That was actually the first immunomodulator I tried and it went very well for me (I was about 14 years old when I first started it)! It led me to the closest form of remission that I have ever been in. Unfortunately, due to some bad circumstances I wasn’t able to take it for over a year (might’ve been two now that I think about it) and I’m sure you’re aware but for those who don’t know, generally after being off any immunomodulator for a certain amount of time, you’re not allowed to take it anymore due to the chances of building up antibodies that make it ineffective (and can lead to severe allergic reactions, including anaphylaxis).
Since then I’ve been on pretty much most of the other ones, I’m on Stelara now and while I’ve been told it’s preventing more damage from occurring, it can’t reverse the damage that has already been done (from things like scar tissue) - even after numerous resections it’s still pretty bad for me.
However, I have noticed that when my depression isn’t so active, then my symptoms aren’t as bad - it’s not a miracle cure by any means and still doesn’t bring me to that previous point of remission, it’s still enough for me to find it worth pursuing.
Of course, multiple doctors have concluded that my on-and-off depression is due to having a chronic illness, and my current psychiatrist is attempting to treat it as if I had BPD (something about the way it works chemically in my brain is probably similar to that of someone with BPD). Hopefully that gets me out of the vicious cycle of my Crohn’s triggering my depression, which triggers my Crohn’s in a catch-22 style loop.
I do find that I certainly have some bad foods (I really miss popcorn) but there are things that affect others supposedly that don’t affect me, such as soda and other carbonated drinks (oddly enough I’ve heard for some Crohn’s patients carbonated drinks can actually help them, so maybe I’m one of those?) - until I reach remission I just continue to try to push on trying as much as I can, since numerous GIs over the years just have zero clue on how to further help me sadly.
(They did make things significantly worse for me by having me on Prednisone for multiple years at a time, but that’s another long story)