- Joined
- Feb 18, 2020
- Messages
- 64
After 11 months on humira, I was told today by my GI that my UC is finally in clinical remission!! My fecal calprotectin is currently 30. He'll be doing a follow up colonoscopy in a year to verify if I'm in endoscopic remission but if things continue to improve, he's confident my scopes will look good.
I am posting this to give others hope and not give up so soon. Since starting, I went through multiple changes in my dose and medication combinations. The combo that finally worked was the following: weekly humira, 50mg/day of azathioprine (imuran), 4 Apriso pills/day and mesalamine suppositories (one in the morning & another at night). I'll be coming off the suppositories in 3 months since my GI things I won't be needing them anymore.
I currently don't have any UC symptoms or side effects to any of my meds. In fact, most days I forget I have UC...I only remember when it's time to take my meds. I am also pretty much back to eating and drinking anything I want in moderation; I continue to keep a food journal to track new foods I try every week. So for those of you feeling hopeless and frustrated, continue to work with your team of doctors. You have options and never lose faith that something will work.
I've only been diagnosed for @14 months and it has been a long road to where I am right now but I'm so happy to finally have my life back.![🙂 🙂](https://cdn.jsdelivr.net/joypixels/assets/8.0/png/unicode/64/1f642.png)
I am posting this to give others hope and not give up so soon. Since starting, I went through multiple changes in my dose and medication combinations. The combo that finally worked was the following: weekly humira, 50mg/day of azathioprine (imuran), 4 Apriso pills/day and mesalamine suppositories (one in the morning & another at night). I'll be coming off the suppositories in 3 months since my GI things I won't be needing them anymore.
I currently don't have any UC symptoms or side effects to any of my meds. In fact, most days I forget I have UC...I only remember when it's time to take my meds. I am also pretty much back to eating and drinking anything I want in moderation; I continue to keep a food journal to track new foods I try every week. So for those of you feeling hopeless and frustrated, continue to work with your team of doctors. You have options and never lose faith that something will work.
I've only been diagnosed for @14 months and it has been a long road to where I am right now but I'm so happy to finally have my life back.
![🙂 🙂](https://cdn.jsdelivr.net/joypixels/assets/8.0/png/unicode/64/1f642.png)