Sclero’ken VZW, or in full the Belgian Association for Scleroderma, aims to involve as many people as possible in our movement.
Together, we can tackle the lack of awareness and understanding that still surrounds the rare autoimmune disease Scleroderma.
We strive to be a source of support for people living with the condition by working together and joining forces.
The activities we organize are as diverse as people with Scleroderma themselves. The proceeds from these activities are used to provide practical support and guidance to patients, as well as to fund and promote scientific research.
As Chairperson and a Scleroderma patient myself, I am incredibly proud to be able to count on a dedicated team of volunteers. Whenever things become more challenging, I know that our association is in excellent hands with our team of professionals and fellow patients.
“Nothing is impossible when we do it together.”
Are you a patient looking for connection?
Would you like to support us?
Do you have a great tip or idea to share?
We would love to hear from you.
Warm regards,
