone, but the damage it leaves behind stays with you forever?
Endometriosis is not one size fits all. Our stories are as different as we are, and because of the progressive nature of the disease, the experience of living and working with endo is diverse.
