About UsASPRDA
Association for the Support of the Patients with Rare Diseases in Albania
was established in Albania in 2024 with the main scope of supporting children with genetic diseases diagnosed as rare disorders and their families in therapeutic and medicinal treatment.
In cooperation with other sister associations, our association seeks to achieve its goal legally and ethically, preserving the principles and rules of the health system and the relevant institutions.
Association for the Support of the Patients with Rare Diseases
ACTIVITYUpcoming Activity
On February 28, 2025
we will arrange a workshop meeting involving specialized healthcare professionals (HCPs), patients and their families, as well as decision-makers from the Albanian Ministry of Health.
