Are painful swollen hands and fingers a PMR flare?
I got off prednisone for PMR after almost 3 years in April. In February I had woken with swollen painful hands and fingers. Because of how I sleep it was diagnosed unseen as carpal tunnel. Finally saw my rheumatologist and she thinks it could be a PMR flare,didn’t look like carpal tunnel. That makes sense to me but she has put me back on only 3mg. of prednisone. I have no strength in my hands and can’t make a fist. Very limited in what I’m able to do.
When first diagnosed with PMR and in terrible pain this same rheumatologist started me on 5mg. of prednisone which did nothing.
Finall got up to 20mg. And got some relief.
Has anyone else had issues with your hands during or after being on prednisone for PMR? I also just found out there is osteoarthritis in my hands.
Thanks!
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I saw my PCP yesterday June 20 and told him about my hand and wrist pain and swelling. Asked if PMR related. He said with inflammatory diseases the symptoms tend to overlap. Could be PMR, arthritis, lupus, etc. So inflammation may not be PMR related. Putting me on Meloxicam which he described as a little mallet compared to the big hammer of prednisone. More to follow when the scrip arrives
Lucky you being able to take an NSAID now that you've ditched prednisone. I hope the Meloxicam helps you and that you don't need to take it for long. Please let us know how you go.
Have you seen the "famous venn diagram" for spondyloarthritis discorders?
"This diagram shows the overlap between Ankylosing Spondylitis and other diseases that occur in the same patient or within families. However, when this Spondyloarthropathy concept was described in Leeds in the UK in the 1970s, the exact link between the conditions was not known."
https://enthesis.info/pathology/spondyloarthropathies.html
The link is the presence of enthesitis in all these disorders.
Yes, I'm on 2mgs daily since May. Pmr since January 24.
My hands and wrists began to hurt v badly since May. Been told it's osteoarthritis
Pls keep us posted about meloxicam. My hands and wrists are nearly useless since May. My PMR is nearly gone, w 2mgs of pred daily now. Fingers crossed. Doc says hands have osteoarthritis. Never knew it could be so painful
I am in much the same situation. But I’m tapering slower. I started at 20 mg four months ago and now at 9 for three weeks.
Painful mornings but I’ll stay on schedule as I’m anxious to get off Pred.
But you might go a bit slower also.
I’m losing all confidence in these doctors who are telling us that this hand and wrist pain is not PMR. We can’t all have just suddenly developed osteoarthritis or some of these other excuses. It has to be a manifestation of the PMR that we all have, and they will never figure out how to address it if they don’t acknowledge it.
No, I do not.
No way it's not related.
We all just developed osteoarthritis in both hands overnight?
Ridiculous
Has your Doc ruled out RA? If so, why (if you know) ?