Who are we?

We are more than an association... We are the beginning of a new journey.

DSCA founding story

The Down Syndrome Charitable Society “DSCA” was established at the initiative of the families of children with Down syndrome and a group of those interested in the field of rehabilitation and training of people with special needs and people with Down syndrome, with the aim of providing various training programs and supporting the entire family to care for their child with Down syndrome. The official registration was made by the Ministry of Social Affairs and was known as the Down Syndrome Charitable Society (DSCA) on 08/14/2002.

DSCA Strategy

Objectives

Developing and providing training, information and support services to families of children with trisomy 21.
Developing and providing education and rehabilitation services for children with trisomy 21 for different age stages.
Financing rehabilitation services, health care, and various needs of children and their families.
Developing practical training materials and programs to qualify trainers and teachers professionally in the field of trisomy 21 and intellectual disability.

Message

Working to achieve the greatest possible degree of self-independence and social integration for individuals with trisomy 21 through developing and presenting specialized training and rehabilitation programs in integration with relevant institutions, whether governmental or private.

Vision

Establishing an expert house that develops local models according to research outcomes in providing specialized services to children, students and adults with trisomy 21 and their families.