So I have been diagnosed with endo during my laparoscopy on November 14th 2017, my specialist has removed as much as he can at the time. I am aware that it can come back at a later date; but for the moment I just want it to be less painful that it's been for years.
the doc said I had lots on my bladder, uterus and a small bit on my bowel also that my bladder was stuck to my uterus and my uterus is attached to my bowel. They've removed endo around and detached the bladder and uterus. I still have some on my bowel which he's said they can do at a later date as they'll need a bowel surgeon, but to note that it will either get worse or stay the same so it's up to me.
Anyone else had the same conversation? What did you decide to do; wait for symptoms or have it removed when you're back to 100% recovered from the first surgery? How long was your recovery? I'm still feeling tired after my first op and I do krav maga so using abs and core is still painful, I'm not looking forward to my first period after as that's supposed to be awful