Scleroderma Webmaster's Association (SWA)
Scleroderma Sites to Surf!

April 1998 — April 2015

First meeting photo

A step back in time! First meeting of the SWA in 1999.

The Scleroderma Webmaster's Association (SWA) encouraged the worldwide development and recognition of high-quality medical information and support resources for scleroderma.

It was founded by Shelley Ensz, and operated by the non profit International Scleroderma Network from 2002 to 2015.

Now that ample quality resources for scleroderma are available, we have switched to simply linking to such sites within

Original SWA member sites that are still in existence remain listed here, in everlasting gratitude for their service to us all.

SWA Main Page
Site Descriptions A-H
Site Descriptions I-R
Site Descriptions S-Z

U.S. Support Groups
Worldwide Support Groups

Scleroderma Sites to Surf (Main Listings) Site by Carol Eustice

(Español/Spanish) Asociación Colombiana de Esclerodermia. Francisco Castellanos.

International Scleroderma Network by Shelley Ensz

Irish Raynaud's & Scleroderma Society by Sheila Miley

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

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 (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

Go to Website Descriptions - A-H

SCLERO.ORG is the world's leading portal for reliable scleroderma information and support. It is a program of the International Scleroderma Network (ISN). The ISN is a 501(c)(3) public charitable foundation providing stellar worldwide research, support, education and awareness for scleroderma and related illnesses, such as pulmonary hypertension. ISN Team Profiles and Volunteer Info.

International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702 USA

Ask for our Welcoming Email
Toll Free US/Canada Scleroderma Hotline
(800) 564-7099
Sclero Forums Online Support, Chats, Blogs and Videos

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Copyright 1998-2015, International Scleroderma Network. AKA Scleroderma from A to Z and SCLERO.ORG. All Rights Reserved.