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Once again, Kelly, you have helped me understand all the blood work they do. I tried just yesterday to explain why it had been so hard for the Dr. to diagnose my RA to some friends-Now, with the help of this information I can do a better job. You are such a great help. Thank you so much.
Hi Kristi, did you read through the links about blood tests on the Do I Have RA page or using the tags list dropdown at page top. If you do have questions, there’s a lot here. Prob. more than you want to know. LOL 😛
My RF is seronegative. My bloodwork always comes back on the high side of the normal range for inflammation. However, I just had to have an xray done of my foot due to an injury and the ER dr compared this xray to ones done last summer. He said I have “significant arthritic changes” in my foot as opposed to last year’s xrays. I have been on Remicade since August and MTX since April a year ago. So much for bloodwork being an indicator of disease activity!
I’m sorry to hear about the new foot damage, Phyllis. But, yes, you’re right. Rf just doesn’t predict it or reveal it. Thanks for sharing your details so others can see.
hey there… i have no blood tests that are irregular..just once in the hight of the initial flare.. crp very very up.. but the pain is more now than at that time.. and in more places.. and more stabbing than crushing/tight. There are changes that were there according to my podiatrist that represent RA before i realized that “sudden severe flare” that identified me as an RA patient..
I didnt feel the RA deterioration in my foot.. yet it was evident on xray.
Darn this sneaking little rascal (RA) .. it is Eons Old.. but it acts like a 2 year old lol
Excellent info for anyone searching Dianne. Delivered w/ humor just how I like it. :yes:
Had to laugh at the statement on the hospital link that said: “The rate at which new advances in care are occurring in RA is mind-boggling!”
It sounds exciting to have RA doesn’t it??
Haha. A life of ease, comfort, and pleasure.
Living on the frontier of an exciting disease…aren’t we lucky! Great post!
Nice way to put it. Shall we get cowboy hats?
I am also seronegative. My RF and ESR are always normal. Once I had an elevated CRP, but I was also sick at the time. The last time my RF and ESR were tested, I literally had burning hot claw hands. In addition, it felt like hot daggers were being twisted into my hips 24/7. Oh, and my feet were stiff, puffy and had stabbing pains in the base of the toes. And still, all “tests” were normal. In my experience, the blood tests have no correlation to the pain.
Or possible to the damage done as well. What did your doc say about that?
You’re right Kelly. I often wonder about the damage that has already been done. So far, I’ve had MRIs of the spine and hips, and neither showed any damage (despite significant hip and back pain). I can only imagine what an MRI of the hands/feet/wrists would show. The hip pain was confirmed to be trochanteric bursitis rather than hip joint pain. I’ve done alot of research on bursitis, and it is definitely related to RA.
Thank you so much for this article, Kelly! I have something else to talk to my rheumy about at my next appt. I now understand why my last rheumy was so slow to do anything – he always talked about my blood work looking good – but I kept showing him the inflammation and telling him how much pain I was in. He took me off meds, the new rheumy has put me on much – irregardless of the test results.
Good luck with your apptointment, Janel. You can click on the orginal studies to print if you like so you don’t have to say, “I read this on a blog”.. LOL.
Don’t you think it can be an extra source of frustration – like we need more on top of pain, meds, lack of awareness… ? :no:
My favorite is a grinding noise I hear in my elbow when it gets stuck or stiff, and I have to push through it to get it to go the “full” range of motion (full is a very relative word in this case). It sounds like metal in a blender is the best way for me to describe it…..thanks for another insightful post, Kelly.
I love the information you bring, but I have to say I love your humour more! Just looking over my records today, in preparation for a move and a change in Rheumatologists – my two prior docs have been focused on swelling. Now I know one aspect of what to look for in my new doc.
THANK YOU ANJ. Glad you get it. :heart: Good luck w/ that new doc! I hope this is a positive move for you.
I wish I could understand more of the medical jargon from these studies, but I do understand some and it helps how you summarized it all. It would be interesting to know if we have this C2C that continues to cause joint damage, and what genetic markers we have also. It makes sense to me now how I am feeling continuous joint damage inspite of my success with mtx and enbrel. My right shoulder specifically, felt normal at diagnosis and has been getting worse as the months go by. It also possibly explains my continued weight loss and muscle loss (REE and FFM). Unless I read it wrong. No wonder I’ve been so confused over what I feel compared to what docs and the hospitals say. So much of what the hospital link says is incorrect. Such as we have safe and effective drugs. They have no idea whether biologics are safe long term. Different sites contradict each other also, which leaves RA’ers even more confused! Thanks for this very interesting and informative post.
Ronda, it is great to have such smart friends as you. I try to make it sound easy & funny, but it is certainly tedious. & Yes, no wonder people are confused with things like that hospital site. I now have a list of “big & credible” sites like that which are plain wrong. 😛
Kelly The only thing my rhemy says is It doesnt look bad! What does that mean? I sit there screaming inside with pain and i hear that..She has never shared any numbers with me..Im learning from you and this site! Thanks for this site or i would have gone crazy along time ago! Well some would say i have already..lol Judi
i was dx 4yrs ago with R.A and S.S i already have had an operation on my knee and when i woke up my doctor casually said, were sorry but we cant always see everything on the MRI and you are going to need a knee replacement. As he left the room i balled my eyes out.I think i realized then that this was only the beginning of things to come. I have already developed nodules in between my fingers. The last few test that i have taken has come back saying that my crp rate is high . i am very worried because obviosly we cannot see whats going on in the inside of our bodies and i thought the thing that causes the dammage is inflammation. Would love to hear back from someone that has some knowledge of this because my rhumy seems to take everything in stride and i am honestly scared of what may be going on in the inside. Thanks and my prayes go out to all of you with this awful disease. xoxo
Hi did you mean muscle loss? I’m certainly not cache xoco!! Thanks for another great article ann
I have a great biologic rheumatologist who doesn’t even do the blood tests to verify disease activity. He bases it on how I am feeling, responding, swelling and pain levels. I haven’t found the sweet spot in meds yet but we are getting closer. My pain levels are manageable and my ability has greatly improved – can do most everything now with only slight limitations.. could not even wash my face without pain prior.
I should point out I get blood work done regularly but that is not used to assess my overall situation..