The Scleroderma Society of Ontario (SSO) is a registered charity dedicated to supporting people affected by scleroderma. Since 2007, SSO has focused on four core pillars: patient support, research, advocacy, and awareness. Through peer-to-peer groups, funding for treatment research, and awareness campaigns, SSO empowers the scleroderma community across Ontario. Their mission is to improve lives through education, support, and discovery of new treatment options.