Wellness. Support. Awareness.

Committed to enriching the quality of life of those living with scleroderma in Atlantic Canada

Support

Providing financial, emotional, motivational, educational, and social support to those living with scleroderma and their caregivers in Atlantic Canada.

Education

Providing education for patients, caregivers, health care professionals, and health care students to increase understanding and awareness of scleroderma.

Awareness

Spreading awareness and educating the public about scleroderma, a rare autoimmune disease, which has no known cause and no known cure.

Research

Supporting research and seeking funding to ensure better treatments are available for those living with scleroderma. Research is essential to finding a cure.

Advocacy

Engaging with medical professionals, government, and media to advocate for those living with scleroderma in Atlantic Canada.

What is scleroderma?

Scleroderma is a rare, progressive, and chronic autoimmune connective tissue disorder that causes excess collagen accumulation. “Sclero” means “hard” and “derma” means “skin”. But hardening skin is just one of many difficult symptoms that those living with scleroderma can experience.

Upcoming Events

Click on an event for more details.

Zoom Meetup | November 22 | 11am (ADT)
Mark your calendar and save the date for our monthly Zoom Meetup. Don’t miss out on this opportunity to connect with others, ask questions, and share your experiences. Send us an email to let us know you’d like to join.

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