World Scleroderma Day 2021

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!

I am my passion not my disease!
Scleroderma and COVID-19 will not take my smile!


June 29th is World Scleroderma Day.

Scleroderma is a rare chronic autoimmune rheumatic disease that affects the body by hardening connective tissue. Skin and internal organs can be damaged by this illness. It can be life threatening and currently there is no cure. However, successful treatments are available for individual organs.

Join our community. You are not alone.

Find out more and help us spread the word.

Again as last years we invite you to share your smiles using the hashtag #sclerosmile on social medias such as Instagram, Facebook and Twitter.We also invite you to help us with spreading the campaign by using #iammypassion

The Federation of European Scleroderma Associations (FESCA aisbl.) is an umbrella support and advocacy organisation composed of the national scleroderma associations of 20 European countries.

Download posters and handouts for distribution

(Please note, that more posters will be available as the campagin continues.)


What is Scleroderma?

Scleroderma researchScleroderma 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.

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