Random burning pain at night: I was diagnosed with sero... - NRAS

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Random burning pain at night

aod75 profile image
8 Replies

I was diagnosed with sero negative arthritis in 2018. I am mostly doing ok, tired but managing. Recently I’ve been getting these painful burning skin sensations at night. They can be anywhere, leg, face, back. They last a short time but can be intense. Has anyone else experienced this and was it due to arthritis? Thanks.

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aod75
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8 Replies
J1707- profile image
J1707-

yes I get this. I was diagnosed with fibromyalgia. Take duloxetine which has helped enormously. I’m serious negative too . Skin in isolated parts feels like an iron is burning or hit poker

aod75 profile image
aod75 in reply toJ1707-

Thanks for the reply! Do you get it during the day too or at night? Sometimes I get a localised hot sensation or a pin prick feeling during the day but the nighttime one is worse. I sometimes get muscle spasms at night too that might also be connected.

J1707- profile image
J1707- in reply toaod75

I get it at both . I don’t get spasms but I use to get an isolated muscle twitch mainly in my thighs . Best go to your Gp or mention it yo your rheumatologist

Runrig01 profile image
Runrig01

Sounds very much like fibromyalgia. Be worth mentioning to rheumatologist or gp.

Joannos profile image
Joannos

Yes and I have slapped at it, it distracts and stops. But see GP or RA nurse it's probably Fibromyalgia it depends on how you want to manage

OSTEOARTHRITISRA profile image
OSTEOARTHRITISRA

See gp as above Maybe a nerve pain needed

You'd need a lot more symptoms for fibromyalgia

And other investigations ruled out before that's considered

Gnarli profile image
Gnarli

As others have advised it would be a good idea to keep a diary of symptoms to show your GP or rheumy team. Diagnosed with fibromyalgia, I get similar symptoms but it was the painful muscle spasms that were the worst. Now, I'm taking duloxitine, and it seems to have calmed it down.

aod75 profile image
aod75

Thanks everyone for your replies!

That’s interesting. Fibro had been mentioned before as a possibility because of some other symptoms I have. I have a rheumatologist appointment in a few weeks. I’ll talk to her about it then.

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