I was diagnosed with RA in the summer and I'm now on Methotrexate and Plaquenil and managed to wean myself off prednisone. In the beginning the mtx and plaq seemed to help and I wasn't "in agony" by any means like the living hell I went through the last time I tried to wean off prednisone which ironically had a silver lining in that it caused me to actually get diagnosed because I couldn't move. So the mtx and plaq meant I was geting just a few twinges. But now the twinges are in more places (I handle with ibuprophen) and the FATIGUE is KILLING ME! I don't know how you're supposed to exercise when it takes everything to crawl mournfully out of bed every day to face the dishes that weren't done yesterday... Anyway, that's not my question, just my rant.
My question is, if and when I go into some sort of remission, can I stop all these freakin' medications? Is that what normally happens? Tell me it is so!
Okay, my second question is do these "increasing of pain twinges" in new joints mean that I will have to "up" the medications now? Is that what normally happens? Tell me it isn't so.
I haven't a clue and I'm too tired to try and figure it out anymore from websites... I see the rheumy next week so I need to ask intelligent questions. None of which I can think of right now other than... pain and pills...
Miserable Hen
Forgot another question...
I had anemia when I was diagnosed but no one gave me any iron or anything. Is the mtx and plaq supposed to handle that? And how do you know if you're anemic tired as opposed to ra tired?
Hello Hen....I am sorry to read you are so fatigued...something that has not happened to me in my journey with RA. So far. You ask in your 2nd post here about RA fatigue and anaemia fatigue. Blood tests will tell you the difference. I am assuming your Doctor has done them but feels you dont need supplementary iron?
When I was on Pred, it was wonderful, absolutely no pain at all. Coming off it, I got ' twinges' also and I was expecting them as the Pred pretty much masked everything. Now, nearly 12 months after coming off Pred, Im doing pretty well and my Rheumy considers I am in remission. I still have some small issues like numb fingers, sore shoulders/wrists on occasion but nothing I cant live with. BUT....I continue with the meds and most likely always will. So far I have not needed MTX or any biologic so Sulfasalazine and Plaquenil did it for me, with the Pred giving me some space from that Godawful pain for a while.