Hi ladies,
November last year I had a very successful third lap for endo removal (and cyst removal from left ovary). Afterwards I was given 2.5mg of Northisterone and had had the coil in for a year along with a diagnosis of Adenomyosis. The coil and Northisterone worked wonders and for a good 5 months I was almost pain free other than the odd flare up.
Back in June for various reasons the coil was removed and I was put on the mini pill which did nothing, I've now moved to Cerazette (on this for a month so far). For the past few months my symptoms have returned gradually which I put down to Adeno no longer being controlled by the coil/N'rone. These past two weeks however I've started to wonder whether the endo has returned. Up until today I've felt I've known that it hasn't, I've felt confident in my surgeon and told anyone and everyone that I'm endo free. Today though I feel a pang in my heart that its the endo causing me grief. The pain is different to the adeno, its higher and more aggressive.
I know you cant tell me whether I'm right or not but its been so long since I've had this type of pain that I'm wondering whether its endo or just the cerazette flaring the tissues? I used to be an expert in my pain, I'd had endo for 8years before diagnosis and had it removed twice before but after my third I was so confident I was rid of it for a good few years. Everything was so good after surgery, my life restarted and I embarked on a great journey, now I refuse to be another statistic of it returning but ...
Truth be told I'm not sure why I have written this. I know I can be given no answers but does anyone have any words of wisdom or experiences they wish to share?
thank you for listening