I have sjogrens disease and I wonder if it causes joint damage. I just started immuran and asked why I can't take one of the newer drugs like Humira and was told that since I showed no signs of RA I can't take any of the biologics. I have migratory pain, no joint swelling but I am still on 25mg of prednisone and can't reduce the amout because of severe pain, burning feet, wrists, knees, hands, ankles, and osteoarthritis in my neck. I started on 100mg of immuran and was told it will take 8wks for results and I am in very bad pain. I started on plaquenil in March, switched to methotrexate in June and this 2wks ago. This is going on too long. I have a new RA doc and wish see would have started new tests and been rediagnosed but she didn't and they are hard to come by in my town. I am in alot of pain and am looking for some help. This hunt for answers started Dec 26th 2008. I am wearing down FAST. Someone HELP!!!!!!!!! I might have something else but what????





My "new" doc won't give me Humira since I tested neg. for RA, I don't know what sero. neg. is but will be looking it up now. I do have osteoarthritris in my neck and maybe my back which is adding to my pain greatly. What I don't understand is the 6 vials of bloodwork and she shows me a half-sheet of blood report and mostly it is on vitamin D level. She tells me I have fibromyalgia and sjogrens and has already spent 20 mins. with me and has to move on to her next patient. I am getting vicodin from my GP but he wants to start cutting it back ASAP. I am on 25mg of prednisone and I try to cut back to 20mg for a few days but I am in so much pain I have to raise it back up. In my town, RA docs are booked until Feb. Thanks for the input. I will keep looking for more feedback. Sandi