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Old 04-03-2014, 12:14 AM #1
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Default CRP and sed rate

So I have been having a flare since all the snow shoveling. I am on 20 mg of prednisone, 2000 cellcept and 660 mestinon a day. MY C reactive protein has always been high and is now back in the normal range but my sed rate is way up to 48. Do any other MGers have high CRP and sed rates or is this my other auto-immune disease (unspecified)?


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Old 04-03-2014, 07:37 AM #2
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Mine have always been in normal range --- and I am seroneg
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Old 04-03-2014, 05:58 PM #3
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I don't know about the crp, but elevated sed rate indicates inflammation somewhere in the body. Don't know that it is a Myasthenic thing or not.
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Old 04-03-2014, 10:43 PM #4
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From what I know with MG your sed rate and CRP should be normal.. if they are elevated it should indicate an inflammatory process of some kind.. neuromuscular wise - like a myopathy.. otherwise - it could be a million other things.. some people just run high normally maybe? Have they tested your adolase?
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Old 04-04-2014, 05:39 PM #5
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Adolase and creatitine kinase are normal. I was in a lot of pain - muscle, joint and tendons. My rapid bowel transit went away for 3 months when they started cellcept but returned with the pain. I also have a vascular rash on my extremities, the rheumy calls livedo reticularis. And a rash on my face constantly - looks like a butterfly to me. They did another bunch of antibody tests including ANA - all negative. But my sed rate sky rocketed, BUN is now slightly high and my urinalysis has moderate wbc, rbc and no bacteria, I am anemic again with very high RDW. I think I might have Lupus too.

They upped the prednisone to 20 mg per day. And the pain and the rapid bowel transit has subsided again. Rash looks the same.

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Old 04-04-2014, 05:41 PM #6
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Does anyone here have MG and Lupus? Do your symptoms and tests look like this?

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Old 04-04-2014, 07:38 PM #7
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Your symptoms do sound like you have lupus as well as MG, but you can't always tell. My daughter had every symptom of lupus that their is. It turned out that each of the symptoms came from a different cause.
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Old 04-05-2014, 02:59 AM #8
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Since both MG and Lupus are both autoimmune, I would imagine it's not uncommon to have them both.. You symptoms sound like there is something rheumatologic going on! Have they run a lupus panel in your bloodwork before? Do your rashes get worse with sun exposure?


I also have livedo riticularis, and a quite elevated ANA.. I also have bowel issues..for three years they thought maybe celiac.. but now that my sibling was diagnosed with crohns and some of my recent testing, they think crohns too... I have rapid transit with the bowels, and malabsorption (bloodwork shows vitamin deficiencies)..

The good news, if you do have something else going on, like lupus, is that MG and Lupus are usually treated in similar fashions... though it's no fun to have one problem, much less more!
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Old 04-05-2014, 06:18 AM #9
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They did a bunch of gastro biopsies and blood test and ruled out gluten, crohns, and celiac. Gastro thinks it definitely autoimmume, waxes and wanes with MG, wanes with prednisones and cellcept. She was thinking lupus, sjorgens or sarcoidosis and sent me back to the rheumy. Rheumy ordered a dozen different antibody test, all negative. That was 6 month ago when I was feeling pretty good. The winter and snow shoveling sent me spiralling down - the fatgue, pain everywhere constantly and the rapid bowel transit returned. The new development was all the rashes and the return of the anemia. I have gotten rashes all my lfe on sun exposure. MY hemoglobin went from 14.5 to 12 in 1 month. Every time they try to wean me off pregnisone, the anemia returns. The rheumy returns from vacation on Monday and I will give him a call. I am concerned with the tests that look like they show renal involvement

keep well
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Old 04-06-2014, 03:13 AM #10
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hummm... how about B12/pernicious anemia?? If your having an absorption issue secondary to your rapid bowel transit, causing malabsorption of vitamins, including B12.. what is your MCV on your CBC profile?

I know when My GI issues are bad, that I don't even absorb my oral meds .. its awful.. and sooo frustrating!

They put me on plaquenil for the joint pains and muscle fatigue - it helps a lot.. though it does have some GI side effects initially....
Good luck!! keep us updated!
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