Living

Women fight every day to receive a diagnosis of endometriosis. Despite this, it takes most women an average of 8 to 10 years to get the proper diagnosis. There is...

Maybe you went to an appointment with the hope and anticipation that they can answer your questions about your recent health struggles, only to be rushed through the appointment and...

It’s a tale as old as dating apps. You’ve been casually meeting some new human beings for a while, going on a few good dates and some bad ones, and...

When I am having an endo flare, my abdomen isn't the only thing that hurts. Endometriosis can impact my entire body, including my brain. Some of my excellent colleagues have...

Research has shown endometriosis is linked to higher levels of stress, anxiety, and depression compared to healthy women. Furthermore, increased levels of stress are related to the severity of the...

I am one year post my second excision, and while my pain is reduced, I still struggle in some significant ways. Before surgery last year, I had lost mobility. My...

For many of us with endometriosis, needing imaging is common. Whether it is an MRI, a CT scan, or an ultrasound, here are some things I’ve learned about how to...

Content warning: this article discusses controlling partners, financial abuse, and other abusive behaviors. Please read with care. If you think you or a loved one may be in an abusive...

An experience that you’ll come across time and time again with endometriosis patients is that they’ve felt ignored, misunderstood, or outright dismissed by medical professionals. The ‘invisible’ nature of endometriosis...

You'll do almost anything to eliminate the pain and discomfort from endometriosis. At times it can feel like it's holding you back in life – exercising, dating, swimming, and even...

I have a confession: I love living alone, and I get to choose what to watch, like reruns of Sex And The City or Captain Marvel for the eighth time...

Throughout the years I’ve been managing endometriosis, I have become skilled at self-advocacy. I am persistent about getting doctor appointments, researching, listening to my body, and not taking no for...

Drinking hot tea is one of the few things I found comforting when I started suffering from endometriosis. Being a Southern woman, I grew up drinking iced black tea. Despite...

Many people struggle with constipation. Living in the rushed world that we do, combined with the great amounts of processed foods that we eat and a global sense of unrest...

Lately, the medication I take to manage certain endometriosis symptoms is leaving me very deflated. I have been on the pill form of the Provera injection for over three years...

My husband knows that I sometimes get pre-menstrual dysphoric disorder, also known as PMDD. We both look forward to day 4 or 5 after my period starts when I usually...

It is pride month and people around the world are celebrating the LGBTQ+ community. Unfortunately, some doctors continue to ignore transgender, nonbinary, and queer people who have endometriosis. I was...

Editorial Note: Nominations for 2024 are now closed. We are very excited to announce the launch of the 2024 Social Health Awards program! The Social Health Awards is an awards...

A year into the pandemic, my anxiety, depression, and chronic pain were at all-time highs. I'd had my first excision surgery to remove extensive adhesions, two big endometriomas, and endo...

"I hate my body and this chronic illness life, and I will never get better," I say to myself as I look in the mirror. A line I have repeated...