TV Video: Hannah - Health Insurance Story. View her fight for insurance coverage for the SCOT Trial, with David Becker, ISN Assistant News Guide.
Tackle Scleroderma! Join/Shop/Donate
SCLERO.ORG by the nonprofit International Scleroderma Network (ISN) is a full-service nonprofit charitable foundation providing stellar research, support, education and awareness
Search sclero.org:

Scleroderma Newsroom
janeywillisHello, I am Janey Willis, ISN News Director and ISN Asst. Webmaster. David Becker, ISN Assistant News Guide researches our Autoimmune News section. Jeannie McClelland, ISN Assistant News Guide, researches Scleroderma Medical and Media News. Assistant News Guide Lisa Bulman posts these stories to our Sclero Forums.
Scleroderma Medical News
Autoimmune News
Media Stories
ISN Website News
Donations & In Memory
New Personal Stories
ISN Donation and Web Site News
Archives 2004: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec
2008 - 2007 - 2006 - 2005 - 2004 - 2003 - 2002
January 2004
Voices of Scleroderma Volume 1: Featured Story #13 of 100
Voices of Scleroderma Volume1 The following story is featured in the ISN's Voices of Scleroderma Volume 1 book. The book has articles by world experts in scleroderma and caregiving, including Dr. Joseph Korn, as well as true personal stories from those affected by scleroderma and related illnesses.
Gio: Progressive Systemic Scleroderma (Italy) I have been suffering from scleroderma since 1990...
Voices of Scleroderma Volume 1: Featured Story #12 of 100
Flora: Systemic Scleroderma with Bronchial Allergic Asthma (Italy) I am a young woman aged 23, and in August of this year (1999), I was admitted to Saint Anna Hospital in Ferrara and diagnosed with systemic sclerosis...
Voices of Scleroderma Volume 1: Featured Story #11 of 100
Dawn: Confirmed Early Scleroderma I am awaiting surgery for a rotator cuff injury. I now understand this might be a symptom of my scleroderma...
Voices of Scleroderma Volume 1: Featured Story #10 of 100
Bobbie Thrasher: Scleroderma I may write a book about my childhood since I am blessed to use my fingers once again...
Voices of Scleroderma Volume 1: Featured Story #9 of 100
Jonty: Son of Scleroderma Patient (Hyderabad, India) In 1997, I secured a seat in a medical college in Hyderabad and enrolled for the MBBS degree course. I then took my mother to meet Dr. Narasimhalu...
Voices of Scleroderma Volume 1: Featured Story #8 of 100
Trish: Spouse of a Diffuse Scleroderma Patient My husband was diagnosed with scleroderma in June of 2000...
Voices of Scleroderma Volume 1: Featured Story #7of 100
Michelle S: Daughter of Systemic Scleroderma Patient I am eighteen years old and my father has systemic scleroderma. He has had this disease for about two years now...
Voices of Scleroderma Volume 1: Featured Story #6 of 100
John: Surviving Son-in-Law of Scleroderma Patient My mother-in-law worked as a custodian and that may be a factor in causing her scleroderma...
Voices of Scleroderma Volume 1: Featured Story #5 of 100
Lisa A: Spouse of Systemic Scleroderma Patient My husband was diagnosed in July 2000...
Voices of Scleroderma Volume 1: Featured Story #4 of 100
Dimitra Stafilia: Daughter of Systemic Scleroderma Patient I am the ISN Greek Translator. My mum has been suffering from scleroderma since 1992...
(Greek Version) Dimitra Stafilia
New Australian Scleroderma Support Group
Scleroderma Support of Mildura, Victoria. This new Australian group is led by Rosemary Doolan. New page 1-14-04.
Voices of Scleroderma Volume 1: Featured Story #3 of 100
(Italiano) Gianna S: Sclerodermia Sono figlia di una signora a cui hanno diagnosticato la sclerodermia in un ospedale della mia città...
Gianna: Progressive Systemic Sclerosis (Italy) Hello, I am writing this story on behalf of my mother, who is not very good at using a computer...
This book has stories from 16 countries and in five languages (English, Greek, Italian, Polish, and Romanian), and all stories appear in their original language, as well as in English.
Voices of Scleroderma Volume 1: Featured Story #2 of 100
Toni: Spouse of Stem Cell Transplant Survivor Jeff is now seventeen months past his stem cell transplant and to look at him you would never know he was sick...
WintervSale in ISN Shops!

ISN Long Sleeve T-Shirt ISN Shops is holding a Winter Sale! Get $4.00 off on any order of $35.00 or more . During order checkout you must enter the code ILOVE2004 to receive the discount. This sale expires 1-16-04 , so hurry now to take advantage of this sale!

It is a great time to get an ISN long sleeve t-shirt and an ISN 2004 Floral Calendar that features the lovely artwork and photography of our ISN artists! Posted 1-8-04.

Voices of Scleroderma Volume 1: Featured Story #1 of 100
Amy: Daughter of Systemic Sclerosis Patient: What is Scleroderma? Imagine for me if you would that in certain areas of your body the skin has begun to thicken and harden...
Surf ISN Style!
ISN T Shirt Nothing is more fitting than an ISN t-shirt to wear while surfing your favorite site! Classy and well-made, your purchase will help to support the nonprofit International Scleroderma Network and helps to raise awareness of scleroderma, too! Our site visitors from around the world are sporting ISN t-shirts and hoodies. 1-03-03.
 
Go to Website News: 2003
 
SCLERO.ORG is brought to you by the nonprofit International Scleroderma Network (ISN). The ISN is a full-service nonprofit scleroderma charitable foundation providing stellar research, support, education and awareness for scleroderma and related illnesses, such as pulmonary hypertension.
  1. Post a message in Sclero Forums!
  2. Email: isn@sclero.org
  3. English Email Form
  4. Español Email Form
  5. Italiano Email Form
International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702
United States
Toll Free Hotline in U.S.
Hours: 9am-3pm CST only.
Please leave a complete message, in English.
1-800-564-7099
Direct Line
1-952-583-5735
We are also known as the Scleroderma from A to Z web site.
© Copyright 1998-2009 International Scleroderma Network
All Rights Reserved