Voicing Identity, Symptoms, Impacts, Barriers, and Lived Experiences in Endometriosis

Courtney deGorterParticipate in Research

Participate in two online surveys (30-45mins each) for adults in Canada living with endometriosis. The purpose of the study is to learn more about how people living with endometriosis experience pain, disability, stigma and identity.

Eligibility:

  • Have confirmed or suspected diagnosis of endometriosis
  • Experience pain for ≥3 months due to endometriosis
  • 18+ years old
  • Lives in Canada
  • Fluent in English
  • Willing to answer questions about their endometriosis and health history, pain and related symptoms, disability, sexuality, and mental health

Participants receive a $5 e-gift card per survey ($10 total), with option to claim or donate to one of the three Canadian endometriosis organizations.

Click HERE for the eligibility survey.

For more information or questions contact Samantha at samantha.levang@queensu.ca