Hi everyone,
I've got endometriosis in my ovarian fossa, diagnosed by a lap 4 years ago.
My pain hasn't got any better and I'm worried it may have spread as I've only had management treatment no surgery.
I'm more concerned now too as I get married next year and would then like to start trying to conceive.
I'm battling to get another diagnostic lap done despite increasing pain and clots during my period. I also can't access surgery in Wales due to no specialists. They are constantly putting me on d tours to avoid a cross border referral.
I'm in so much pain. I was an avid gym goer and now I can't go cause it completely drains my energy and on top of my job role I couldn't face being in bed at 6 each evening!
I guess I just want to hear if anyone else has ovarian fossa endo. What are your symptoms? What have they done to treat it and what have they said about fertility?
My consultant told me - in her words - get pregnant now and have my insides removed...!
Thank you