As a university alumna, I still have access to medical journals and I've been reading through them to gain a more indepth understanding of the research being currently done. One thing is quite clear, the biggest factor in the treatment of endometriosis (specifically surgery) is the surgeon!
As Ticked said above, it is worth doing whatever you need to do to get an endometriosis specialist, not just any gyno. I'm not saying miracles can happen with a specialist, endo is endo, but at least you'll be in better hands and have the opinion of the best in the field.
i live in minnesota. there is nothing here other then maybe the cities and that still about a 5 in half 6 hr drive...
My suggestion? Find a new doctor. You need to find and Endometriosis specialist.
I had stage IV endo and I had it all over, my ovaries were wrapped around my uterus and Fallopian tubes, it was all over my intestines and bladder, kidneys and I had a rectovaginal cyst. He removed all the endo and I have been on the BCP continuously since 2007 with no pain.
I am not saying everyone will become free of pain because I still have times where I do get pain but I dont get a period so I really dont get pain like that anymore.
Regular Gynos really dont know alot about endo and most of them feel the best choice is a hyster and i disagree.
I do want a hyster and he wont give me one. I also have high grade lesions on my cervix and since I am done having children and because of the endo I want it all out. Well unless I get another doctor to okay it he wont do it.
He is the only doctor I want doing my surgery because he is the best of the best. Trust me you want someone who knows their stuff and can work with you. If I was going to have another baby he would be all over this because right now my uterus is anteflex and retroflex. and I know its stuck to my intestines. I can feel it.
Where do you live? I can help you find a good one.