World Scleroderma Day 2018
Scleroderma is a rare autoimmune disease that stiffens the skin, turning simple daily activities into real challenges. It can affect all organs in addition to the skin, and while treatments exist, there is currently no cure. More research is urgently needed. Help us to keep smiling by donating to research!
Scleroderma will not take my smile
We invite you from all over the world to post a picture/video with smiles on social medias like twitter, facebook, instagram etc with the hashtag #ScleroSmile
Scleroderma is a rare autoimmune disease that stiffens the skin, turning simple daily activities into real challenges. It can affect all organs in addition to the skin, and while treatments exist, there is currently no cure. More research is urgently needed.
Also known as Systemic Sclerosis, scleroderma is a chronic disease of the connective tissue, immune and vascular systems, and presents a major management problem for patients and their doctors. Early diagnosis is essential. New research has brought important improvements in therapies and care, so please join patient organisations and families as they spread awareness and support research.
Help us to keep smiling by donating to research!
DOWNLOAD
Download posters and handouts for distribution:
World Scleroderma Day 2018 A3 Poster
World Scleroderma Day 2018 Roll up
World Scleroderma Day 2018 A5 Handout
What is Scleroderma?
Scleroderma is a chronic disease characterized by excessive deposits of collagen in the skin or other organs. The localized type of the disease, while disabling, tends not to be fatal.
Diffuse scleroderma or systemic sclerosis, the generalized type of the disease, can be fatal as a result of heart, kidney, lung or intestinal damage.