Hi, I’m Casey
Founder, EndoCare Health Co.
I’ve lived with endometriosis for most of my life, and like so many others, it took years of pain, confusion, and misdiagnoses before I got the care I needed. That experience — the long, frustrating road to answers — now drives my work with EndoCare™ and the Endometriosis community.
Together with the EndoCare Health Co. team, we are here to make sure no one walks this journey alone. Whether you’re experiencing symptoms, navigating a diagnosis, or supporting someone who is, we are here to offer guidance, encouragement, and connection.
Our voices together are loud!
My Story
As a teenager, I began experiencing severe pelvic pain and debilitating periods, accompanied by nausea and frequent absences from school. I was often told it was just part of being a woman. Over the years, my symptoms escalated to include GI issues, fatigue, sciatic pain, heart palpitations and even loss of function of my left leg.
After numerous misdiagnoses over more than a decade, I was finally diagnosed with endometriosis in 2013. By that time, the disease had significantly spread, leading to multiple surgeries that removed my uterus, ovaries, and fallopian tubes. While I experience less pain now, endometriosis remains a challenge. It's important to understand that this condition is not just about "bad periods", it's a complex disease that persists even after menopause or surgery.
I share my journey to shed light on this issue and to let anyone facing similar struggles know: you are not alone, your feelings are valid, and you deserve better.
With care,
Casey