Anyone else waited months for their post surgery appointment and feel let down by everyone? My Laparoscopy was in May and my apt in September so I can barely remember all the questions I had back then! Anyway, as sympathetic as the doctor was she basically said they don’t give endometriosis a stage and they don’t refer for a second lap, even though my pain has doubled since the surgery. She also told me I have it on my bladder, but didn’t elaborate on what this means. I have it on my POD, both sides of my pelvic walls, on my womb and the uterovesical fold. I also have adenomyosis. She basically told me I am the way I am because of it all...tell me something I don’t know! She has referred me to the pain management team and has prescribed me some tablets for the first few days of my period. Is this similar to anyone else’s experience?