Fatigue and what I can only describe ... - Scleroderma & Ray...

Scleroderma & Raynaud's UK (SRUK)

10,985 members5,510 posts

Fatigue and what I can only describe as back stiffness

-missymoo profile image
2 Replies

Hello everyone, I have Limited Cutaneous Systemic Sclerosis and secondary Raynauds. My diagnosis came in January 2017, I’m still getting to grips with all the changes and one of them is the fatigue, how do you cope? If I sit down for 1/2 hour, I’m asleep, just ridiculously tired all the time. I have to keep active and go to the gym four times a week, but finding this really hard to do. Also, I’ve been suffering with my back, feels very stiff and movement is getting limited, doing shoe laces, putting socks on, standing for too long. I can’t seem to find an actual link with ssc and back pain?!

Anyone else suffer? X

Written by
-missymoo profile image
-missymoo
To view profiles and participate in discussions please or .
2 Replies
Ajoshi profile image
Ajoshi

I have limited scleroderma too. Suffer with severe back and also neck pain. MRI scan normal. Tried accupunture helped briefly. Now back to square one with severe pain. Just manage on day to day basis

Patr1c1a profile image
Patr1c1a

I have that problem and find streatching exercises and gentle Pilates helps. Exercise and heavy work seems to make it worse and I stiffen up if I sit too long as well. Don’t know if this will help but it is so frustrating isn’t it.

Not what you're looking for?

You may also like...

Fatigue and joint and body pain- what helps?

Hi everyone. I received my formal diagnosis of limited systemic sclerosis last week and am waiting...

what can i do?

I know i asked a question a few days ago, but i went to the doctors today and ive been put on some...

I have only just joined up and have loadsa questions....

Hello guys iv just been told i have mixed connecting tissue disorder with signs of limited...

Please help

I have limited systemic scleroderma/raynauds/calcinotis cutis and I’m a 36 year old woman.Being in...

Confused 🤷‍♀️

I was diagnosed with limited cutaneous systemic sclerosis 12 years ago but I’m really confused. I...