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I was on 2 different doses of prednisone for the rash that I have, & finally, 2 weeks ago, I convinced my ANP that I needed to be tested for lupus. And, now I'm on 200 mg of Plaquenil. So far, the rash isn't going away, but it's not spreading either, plus she gave me a cream that helps with the itching. But, for over a year now, I've complained about having sweaty episodes, that literally leave me drenched with sweat, plus very fatigued. So, I am figuring out that I have basically been ignored for the most part. Since I have no insurance, I use a clinic that is tax payer funded, & they only take uninsured people. So they don't have a lot of doctors available that are experienced in some areas. But, after the lupus blood test, she showed my chart & the results to the doctor that is over the clinic, & he immediately told her to start me on the plaquenil. But, she was hesitant about it because she said it's a dangerous med. I told her I'd rather take my chances & see IF it helped me, or not. And, the pamphlet I got from the pharmacy with the side effects, lists a lot of the effects that come with lupus already. I do have to go back in 6 weeks to get my blood tested again, (the CBCs though, not for the lupus.) It just really ticks me off that I've been fighting with this for over a year, & the only reason they checked me for lupus was because I asked about it. That was what I was hoping they were going to reform in the health care system, but so far, no changes in that area! But, I refuse to give up, & ramble all you want! I can understand, & sympathize with you totally.View Thread


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