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MS AND Lupus?

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    MS AND Lupus?

    I am restarting this thread here. Think I put it in wrong area first time.:

    I may have posted this before, but am now reading symptoms of Lupus with new "eyes". BEFORE now, I wanted to disregard any symptoms, but my s/o is insisting I review them and talk to my PCP to get her to refer me to a Rheumatologist. The more I read up, the more I see symptoms that I really DO have.

    One of the things mentioned is that Sjogrens is linked to Lupus. I have dry eyes/mouth, limited ear wax & very little oil production on my hands as evident by my inability to pick up most ANYTHING with out first moistening my fingers on a towel (can't lick them b/c of limited sputum/spittle production).

    Damage to organs is serious & I already know that I am experiencing heart rhythm problems. Kidneys damaged can cause frothy urine (which I do not have, but am sharing in case anyone else has this).

    Lupus can, eventually (and does) cause organ shut-down. Another thing I wanted to share with everyone.

    If anyone can share links here, I would be grateful. Here is one:
    http://www.smartlivingnetwork.com/im...he-connection/
    Live simply. Love generously. Care deeply. Speak kindly.
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