I'm on some of the other forums, Polymyalgia, osteoporosis,...
My Rheumy put me on both Plaquinel and Sulfasalazine. I do NOT have RA markers. She think the DMARDS help one reduce the Prednisone. I do not think it helps. I felt somewhat better for a few months, but I think it's more due to other things, meditation, gentle yoga, shift in attitude.
Problem is, I still harbor fear...fear of all the drug side effects.
I want off the drugs. Doctors do not support this, they just push more drugs.
Who knows.......... I think everything requires tapering off a little at a time. I agree, all the drugs are wretched. The sharp, constant, tear producing pains were worse. Long term, I have no idea what will happen. It's a bit like being in a dark and scarey fun house at the amusement park as a child. Of course, the fun house has an exit....... RA is forever. How did this happen to all of us?
She has never said, just says the prednisone could be masking underlining problem. I thinks that's why doctors want us off the drug. But I don't have other symptoms really other than PMR pains. But my mother does have RA bad in her hands. Is it always hereditary?
With havng osteoporosis now I'm really, really working on good diet (including anti inflammatory) and trying to get back to exercise, slowly.
RA is not hereditary as such- it isn't automatically passed on. But having someone in the family with RA is an indicator to help them diagnose.
Pred is the usual treatment for PMR - and usually PMR has a limited time frame from what I ve read. It s the med that has affected me most with side effects- but needs must to get down the pain and you can taper off eventually ( I just have) long term use of pred can lead to osteoporosis .my rheumy said to have calcium and vit d tablets prescribed by GP.
But don't worry too much about the side effects of sulfasalazine. It s one of the most tolerated DMARDS and so is plaquenil.
Hello Layne Texas I read what you wrote and you are very close to me; oh by the way I live in east Texas in Tyler. What I have been diagnosed with RA, osteoporous, and fibromyalga. I have been prescribed only imixatrae, and folic acid. My doctors did give me a TB test I passed and now I can use humira. My biggest problem I have a lot of pain I am going to talk to my doctors about medicine for it. I do take lyrica, trazodone, zanaflex, tramadol, clonazepam. So I am getting some relief. Like I said I will talk to my RA doctor and see if he thinks the medicine needs to move the MG needs to go up or whatever. Sorry I wrote a months worth of a letter but this is my first time on this forum.
Maybe that s because the methotrexate was working- but stopping it caused a flare . In other words the problem was stopping the mxt not taking it ! I understand the reluctance we all have to take meds- but leaving the RA auto immune condition untreated is far worse( pain, joint destruction, more likely to have heart or lung affected too) I know folk are wary of mxt as it is a ' chemo therapy drug' . But it s used for RA at a tenth of the strength for cancer. Unfortunately it does affect some badly which is why we have regular blood tests to check liver is ok - and why you ll find some posts on here where mxt caused problems or the side effects were too great. Many people on mxt have sustained help from it( ...and no...I don't work for a drug company ! )
i totally agree with you about people s perception of RA- some people call it rheumatoid disease to take the arthritis confusion out of it.