Urinary Urgency with Endo: Anyone Else?

Don’t know if it’s because of my endo or because I’m super prone to kidney stones, but every time I get a UTI, it doesn’t burn so I don’t know I have it until I get majorly sick and it spreads to my kidneys and I wind up in the ER.

I feel like I have a UTI more often than not sometimes. It’s definitely possible that it’s related to the potential endometriosis. Also, I had a laparoscopy done to confirm the presence of endometriosis in January 2020, and let me tell you—the recovery isn’t very fun, but if they DO find endometriosis, they will remove whatever they can and you WILL feel relief. I had chronic pain and nausea horribly, as mine was growing around my pelvic and abdominal cavity (dude, my intestines were quite literally looking like a rollercoaster because of the amount of tissue that was wrapped around it), and it doesn’t cure you…but it makes it much much less severe. Hope this helps, good luck with the surgery!!!