Want to keep this short. Had a laparoscopy last year when I was 17. They found a deep nodule of endometriosis on left Kidney tube (ureter). Got referred to a specialist, he didn't do anything apart from offer the prostap injection. My new Doctor in a CEMIG center said I need surgery to remove this nodule as the previous surgeon should have kept an eye on it as it is on such a vital area. I am getting all the symptoms related to Ureteral Endometriosi, including need to go to the toilet often (feel like I have a bladder of a child) and horrible back pain etc.
Want to know if anyone else has had experience with Ureteral Endometriosis or any endometriosis on their kidney tubes (ureter).
Thank you. Would appreciate any reply.