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Sclerodermia... my morphea story

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#1 Babi



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Posted 09 March 2008 - 11:16 AM

I'm a 27years old italian girl. I hope my English will good for this topic.
Last year it has been diagnosed me a "sclerodermia" --> morphea.

I met doctors that told me to make a cure made of cortison and other doctor that thought was null to make, therefore as the disease has arrived to me it had to go to pass. 4 months ago my family doctor prescribe me one box of antihistaminics.. one a day before go to sleep.

I had a thickened brown layer of derma on my belly 15x4 cm.. I took 20 tablets of the antihistamine and the thickness is disappeared! It remain only the skin a little brown.. but with a little bit of cortison cream and hydrating cream, my belly now is nearly like how it was first of the disease.

I don't know if I'm completly recovered.. maybe next year I discover the morphea in other part of my body. Is there somebody that try with the antihistaminics?

In this year I made 2 times the blood test but every time I was negativ to the anticops Ana, Ena, C+ etc...

I wait your reply.. thanks to read me.

Bye!! Barbara

#2 Shelley Ensz

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Posted 10 March 2008 - 08:44 AM

Hi Barbara,

I'm glad you've joined Sclero Forums. I'm sorry you have morphea, but happy that your treatment has seemed to improve it so far.

As it happens, morphea often improves or goes away within the first five years of onset, even without any treatment at all. However antihistamines are frequently prescribed to help reduce inflammation, itching, and swelling associated with many skin diseases. My guess is that it hasn't "cured" you but has really helped.

And just by the passage of time, you may even see more improvements, although it may not ever clear up entirely. There's just no telling for sure, as the course of the disease is different in everyone.

For more information on Morphea and morphea treatments, please see our main site at:

Warm Hugs,

Shelley Ensz
Founder and President
International Scleroderma Network (ISN)
Hotline and Donations: 1-800-564-7099

The most important thing in the world to know about scleroderma is sclero.org.

#3 Sweet


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Posted 10 March 2008 - 08:49 AM

Hi Barb,

Welcome to the Sclero Forums. I'm so happy to hear that at this time you are not having any problems with your Sclero.

Looking foward to knowing you better.
Warm and gentle hugs,

ISN Support Specialist
International Scleroderma Network (ISN)

#4 Guest_SADIE_*

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Posted 10 March 2008 - 10:05 AM

Barb, Welcome!! I'm a newbie too. This is a great place! Glad to hear that you are doing well! I have Diffuse SD. I've had it 18 years now. Wish I could answer your question.
Take care,
Sadie :)

#5 jefa


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Posted 10 March 2008 - 11:20 AM

Hi, Barbara. So glad you found us. Shelley has given some excellent advice. Please feel free to ask anything else that may concern you. I look forward to reading more of your posts.
Warm wishes,

Carrie Maddoux
(Retired)ISN Sclero Forums Support Specialist
(Retired)ISN Sclero Forums UK Chat Host

International Scleroderma Network (ISN)

#6 Babi



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Posted 12 March 2008 - 08:20 AM

oh... friends!! I'm really happy to read our reply!
also because I never meet somebody that have my (our) problem...
so, in this website, I'm not feel alone.. it's not a good thing because it means that therse a lot of people with SD, but fight in group is better that fight alone...
Now my morphea seems desappeared... but if it would like to come back I will made a tour in this forum.. it's sure!
An embrace... Barbara