Help Aveeve raise money

Endometriosis has affected my life in so many painful ways. I was first diagnosed after a ruptured cyst sent me to the emergency room in my early 30s. Little did I know that this disease had quietly been wreaking havoc in my body for decades. It takes on average 7 years after symptoms start to get an Endo diagnosis, so the delay in diagnosis isn't surprising. I had already been diagnosed with IBS, then with infertility and diminished ovarian reserve. Endo had destroyed my ovaries and I struggled to build a family after multiple rounds of IVF. I developed chronic abdominal pain and constant fatigue that left me barely functioning. I remember struggling to get up to play with my young daughter and wondering if this was going to be the rest of my life. After extensive surgery and ongoing medication I am one of the lucky ones that can manage my chronic symptoms. I'm running for change. I'm running for awareness. I'm running for a cure.