Has anyone with UC tried Xeljanz? Been in the trials?...
It should be noted that you may get worse on Entyvio while it begins to work, increasing your chances of worsening the flare to the point where you can't get out. Remicade works very quickly, so...
I am curious about this as well. I've been on Entyvio since early August, but I haven't made a whole of progress (or any at all), so I'm wondering what my next options are. I did well for ~2 years on...
I know Aspirin, Excedrin, etc. can be troublesome, but I'm curious as to what your experiences have been with Tylenol? It seems to give me a lot of trouble....
I've been getting Entyvio since 8/11, and I think things are getting better, albeit very slowly. That being said, I've had a lot more pain and soreness than I've ever had. I can barely even move my...
I've been on Entyvio since August, and the only effects I've noticed are headaches and fatigue. On the days that I don't exercise, even if I get eight hours of sleep, I'm still exhausted....
Have you talked to your doctor about upping the frequency of your dosing to every four weeks? I'v read a few different things that say this can make a difference....
I just wanted to check in to see where everyone's at? I don't know if I've hit my baseline, but I've pretty much flat-lined as far as improvements go. I'm hopeful, though, because I know this drug...
I am at week 8, and things are really looking up. I can tell there are some very positive changes happening, so I'm hoping that continues. It really didn't seem like anything at all is happening in...
I moved on to Entyvio because Remicade really didn't get me into full remission. We wanted to see if Entyvio would accomplish that rather than upping the Remicade dosage, which is something I'd...
Like you, I received Remicade during a bad flare. Like you, it immediately turned my symptoms around. I wouldn't worry too much about your symptoms right now. See what it's like after you get your...
Things seem to be moving in the right direction VERY slowly. Each week is a little different than the last. I'm going to see where I'm at over the next few weeks....
Thanks for your thoughts....
Longtime lurker, first-time poster. I've had UC since May of 2011. I was on Remicade until this past summer, switching over to Entyvio on August 15th. I just finished my third infusion last week, but...