Thank you for joining the National Scleroderma Foundation on Feb. 29, to call attention to rare diseases, for Rare Disease Day....
The 2023 National Scleroderma Conference and Kids Get Scleroderma, Too! scholarship application is now available! Download the form and email it....
Amazon will be discontinuing its AmazonSmile program on February 20, 2023. Here are 3 ways you can continue your impact.
In observance of the Presidents Day, the National Scleroderma Foundation’s national office will be closed Monday, Feb. 20. We look forward...
CEO Mary J. Wheatley shares a message reflecting on the 25 years of support the National Scleroderma Foundation has provided to...
The National Scleroderma Foundation encourages appropriate vaccines and treatments to protect individuals within the scleroderma community from the serious complications that...
Eight new and established researchers receive grant awards DANVERS, MASSACHUSETTS – On Thursday, Feb. 2, the National Scleroderma Foundation announced its...
We are grateful to our partner HealthWell Foundation for launching a new Patient Assistance Program for SSc-ILD! Learn more at HealthWell’s...
Our 2022 Annual Report is now available on our website! This report serves as a summary of the Foundation’s activities over...
