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Rheumatoid Arthritis
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Beth,
I, too, recently tested strongly positive on the anti-ccp test. I then went to see a Rheumatologist with my test results. She said that with my symptoms (which sound very close to what you are experiencing) and test result, she wanted to treat my RA quite aggressively and started me on methotrexate immediately. Each one of us is so different, but it sounds like you are already have RA (only my opinion- I am no doctor, just in a similar situation). The test would likely be a predictor if you were asymptomatic (again, only my opinion). Now with your syptoms plus test results, wouldn't that mean you have active RA? I advise you to see a board certified Rheumatologist. Mine really helped me understand where I stand, and where to go. By the way, I was told my syptoms + strong positive anti-ccp means I have Rheumatoid Arthritis. I have been doing lots of research and it also is helping me. One thing I have read is that the higher the number on the anti-ccp test, the more likely for aggressive disease. Again, a good Rheumatologist would be the ideal way to find the answers you are looking for. I will say a prayer for you. Hang in there! Best Regards
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| Posts: 2 | Location: Minnesota | Registered: 04-14-2008 |    |
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Yes, i did read somewhere that a positive Anti CCP Antibodies test means you have RA. I have a follow up appointment with the Rheumatologist on Wednesday, the 16th of this month (in a few days). While I am there I am going to get a copy of all my blood work for me to review. I want to see exactly how positive my Anti CCP Antibodies test was. For the last 4 weeks my wrists have only really swelled up twice, once when bowling (right hand) and once when playing cards( again, right hand). In fact, my wrists for the most part do not bother me at the moment. However, I seem to have developed something else. My hands at times, have a tingling sensation, a burning sensation, and turn red, and sometimes sore when i make a fist. I am not sure if i would call them "stiff" About 5 days ago i noticed the tingling and burning sensation on the soles of my feet to a lesser degree. My hands have never stopped feeling wierd since March 3rd. I have found that my hands feel better when I ice them. which i did some internet search and came up with erythromelalgia, and the symptoms were similar. However, my symptoms could match many things! So, is the medication doing you some good? I hate to go on medications....but i have heard that early aggresive treatment is better if you are in the early stages of RA. Please tell me if you are getting some relief. Thank you. sorry for the long post!
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| Posts: 3 | Location: Southern California | Registered: 03-18-2008 |    |
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Beth,
I have just join this board and I have a strong positive for Anti-ccp which was 162 and normal I think is below 20. You sound like you have symptoms of RA. My Rheumatologist started me on Humira which helps but the methotrexate makes me sick to my stomach. I do have/had tingling and burning sensation in my hands and feet but I don't know what it is. The tingling is better in my hands but I still get the burning. Mine doesn't not turn red or swell. I have never had any swelling at all. Remember that everyone is different and hang in there. Get a Rheumatologist that is aggressive with your treatment.
Renee
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