Limited Cutaneous Systemic Sclerosis!... - Scleroderma & Ray...

Scleroderma & Raynaud's UK (SRUK)

11,028 members5,554 posts

Limited Cutaneous Systemic Sclerosis! Is rash connected?!

-missymoo profile image
8 Replies

I’ve had this rash apear, more aggressive on hands in between fingers and feet, but bumpy rash all over my body. Anyone know if this could be connected to LCSS?!

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

My daughter has an itchy rush like that from time to time on her feet. We showed it to our SS “specialist” she didn’t know what it was. It normally goes away in a week or so...

8whitetoes profile image
8whitetoes in reply toSVBO

I get this rash too ....

My Rhematologist and gaggle of doc's ..., All Tell me ""this is an autoimmune reaction inside your body"" an indication you are having a FLARE up....

The tiny blisters drive me nuts because they itch so badly !!!! I know I shouldn't *scratch them* but I do anyway and this is gonna sound *Painful* an it is ..., But I will Use *table salt* TOO help dry the things up.... (I'm alergic to benedryl) ....

OH...., I want too say I have seen worse the size of dimes and nickels.... On people who have contacted **LYME DISEASE** .... And again refered too as **auto immune system reaction**

Wengc profile image
Wengc

I have limited Ssc, I've never had this but do get random allergies that can appear anywhere, either as hives or a set of itchy bumps, I take anti histamine when these crop up. What does your doc think?

-missymoo profile image
-missymoo in reply toWengc

Hi the Wengc

So the rash got so much worse and spread across my entire body, face and eye swelling. Really nasty. My doctor believes it’s a delayed reaction to the Hydroxychlorquine I started about 3-4 weeks ago. I’ve obviously stopped these immediately and am currently day 3 into a course of steroids. I’m see Professor Denton next Friday so will get his opinions too 🙌🙌

X

Wengc profile image
Wengc in reply to-missymoo

Eek - that sounds terrible, I hope the steroids are giving you some relief. I did get an itchy rash across my fingers when I started Hydroxychloroquine but it didn't spread and lasted only about a week. Good that you're seeing Prof Denton, I'd be interested to see what he says. 😃

-missymoo profile image
-missymoo in reply toWengc

I will let you know the verdict 😊 x

tammyrae66 profile image
tammyrae66

Pustulosis psoriasis. Cured with UV light, so you can go get a tan...or buy a UV lamp.

Jevrvdisn profile image
Jevrvdisn

This is a year ago now but maybe this will help, I’ve been told my rash exactly like that was dyshidrotic eczema

Not what you're looking for?

You may also like...

Limited cutaneous systemic sclerosis and lung involvement question.

Hello to anyone reading. I just wanted to get a general feel for how many people diagnosed with...
-missymoo profile image

Butterfly rash with systemic sclerosis/Raynauds?

Hi all,I was diagnosed for sure with scleroderma (limited) and secondary Raynauds in June via nail...
san61 profile image

systemic sclerosis

hi everyone ive had raynauds for about 5years now in december last year I developed ulcers on 2...
franky1965 profile image

Limited cutaneous systemic sclerosis, secondary Raynauds and IEM versus COVID-19

Hello Reading confusing reports about this, should we who have this be self isolating? I have no...
-missymoo profile image

Systemic sclerosis

I just wanted to say that anything is achievable if you prepared to work towards it. Yes it's hard,...

Moderation team

AnnabelSRUK profile image
AnnabelSRUKAdministrator
Chicunique27 profile image
Chicunique27Administrator
SRUKadmin profile image
SRUKadminPartner

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.