'A name to the pain': A mixed methods analysis of diagnostic delay and perceptions of diagnosis importance in Australians with endometriosis
Australian endometriosis patients experienced a 12.3-year diagnostic delay, often due to medical dismissal, with diagnosis being crucial for effective care and shorter delays linked to recent symptom onset and younger age.
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Cited by (13)
- “Belittled” and “Broken”: Distressing Medical Interactions in Endometriosis Healthcare: A Mixed Methods Study 2026
- The Endometriosis-Related Healthcare Experiences of Regional Australian Women: A Qualitative Systematic Review 2026
- Endometriosis and the mental health burden: a registry-based study of redeemed prescriptions and psychiatric hospital contacts before and after diagnosis of endometriosis 2026
- Patient Perspectives on the Missed Opportunities and Barriers During the Diagnostic Journey: A Mixed Method Cross Sectional Study on Endometriosis in Australia 2026
- Preliminary Materials for a Situated Knowledge of Endometriosis 2026
- Endometriosis at the Intersection: Trauma, Identity, and the Struggle for Equitable Care—A Narrative Review 2026
- Pain Self-Efficacy, Pain Acceptance and Quality of Life in Endometriosis 2026
- The Long Road to Endometriosis Healthcare: The Experiences of Regional Women Living in Australia 2026
- The needs, preferences, and priorities for supportive healthcare in people living with endometriosis: A qualitative exploratory study 2026
- Comparing psychological distress, health-related quality of life and pain in people diagnosed with endometriosis and those suspected to have endometriosis 2025
- The Experiences of Endometriosis Patients During Primary Healthcare Encounters: A Systematic Review of Qualitative Evidence 2025
- Yonder: Menstrual cups and IUD displacement, deprived area GP retention, endometriosis diagnosis, and patient assertiveness 2025
- Debunking the “Mystical Condition” of Endometriosis: What People Living with Endometriosis Want You to Truly Understand 2025
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