Shoulders are killing me..: My shoulders have been... - LUPUS UK

LUPUS UK

32,252 members28,614 posts

Shoulders are killing me..

Natura profile image
11 Replies

My shoulders have been stinging lately. My right shoulder blade actually clicks when I move my arm around. I use a back massager with heat, and it helps a little. I don't want to take aspirin every time my back hurts. I can't take ibuprofen because of my kidney problems. I have had it bad the past two days. Ugh! Every time I think my symptoms subsided and I actually feel good for a couple of hours, something comes up.

Written by
Natura profile image
Natura
To view profiles and participate in discussions please or .
Read more about...
11 Replies

It's all joint inflammation, and just another one of those lupy things. I have had many steroid jabs to my shoulders and surgery too. The jabs do give some relief, as did the surgery, but it isn't a cure as, obviously, the lupus is the cause.

Natura profile image
Natura

Thanks 6161..that is what I figured. So painful sometimes. It finally lessened, but always there..sometimes dull, sometimes stinging. Just have to live with it. Was wondering if warm compresses would help alleviate the pain. I know lying down helps, but don't want to spend so much time doing that either.

in reply toNatura

For me, I have those 'cracked wheat' bags, that you heat in the microwave. Putting something hot on a hot joint, seems strange, but for me it works.

Natura profile image
Natura in reply to

thanks 6161...I am going to pick one of those up....

Slowmo profile image
Slowmo

Hi Natura, I too have had steroid injections on several occasions to my shoulders, as well as to my hips, as said they help in the short term with pain relief but don't address the underlying SLE problem that causes the pain, and don't stop if from returning. My shoulders would get so bad that I would be unable to use my hand/arm, sometimes for several months. If this continues for you it may be worth getting it checked out.

BellaC79 profile image
BellaC79

I had severe shoulder pain- enough to go to my gp and complain. At my next rheumatology appointment he mentioned it could be vitamin d deficency and it was. Six months of high dose tablets and a little sunshine when the summer came (i know we all avoid it and we get very little sunshine in Manchester ) I felt a difference within a month!

Natura profile image
Natura in reply toBellaC79

thanks cath_c... I do take vitamin d. I don't remember to take it everyday though. Could be why I feel good most of the time, but the pain shows up out of nowhere. And I am a sun lover...I try to get out as much as possible. I know the UK can be rainy, but NY has been awful lately. Lot of cloud coverage.. and still cold...I am going to have to make sure I have my sun hat on all the time now.

Bebe76 profile image
Bebe76

Ice pack and naproxen work for me, along with a massager.

Natura profile image
Natura

Thank u everyone...will try...pain is not there today..go figure...

jsdrjohnsamuel profile image
jsdrjohnsamuel

homeopathy medicines give relief for fore arms like shoulder syndrome ,consult a homeopath.

Natura profile image
Natura in reply tojsdrjohnsamuel

Thanks,...i already spend much on vitamins and supplements i cant afford. I cannot afford to go to a homeopath. Thanks

Not what you're looking for?

You may also like...

Me again 🥰

Thanks for all your replies on my last time Post really appreciate you all taking the time to write...
Buckley123 profile image

Fatigue is killing me

Please please any advice on addressing extreme fatigue . I’m sleeping for about 16 hrs a day and...
Harry19 profile image

Almost feel like im killing myself with the fatigue

Hi their I have had lupus since 2012 June time am now 20 and seem to be struggling slightly as time...
Danielle2419 profile image

Are these symptoms lupus?

Hello, I'm Suzanne, 43 years old. I have narcolepsy with cataplexy, I've also been recently...
mumsyme profile image

An Hallelujah from me

My Rheumatology consultation by telephone today was such a positive experience. I cannot express...

Moderation team

See all
Debbie_kinsey profile image
Debbie_kinseyAdministrator
chelseawong profile image
chelseawongAdministrator
michaellasmith profile image
michaellasmithAdministrator

Top community tags

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.