I got diagnosed with endometriosis in my ovaries with an MRI scan in September. I am due to have a surgery in December to confirm the diagnosis and take out any endometriosis. I have had a few rounds of severe pain and was told it was ovarian cysts bursting and leaking in to my pelvis. I have been off work since August with the constant pain and the in unpredictable flare ups of burst cysts.
I guess i am looking for any tips from your experience with surgery and how you felt and what i should do to make things easier. I am terrified of the surgeon going in to my pelvis and not finding anything. I read that endometriosis can only be 100% diagnosed through surgery. I do not want for my pain to have no definitive because as it’s hard to get people to believe my pain if the cause is not known. I have already been through that, no one believed the pain i was in before the diagnosis.