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Type: Posts; User: ljames

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    I am sorry to hear your troubles. To me you,...

    I am sorry to hear your troubles. To me you, Tgal, seem to be very knowledgeable and very forthcoming. Can you answer for me? Why does the medical community shy away from diagnosing lupus? ...
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    My doctors said that the elevated sed rate is...

    My doctors said that the elevated sed rate is indicative of inflammation or infection. My response was something like - isn't that what the joint pain is? Inflammation in the joints?

    I don't...
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    My ANA tested positive for the first time this...

    My ANA tested positive for the first time this August. Based on my symptons, my GP thinks I have lupus. The first rheumy said "it could be lupus, it could be fibromyalgia, it could be malignant. ...
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    Vitamin D deficiency

    I went to a new rheumy last week and she said that my joint pain is not lupus but a severe vitamin D deficiency. Has anyone else heard of this?
  5. Thread: Thank you all!

    by ljames
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    Thank you all!

    I am new to lupus and new to this site. I have found all of your messages and threads to be very helpful. I am not crazy. My issues are real. My pain is real. My fog is real.

    Actually, I...
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