Scleroderma will not take my smile

May 13, 2017 | Scleroderma Day

Scleroderma will not take my smile

World Scleroderma Day 2017

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 turns simple daily activities into real challenges. It is life-threatening and currently has no cure. But patient organisations are fighting back. Join us as we spread awareness and support research. We refuse to lose our smiles!

World Scleroderma Day

Also known as Systemic Sclerosis, scleroderma is a chronic disease of the connective tissue, immune and vascular systems, and presents a major diagnostic and management problem for patients and their physicians. Despite this, the past two years have witnessed important improvements in therapies and care. Early diagnosis is essential, and the first symptom is nearly always Raynaud’s.
Help us to keep smiling by donating to research!

The Federation of European Scleroderma Associations aisbl. (FESCA) is a focal umbrella support and advocacy organisation composed of the national scleroderma associations of 19 EU countries.

The Federation of European
Scleroderma Associations aisbl.

FESCA news & eventsnews & events

This is Living!

This is Living!

FESCA is proud to be a partner of a the new This is Living campaign launched last month by Boehringer Ingelheim.

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