Raynaud’s disease : I have lupus and... - Scleroderma & Ray...

Scleroderma & Raynaud's UK (SRUK)

10,935 members5,467 posts

Raynaud’s disease

djsema profile image
5 Replies

I have lupus and been diagnosed with Raynaud’s disease. My feet are always cold but when it’s touched it feels normal.

Is this normal please?

Written by
djsema profile image
djsema
To view profiles and participate in discussions please or .
5 Replies
marie5454 profile image
marie5454

Mine are the same, I have raynauds, also my feet and hands are boiling hot sometimes but if I take off socks, gloves etc I get raynaud attacks. The rheumatologist didn't seem concerned at the time because bloods were ok, that was 5yrs ago. Try to keep yourself warm and mention it to the doctor next time you go, good luck x

djsema profile image
djsema in reply to marie5454

Thanks for your advice. And I will do xx

Sanmateogirl107 profile image
Sanmateogirl107

HAS YOUR DOCTOR DONE ANY BIOPSY OF YOUR SKIN TO CHECK FOR SMALL NERVE NEUROPATHY. ASK ABOUT PRAZOSIN 1MG, I CAN NOT FEEL MINE I GET PINS AND NEEDLES IN THE BATH ITS VERY PAINFUL, HANDS WHEN I PUT THEM IN WATER SAME THING. THE DOCTORS WILL START ME ON IMMUNOTHERAPY FOR CREST, LUPUS. ASK YOUR DOCTOR FOR HELP AT HOME MAKE NOISE ABOUT IT. GET SUPPORT, GET YOUR FAMILY INVOLVED ALSO. THE LOVE YOU RECEIVE ITS WONDERFUL. GOOD LUCK I AM PROUD OF YOU. LOVE AND HUGS JULIEANNA

djsema profile image
djsema in reply to Sanmateogirl107

Thank you xx

djsema profile image
djsema

Thanks you xx

Not what you're looking for?

You may also like...

Anyone have these Raynaud’s symptoms?

purple when sitting at my desk and not moving for about 20 minutes or when being exposed to cold....

Worsening Raynaud’s

here in about a year, but have since been diagnosed with UCTD, secondary Raynaud’s and Sjogren’s....

Red nose after Raynaud’s diagnosis

Morning all 😀 I was diagnosed with Raynaud’s last winter and have since been experiencing horrible

Anyone continually being diagnosed with more and more auto-immune diseases?

I have been diagnosed over a lengthy period of time with Mixed Connective Tissue Disease, Morphea...

Chronic Kidney Disease

anyone else been diagnosed with CKD in relation to Scleroderma or connective tissue disease. What’s...