Laparoscopic Surgery for Endo: A Patient’s Perspective Laparoscopic surgery is often described as the gold standard for diagnosing and treating endometriosis. But what does the experience really feel like from a patient’s point of view? I want to share some…
Endometriosis Books That Helped Me Understand My Body Living with endometriosis can feel confusing and isolating — symptoms vary widely, and answers can be hard to come by. One of the most empowering steps I took on my journey was…
What I Wish I Knew at the Start of My Endo Journey Starting out with endometriosis can feel overwhelming. I remember feeling lost, confused, and sometimes completely alone. If I could go back, here are a few things I wish…
Why We Started This Blog Endometriosis affects millions worldwide, yet it remains widely misunderstood, underdiagnosed, and underfunded. We started this blog to help change that. Our aim is to provide a trustworthy and compassionate space where people living with endometriosis,…
My Endo Journey: From Symptoms to Diagnosis Endometriosis is often called a ‘silent disease’ because its symptoms can be misunderstood, overlooked, or dismissed. My own journey from the first signs of pain to finally receiving a diagnosis was long and…
Living with Endometriosis as a Nonbinary Person Endometriosis is often framed as a “women’s health issue,” but it affects many people beyond the gender binary, including nonbinary, genderqueer, and trans individuals who have uteruses or pelvic organs affected by the…
What I’ve Learned from Sharing My Story Publicly Sharing my endometriosis journey with others—whether online, in support groups, or with friends—has been one of the most powerful and vulnerable things I’ve done. It’s taught me a lot about connection, courage,…
How the Endo Community Got Me Through My Worst Flare-Up Endometriosis flare-ups can feel isolating and overwhelming. During my worst flare-up, when pain and exhaustion made everyday tasks almost impossible, it was the support of the endometriosis community that truly…
