PMR in Hands and Wrists
Posted , 12 users are following.
I am interested in hearing from others about PMR traveling into the hands and wrists. Mine migrated from my thighs to my shoulders and now into my hands. Mostly my right hand. My doctor concluded that instead of PMR i might have late onset rheumatoid arthritis (LORA). Numerous tests within nuclear medicine (I now glow at night) seemed to prove otherwise even though PMR is not "known" to affect the hands.
So...I'd be intersted in hearing from others about whether your experiencing swelling in your hands. One hand? Both? And someone out there commented on calcium as being a culprit...meaning too much calcium being consumed to offset bone density issues. Any thoughts?
Much appreciated.
0 likes, 56 replies
marian-colorado Daniel1143
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maid_mariane Daniel1143
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When finally diagnosed and on prednisone it is better but are swollen if i over use or repetitive actions.
I hope this helps
Mariane Canada
MaggiGrace Daniel1143
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I had a period of several weeks where my hands and wrists were hit with a vengeance. They eventually settled down, but during that time the pain was excruciating. I wasn't taking any calcium at the time.
I continue to have some mild swelling in both hands, especially between my first knuckles near the palms of my hands...slightly worse in my right. I only notice wrist pain if I "over bend" or lift something heavier than I should. Hand/wrist pain is worse in the AM and gets better as the day progresses.
My rheumy also suspects LORA, though tests were sero negative for RA.
I'm presently on 2.5 mg of pred with 200 mg Plaquenil. The RX was for 400mg Plaquenil but that dosage made my ears ring so badly that I couldn't sleep, so I reduced to 200 and seem to be managing.
I was diagnosed w/PMR in March 2015
Daniel1143 MaggiGrace
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MaggiGrace Daniel1143
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donna60512 Daniel1143
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renee39320 Daniel1143
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I have problems with my wrists too. I'm down to 3 mg of prednisone after 16 months. I can't lean on them when getting up. My rheumy told me to soak them in Epsom salts and warm water in the morning. It seems to help.
donna60512 renee39320
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Anhaga donna60512
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You should not go down by as much as five. There is a way to go down by five in the same amount of time. Say you are given a month to reduce from 20 to 15. Try dropping by 2.5 for a week or two. If that works, you can try a further drop of the same, although I'd be tempted to reduce by only 1 mg per week. Do you have 1 mg tablets? The standard is never to reduce by more than 10% at a time, and to make sure you are stable with the pain under control at each level before reducing further.
Daniel1143 donna60512
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Donna, your rate reduction is much too fast, if you're not careful you will suffer the consequences. Lots of discussion on these threads about tapering very very slowly. Those of us who've tried to accelerate the process live to regret it
donna60512 Daniel1143
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Anhaga donna60512
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If pain returns you have to up your dose again. This sometimes makes the next attempt at reduction more difficult. By all accounts the smaller the reduction each time the more successful. As I pointed out above you can probably achieve this 5 mg drop in a month but in smaller steps. If you are expected to drop 5 mg in a week and then another 5 mg in another week, then I don't think anyone can make suggestions that can help you. I live in Canada and from my starting dose of 15 mg I was advised to drop by only 1 mg increments, weekly. At 10 mg I had to start the dead slow nearly stop taper, with my doctor's blessing, and have so far successfully reduced to 3.5, now tapering to 3. This has been since my start thirteen months ago. I may be nearing my lowest possible dose, but so far so good.
Anhaga donna60512
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If pain returns you have to up your dose again. This sometimes makes the next attempt at reduction more difficult. By all accounts the smaller the reduction each time the more successful. As I pointed out above you can probably achieve this 5 mg drop in a month but in smaller steps. If you are expected to drop 5 mg in a week and then another 5 mg in another week, then I don't think anyone can make suggestions that can help you. I live in Canada and from my starting dose of 15 mg I was advised to drop by only 1 mg increments, weekly. At 10 mg I had to start the dead slow nearly stop taper, with my doctor's blessing, and have so far successfully reduced to 3.5, now tapering to 3. This has been since my start thirteen months ago. I may be nearing my lowest possible dose, but so far so good.
marian-colorado donna60512
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I do not think there is a "protocol" in the US as you say. It is just that doctors here are less informed than in the UK since there are more people in the UK with this disease. My doc knows the slower the better chance of succes.
donna60512 marian-colorado
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I am glad to hear that. I will talk to my rheumatologist about this. I found out this past week that my primary care doctor's nurse has PMR. I am sure she was tempted to talk to me when I first went in with all of my pain in my legs, upper arms, and shoulders, but of course she did not. Anyway, when I saw her last week and told her that I had been diagnosed in early June, she told me that she has had it for two years. She is down 6mg. Her doctors is from an eastern European country and was trained in the UK. She has been reduding her by 1 mg a month. I would love to do it that way and will discuss it with my doctor. I have been on 20 mg for about five weeks, so not sure what be the usual time to begin reducing. Do you know? The doctor wanted me to be at 15 by the time I see him again in early August. I have been pain free for one week, only because I started splitting my dose, breakfast and dinner. By doing that I wake up pain free. What do you thing? I love that I get so much help on here. Thanks, Marian I apprecite anything you can tell me. Donna
Anhaga donna60512
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marian-colorado donna60512
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donna60512 Anhaga
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Thank you so much, I have been feeling so good. I don't want to be overyly optimistic, but still want to be hopeful. I agree that a person should listen to their own body. I know that we are all different. I appreciate your help.