New to group: Hi all, Was diagnosed... - Scleroderma & Ray...

Scleroderma & Raynaud's UK (SRUK)

11,131 members5,646 posts

New to group

Stevenorthernsoul profile image

Hi all, Was diagnosed with limited a couple of years ago and straight after things seem to calm down. In the last couple of months the skin around my mouth\chin has thickened and I'm developing deep lines, which is making me very down Also, my nails have become almost chalk like. Not really sure what to do or where to go from here. I'm thinking of trying Intracell treatment and would welcome any thoughts on this

Written by
Stevenorthernsoul profile image
Stevenorthernsoul
To view profiles and participate in discussions please or .
4 Replies
Bagpuss1972 profile image
Bagpuss1972

Hello stevenorthernsoul, Sorry I can't really advise as I've only recently been diagnosed with systemic sclerosis myself but am personally experiencing thickening of skin on my feet which is causing me a lot of pain and difficult walking. Completely understand about feeling down due changes in our body from this condition. Stay positive and take care.

Stevenorthernsoul profile image
Stevenorthernsoul in reply toBagpuss1972

Thank you for you're reply am sorry to hear about the problems you are having. It is difficult to stay positive when my mouth and chin are starting to resemble that of someone 40 years older, but I suppose we all have to live with this condition as best we can. Take care

zenabb profile image
zenabb

I have those lines and I think that they are caused by the excess of , sorry I can't remember the word. But some people who want to look more beautiful inject themselves with Botox.

LucyJean profile image
LucyJean

Hello there Steven, sorry to hear how things are at the moment. Can you say a little bit more about what this Intracell is? Is this something your Rheumatologist is prescribing for you to help with the skin fibrosis around your mouth? I think if your symptoms seem to suddenly be accelerating, or changing then, if you haven't already done so you need to contact your Rheumatologist and /or GP to discuss this. Flare ups can take many forms but you need to see if you can nip them in the bud. Are you on any immunosuppression? All my best Lucy

Not what you're looking for?

You may also like...

New to the group

Hi I was diagnosed with diffuse systemic sclerosis earlier this month. I was informed by a 5 minute...
Rebecca99 profile image

New to all this and looking for some guidance from those with more experience

I'm a previously fit and healthy man of 58 and have gone from a sore knee, then a swollen calf less...
scjh profile image

New To Scleroderma

Hello, I have been to 3 different dermatologist and they have done byopcies. Finally got a...
Rosamylio profile image

New to all of this,,

Hi all,, I'm new to all of this was diagnosed nearly 4 years ago with scleroderma and Raynaud's but...
kel87 profile image

new to the group with a query

Hi everyone, I have had Raynaud for a 4-5 years both in the hands and feet. This year it is...
itexpat profile image

Moderation team

See all
JillWillSRUK profile image
JillWillSRUKAdministrator
AnnabelSRUK profile image
AnnabelSRUKAdministrator
Chicunique27 profile image
Chicunique27Administrator

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.