Contact Us

The National Scleroderma Foundation is the leading national patient advocacy organization serving people affected by scleroderma. Whether you’re newly diagnosed with scleroderma, a loved one helping support someone living with scleroderma, a researcher or healthcare provider leading the charge for better understanding and patient care outcomes, or a donor ready to help put the Foundation’s mission into motion, the Foundation is here and ready to support you.

Don’t know where to start? Call our free HOPE Line using the number below or email us at info@scleroderma.org to connect with a Foundation team member who is ready to help.

General Information

If you’re looking for information about specific Foundation resources, programs, or services, please use the staff directory below to find the best point of contact. Click on a team member’s photo to view their area of expertise and access their email link.

The National Scleroderma Foundation Team