Advancing and supporting research into SLC6A1
Standing up for the inclusion of people with SLC6A1
Contributing to the social protection of people with a pathogenic variant of the SLC6A1 gene and other rare diseases, taking into account additional factors of social exclusion such as disability, childhood, youth, gender or immigration.
- Promoting medical and care services
- Promoting educational services
- Promoting employment, residential and social services
Support and guidance
Providing support and guidance to people with SLC6A1 and their families in every area of their lives, including care, as well as their social, educational and professional inclusion.
Raising awareness and sharing knowledge
Promoting and sharing knowledge about SLC6A1 among affected people, families, associations, professionals and institutions. We are also concerned with intervention and treatment for rare diseases and neurodevelopmental disorders.
A trusted voice
Acting as a recognised representative before public and private bodies at local, provincial, regional, national and international level, on matters of common interest affecting people with SLC6A1 and other rare diseases.
