What barriers can one encounter when seeking endometriosis care? How can parts of one’s identity contribute to further difficulties accessing such care? What language should we use when speaking about endometriosis to ensure inclusivity? With Nikita Aaashi Chada, Cara E. Jones and Beth McCowen we discuss how various aspects of our identity (i.e. race, gender, sexuality, age) may further contribute to the delay in receiving a diagnosis, and the quality of care one receives.