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During the annual conference dedicated to people living with rare conditions and diseases, the Minister for Health and Active Ageing, Jo Etienne Abela announced that the Ministry has worked on the first National Strategy for Rare Diseases which will soon be launched for public consultation.
Minister Jo Etienne Abela confirmed the Government’s commitment to people living with rare diseases, while emphasising the importance of cross-border healthcare as a means of improving diagnosis, care and quality of life. “While each rare disease affects a small number of people, together these conditions affect around 30,000 people in Malta. This means thousands of families who face uncertainty and real challenges every day,” said Minister Abela.
He explained that 80% of rare conditions are genetic in nature and often require highly specialised care and expertise. “Not every service can be available locally. Therefore, cross-border healthcare is not just an option but an essential part of our commitment to leaving no one behind,” reiterated Dr Abela.
The Minister highlighted Malta’s role in the European Reference Networks (ERNs), through which Maltese clinicians can consult with leading experts in Europe on complex cases. “Through these networks, we are bringing the best expertise to Malta, without always having to travel for the patient.”
He also referred to the digital eHealth services, including the exchange of patient summaries and electronic prescriptions, which enhance the continuity of care abroad. He said that European cooperation is crucial, but at the same time the Government is continuing to invest in national capacity, in early diagnosis, in the training of professionals, as well as in research. “Our vision is clear, that rare diseases no longer mean rare treatment or rare hope. We will continue to work to build a health system that places the patient at the center, with dignity and compassion,” concluded Minister Abela.
