EndoFound's online magazine.
A new review by clinician Dr. Calbeth Alaribe finds that research has largely overlooked how endometriosis may affect preeclampsia risk for Black women, and she makes the case for why that gap matters…
This November, 70 runners will take on the New York City Marathon as Team EndoStrong, the largest team in its history, with a goal of raising over $400,000 for endometriosis awareness, education, and…
Early signs of endometriosis, why they matter, and how to advocate for yourself in school this year.
For anyone stuck in what Kate Downey calls "diagnosis limbo," CRAMPED offers information, community, and the relief of hearing someone else describe the pain you know.
Alexandra Henry spent ten years fighting for a diagnosis of thoracic endometriosis, only to be dismissed by every doctor she saw. Today, Alexandra reconnects with the doctor who finally believed her,…
Inside Summer Bloom, the Sag Harbor fundraiser where art and advocacy came together—and where a disease as misdiagnosed and underfunded as endometriosis found a room of new champions.
Diagnosed with stage IV endometriosis after years of being told she had "bad periods," Leslie Mosier has spent the last several years sharing what that life actually looks like, including the summer morning…
In February 2026, Congresswoman Nikema Williams (GA-05), Co-Chair of the bipartisan Congressional Endometriosis Caucus, sent a letter to the U.S. Secretary of Labor urging the Department to name endometriosis…
By signing up at the NASN Annual Conference for ENPOWR Programming, school nurses have positioned themselves as advocates for roughly two million students who need better care.
Endometriosis Patient and Advocate Melissa Boudreau Finds Gratitude Through Chronic Illness in New Memoir
