Entyvio

Hello everyone. I'm new to the forum but have read the threads with interest and gratitude.

I was diagnosed with UC three years ago. I'm not taking anything for it just now with the exception of various natural remedies. Because I fear that these remedies aren't helping enough, I am considering starting Entyvio
(mesalamine wrecks my liver, and I'm not a candidate for immunosupressants like Humira). I see that many of you have taken it, but so far as I can tell (on the threads I've read), no one has reported on the long-term use/effects of using the drug.

Can anyone tell me about their experience using this drug long-term? I'm interested to know how it's working and what the side-effects have been.

Thank you,

Ward

Thanks for the reply, Chickenwings. Much appreciated. I will ask my doc about the study you cited and see what he knows. Best, W.