Guest guest Posted July 18, 2008 Report Share Posted July 18, 2008 I have been diagnosed with Primary Sjogren's for almost 14 years. My rheumatologist still believes that I have Sjogren's but because of the appearance and pattern of my joint pain, he put the primary diagnosis as Inflammatory polyarthritis, not specified and ordered even more tests. I know that my RF has been negative for more than 14 years, and even my sed rate is never elevated (although I have been on DMARDS for 11 years too). I was started on MTX last month and he was seeing me this month to check on the medication change. I was saying that I think it is helping me and then he noticed my hands and didn't like the way they looked. He said my joints look swollen and when he checked them, many of them did hurt. Of course, they have been hurting on and off for over 14 years, along with having stiffness, and very occasional redness and heat. So now I am asking what are all the different forms of inflammatory polyarthritis and how much difference does it make if I was incorrectly diagnosed all these years? I have been on plaquenil for over 11 years and been on cortisone in one way or another on and off (mostly on these last 4 years in low doses). I am now on MTX at 10 mg. once a week. TIA in Space Coast Quote Link to comment Share on other sites More sharing options...
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