Guest guest Posted November 21, 2008 Report Share Posted November 21, 2008 Hi everyone, I was diagnosed with PA in the last week after 6 weeks of Prednisolone and Mobic. While they gave mild relief, the rheumy says it is time for Methotrexate (3 pills per week). He said it might take 3-4 weeks to kick in. Just wondering what good experiences you guys have had. How long did it take to kick in and how good did you feel afterward? At present my feet and wrists/hands are very weak and sore. Cheers all, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 22, 2008 Report Share Posted November 22, 2008 Hi Methotrexate actually put me on my feet literally. It took about four weeks the doctor Told me that six weeks is usually when it kicks in. Like you I started out at 3 pills. I am Now up to six and doing well. Hope this helps. Jolene Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 23, 2008 Report Share Posted November 23, 2008 It helped slowly for me. Probably kicked in some within the first month but took 3 months for the full effect to be felt. If you are still taking the pred it might not seem so slow for you. If you stop the pred you are going to feel worse before you feel better. If you don't feel a lot better within 10-12 weeks, ask the rheumy about one of the newer meds. regards, sherry z > > Hi everyone, > I was diagnosed with PA in the last week after 6 weeks of Prednisolone > and Mobic. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 24, 2008 Report Share Posted November 24, 2008 Hi , I have been on MTX for years. It has helped me tremendously. I take ten pills per week. In addition, I am on Humira, having been on Enbrel since 2000, I switched about 2 mo ago, and I Love it. I am also on prednisone - 5 mg/day down from 10 mg. I've been on prednisone for 20 years, and so happy to be getting lower. Don't know if I will ever be able to ditch it entirely. You should know that I was diagnosed in 1973, have been on nearly everything. My choice to use steroids wasn't made lightly, but I couldn't move. It has given me a long period of reasonable comfort. Not without side effects, which I made a conscious choice to deal with. My case was a particularly rampant one. I hope the MTX works for you. Give it a try - do your lab work - years ago, my liver numbers were too high and so I got off the MTX. The pain was so horrible, my doc allowed me back on it, and I have been ok since. Give it a try, and we shall all stay optimistic for you. Libby in New Mexico Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 24, 2008 Report Share Posted November 24, 2008 Libby: am curious as to why the switch from Enbrel to Humira and what do you think are the advantages of Humira? I'm asking only because I'd only been on Enbrel for about 8 months (started taking it right after I was diagnosed) and it was working beautifully for me but my doctor - out of the blue and for no reason I could discern - asked me if I wanted to switch to Humira. I told her no since Enbrel was working fine and I've heard others say that sometimes a PsA drug will no longer work for you and you have to switch. Joanna Hoelscher Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 25, 2008 Report Share Posted November 25, 2008 Hi Sherry, Yes I am off the prednisone and you are right...I am feeling a bit worse having only been on MTX for one week. Anyway my chin is up and I look forward to feeling better with MTX. Cheers. " ayrton192068 " <vk2vhf@...> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 27, 2008 Report Share Posted November 27, 2008 Looking back on my MTX treatment I would probably say that my previous rheumy didn't increase the dose quickly enough. He kept me on 7.5 mg for a long time, about 6 months, then increased it to 10 mg when I also had a shoulder problem. When I saw the second rheumy he increased it to 15 mg, saying an extra 2.5 mg wouldn't make enough difference. Then I was increased to 20 mg. Then after having NSAID esophagus problems, he's added 10 mg Arava. So I suppose I cant really say how long it takes to work. Its meant to take about 6 weeks I think to take effect, so maybe discuss with your rheumy after 2 months or so. I did mention to my dermy that I would have thought that 20 mg MTX should have helped my skin more, but she said some people don't respond that well. Another thing, while I was taking the MTX I was on NSAIDs too, so that sort of masks the pain and inflammation (rather than preventing joint damage). So in a way, I think you cant really tell how well MTX is working until you stop the NSAIDs like I had to. regards max Quote Link to comment Share on other sites More sharing options...
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