Would you like to take part in a study about experiences of endometriosis?

Taking part in the study will involve being interviewed about your experiences of endometriosis. This could include discussing what your experiences of symptoms, treatments and healthcare have been like, the impacts on you, how you have found information, how you made decisions, and anything else you would like to tell us.

We will publish the study findings on www.hexi.ox.ac.uk, an award-winning website that provides access to the experiences of others who have faced the same concerns. On the website you can read, hear or watch the accounts of people describing their experiences of many different health conditions.

HEXI is used to help support others going through similar experiences, and help train doctors, nurses, GPs and other health professionals to understand people’s experiences of endometriosis or suspected endometriosis.

We are particularly interested in talking to:

• people from racially minoritised groups
• those who speak English as a second language
• trans, non-binary, or gender diverse individuals
• people living with a disability
• people facing challenges such as poverty
• and individuals experiencing homelessness

If you would like to take part, a researcher can interview you at your home or elsewhere if you prefer, or can arrange an interview by phone or online.

For more information on taking part, please go to our website: Experiences of endometriosis — Nuffield Department of Primary Care Health Sciences, University of Oxford

Or contact the researcher, Rachel:

Email: endear@phc.ox.ac.uk

Telephone: 07598 064 496

Address: Medical Sociology & Health Experiences Research Group, Nuffield Department of Primary Care Health Sciences, University of Oxford, Radcliffe Observatory Quarter, Woodstock Road, Oxford OX2 6GG.