Guest guest Posted June 16, 2004 Report Share Posted June 16, 2004 Hi Beth - Welcome to the group from another Beth. I was diagnosed about 5 1/2 years ago, and spent 2 years on Enbrel before switching to Remicade. I made the switch because Enbrel stopped working for me, and didn't have huge success with Remicade. It didn't start working for me until after the 3rd infusion, and then quit working by the 7th or 8th one. On the other hand - I had no side effects at all from Remicade, and actually enjoyed the experience since there were always several of us getting infused at the same time. I always brought things to read and spent most of the time talking with the other patients. I hope it works for you - best of luck! Beth > hello all! > > I've been lurking for a few weeks now.... I'm Beth and I've had RA > for 15 years. I've been on Enbrel for the past 4 years, and now, > this week, I will be starting Remicade. I've been struggling w/ a > very bad case of scleritis and living on major doses of prednisone... > and my opthamalogist says that remicade seems to have a pretty good > track record in dealing w/ the eye problems. So, I'm going to give > it a try. > > My questions are: What side effects have you experienced? How long > does it take to " kick in " ? > > Thanks for your help and shared wisdom! > > Now, back to lurking > > Beth Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 18, 2004 Report Share Posted June 18, 2004 Hi Pat, After failing Enbrel and Remicade, I'm currently on Kineret. We decided to try it since it works against a different thing (IL-1) then Enbrel, Remicade and Humira (which work against TNF). I also changed from Methotrexate to 10 mg Arava a couple of months ago to see if that helps. I'm also on 10 mg of Prenisone daily, which I desperately want to lower or drop, but haven't been able to (I was down to 6 mg earlier in the year but had to up it again). My rheumy has mentioned that I'm running out of options, which is a real concern. One thing that has started to help is that I cut back my work hours about 3 weeks ago. I had been working around 10+ hours / day for the past 5 months (just your normal corporate full time schedule) and I had my doc put me on reduced hours at 6 per day. I do feel more rested and relaxed, and my life feels better in balance. I haven't been able to cut back on the drugs yet, but hopefully that will come. I enjoy my job, and carry the family benefits so it's important that I work, but I really hope I can stay at 6 hours for good - it really is nice! How is Remicade working for you? Have you tried anything else? Beth > > hello all! > > > > I've been lurking for a few weeks now.... I'm Beth and I've had RA > > for 15 years. I've been on Enbrel for the past 4 years, and now, > > this week, I will be starting Remicade. I've been struggling w/ a > > very bad case of scleritis and living on major doses of > prednisone... > > and my opthamalogist says that remicade seems to have a pretty > good > > track record in dealing w/ the eye problems. So, I'm going to > give > > it a try. > > > > My questions are: What side effects have you experienced? How > long > > does it take to " kick in " ? > > > > Thanks for your help and shared wisdom! > > > > Now, back to lurking > > > > Beth > > > Quote Link to comment Share on other sites More sharing options...
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