I was diagnosed with GCT two and a half years ago. I was stage 1a and had a TAH/BSO at the age of 50. I am involved with the Granulosa Cell Tumor Foundation (www.gctf.org), along with the New Zealand branch (www.gctf.org.nz), which are desperately trying to raise funds for research on this woefully under-researched cancer. Please go onto these websites for lots of information. This kind of ovca is so rare that the doctors don't know what to do with it and treat women with chemo that has been only tested on other, more common ovca. Also, on the (www.ovca.net) website, there is a very active thread on the message board for GCT. I have received so much info there from women who have been dealing with this frusttrating cancer. As far as ovca goes, I guess this is the kind to get because it grows so slowly (but not always!) Good luck to you all! Cindy