Catherine Vanacore s an aspiring healthcare technology executive based in Kansas City. She holds an MBA from Northwestern University's Kellogg School of Management and hopes to use her professional background and personal experience to improve care for endometriosis and other chronic diseases.
It is no secret that there is a significant need to increase the amount of research done on endometriosis. As patients you can help research efforts by participating in clinical trials. If you’ve never participated in a clinical trial…
One of the most empowering things a person with endometriosis can do to take charge of their health is learning how to find and interpret new research findings. It takes an estimated average of 17 years for new research findings to be implemented…
One of the hardest things I have dealt with in my endometriosis journey is the struggle to speak up for myself during doctor’s appointments. Over the years, I let doctors dismiss my severe symptoms and convince me that I had a normal…
I’m 29 years old and finally just got my definitive diagnosis of endometriosis—and during a pandemic, no less. My journey from the onset of symptoms to diagnosis has been similar to that of many other women: it took 15 years. My…