Just found out it's what my mum has. According to my google research it's very rare (1-2% of all ovarian tumours) and very aggressive and prognosis is very poor. My mum had her surgery about a month ago and now undergoing another round of chemo (she had four before the surgery). We think the cancer is all out of her following the surgery although having scared myself brainless with all my googling I realise that there are so many variations and meanings to that phrase. The only thing that sticks with me is how poor the prognosis is conveyed online. I haven't been able to speak to her doctors. I need someone to tell me that it isn't that bad for everyone. Has anyone been unfortunate enough to be affected by ovarian carcinosarcoma (also known as ovarian MMMT)?
I was feeling so happy at her progress after her surgery and now having read her pathology report I just feel terrified and sick to my stomach.
Mayski
xxx
