← Return to PMR's effect on my hands

Discussion
zkeith avatar

PMR's effect on my hands

Polymyalgia Rheumatica (PMR) | Last Active: Jun 12 7:29am | Replies (49)

Comment receiving replies
Profile picture for cheraloha @cheraloha

I'm down t 3 mgs of Prednisone and also on Kevzarra. Unfortunately, my hand pain remains excruciating. The tapering makes it worse. From what I understand, 30% of PMR sufferers experience hand pain. I'm not positive, but I don't think it is Carpal Tunnel or RA as there seems to be a direct link to tapering. It's constant, though worse at night and in the morning. I don't want to increase the dosage of prednisone, so trying to tough it out.

Jump to this post


Replies to "I'm down t 3 mgs of Prednisone and also on Kevzarra. Unfortunately, my hand pain remains..."

@cheraloha
You and me both. I feel the same way. My hands hurt in the morning and slightly get better by evening. My rheumatologist told me to stop Kevzara (and come back in 6 weeks) because of low wbc and anc. Not sure how that’s going to work.

I think there is more unknown about PMR than is known.