The Scleroderma Patient-centered Intervention Network (SPIN) is taking another step towards fulfilling its mission of supporting people living with scleroderma from around! SPIN is thrilled to announce the launch of the SPIN-SHARE platform, through which toolkits will be released publicly after being tested through the SPIN Cohort.


To have access to SPIN online toolkits, login or register at: SPIN Cohort users can login directly and public users will need to register first, in 4 easy steps.

Check out our NEW resource page. It is common to feel overwhelmed when first diagnosed with scleroderma. A typical result to a new diagnosis or to new and frightening symptoms is to seek information online. We've also included our quarterly newsletter in the readings section for you to see what's happening at SSO.

If you would like to extend your support to the SSO by making a lasting impact, there are several monthly or one-time donation options to choose from.

To donate, go to 

or call 1-888-776-7776.

Where and how do you find information about eating well with scleroderma?


SPIN is looking for people with scleroderma to participate in an online focus group about their experiences with trying to find information about diet and nutrition.  Please click the button below to register. 


SSO Swim-a-Thon
June is Scleroderma Awareness Month so Charlotte organized a swim-a-thon on June 27 with a few family members. Please donate by July 3rd, 2020. Thank you!
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41 King William St., Suite 202
Hamilton, Ontario L8R 1A2 |  1-888-776-7776

©2020 Scleroderma Society of Ontario