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PMR's effect on my hands

Polymyalgia Rheumatica (PMR) | Last Active: 9 hours ago | Replies (47)

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Profile picture for barjohnson62 @barjohnson62

Male, 63, second go-round with PMR (first at 55 y/o).

Pain primarily in hands and shoulders. Currently only hand pain, but managing it fairly well.

Tapering prednisone (4mg) @ 1mg/2wks. and injecting Kevzara every other week. Started at 20mg prednisone in early January after 2+ months of substantial pain.

So what's helped my hands besides prednisone...

Occupational therapy gave me various exercises and a hot wax dip. Pretty simple, but it helps. I find myself doing the exercises all the time when hands start bothering me.

Acupuncture has helped a great deal. Hands actually gripping better than I have in years at times, since my first PMR bout -- usually the few days after a session. Not sure it helps with other parts of my body, but it has been notable on my hands.

That's about it, but so far so good. Hands are definitely the first to feel it when tapering. Determined to take it slow through the summer and be off the prednisone.

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Replies to "Male, 63, second go-round with PMR (first at 55 y/o). Pain primarily in hands and shoulders...."

@barjohnson62
Thanks for this info! I'm doing great on 20 MG prednisone, but my hands are getting worse. Everything else is like it was 30 years ago. No pain in shoulders or neck, etc.

I have to go back to acupuncture! I used to get it for my back and it worked wonders. I'm curious: What kind of occupational therapy do you use? Are there any resources for that?

Thanks again, and glad to know you're doing better.