Do race and ethnicity affect endometriosis diagnosis rates?

Endometriosis can affect people of every race and ethnicity, but diagnosis is not experienced equally. Many patients who are Black, Hispanic/Latine, or Indigenous face lower diagnosis rates and longer delays, even with similar symptoms.

These gaps are often driven by systemic barriers such as reduced access to specialized care, implicit bias in healthcare settings, and symptoms being minimized or misattributed. If you feel your pain or bleeding concerns haven’t been taken seriously, our team can help review your history, validate your symptoms, and outline a clear path to thorough evaluation and next steps.