Does anyone here experience having a small endometrial cyst (around 1.2 cm now, from originally 4 cm), with adenomyosis and PCOS, but still experience severe pain?
I recently had my TVS, and my doctor said she couldn’t connect the severity of my pain to the result of my ultrasound. She said it doesn’t make sense that despite not having my period anymore and already taking Dienogest for 3 months, I’m still experiencing intense pain.
I honestly feel frustrated because my ultrasound results don’t seem to match what I physically feel every day. What my doctor said also felt a bit invalidating—to the point that I started questioning myself and wondering if maybe I’m just being dramatic or if it’s all just in my head.
I’m so tired of constantly having to explain and justify my pain to people.
Has anyone else experienced something similar? Please help me feel less alone in this.