CRAMPED: The Podcast Asking Critical Questions About Period Pain
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.
The Blossom
EndoFound's online magazine.
Overlooked, Not Rare: Thoracic Endometriosis Outside the Textbook
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,…
Over $50,000 for Endometriosis Research, Raised in a Sag Harbor Gallery
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.
Showing the Full Picture of Pain: Leslie Mosier on Navigating Cannes Lions During an Endometriosis Flare
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…
No One Should Choose Between Their Health and Their Paycheck: Congress Pushes for Endometriosis Recognition Under FMLA
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…
ENPOWR Signs Up Nearly 4,000 Schools at the National Association of School Nurses Conference
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.
Melissa Boudreau on Finding the Small Wins in a Life with Endometriosis
Endometriosis Patient and Advocate Melissa Boudreau Finds Gratitude Through Chronic Illness in New Memoir
Remembering Dr. Asgi Fazleabas: A Pioneer in Uterine Biology and a Dear Friend to the Endometriosis Community
His baboon model transformed what researchers could observe about endometriosis. His mentorship transformed the next generation of researchers. A tribute to a member of EndoFound's Scientific Advisory…
The Bodies We Mourn, The Selves We Become: Endometriosis, Queerness, and Grief
In a powerful personal essay, public health professional Frieda Walsh-Seaman poignantly traces their experience navigating their endometriosis diagnosis as a teenager while later coming out as queer.
A New Endometriosis Research Initiative Dedicated to Genomics
The Our Daughters Foundation, launched by the parents of daughters with endometriosis and adenomyosis, partners with EndoFound, supporting research at the Seckin Endometriosis Research Center at Cold…
