My year my story stage 3c ovarian cancer

Hi there firstly I'd like to think my story so far will bring hope faith and a positive outlook to anyone who has a similar diagnosis. 

November 2020 I went to hospital with what I thought was appendicitis, turned out to be stage 3c Ovarian Cancer I was told I had weeks to a few months to live and there was nothing they could do. Long story short I changed their minds and went to see my surgeon who explained the risks and my 2 options. Given the high death rate of the surgery I was going to have and given most opted for 3 rounds of chemotherapy prior I decided to go straight for the surgery, I felt I would be at my strongest and would be in with a better chance.  Surgery was one of the biggest they had done 25 hours, lots removed, full hysterectomy, bowl, appendix, partial bladder, stomach, liver and stripping  of my diaphragm along with a few other bits and bobs.  2 months in hospital due to a few set backs, once home this is where I began to heal, given my wound had to be opened up due to infection I had been fitted with a vaxpack then as this healed a picco machine.   On to chemo well what can I say about that other than this is what made me ill and I could understand why most did not survive the type of surgery I had never have I felt so weak and frail, on top of this I had 2 covid jabs. After chemo I began to get my strength back started walking slowly but always on the up.   Next the maintenance therapy Niraparib  now once again I struggled I found the side effects of these worse than chemo so my dose was lowered from 300 to 100 which I am fine with, my CA125 remain at 11 and for the last 4 months I've felt great, taken up flying and started to live my life again. I swim go for walks eat well and laugh loads I even took up singing to help heal my lungs (it worked). 1 year ago I was told I had no chance but here I am doing well feeling good and feel sure I will be OK.  The other thing too that concerned me was covid and given I had my jabs during chemo unsure if I was protected, I decided to join a trial and I now do regular antibody tests and so far I have good antibodies not yet had my booster as need to research more given the blood clots side effects. So my advice to anyone have a few extra pounds on your bones prior to treatment they will give your body something to feast off whilst you are ill, eat healthy and eat what you you need to repair, do things that give you joy and tell yourself you can do this.