I had endometriomas blocking my ureters and had to have stents placed and later removed...

I have/had it on my bladder, but my doctor said having it inside the bladder is rare.

I also have endo on my bladder. It is so painful for me to pee.

I have endometriosis on my bladder.

Yes I had endometriosis of the bladder and endometriosis in my intestines so bad I had to get a double intestinal resection surgery done April 1st. Now it is possibly affecting organs in my upper abdomin. Today, I finally got an abdominal ultrasound done on my liver, spleen, gulbladder, pancreas, and whatever they check for in that area. I've had pain there for over 5 years and they are finally checking into it after my bloodwork is coming back funny. All kinds of rare stuff seems to run in my family though.