The National Scleroderma Foundation’s mission is to advance medical research, promote disease awareness, and provide support and education to people with scleroderma, their families and support networks. Our vision is to be a relentless force in finding a cure and improving the lives of people affected by scleroderma.

Mary J Wheatley - Chief Executive Officer (CEO) Send email

Aligned PRO Users:
Alice Alvarez [[email protected]]
Online and Virtual Assistance

Connect with Others on a Similar Journey

As support is one of the main pillars of the National Scleroderma Foundation’s mission, we are happy to share that there are more than 100 Foundation-affiliated Scleroderma support groups around the US. Our support group leaders are trained volunteers committed to creating safe, welcoming, and inclusive environments where all can share their journey with scleroderma.

Click here for a list of support groups

Free

Dates & time vary with each group
Updated within the last 5 months.

The National Scleroderma Foundation’s mission is to advance medical research, promote disease awareness, and provide support and education to people with scleroderma, their families and support networks. Our vision is to be a relentless force in finding a cure and improving the lives of people affected by scleroderma.

Click here for more information.

Updated within the last 5 months.