Children with Cockayne syndrome – type B (CSB) need special care and support, but there is no cure yet. That’s why we are asking for your donation today. Your generous contribution will help fund research and treatment for this devastating disease. You can make a difference in the lives of these children and their families. Please donate now and show them that you care.

Please contact us at if you prefer to donate offline.

Donation directly to our bank account:

Account: IBAN SI56 0400 0027 7357 570
Organisation: Viljem Julijan Association for Children with Rare Diseases, Cesta Leona Dobrotinška 2, 3230 Šentjur, Slovenia, EU