Nina Foundation

The Nina Foundation is a charitable organisation focused on Angelman syndrome, a rare genetic condition. Its two main goals are to fund research into the syndrome and to share available knowledge with families, professionals and researchers. The foundation supports projects addressing treatment, diagnosis, communication, sleep and the cognitive challenges associated with Angelman syndrome. Its past initiatives have included testing medicines, investigating whether the condition may be reversible, exploring stem-cell research to reactivate UBE3A, and developing support for children and their families.

The foundation also highlights the Angelman Syndrome Clinic, described on its website as the world’s first expertise centre for the condition, where more than 100 children, young people and adults had received care. It provides information for parents about treatment and connects visitors with scientific articles, laboratory updates and organisational resources. Supporters can contribute through donations, partnerships or volunteering, with options for both individuals and businesses. Through research funding, knowledge-sharing and practical projects, the Nina Foundation works to improve understanding and support for people affected by Angelman syndrome.