I would like to leave this post for anyone diagnosed with Leiomyosarcoma of the cervix. Please ignore the horror stories and low statistics online. When I was diagnosed at late stage 2 12 years ago I was petrified after reading the poor prognosis rates. I would just like to say I had surgery and I am still here and fighting fit after 12 years so please stay positive if you're in this position. Please don't ignore symptoms and don't be fobbed of by doctors. You know your own body and you know when something  isn't right.  Please feel free to write if I can be of any help. Good luck everyone. xx