5 CRP tests resulting as High, but no Dx!
I have had (5) CRP tests come back High, ranging from 5.9 to 8.5, with no Dx yet! The last test ordered by Mayo neurologist. I pointed out to him the result of 5.9 - High, along with the other tests ranging from 5.9 [twice] to 8.5 [three of the High test not indicating as so!] and he told me to speak with the Mayo rheumatologist I had seen. Contaced the rheumatologist thru the portal and he said to discuss the results with the Dr who ordered the test! LOL! I have had many Drs, including a dentist regarding delayed healing and my retinal specialist, indicate "inflammation" as part of my problems, but no one seems to want to get to the bottom of it. Frustrated and worried! I will sign this as "P".
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Thank you so much for responding to me. I really appreciate that. I have told many Mayo employees that I think there is a stipulation that each employee must display before they are hired........that is KINDNESS, and I truly mean it. Thank you for your kindness. I just wish the Drs, too, would be required to meet that stipulation. I am on a "break" right now because I got so frustrated with my Drs [neurologist, rheumatologist and GI], but I may do a follow up when I feel I have built up my strength. I really do appreciate you and the info you provided me.
P
SIX neurologists! You poor thing! I thought I had many with 4, one of which I no longer see at all. Actually, I am seeing none of them right now because I am so disgusted with how they treated me. The main Mayo neuro even quoted me an incorrect Dx thru the portal. One I KNOW I do not have, one not even related to my symptoms, and one he NEVER EVEN MENTIONED TO ME BEFORE! If he had done so, I would have argued with him because I have had this Dx before, I know the symptoms, and it is nothing like the symptoms I have related to him. I would know it if I had the Dx he just recently quoted. Sometimes I think they believe we are dummies that they can say anything to us and we will just swallow it. First of all, you gain a lot of knowledge just with your medical experiences. You gain a lot of knowledge researching the symptoms that the Drs don't pay attention to. And, my career was in the medicaal field for years! Not that I know more than the Drs, or that I am a "know-it-all", but there are things they just cannot get by me! 😉 Hang in there! You have my sympathy.
P
The GI who told me to "learn to manage my expectations" is not a Mayo Dr. I wanted to make that clear. He is just an idiot Dr I went to before Mayo. Believe me, I have gotten many laughs and puzzled reactions when I relay that story! LOL! You just have to keep laughing! Otherwise, it will really get you down. Thanks for your response and it sounds like you have your share of "you know what" to manage. I am sorry for your experiences. We deserve better.
P
@walk4life Please read up on the cortisol test, I understand that the blood draw needs to be done early in the morning. My endocrinologist looked at the time of day on the blood draw for me I literally just made it under the wire. My PCP had ordered it and apparently did not know time of draw was critical and neither did the lab doing the draw. I live in the Dallas area and these are doctors and labs of major health providers, so not a small town by any means. Thankfully my endocrinologist knew to check.
Also, have you had your Sed Rate tested? https://www.mayoclinic.org/tests-procedures/sed-rate/about/pac-20384797
Sed Rate and CRP are the two inflammatory tests. They are both non-specific and do not directly lead to a Dx they simply tell doctors about inflammation in your body. Your rheumy should be able to identify/eliminate an autoimmune problem.
I will look into the cortisol test. What exactly is the test looking for? No Dr has ever mentioned cortisol to me, so I am not educated on it. Yes, I have had the sed rate tests and some have been high, some not. Actually, the sed rate tests were not done looking for imflammation. I have these stabbing pains in the R temple area, leaving me with swelling, like a bulging vein, or something and extremely tender for awhile. They were looking for temporal arteritis, or giant cell arteritis, and like everything else, it was just dropped. I still have the temporal pains.
Thanks for the info about the cortisol test. Yes my sed rate was elevated. CRP elevated -all the ither tests were normal .
I am not a doctor- but several years ago I was diagnosed with PMR, polymyalgia rheumatica. It is a default Dx based on them not being able to find another cause for your inflammation markers being high plus other symptoms. https://www.mayoclinic.org/diseases-conditions/polymyalgia-rheumatica/symptoms-causes/syc-20376539
Mayo Connect has a group focused on PMR. If you do get a Dx of PMR you might want to join the group.
And I forgot to mention not only was my CRProtein high, but so was my protein in my spinal fluid.
Got no answers for that one either