During the annual conference dedicated to individuals living with rare diseases and conditions, the Minister for Health and Active Ageing, Jo Etienne Abela, announced that the Ministry has developed the first National Strategy for Rare Diseases, which will soon be launched for public consultation.

In his address, Minister Jo Etienne Abela confirmed the government's commitment to those living with rare diseases, emphasizing the importance of cross-border healthcare as a means to improve diagnosis, treatment, and quality of life. He noted that while each rare disease affects a small number of people, collectively these conditions impact approximately 30,000 people in Malta. This represents thousands of families facing real challenges and uncertainty every day.

He explained that 80% of rare conditions are genetic in nature and often require highly specialized care and expertise. Since not every service can be available locally, cross-border healthcare is not just an option but an essential part of the commitment to leave no one behind.

The Minister highlighted Malta's role in European Reference Networks (ERNs), through which Maltese clinicians can consult with leading experts in Europe on complex cases. Through these networks, the best expertise is brought to Malta without the patient always needing to travel.

He also referred to digital eHealth services, including the exchange of patient summaries and electronic prescriptions, which strengthen the continuity of care outside of Malta. He noted that while European cooperation is crucial, the government continues to invest in national capacity, early diagnosis, professional training, and research.

Our vision is clear: that rare diseases no longer mean rare care or rare hope. We will continue working to build a healthcare system that places the patient at the center, with dignity and compassion, Minister Abela concluded.