First Entyvio infusion

I finally got the infusion nurse to call me back and my first infusion is Thursday morning. I'm torn between excited to get this started and the normal hesitation at a new med. Wish me luck!

Good luck, I'm sure it'll go well. I've been on Entyvio a year and a half and am doing great on it. Two fistulas closed since I've been on it! Just be prepared for it to take a long time to start working.

I was scared too - due to allergic reactions to many drugs - but so far so good. And side effects post-infusion for Entyvio have been far less than Remicade for me (until I had to stop).
So try to think positively. I hope the infusions go well. I've been nervous each time & then very relieved after because it went so well. Five so far.

I was on entyvio and the infusions were a piece of cake. It didn't do anything for my inflammation unfortunately, but I also didn't have any side effects.

lamb...have you tried a cholestyramine / Questran for the excessive D? I have totally lost track of who has tried what anymore! I know not everyone can tolerate it, but for me it lets me live a relatively D free life. My husband says its the thing that lets me leave the house. I actually use less than what was originally prescribed...but I use it every day. Maybe you could use it intermittently as needed???

Hoping Good Friday is a good Friday for you!
Take Care