Endo + Chronic Illness?

It is probably the dumbest understatement ever to say having endometriosis has been a JOURNEY, but it really has. From the moment I suspected I had it (probably about a decade ago now), to the moment I was surgically diagnosed with it, to writing about it excruciatingly publicly, to my second surgery to treat it, to now, I've learned so much. After writing my series about it in 2016, I learned that I'm part of an incredible community of strong, resilient women -- a community that has largely gone unseen and unheard by the general public and doctors alike. So with this page I plan continue writing not just about the medical experience of having endo but about the day to day experience of what it's like to have your reproductive system hold your life hostage in tandem with other chronic illnesses.