17 years of pain, help me find treatment

My name is Emma. In 2009, my life changed forever after treatment I received in the UK following my first pregnancy. I was told I needed an ERPC after a scan showed no heartbeat.

After the procedure, I stopped having periods and was later referred back for surgery. As I was coming round, I was told nothing more could be done and that my only options for having a child were surrogacy or adoption. I was 29. My womb had been severely scarred.

Over time, my health has continued to deteriorate. I now live with severe chronic pelvic pain, bowel-related pain, and symptoms consistent with internal scarring and pelvic tethering. I have since been diagnosed with Endometriosis, Adenomyosis, and Asherman's syndrome, and have been told I cannot have children naturally.

The pain is debilitating. At times, I cannot stand, sit, or even go to the toilet without severe pain. It affects every part of my life.

Despite multiple scans, the full extent of the damage remains unclear. I now need specialist investigation and treatment, potentially overseas, to find answers and relief.

I am seeking support to access the care I urgently need. Any help or sharing means more than I can express.