Based on my blood tests it indicated I have Sjogrens but my doctor wants me to have the biopsy to be completely sure. My issue is I do not have that much of a problem with dry eyes or mouth. I have it occasionally but I am wondering for those of you with a definite diagnosis how you are with dry eyes and mouth? is it not much of a problem or is it very noticeable? I have the other symptoms of Sjogrens but that also goes along with Fibromyalgia and my possible lupus diagnosis... any thoughts? Do your eyes/mouth always have to be dry to have Sjogrens?
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