Luckily my GI doctor is a part of my ER system - When I go, I'm strictly under her care.
I just saw her PA today - Looks like we're going to try some steroidal enemas to see if that stops the bleeding. We'll try them until the end of the week, if anything, she'll start me back up on tacrolimus (pill biologic) until I can lean on the Entyvio a little bit more.
In the meantime, they're checking my levels to see how my liver enzymes are doing (Remicade TRASHED my liver), and to make sure I'm not going anemic (again).
Since I've been off of tacrolimus for a little over a month now, she's thinking that if the Entyvio wasn't doing some part of it's job, that my UC would've come back full force, and quickly, that it'd be more than just a little blood and some slight aching.
So. Here's hoping I'm not within the 30% of people that Entyvio doesn't do jack for.