“Endometriosis Stole My Life”: What It's Really Like to Live With the Condition

While many people may feel a sense of relief, after living with endometriosis for over a decade, Yaël says, “It felt like a part of me died on the table in the OR.

“I was overcome with grief. It’s like, for 10 to 12 years, you’re told that you’re not seeing the world in blue. You’re crazy. You need to take this medicine. You start questioning yourself. Am I crazy? And then one day, someone says, ‘Actually, we figured out that your eyes are different and you are seeing the world in blue.’

“There’s something so insane about something being tangible and being invisible. That is the fucked up thing that no one can see endometriosis, and people are invalidated and gaslit all of the time.”

According to an Alliance for Endometriosis survey, 90 percent of people with endometriosis say they are “disbelieved, dismissed, or ignored by others at least monthly.” The survey also found that many people with endometriosis symptoms are told that their struggles are a “normal part of being a woman” by family, friends, or employers as well as health care professionals.

“Endometriosis steals your life,” Yael says. “And it has stolen mine.”

Yaël Krinsky crying, in pain, over her symptoms.

Sex and Endometriosis: Breaking the Taboo

Then there’s the part that people don’t often talk about openly—not with their friends, family, or even intimate partners. When you have endometriosis, it can be incredibly painful to insert a tampon into your body, let alone engage in sexual activity.

Glamour’s commerce producer Leilani McQuay was diagnosed with endometriosis at 19, but her symptoms began in high school. “I remember missing school because of my period,” she says. “I would get in trouble and be told that I’m over exaggerating, or they thought I was doing it to myself and making myself throw up.”

“With one of my boyfriends,” she continues, “I threw up on him while we were having sex, which is so painfully embarrassing to even talk about. But I didn’t want to tell him how bad it was hurting.”

Experiences like this, as well as societal pressures that prevent women from having honest conversations with men about sex and their pleasure, led to Leilani feeling like, “Am I just being weak? Is this how sex is supposed to be?”

Yaël also recalls having similar challenges when engaging in sexual intercourse. “I have to go to therapy because sex has been painful ever since I became sexually active,” she says. “Crying, screaming in pain, never feeling safe or comfortable.”

The majority of the women that I interviewed for this article stated that they have had intense and painful experiences during sex with partners. Studies indicate that more than half of people with endometriosis experience dyspareunia—that is, vaginal pain during sex. A study published in 2020 in the journal Sexual Medicine recognizes that dyspareunia is a neglected symptom of endometriosis, which is attributed to “embarrassment and normalization by clinicians and patients.”

In Leilani’s case, on top of sex being extremely painful, she was also told by medical professionals that getting pregnant might be extremely difficult. “A doctor told me that I would be infertile because I have endometriosis,” she says. “I remember, thinking, ‘Okay, so I’m just not going to have kids.’ When you hold shame for that long, and you think, ‘I’m not good enough as a woman, or I’m not able to give my partner this,’ it starts to cause a lot of emotions within yourself.”