Wellness. Support. Awareness.
Committed to enriching the lives of those living with scleroderma
in Atlantic Canada
Providing financial, emotional, motivational, educational, and social support to those living with scleroderma and their caregivers in Atlantic Canada.
Spreading awareness and educating the public about scleroderma, a rare autoimmune disease, which has no known cause and no known cure.
Engaging with medical professionals, government, and media to advocate for the those living with scleroderma in Atlantic Canada.
Providing education for patients, caregivers, health care professionals, and health care students to increase understanding and awareness of scleroderma.
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.
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Join Us To Make A Difference in The Lives of Those Living with Scleroderma
Atlantic Canadians are going to MAKE A MOVE FOR SCLERODERMA. This year, we are hosting both Virtual and In-Person Walk Run in the Park Events starting on May 2nd and ending on June 30th.
To join the Zoom Meetup email us ▶️[email protected]
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