The Marigold Foundation is the pioneer in Malta in raising the voice of patients with a rare disease or condition. In 2016, it founded the first ever National Alliance for Rare Diseases Support – Malta (RDM) bringing together patients, doctors, researchers, carers and pharmaceutical entities. Through this movement it was possible for Malta to raise the issue to European level during Malta’s Presidency in the Council of Europe in 2017 thus putting forward the issue on a European and International level. Currently RDM is full member of EURORDIS and full member of Rare Diseases International. Through the latter platform, RDM was chosen to form part of the ECOSOC Committee on Rare Diseases at the United Nations which in the December 2021 has successfully pushed forward the Agenda of Rare Diseases for a UN Resolution that will see that rare diseases are given the attention they deserve with the aim of reaching the sustainable development goals by 2030. RDM Malta through its Co-Founder, The Marigold Foundation, will continue to advocate worldwide and also on a National basis so that Maltese rare disease patients are given the necessary attention and services through the setting up of a National Action Plan. With regards to its members RDM and Marigold collaborate on a regular basis to provide patient members with psychological support, communal networking and access to clinical trials, access to medicinals and services, and to serve as their voice.
Our Chairperson has served as Patron of Eurordis for the last ten years and continues to engage personally on a one to one basis with patients.








