Scleroderma Sites to Surf!
The Scleroderma Webmaster's Association is a free service of the nonprofit International Scleroderma Network. We all work together to make it easy to find scleroderma resources worldwide!
Scleroderma Sites to Surf! (Main Page)
—Site Descriptions A-H
—Site Descriptions I-R
—Site Descriptions S-Z
International Support Groups
United States Support Groups		 For Scleroderma Webmasters:
—Invitation for Webmasters
—Apply for SWA Membership
—Instructions, Logo & Listing
—Awareness Banners
—April, May, June
About.com/Arthritis Site by Carol Eustice
(Español/Spanish) Asociación Colombiana de Esclerodermia. Francisco Castellanos.
Bunny's Place by Bunny Gardner
Doris Reichard's Internet Haven by Doris Reichard
International Scleroderma Network by Shelley Ensz
Irish Raynaud's & Scleroderma Society by Sheila Miley
I Survived Scleroderma by Kirstin Wallin
Juvenile Scleroderma by Dr. Thomas Lehman
Juvenile Scleroderma by ISN
Mare's Home Page by Marion Pacy
Psychosocial Aspects of Systemic Sclerosis by Dr. Vanessa Malcarne
Pulmonary Hypertension Registry of Scleroderma (PHAROS)
The Rombergs Connection by Marilyn Neal
Roseewriter.com by Judith Devlin
Go to Roseewriter.com Sclero Forums, Chats, Blogs and Videos by International Scleroderma Network
Scleroderma and Life Insurance by Steven H. Kobrin, LUTCF
Scleroderma FAQ by Ed Harris
Scleroderma Friends and Family by Diane G.
SCLERO.ORG by International Scleroderma Network
Scleroderma Family Registry and DNA Repository by Dr. Maureen Mayes on ISN
Scleroderma Meets Sjögren's by Natasha Lubin
Scleroderma Society by Kim Fligelstone
Scleroderma (Systemic Sclerosis) by Dr. Debabrata Bandyopadhyay
SCOT: Cyclophosphamide or Transplantation by NIH/NIAID
SD World in memory of Judy Tarro
Sjögren's Syndrome by Lynne Messina
Thanks to Judy Tarro!
SD World Email ListSpecial thanks, in memory of Judy Tarro of SD World for her SWA site design assistance.
 
Go to Website Descriptions - A-H
 
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.
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