Scleroderma Information This is your Project Page. It's a great opportunity to help visitors understand the context and background of your latest work. Double click on the text box to start editing your content and make sure to add all the relevant details you want to share. 01 Project Name This is your Project description. Provide a brief summary to help visitors understand the context and background of your work. Click on "Edit Text" or double click on the text box to start. 02 Project Name This is your Project description. Provide a brief summary to help visitors understand the context and background of your work. Click on "Edit Text" or double click on the text box to start. 03 Project Name This is your Project description. Provide a brief summary to help visitors understand the context and background of your work. Click on "Edit Text" or double click on the text box to start. 04 Project Name This is your Project description. Provide a brief summary to help visitors understand the context and background of your work. Click on "Edit Text" or double click on the text box to start.

My Scleroderma Story My Scleroderma Story Scleroderma Society of Ontario launched "My Scleroderma Story" in June 2022 to support our largest fundraising campaign of the year, Make a Move for Scleroderma. We were thrilled to see how much momentum the trend carried and the support we received from our community. By sharing scleroderma stories, we can amplify awareness and knowledge of the disease growing our community of supporters, one scleroderma champion at a time! You can share your scleroderma story, even if you don't live with scleroderma yourself. For example, you could be... A friend or family member supporting someone who lives with scleroderma A doctor who supports patients who live with scleroderma, or a doctor that is/has researched scleroderma An individual and/or volunteer who is passionate about supporting and spreading awareness for scleroderma Anything! Ready to share your story? Submit your story through this form . Email us at info@scleroderma.ca to learn more. #MySclerodermaStory shared by SSO Board Member, Silvia Petrozza.

About Us 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. Patient Support Research Advocacy Awareness 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. Mission The Scleroderma Society of Ontario is committed to promoting increased public awareness, advancing patient wellness, and supporting research efforts to discover treatment options. Vision Improved quality of life for scleroderma patients and their families through education, support, research and increased public awareness. Contact Us We'd love to hear from you! You can reach us via email, telephone, or on social media. Email: info@scleroderma.ca Telephone: (905) 544-0343 Follow us on social media!

Explore our services and get in touch Our Services Nothing to book right now. Check back soon.