EndoPhoto

In 2023 we asked 22 South, Southeast and East Asian women living in British Columbia, Canada to share their stories of having endometriosis during the Covid-19 pandemic through photography.

We found that their intense and inspiring experiences represented the many lives they led including Daily LifeConnected LifeReflective lifeHealthcare Life, and ultimately A Resilient Life.

Throughout this exhibit, please keep in mind that some photos depict sensitive subjects such as fertility, mental health and medical trauma.

If you are experiencing endometriosis, remember that you are not alone, your pain is real and there are treatments and resources available.

This project was co-developed by the University of British Columbia’s (UBC) Endometriosis Pelvic Pain Laboratory and the UBC Endometriosis Patient Research Advisory Board. It was funded by the Canadian Institutes for Health Research and Michael Smith Health Research BC which had no influence over the process or outcome of the project. Ethics approval was provided by the UBC Childrens and Womens Research Ethics Board and all participants provided informed consent.

At the UBC Endometriosis Pelvic Pain Laboratory we believe in a trauma-informed and patient-oriented approach to healthcare research.

The Daily Life

Endometriosis can impact every facet of someone's life from their daily activities to careers to social activities.  It can challenge their physical strength and emotional well-being. Despite the pain, isolation, loneliness, grief and hope, people with endometriosis are strong.

The Connected Life

Though it looked a little different during the pandemic, connection was found to be an essential component of the lives of people with endometriosis.

Many described both the benefits and challenges of navigating the social world with endometriosis.

Trigger warning - some photos and captions depict images of fertility.

The photo shows a pink rose-patterned mug of hot chocolate, with a cat curled up on the couch and a heating pad behind it. This scene captures the cozy, confined comfort of home life during the pandemic and the challenges of managing uncertain endometriosis pain.
A large body of water, with cranes and mountains in the distance, features a person sitting at the bottom of the frame, looking down at the water. The dark blue hues of the person and the water create a unified but melancholic scene, emphasizing the feeling of uncertainty and disorientation in dealing with endometriosis.

The Reflective Life

People found comfort in learning about endometriosis, their own bodies and self-management strategies that could help.
The extra time during Covid-19 helped some to research their experiences and become more prepared.

The Healthcare Life

People with endometriosis had varying experiences with the healthcare system.  Many experienced long delays to diagnosis and struggled to receive appropriate and timely care.

They experienced mixed emotions including fear, disappointment, shame, promise and hope. 

Content Sensitive Images – some images may depict medical trauma.

A portrait of a person sitting on a stool with their legs up and crossed, holding their hands, is overlaid with words and phrases such as "bad patient," "weak-minded," "negative," "my fault," "unworthy," "difficult," "defective," "too complicated," "disappointment," and "shame." These words symbolize the labels and barriers often placed on individuals with endometriosis.

A Resilient Life

Despite the challenges faced by people with endometriosis many described a strong sense of resiliency noting that there was hope for the future.