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!
Interested in more discussions like this? Go to the Polymyalgia Rheumatica (PMR) Support Group.
Hi @kmw24, Welcome to Connect. I have carpal tunnel in both hands but worse in my left non dominant hand. My PMR is currently in remission for the second time but I remember when my second flare up occurred it was similar to my first time with pain more in my shoulders and legs with some stiffness in the hands but no real pain. I've had 2 steroid injections in my left hand that helped a little but I still notice the carpal tunnel symptoms. I think it's great that you have an appointment with your hand doc before your appointment with your rheumatologist.
Can you provide an update after your appointments?
@johnbishop thank you for your reply. Good to hear that you’re in
remission. I’m not excited about hand injections, especially if they don’t
give a lot of relief. I’ve had quite a few injections, different joints and
the worst was the foot so I can’t imagine that the hand would be any
better! I will post an update after seeing both physicians.
Kristen Waller
Here's a link to an article about swelling in wrists and hands with PMR. I hope you feel better soon. https://pubmed.ncbi.nlm.nih.gov/8546741/
As I tapered from 10 mg to 9 mg would wake up with extreme pain and numbness in wrist, hands, and fingers. Discussed with rheumatologist and because the finger pain was specifically to my middle three fingers he suggested it may be carpal tunnel. Suggested sleeping with wristbands. It is now a month later and it has much improved (now on 8 mg). They are still ‘sore’ in the morning, but nowhere near the pain I had been experiencing.
@scpartain, thank you for the article regarding hand swelling. I’ll take a look today.
I have seen a few posts where people mention that their bilateral hand pain and stiffness started to resolve once they got down to 5mg Prednisone. Curiously i have just dropped to the 5 mg range and woke up this morning able to move my hands without the usual pain and stiffness for the first time since October last year (not gone but at least 70% better). Is it a coincidence ? I am 7 weeks on Hydroxychloroquine which seems to be helping with the PMR pains. I also stopped taking the D3/Calcium/K2 supplement last week because i was worried about calcium deposits in the joints and arteries and started back on the Tumeric supplements ?? Something is finally working at last !!!!
Wow! Thx!
I had hand and wrist pain between 8 and 6, now down to 5 and it is essentially gone. Hang in there…it will get better !
I am on my third flare in 10 years, and already down to 2 mgs per day prednisone. Yesterday my hands began hurting so badly and I'm having difficulty w daily routines.
The past two bouts of PMR never affected my hands, just the v typical hips, shoulders.
Anyone have similar issues w hands?
I could barely grip anything. It didnt seem so bad in the knuckles but I completely lost my grip without pain.