ANA and ds-DNA results & symptoms
Answered by
Kevin Pho, MD
Boston - MA
This forum is for questions and support regarding arthritis issues such as:
Arthritis, Autoimmune Disease, Bursitis,
Fibromyalgia, Gout, Juvenile Rheumatoid Arthritis,
Lupus, Myositis, Neuralgia, Osteoarthritis, Polymyalgia Rheumatica, Rheumatoid Arthritis, Sciatica, Tendinitis, Vasculitis.
Do you think it would be useful to repeat the ANA test? Also, what should I be looking for in a urine test? Thanks,
ANA levels fluctuate, so if you are having diffuse joint pain and any other symptoms, I would follow up and have your ANA repeated as well as the other autoantibodies that are tested for the various connective tissue diseases. The best person to do this would be a rhematologist if you haven't already gone to one. So don't freak out thinking you have lupus just because your ANA was 1:80 (not saying you can't have it, just that that titer doesn't mean you do, especially with the negative double-stranded DNA). I made the same mistake 13 years ago when I first got sick. I read somewhere a positive ANA was linked to lupus and immediately thought I had lupus. It's not that black and white/clear-cut. Usually much higher titers are seen with lupus 1:640, etc., but of course they can fluctuate up and down. My ANA has fluctuated between 1:40-1:160.
At some point, we all face a health issue. Having someone share their health experiences, fears, afflictions and triumphs can provide you with insight, confidence or hope to tackle yours. If you are interested in having your story told in a more open and interactive forum, I'd love to hear from you.
At 21 I began to pain all over my body, not knowing what it was I tried my best to continue with my daily activities. Friends and family would always ask me how was I feeling and the only way I could describe it was I'm 21 stuck in and 90year old body. I would laugh they would laugh and on with my day I would go. As the days past I was takin more days off work, trying to relax by the pool get my energy up, not knowing that the sun was only making matters worse. All that sun bathing caused the buterfly looking rash on my face, which I shrugged off as a real bad sun burn. One day I decided I had to get some help so off I went to th Hospital, only to wait 15 hours and be sent home. Few more days past, now for some strange reason I was menstrating dangerously heavy, along with all my other symptoms off again to the same hospital, this time waited 11 hours the gave me a pill sent to for some blood work and off home I went still with no answers to why I was feeling like sh**. Again some days past and still getting worse, now I was barely able to dress myself, it was a struggle to get out of bed to walk to pretty much do anything. This time my mom insisted I go to the hospital and this time we went to another one. As soon as I walked in to triage, the nurse told me that it looks like I have lupus.
So long story short that what it was. My symptoms consisted of fatigue, joint pain, rash, loss of appetite( a few other I can't remember) and shortly after a positive ANA.
Anyhow today I have a few more added symptoms, and you know what I'm still living. I have my days, but its not so bad really, I think of all those other ppl out there in more serious situations with life threatening diseases. Well my dear not sure if my story helped. If you do have lupus, don't worry it will be ok. Hang in there and your in my prayers
God Bless