The Association primarily aims at:

• the protection of the rights and improvement of the quality of life of the thalassemics through the systematic intervention and pressure exerted on the state and other responsible authorities.
• the encouragement of any kind of effort to develop the institution of voluntary blood donation and to awaken the public opinion on matter of blood donation.
• the education proficiency and rehabilitation of the patients, in order to achieve the social integration of the thalassemics.

The targets of the Association are also:

• to inform the public and the thalassemicis on issues concerning the problems and complications of the disease an their therapeutic treatment.
• to secure the right medical follow-up and treatment of disease with the use of the latest protocols.
• to inform the thalassemic patients of the latest treatment-methods, the newest medical protocols and data.
• and to inform the public, in order to prevent more children being born with thalassemia, so that in the long run the disease will be extinct.