1. Activities for influencing the decisions of the Commission of Health working at the Parliament as well as the Ministry of Health in order to assure a social protection for people having cleft lip and/or palate and other facial abnormalities as it is organized in EC.
2. Creating a National network of ALA with represent in every big agglomeration in order to assist patients and parents closely.
3. Activities towards the Ministry of Health to recognize the Plastic and craniofacial Unit as a National Centre specialised in care of facial abnormalities.
4. Facilitate and collaborate the medical and paramedical specialists in their work.
5. Elaboration and participation to projects leading to collection of funds for the families and the specialised centres.
6. The improvement of the knowledge of the neonatologists, gynaecologists, midwifes, nurses and of staff working at orphanages in problems related to the facial abnormalities. Better inform the entire society about theses problems. Decrease the number of the abandoned children with cleft lip or palate.

1. Establish a national register of the children born with facial abnormalities in Bulgaria.
2. Receive the status of a National Centre Specialised in care of facial abnormalities.
3. Apply the standards proposed by EUROCLEFT in the file records of every patient.
4. Improvement of the quality of the care of every patient especially the treatment of the otitis by the means of transtympanic drains.
5. Collaborate for the organization of courses for orthodontists, speech therapists and "target" doctors.
6. The development of the orthognatic and craniofacial surgery.
7. Take part in the fundamentals studies of EUROCRAN on the genes, environmental factors, etc…
8. Take part in multicentric clinical studies inside the EUROCRAN network.
9. The development of the cranio-facial and orthognatic surgery.