18/04/2026
A new paper from Rachelle Bonner amd Jodie Wilson Avery: “Endometriosis at the Intersection: Trauma, Identity, and the Struggle for Equitable Care”
This piece challenges the idea that endometriosis is *just* a biomedical condition. It isn’t.
It sits at the intersection of trauma, structural inequality, and whose pain gets believed.
They argue that:
– Diagnostic delay isn’t accidental, it’s systemic
– Trauma doesn’t just coexist with endometriosis, it shapes how it’s experienced and treated
– Entire groups (First Nations people, trans and gender-diverse people, people in larger bodies, people with disabilities, and racially marginalised communities) are routinely erased from research and care
– Patients are forced into self-advocacy because systems continue to fail them
It’s not a light read. But it’s an important one.
At its core, this is about pushing for care that is more human. Care that actually recognises the full reality of people’s lives, not just their symptoms.
If this is something you care about, whether professionally or personally, I’d love you to have a read and tell me what you think.
🔗 Read it here: https://doi.org/10.1080/23293691.2026.2636611
Robinson Research Institute
Endometriosis is a chronic inflammatory condition affecting millions worldwide, yet it remains underdiagnosed and undertreated—particularly among marginalized individuals. Drawing on medical sociol...