CRP levels “ off the scale “: Hi ! Have managed to... - PMRGCAuk

PMRGCAuk

21,317 members40,425 posts

CRP levels “ off the scale “

Geordieland profile image
14 Replies

Hi ! Have managed to reduce to 5mgs of Prednisolone from 20mgs prescribed March 2020 . Had a recent blood test done and hip and lower back X-ray because of increased pain in both . Both X-rays showed deterioration but my concern is that my CRP levels were above 340 !! Apparently the normal range is up to 20 ? I had an appointment with a rheumatologist in December but that has now been cancelled - advice please as to what I should be doing about these very high levels !! I have osteoporosis , PMR , scoliosis and RA ( with a bit of bursitis in my hip ) such a lucky girl 😂

Written by
Geordieland profile image
Geordieland
To view profiles and participate in discussions please or .
Read more about...
14 Replies
DorsetLady profile image
DorsetLadyPMRGCAuk volunteer

The only thing, is back to GP and get them to do any other tests they think might help to resolve what is causing such high levels, maybe testing CRP first, to make it sure it wasn't a one-off blip. so don't panic, but get it checked again. It can be caused by many things, including your other issues. What where your level at diagnosis?

Have a look at this post -

healthunlocked.com/pmrgcauk...

Geordieland profile image
Geordieland in reply toDorsetLady

Hi 😊 will need to get the previous results from my GP - this was a locum who actually offered to print off my results for me 👍 but will defo pursue it 👍👍

SheffieldJane profile image
SheffieldJane

As you have probably heard PMRPro explain, many things can raise our CRP levels quite considerably even the common cold can make them skyrocket and the “common” colds we have around currently are far from ordinary. Any kind of infection or inflammation will see them rise so this is not an indicator of trouble for our central diseases necessarily. Is your Rheumatology team aware of your current state of health? They may reconsider their priorities for appointments. Failing that your GP should be able to advise you. Commiserations, I hope you can access the help you need, quickly.

Geordieland profile image
Geordieland in reply toSheffieldJane

Thank you ! I’ve only had 1 previous appt with the rheumatology team so I don’t feel connected to them at all ☹️ Am considering paying a one off consultation privately just to get a handle on things .

DorsetLady profile image
DorsetLadyPMRGCAuk volunteer in reply toGeordieland

Might be worth but you are quite likely to seem same consultant if you go locally….but why not give your GP a chance - if you can get an appointment that is! Provided you don’t have complex issues, they are quite capable of treating PMR. Don’t always require a specialist.

PMRpro profile image
PMRproAmbassador in reply toGeordieland

Are you really living in Geordieland? Who/which hospital are you under?

Geordieland profile image
Geordieland in reply toPMRpro

😂 no - born in Newcastle and lived in the northeast until I was 11 then moved to Ilkley - now live in the southeast but love my roots 😊

PMRpro profile image
PMRproAmbassador in reply toGeordieland

Makes a difference to what I would suggest! Gateshead QE hospital rules ;)

Geordieland profile image
Geordieland in reply toPMRpro

As far as I’m concerned the” North East “ rules 😂 Have managed to arrange a chat with a GP on the phone so any suggested questions would be gratefully received 😊

PMRpro profile image
PMRproAmbassador in reply toGeordieland

Maybe a new post asking for some guidance so everyone sees it?????

Geordieland profile image
Geordieland in reply toPMRpro

Will give it a go 👍 thanks

phebamom profile image
phebamom in reply toSheffieldJane

True! I have PMR/GCA. I also have a blood condition called MGUS. I carry a protein in my blood. I see an oncologist for this condition. The protein in my blood makes it difficult to assess my SED rate. The MGUS does not elevate my SED, but the protein in my blood makes it difficult for the blood to settle in the test tube, making my SED look higher than it really is. My rheumatologist goes more on how I say I am feeling, than my blood work.

PMRpro profile image
PMRproAmbassador

You need it to be checked in a couple of weeks to be sure it isn't a lab error - but as SJ has explained, all sorts of things raise it and if you have bursitis it could be that or the RA not being adequately controlled.

Your GP needs to get their thinking cap on.

Geordieland profile image
Geordieland in reply toPMRpro

Will be ringing my GP for a call back ( no face to face available ) and make sure I have a list of questions !

Not what you're looking for?

You may also like...

CRP levels

I am now off Pred since June and feeling good. I need some help regarding my younger sister who has...
Middleton22 profile image

Off the scale

I have been immobilised for the last five days with excruciating pain in my left buttock, outer...
bBarnabus profile image

CRP levels raised

I was diagnosed with PMR in April 23 , starting on 15 mg Prednisolone reducing to 8mg. Then...
Agapanthous profile image

ESR and CRP levels

Yesterday I had a blood test for ESR and CRP levels - results are: ESR 2mm/hr Serum C reactive...
Miserere profile image

CRP/ESR and calcium levels

I have had Polymyalgia for three and a half years now, and after many ups and downs am now on 6mg...
Purplegloss profile image

Moderation team

SophieMB profile image
SophieMBPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.