So, I finally got in to see my rhuemy and asked him my lupus question. What he said seemed to contradict a little what was posted here previously. Here's how it went:
"I was wondering if I've ever been tested for Lupus?"
"there's no test for lupus..."
"Oh? I thought there was."
"Well, there's the ANA (I think that is what he said) and yours has been positive."
"It has? So, what does that mean?"
"It could mean anything."
"?"
"Lupus is a clinical diagnosis based on what the doctor can see."
"Okay.....and...?"
Then that was it. He didn't offer any more information on the subject.
So, I don't know. He has dissed the previous doctors' dx of PA saying I only have RA - BUT that it doesn't matter because I'd be treated all the same.....based on that "clinical diagnosis" comment re:lupus, he didn't see all the problems I had years ago clearly indicating the psoriatic arthritis. I think it matters in the DX because of the other issues I've been having & certain dr's have been blaming the "obvious" PA symptoms. That is my question w/Lupus....I'd rather not have it, but if I DO, aren't there other precautions that need to be addressed if additional problems I'm having could be caused by it?
Also, he was very mad at me for not starting Enbrel yet. Basically said my reasonings were wrong and I am misguided by my fear of getting sick again (though he understood - ahhh, a little bedside manner!)....but, that he'd make a deal with me. Get blood work drawn in 2 weeks, then again in 5. Currently, my RA factor has been normal and my white blood count low - if my WBC is normal and my RA factor is high, then he wants to put me on a new drug they are testing (infusion - I think we've discussed it here previously) - if I do NOT qualify for the study, then I have to start taking the Enbrel. I agreed.
Thoughts? Am I stressed over nothing?
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