Scleroderma Hotline and Email Support Specialists are eager to help people affected by scleroderma and related illnesses, such as pulmonary hypertension. Simply email [email protected] or call our Hotline at 1-800-564-7099. Ask for your free information packet! Posted 09/26/2017.
Sclero Forums offers stellar online support, with forums, chats, and blogs for people who are interested in scleroderma. It is a free service of SCLERO.ORG, by the nonprofit International Scleroderma Network. Posted 09/23/2017.
The International Scleroderma Network thanks Genentech for their sponsorship support! Posted 09/21/2017.
The International Scleroderma Network thanks Gilead for their sponsorship support! Posted 09/14/2017
Would you like to help scientists find a cure for scleroderma? Dozens of clinical trials for scleroderma and pulmonary hypertension are actively recruiting now. Review them and be sure to ask your scleroderma expert about the ones you are interested in. (Also see Current Clinical Trials and Scleroderma Experts) Posted 09/09/2017.
Did you know you can help raise scleroderma awareness? The nonprofit International Scleroderma Network offers scleroderma awareness bracelets! Bracelets for just $2.50 each with free shipping and handling! They say "scleroderma" on one side and "sclero.org" on the other. (Also see Get Scleroderma Awareness Bracelets) Posted 09/07/2017.
The International Scleroderma Network thanks United Therapeutics for their sponsorship support! Posted 09/06/2017.
In loving memory of Arlene Marie Petulla, a donation has been made by Robert Polk to the nonprofit International Scleroderma Network. (Also see Sclero Shop/Donate) Posted 09/05/2017.
Shop at AmazonSmile and Amazon will make a donation to the nonprofit International Scleroderma Network! Posted 09/04/2017.
The International Scleroderma Network thanks Actelion Pharmaceuticals US, Inc. for their sponsorship support! Posted 09/02/2017.
SCLERO.ORG was the world's leading nonprofit for trustworthy research, support, education and awareness for scleroderma and related illnesses from 1998 to 2021. It was a grassroots movement from the original Scleroderma from A to Z web site, which was founded by Shelley Ensz. We were a 501(c)(3) U.S.-based public charitable foundation. We closed this web site and our nonprofit agency in April 2021.