Improving pain management support for endometriosis pain

[Emmaheather]

Endometriosis UK, and the universities of Oxford and Edinburgh are carrying out a survey to help design research for a pain management intervention for those with endometriosis and persistent pain. Really important that they hear from as many people as possible. You can have your say here:

https://twitter.com/Ox_wrh/status/1788178937152958786?t=Gb9aTvWhSjUaJFIg-uaHWQ&s=19

Thank you op. It’s shocking that women are still waiting for effective relief in this day and age.

I hope this research means less women suffering in the future
https://vm.tiktok.com/ZGeCdsQx5/

I will have a look thanks op. I felt I was left completely alone and unsupported with no diagnosis for about 7 years and then a 2 year wait for surgery, with no pain relief at all during that time. Surgery was a few years ago and I can feel my symptoms returning but I know they'll probably brush me off and make me wait years again to do anything about it so I'm reluctant to even go back to the gp