So I will begin with... I am new to endometriosis. For 4 years I have been told I have IBS but I kept going back because something just was not right. In December my new gp agreed I have endometriosis although not diagnosed as waiting laparoscopy to see if I really have it.
I am very convinced I do, I know my body very well. For pain management they gave me Naproxen, codeine and co-codamol
Any lifestyle advice you can give me re how to make it less painful for me?