HOW SOCIAL PERCEPTIONS SHAPE WHO GETS AN ENDOMETRIOSIS DIAGNOSIS Centring LGBTQ+ experiences of endometriosis: A critical mixed-methods analysis
What is endometriosis? Imagine you are in chronic pain. You’ve been waiting around eight years for a diagnosis. Then, after years of your symptoms being normalised and not being believed by family, friends, colleagues, and healthcare professionals you finally receive a diagnosis, only to find the cause is unknown and there is no cure. That’s the reality for people with endometriosis.
What do you research? My PhD is about trying to improve the understanding of factors that contribute to this delay in diagnosis, specifically for LGBTQ+ patients, using a mixture of both quantitative and qualitative research methods. My work aims to broaden who is involved in creating knowledge about the experiences of endometriosis diagnosis.
VISIT OUR WEBSITE TO LEARN MORE ABOUT ELLEN’S RESEARCH! leedspostgraduatereview.wordpress.com
A very exciting new research spotlight has been uploaded to our website!! Written by @eldoespsyc.bsky.social the post explores how social perceptions shape who gets an endometriosis diagnosis. You can get a taste of Ellen’s research here leedspostgraduatereview.wordpress.com/ellen-frost-...