EndoPhoto
Under The Mask
I even feel okay to wear mask when I go out. It’s just like a new normal for everyone. I can hide my feelings from anyone under the mask.
Dark Unknowns
Endometriosis is an invisible disability at times because someone can look so vibrant on the outside, while suffering with deep darkness physically and emotionally as the disease exists inside my body.
Tracking Symptoms
As my symptoms worsened, I began to document them. I used an app ….. to track my symptoms.
So Many Soaks
When a hot bath is the only pain relief that seems to work, there are days and hours spent soaking in the tub – unable to do much else. Sometimes, the pain is so debilitating I take my work calls, tend to emails, and try to continue on with life the best I can from the comfort of this little porcelain cage … without my usual coping methods available during the pandemic there is nothing but time to sit with it.
Date Night
A date with my husband has a plan B in case of how I end up feeling. Plan B is hanging out on the couch with a heat pad, movie, hot chocolate and our cat.
Tiny Barnacles
A lone encrusted post in the ocean. Creepy crawling feeling when I look at it, reminding me of the first endo photos I saw when I got the diagnosis. Feeling like my organs are encrusted in tiny barnacles, rusted and useless.
Self-Portrait
This self-portrait depicts the emotions, thoughts, and fears that have accumulated from my interactions with the health care system. As a person living with Endometriosis, the process of seeking thorough and compassionate care has, at times, been a dehumanizing experience that has impacted my sense of self. However, I know that I am so much more than my illness.
Grounding
Spending time in nature has been a source of resilience and groundedness throughout this journey. However, at times the only way I have been able to enjoy this is through the photos I have captured on the days when I felt good. These photos are a reminder to maintain hope even on the bad days – that there is still so much beauty around me even when things are tough.
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 Life, Connected Life, Reflective life, Healthcare 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 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 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.