RA and hand palm pain: Hi, been diagnosed more than 1... - NRAS

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RA and hand palm pain

virginied profile image
28 Replies

Hi, been diagnosed more than 10 years ago with RA. Had extreme pain inside my hand for many days ( palm) . I find it hard to open my hand and fingers as it.hurts too much inside hand , especially big middle finger. It feels like the tendons can't stretch anymore .

Anybody with same thing ? Is that linked with RA ? Is it tendinitis?

Thanks

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virginied profile image
virginied
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28 Replies
Madmusiclover profile image
Madmusiclover

Might be. Or tenosynovitis. Or trigger finger. Been getting injections in my ring finger palm for years for tenosynovitis. You need to visit your GP.

virginied profile image
virginied in reply to Madmusiclover

Ok thanks , does it feel better when your wrist is closed and painful when you open your hand ? Do you always have tenosynovitis or is it some flare up which last a few days and go ?

Madmusiclover profile image
Madmusiclover in reply to virginied

Yes always have it. Worse when RA flaring. You need to get a proper diagnosis.

Vonnie69 profile image
Vonnie69 in reply to Madmusiclover

Do injections help?

Madmusiclover profile image
Madmusiclover in reply to Vonnie69

They did. Had quite a few over the years but last one didn’t.

AgedCrone profile image
AgedCrone

Ask your rheumy’s advice…..could be compressed nerves …or osteoarthritis…both cause pain the the palm if your hand.

Old_Sceptic profile image
Old_Sceptic

Hello,

I don't know if it helps but I had a similar issue a few years ago and my neurologist diagnosed it as vitamin D and Calcium deficiency. Mine was related to Phenytoin which causes a deficiency of both but it might be worth asking if your levels are ok?

Perhaps your GP will run some bloods for you

Anyway good luck and I hope you find relief soon

virginied profile image
virginied in reply to Old_Sceptic

Thanks for those advise. I'll wait a few more days and contact my gp. Its very difficult to get a reply from my rhumatolog so I will not even try . Thanks

welsh12 profile image
welsh12 in reply to virginied

Don't you have a nurse helpline? At Rheumatology

virginied profile image
virginied in reply to welsh12

I do but it's an answer phone and she never phone back. Phoned a couple of time in 10 years time and never had a reply ... very bad

welsh12 profile image
welsh12 in reply to virginied

That's bad I have an email system goes through to admin and they pass to rheumatology

JulesCurrie profile image
JulesCurrie in reply to virginied

I find the same at my hospital . RA helpline has been useless however has improved the last year. They very often say the helpline is closed and say don’t leave a message will reopen later today . What use is that … I did keep calling and was able to leave a message on the last occasion ..

Hippo1234567 profile image
Hippo1234567

I get his sometimes too. It comes and goes.

Lizard28 profile image
Lizard28

I’ve had tenosynovitis and I can feel your pain, I suffered for months before trying to get a doctor to look at it. My GP gave me a weeks steroid tablets and referred me urgently to see my rheumatologist. 6 weeks later I finally saw her, she gave me steroid jabs which didn’t work, the pain got worse I had to go on steroids for about six weeks for it to eventually ease up. She sent me to a physio who did an ultrasound and told me to squeeze my hand till it hurt, he did it and I almost punched him it was so painful. I’ve lost movement in my ring finger and altho the severe pain has gone down there is still swelling in my finger, can’t wear my rings. I do keep trying to squeeze my hand all the time but I don’t think it will improve now. My advice to you is try to see your Rheumy as soon as possible.

virginied profile image
virginied in reply to Lizard28

Wow, that sounds painful, thanks for the advice 👍

Hairbraid profile image
Hairbraid

hi I get this too always worse in a flare and when my medication isn’t working yes opening hands so painful and throbbing burning pain hurts more if do anything

1973hillview profile image
1973hillview

Hi. I had the same for many years each time I had a flare up. My palm would start hurting, become tight and eventually my middle finger would be curled over and locked. It was mainly treated with steroid injections into my hand and a splint on my fingers but then became more regular affecting all aspects of day to day life along with being extremely painful. My rheumatology Dr referred me to a orthopaedic hand surgeon and I ended up having surgery and my tendon cut to stop it reoccurring and locking. I still get the pain but it does not affect my finger locking. I was told it was due to nodules on my joints catching on my tendon and the inflammation compressing the tendon. Hope that helps and you improve and get some relief.

JulesCurrie profile image
JulesCurrie

I do get something similar to you . When I have a bad flareup I am beside myself with pain in my hands a wrists. It’s so hard to explain so much more than the normal joint flares. It’s like a surging thrusting burning pain, I just can’t sit down or settle finding myself to constantly walking around swinging my arms to get a slight around of relief. . Pain killers and even oramorph, did nothing to help. I fingers like sausages hands wrist and arm hot and swollen, finger tips cold find myself pacing around unable to sit down , It generally starts in evening and continues all night, The pain can be that intense that I wan to have my arm amputated…. You might think she has a low pain threshold,.. I don’t had my first child without any gas air or pain relief, not wanting to be a hero it’s just the way it happened., suppose I was lucky. .. I have just been put on another course of steroid which has instantly helped. Left with numbness in finger tips Thank goodness for steroids but I do hate taking them .

virginied profile image
virginied in reply to JulesCurrie

Sorry to hear that , ita difficult to explain this pain especially with people who don't have RA.I'm the same as you , I do not like taking steroids, all the best

Welshwomanprestatyn profile image
Welshwomanprestatyn in reply to JulesCurrie

I have experienced pain like this in my hands. Starts late evening and carries on into the night. Horrible pain I cant sit still have to keep moving my hand about. Usually happens with a flare up

Gaz227 profile image
Gaz227

might be a form Dupuytren's contracture , Google it , a have a mild form of it and my friend had the op to free up the tendon sheaths 👍

Clariana profile image
Clariana

Palm pain was one of the first symptoms I noticed.

Tiverland profile image
Tiverland

get it checked first. Mine is identical and diagnosed as RA. I take my RA meds plus Vitamin D as suggested by RA nurse and curcumin C3 ( simple supplement) works wonderfully for my hands. I tried stopping it and the pain/ tightening came back. Another suggestion from my RA OT support gloves (Amazon) This relieves the pain I wear overnight so my hands are free in the morning. Good luck hope this helps. But speak to RA nurse first

Angels54 profile image
Angels54

Hi , I have experienced this several times , I put my hands in water as hot as I can bear it , massage , get some support gloves for rhuematoid, you might get them off Amazon👍

virginied profile image
virginied in reply to Angels54

Thanks, yes I do have them and also wear splint at night

Green230461 profile image
Green230461

I have had the same thing since Christmas excruciating pain especially at night!

Vonnie10 profile image
Vonnie10

I had similar symptoms rheumatology diganosed carpel tunnel and osteo was added into my ra . I have resting splints for it waiting a op on my catpel tunnel

virginied profile image
virginied

Thanks for all those comments , although it doesn't make things better ,it feels good to see I'm not the only one ( although it will probably sound wrong saying that) ...... All the best xx

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