To advise, support and accompany individuals directly or indirectly affected by the SLC6A1 gene mutation. To provide information to interested parties, medical personnel or other professionals and authorities. To defend the interests of affected individuals in front of the community. To collaborate with associations for the SLC6A1 gene mutation present in the rest of the world. To collect funds for research and activities useful to the association. To contribute to the creation of a collaborative network of researchers, medical personnel, representatives of the pharmaceutical industry in Switzerland and abroad. To raise public awareness of the consequences of rare diseases and more specifically of the SLC6A1 gene mutation.