Hi everyone.
I'm currently 29 and have been through severe period pain since I started my periods at 12 and ended up going on the pill and having severe pain, heavy bleeding and becoming anaemic. I still had pill breaks but the bleeding did get a bit lighter but the pain was still bad and progressively got worse.
I had tried to query this with doctors over the curse of several years but it amounted to nothing and 5 years ago I was told to take the pill continously which did help for the time I did this.
I then came off the pill to try for a family in early 2022... the stress that came with that and having normal periods again was terrifying. My periods were much worse, I had breast cysts pain for 2 weeks prior and severe pain going to the toilet etc. and I knew something was wrong for sure.
January 2023 investigations started but took so much time in which things forgot worse until I eventually went back on the pill in August. after no luck trying just to have a break. In September 2023 I was finally diagnosed with endo through our ivf clinic... but in October 2023 I ended up in hospital through a and e after having a pill break due to bleeding intermittently. Inflammation so high I was told initially it had to be pelvic inflammatory disease and sepsis or ectopic pregnancy and I was straight in for surgery.
This is where they found end stage endo, frozen pelvis, both tubes blocked and squashed, extension out into bladder ans bowel with all gaps covered in adhesions... here I was told I will never conceive naturally and IVF is our only hope. I was also diagnosed with adenomyosis in my womb.
We're starting IVF in Jan after almost 2 years of waiting and reviews and following this I know I need specialist surgery due to the frozen pelvis.
I know this is a but of a waffle but I've never shared my story and feel like people here will be able to relate with some part of it. Just taking things day by day for now and looking forward to the day I can get back in the gym for some exercise