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Biomarker for Diffuse Scleroderma skin has been discovered!


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#1 Hazel

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Posted 11 July 2010 - 04:23 AM

Hello all, I am new to this forum, I have Scleroderma Morphea and have had it for 47years. Just wanted to say Hi, I am now going to trawl my way through alot of this forum and other things on the Scleroderma site.

#2 janey

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Posted 11 July 2010 - 05:55 AM

Hazel,
Welcome to the Sclero Forums. I love that you found us and are headed to doing some trawling! If you are looking for something specific, be sure to use the search function. It does a great job is helping you navigate this site. We have over 1500 pages, so it's a lot to navigate, but well worth the time. Let us know if you can't find something specific and we'll get you there.

Hope to learn more about you in future posts.
Janey Willis
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International Scleroderma Network (ISN)

#3 Amanda Thorpe

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Posted 11 July 2010 - 06:33 AM

Hello Hazel

Welcome to the forums! I have diffuse systemic sclerosis as well as morphea and bullous morphea, very rare you know, clearly I'm greedy! :lol:

Take care and keep posting.
Amanda Thorpe
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#4 Jeannie McClelland

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Posted 11 July 2010 - 10:49 AM

Hi Hazel,

Welcome to the Forum! Have fun with your trawl. There's loads of interesting things. I hope to see you around here often.

Best wishes,
Jeannie McClelland
(Retired) ISN Director of Support Services
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International Scleroderma Network

#5 Shelley Ensz

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Posted 12 July 2010 - 07:35 AM

Hello Hazel,

Welcome to Sclero Forums! With all your many years of experience with morphea, I hope you stay involved especially to help newcomers with morphea.
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.

#6 Sweet

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Posted 12 July 2010 - 09:08 AM

Hi Hazel!

Welcome to the forums. I look forward to knowing more about you. :flowers:
Warm and gentle hugs,

Pamela
ISN Support Specialist
International Scleroderma Network (ISN)