Hi! So pretty much since I was diagnosed with Crohn’s, my doctor has pushed for me to take mercaptopurine (6MP). I have been taking it for a few years and having weekly , monthly, and then more sporadic blood work to monitor the levels. Recently, my liver enzymes came back as elevated so she wants me to stop taking it. I’m starting to have some symptom flare up. And Now I am only getting Entyvio infusions every 8 weeks. Has anyone else experienced something similar? I’m just feeling like no matter what I do nothing changes. Even when I was on 6MP, budesonide(Entocort), and Entyvio, my crohn’s still stayed the same.
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