Hi! I’m a student doing an Extended Project Qualification (EPQ) on gender inequality in endometriosis diagnosis and treatment in the UK.
I’ve created a short, anonymous survey to collect real experiences of people with endometriosis. It takes around 5-10 minutes, and you can skip any question.
Here's the link: https://docs.google.com/forms/d/e/1FAIpQLSdm6yV...
Thank you so much for helping - your voice is really important to this research 💛
Thank you for your comment @A MyEndometriosisTeam Member! You are more than welcome to participate if you do not live in the UK. However, only data collected from participants who answer 'Yes' to the question 'Are you from the UK?' will be included in my final report. That being said, I'd still love to hear from of those living outside the UK to further my understanding, and provide sufferers with a chance to express their opinions. Let me know if you have any further questions!
Is this only for folks who live in the UK?
Amazing work you're doing here! Regardless of if I'm able to participate or not, good luck! ❤️
Your research into gender inequality in endometriosis diagnosis and treatment is addressing a critical issue. On average, it takes about a decade of pain and symptoms before women receive a correct endometriosis diagnosis, highlighting the systemic issues in healthcare recognition and treatment. While your interest in Show Full Answer