The Scleroderma Education Project is registered in the United States as a 501(c)(3) tax-exempt organization. If you are financially able to do so, please consider making a donation to help us to expand our educational, patient advocacy, and research activities. (See the About page for more information on our Mission.) 100% of all donations go to supporting these goals – not for administrative salaries.
Spread the Word
If you belong to a local, regional, or national Scleroderma support group or organization, tell the leaders of the group about the site and urge them to notify all of the chapter members, both by email and by adding it to the next newsletter or announcing it at the next meeting. Also, if the group has a website, ask them to put in a link to the Scleroderma Education Project website: SclerodermaInfo.org. Here is some suggested descriptive text for the newsletter or website link:
The Scleroderma Education Project website is a comprehensive, up-to-date, unbiased, and research-based source of information for scleroderma patients and their providers. While the website thoroughly discusses all aspects of scleroderma diagnosis and treatment, everything on the website is written in a language that is easy for patients and their families to understand.