Scleroderma/Lupus Support Society, Inc. of Newcastle, New South Wales
Most people with Scleroderma and Lupus have experienced feelings of loneliness and sometimes despair while undergoing numerous tests over a lengthy period. To finally arrive at a diagnosis brings relief but also fears for the future. The benefits of mutual support have greatly improved our quality of life, and we invite you to join us.
Autoimmune Resource and Research Centre
For scleroderma support group meeting information in Newcastle, please visit our website, at: HAPS Scleroderma/Lupus Support Group.
HAPS website down, changed to Autoimmune Resource and Research Center. 04-24-13. SLE.
Group contact information updated 11-19-10 per Robyn Sims. SLE.
See ISN News
for recent donors, including memorials for
Patricia Ann Black, Gayle Hedlin, Janet Paulmenn and Lilian Stiles.
SCLERO.ORG is the world leader for trustworthy research, support, education and awareness for scleroderma and related illnesses, such as pulmonary hypertension. We are a service of the nonprofit International Scleroderma Network (ISN), which is a 501(c)(3) U.S.-based public charitable foundation, established in 2002. Meet Our Team, or Volunteer. Donations may also be mailed to:
International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702 USA
Email firstname.lastname@example.org to request our Welcome email, or to report bad links or to update this page content.
TOLL FREE HOTLINE 800-564-7099
Free to U.S. and Canadian Callers. Ask for our Free Info Packet by mail or email!
Scleroderma, Pulmonary Arterial Hypertension, and related illnesses.
The most important thing in the world to know about scleroderma is sclero.org!