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If I were you I'd get a 2nd opinion, or push for more tests. You don't have to " LOOK " like an RA patient to have it. Or you can " LOOK " healthy and still have it. I just got a finial diagnosis of RA friday, and I have no outward signs of it except my left elbow is a little bigger. I'm a 49 yr old male, look about 35, and I " look " perfectly healthy. You couldn't tell by looking at me that I had anything at all. But... I was in severe pain 24/7. ( read my Thread here - titled " Pain..." ) Get more tests Funnygirl. My rumey even tested me for hepatitis in all the blood work he did. He said sometimes it would mimic RA, but I came back neg on that and positive for RA. And I have it in most of my joints. But you couldn't tell just by " looking " at me. Now he's got me on 4 med's and in just 2 days of it I feel almost 100% or maybe 90%, LOL Any thing is better than the pain I was going through. Anyway... My advise to you is - Tests ! Insist on more tests ! Good luck to you... and let us know how things go.
Sudden decrease or loss of hearing has been rarely reported in people taking PDE5 inhibitors, including VIAGRA. It is not possible to determine whether these events are related directly to the PDE5 inhibitors or to other factors. If you experience sudden decrease or loss of hearing, stop taking VIAGRA and contact a doctor right away.
Further, lupus is spectrum with varying degrees. In classic systemic lupus (SLE), ANA is positive maybe 95% to 97% of the time (I've seen various figures). But in the intermediate subacute cutaneous "subset" (SCLE), that figure goes down to maybe 70%. In the mildest group, "discoid lupus" (DLE), that percent is even lower.
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