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Scleroderma Newsroom
Janey Willis, ISN News GuideHello, I am Janey Willis, ISN News Manager and ISN Asst. Webmaster. David Becker, ISN Assistant News Guide researches our Autoimmune News section. Assistant News Guides Lisa Bulman and Judy Tarro post these stories to our Sclero Forums. Stephen Dickson prepares our RSS Newsfeed.
Scleroderma Medical News
Autoimmune News
Media Stories
ISN Website News
Donations & In Memory
New Personal Stories
October 2008 ISN Donation and Website News
Archives 2008: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov
2008 - 2007 - 2006 - 2005 - 2004 - 2003 - 2002
Venezuela Revista: Esclerodermia y Algo Mas (FLASH Document) —Gratis!

Revista: Escleroderma y Algo Mas(Español/Spanish) En la Grupo de Apoyo de Venezuela contra la Esclerodermia: Revista:Esclerodermia y Algo Mas (FLASH Document) —Gratis! Esta es una publicación en español, 41 paginas.

(English) The Scleroderma Support Group of Venezuela (which is an affiliate of the ISN) has published a 41-page online FLASH magazine, in Spanish, Escleroderma y Algo Mas, which is free! Posted 10-29-08.

Tackling Scleroderma!
Tackling scleroderma through donations, memberships, books, brochures and awareness bracelets:
Shop/Donate
Running for SCLERO.ORG!
I'm running for those who can't, SCLERO.ORG
Running for SCLERO.ORG: Sponsor Earl Manns in Chicago Marathon, October 12, 2008! I'm running in honor of my daughter Mya, and in memory of Sherrill Knaggs. (Also see Donate Now, Earl Manns, and Sherrill Knaggs ) Reposted 10/01/08.
Scleroderma Can Koozies Now Available!
Scleroderma KooziesScleroderma Can Koozies! Keep your hands warm with cold pop cans, $2.50 each, minimum order of 4 ($10), please. Reposted 10/01/08.
In Loving Memory of Maxine Gail Mackler
The nonprofit International Scleroderma Network thanks Gerald Mackler for his donation in loving memory of Maxine Gail Mackler. Posted 09/15/08.
New Personal Stories
Alana: Scleroderma (Peru) I cannot open my mouth completely, I have lost strength in my hands, I have breathing problems, my face looks different, my skin is really tight and I have lost my appetite...
(Español/Spanish) Alana: Paciente Nuevo con Esclerodermia (Peru) Le dije que ya no podía abrir la boca completamente, he perdido la fuerza de las manos, tengo problemas respiratorios, mi rosto está diferente, mi piel está dura y he perdido casi el apetito...
Kristy C: Generalized Morphea The only place where I do not have any morphea is my face, which I am very thankful for...
(Update) Raymond: Surviving Son of Scleroderma Patient On October 19th, the Herbert family lost another member of the family to scleroderma. My uncle Edmond has passed on...
Sharon H: Scleroderma/Morphea It has been thirty-two years living with this and it has progressively gotten much worse and has spread...
Teena: En Coup De Sabre My mother and I went to Johns Hopkins Hospital. They did what was called 'Grand Rounds' where about fifty doctors were looking at me taking pictures and videotaping me...
More New Stories: November 2008
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Go to ISN News: September 2008
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International Scleroderma Network (ISN)
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