EndoFound's online magazine.
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
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…
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.
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…
Endometriosis shaped Monroe's career, her losses, and her life, yet almost no one talked about the condition.
