AAAAAAAAAAAAAAARRRRRRRRRRRRRRRRRRRR Capt Deb,
We share a common ground here. We have bot had middle fossa and have screaming headaches. Fortunately, you have not had regropwth whereas I have.
Ok, I had surgery Nov 2002. I was told (lied to) that they got all my tumour out. I scheduled annual MRI's even though I was told that i did not need one for 5 years, and at the 3.5 year mark, I was devastated (although i had an inkling) that my growth had returned. It was about 19mm and still is.
I dumped that neurosurgeon and went for the no.1 guy here in Sydney (couldn't see him the first time because he was over booked) and he is our most experienced one. He agreed for me to see him going forward and he has told me that, baseing his decision on experience and a number of overseas studies (Norway I think) that he no longer does middle fossa because of all the post op complications and the apparant high chance of growth return. He cited headaches as a major by product.
He now waits until either the growth starts to grow - trans lab or watch and wait.
He was very apologetic to me saying that he wouldn't have operated - he even suggested radiation as an option, which he doesn't do.
All in all. My next attack on my growth will be gamma knife. last resort is surgery.
Laz