Hello, I hope you are all well! I have posted a few times about being frustrated lately with difficulty getting assistance from my doctor with my current pain. I finally decided to go to the nearest university hospital with a dedicated IBD center for only Crohn's and UC patients. I am optimistic about their ideas and am likely going to transfer my care. This doctor is a little over an hour away. I am only concerned about where I will get my infusions now if I leave my current doctor, who does them in the office. Does anyone have advice for arranging infusions elsewhere when your doctor is far away, or how does one go about home infusions? Do many insurances cover that? Thank you so much for your insights!