Hi there I’m new to this was just wondering if anyone no what the best treatment would be And have been through it themselves ,I have just received my letter regarding mri results I have adenomyosis throughout my womb and endometriosis in another place Was also just wondering how it would effect me if I was to ever want more children. Thank you very much
Adenomyosis and endo : Hi there I’m new to... - Endometriosis UK
Adenomyosis and endo
Iv just been diagnosed with adenomyosis. Heavier periods but manageable. But 3 years of unidentified pelvic pain! Spinal consultant injected me with steroids thinking was coccyx. A colon rectal consultant sent me for pelvic floor physio. And finally off my own bat I saw a gynaecologist and within ten min he examined me and showed me on a scan, what looked like a mass inside uterus with own blood supply! My uterus was 50% larger on one side. He said he thinks this was have caused most if not all of my pain and discomfort! 3 years of sitting on rubber rings! 3 years of telling them that it’s not my coccyx and it has always felt that it was my womb and something growing / inflamed! No one listened! And I truly mean that! I’m going on mini pill to reduce aestrogen levels for 2 months on the hope this solves pain and avoids removal of womb! I’m still trying to get head around not maybe being able to have second child! I’m 42 so this was my last chance. But my issue is diff to yours on that my pain is not sustainable. I believe if it’s not causing u issues that you can still have kids. So def y’all to your doc about that