Hi everyone. I’m finally home from the hospital. They did another colonoscopy while I was admitted and found that my UC is much more severe now than it was a couple months ago, and now I’m possibly looking at a Crohn’s diagnosis as well but waiting on pathology to confirm. I’ve been on Prednisone, Mesalamine, and Entyvio since I was last hospitalized. They officially declared that I failed mesalamine and Entyvio and I got my first Remicade infusion on Monday. I haven’t had time to research Remicade like I want to, so I was hoping y’all might have some advice/tips/info about Remicade and things I can expect (side effects, etc.). Thanks in advance.😊