Who We Are
Scleroderma Society of Ontario (SSO) is committed to promoting increased public awareness, advancing patient wellness and supporting research in Ontario's scleroderma community. SSO is a registered charity and was established in 2007 with one main priority: support people with scleroderma in their quest for information, community connection, advice, and yes, a cure!
Our Core Pillars
Since being established as a registered charity, SSO has developed and committed to four core pillars which help guides our mission, vision, and our everyday work.
Using our Core Pillars as a guiding measure, SSO will work towards:
1. Developing continuous resources for patients and facilitating patient-centred peer-to-peer support groups.
2. Facilitating and granting funding requests for external research geared towards scleroderma treatment.
3. Increasing awareness of scleroderma through annual campaigns and fundraising events across Ontario.
The Scleroderma Society of Ontario is committed to promoting increased public awareness, advancing patient wellness, and supporting research efforts to discover treatment options.
Improved quality of life for scleroderma patients and their families through education, support, research and increased public awareness.
We'd love to hear from you! You can reach us via email, telephone, or on social media.
Telephone: (905) 544-0343
Follow us on social media!