Donation
Donate for children with Cockayne syndrome type B
Children with Cockayne syndrome type B (CSB) need special care and support, but there is no cure yet. Your donation funds the research that can change that.
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 helps fund research and development of gene therapy 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 csb@viljem-julijan.si if you prefer to donate offline, or if you are a company or foundation that would like to support the project.
Bank transfer
Donations from anywhere in the world. Please state “Cockayne syndrome” as the payment reference.
- IBAN
- SI56 0400 0027 7357 570
- SWIFT / BIC
- KBMASI2X
- Beneficiary
- Viljem Julijan Association for Children with Rare Diseases, Cesta Leona Dobrotinška 2, 3230 Šentjur, Slovenia, EU
Where your donation goes
Funds raised through this campaign support the research and development of gene therapy for Cockayne syndrome type B carried out by our partner research groups in the USA and Portugal. The campaign is run by the Viljem Julijan Association for Children with Rare Diseases, a registered non-profit in Slovenia, EU.