General fatigue and pain ideas please: Good... - LUPUS UK

LUPUS UK

31,688 members28,071 posts

General fatigue and pain ideas please

johare profile image
5 Replies

Good afternoon everyone.

I am hoping some of you may share your experiences with me, I am not asking for an online diagnosis, as I have a GP phone call on the 10th, however, this is a thyroid check, not to discuss what is below.

I've had lupus, plus other issues for over 20 years and am used to the pattern to my lupus lows. However, last February I had a virus, along with my family. As usual, they picked up and I was left with chest pain(muscular) probably costochondritis and a sore throat and heavy feeling on my chest, that went on for months. But I picked up otherwise. Then just before xmas I began to develop alot of muscle pain. An example is putting on a jumper and feeling like I had pulled a muscle in my shoulder, the pain would go on for days. Then another area would become painful. I feel, even more brain fog, nausea, weakness than usual. All of my usual symptom exacerbated.

The only thing changed recently was increasing Levothyroxine from 25mcg to 50mcg in November. Such a low dose I doubt it would cause this.

I am now unable to do very much at all without feeling like im going to collapse.

I recently have had cardiac and gastro tests, for the heavy feeling. All fine.

I have, previous to this, always been as active as Lupus would allow.

Any thoughts would be appreciated

Written by
johare profile image
johare
To view profiles and participate in discussions please or .
Read more about...
5 Replies
Hamptons profile image
Hamptons

Niacin or B12 supplements can help energy. I use heat pads, hot water bottles for pain. Support gloves and bandages for wrist, elbow and knee pain. Tens machine eases muscle pain. Pacing helps with fatigue, lots on internet in that at mo.

johare profile image
johare in reply to Hamptons

Thankyou for your support.

MrsMouseSJ profile image
MrsMouseSJ

Hello, and I'm sorry that you are experiencing this. I guess the call with your GP will shed more light - and perhaps whether this might, for example, be Fibromyalgia.

In terms of what you can do in the meantime, as Hamptons says pacing is key here. I attach a link to, hopefully, a PDF on this. Whilst written for the charity Action for M.E. (sometimes called Chronic Fatigue Syndrome by some people), I think it is relevant for a wider audience, myself included.

actionforme.org.uk/uploads/...

If you are open to trying a dietary supplement, and there are no medical reasons why not, then it might perhaps be worth trying some magnesium powder - in a readily absorbable form. I use a magnesium citrate and malate mix, sold by a reputable brand (two words, ends in Care). Hopefully this wouldn't be prohibitively expensive. I also take Ubiquinol and D Ribose, which are far more expensive but which work very well for me; plus vit C and D each morning. If you want any pointers about where to buy at a reasonable price, PM me - I'm not sure I can mention here on the open forum.

Finally, how's your sleep? If it has deteriorated over the past year/months, that might be a contributing factor and worth looking at in detail.

Good wishes

johare profile image
johare in reply to MrsMouseSJ

Sleep is always poor due to peripheral neuropathy and now menopause! I'm also wondering whether the increase in gabapentin to combat this could be a factor.I take some supplements ie vit c/d the usual line up but will have a look at what you suggested.

Trouble is you wait a while to see if it's a bug, then is it lypus hanging on to a bug. Finally, you hope it's not a new state of normal, so you look for new reasons.

Thankyou.

I have all the same symptoms, and am being evaluated by a Rheumatologist. I use a heating pad, all the pain creams available, hot baths, yoga, but the pain is really incomfortable. I have trouble getting dressed also. My chiropractor helps a lot she uses TENS and heat, and massage. It's hard to get used to the constant discomfort, I am doing my best but some days I am so weak I can barely walk, the next day I can walk fast five miles. Old age is really quite an experience.

You may also like...

Cyclosporine ,Pain and fatigue

felt so ill since diagnosis it feels like the worse case of flu Iv ever had , everything aches from...

Dealing with family/friends/general life whilst investigations are pending - Please help!

for that long you'll end up feeling worse the next day. The one I feel for is my partner because he

General question please guys

Hi people, I would like to know your general opinions! I have been suffering with pains IB my joints

Any ideas with worsening weird rash please?

Hello, anybody had anything similar to this photo or got any ideas please?! I’ve had it 3 times over

in pain and so fatigued. pain killers useless.

trying. I had bloods done again last week and so surprised s.l.e. rate has improved. why is my pain...