Project Description

Serbian Society of Autism
SERBIA
Serbian Society of Autism was established in 1977. 16 local associations operate within the Society, and this network is constantly expanding. Society is a non-profit organization and all active members, parents and professionals are volunteers. The General Assembly and Managing Board consists of parents from all over Serbia, making all decisions regarding the operation of the Society
The Society also has a Team of experts, which is composed of: therapists, teachers, special educators, psychologists, psychiatrists, caregivers, nurses etc.
The financing of SSA work is carried out through projects and donations. Society is a member of National organization of persons with disabilities of Serbia and is a full member of Autism Europe.
The mission of the Society is improving the quality of life of people with autism and their families with a focus on preservation, protection, enhancement and promotion of internationally established standards in the field of human rights and civil liberties.
The Society is continuously working on solutions for the rights of people with autism to:
- Adequate diagnostics
- Education
- Right to work
- Quality medical care
- Social care
- Help their families
Society is working on:
- Representing the rights of people with autism and their families
- Providing advocacy services for people with autism and their families
- Empowering families of people with autism
- Educating parents and professionals
- Creating and implementing of support services
- Initiated the opening of the first daily centers in the country (since 1989.)
- Respite care service
- Weekend program
- Family assistant
- Advisory and therapeutic support services for parents
- Help line
- Informer for the exercise of the rights and procedures of people with autism and their families
Society was also actively involved in making and adoption of:
- The Law on inclusive education
- The Law on rehabilitation and employment of persons with disabilities
- The Law on Health protection
- The Information Law
Mid-term objectives of the society:

- The formation of a National Registry that would allow a precise insight into the number of people with autism in Serbia. The Register would also facilitate the implementation of the rights of persons with autism, the state budgeting and resources.
- Adoption of a National Strategy for autism, which would cover issues from the earliest (diagnostics) to eldest age (health treatment) of persons with autism.
- Respecting and practicing all adopted laws protecting the rights of people with autism.
- Development of support services such as daily care centers, family assistant project, respite care services, supported living and their implementation in the system.
- Higher education and the existence of adequate occupations for people with autism, so employment in the labor market conditions becomes possible.
- Greater education of health workers to treat illnesses that are not a consequence of autism, such as diseases in cardiology, neurology, oncology, gynecology, etc.
- The inclusion of individuals and groups directly affected by autism (parents and associations) in the process of adopting laws, policies and decisions