A perfect combination of valuable life

The association aims to implement preventive strategies to reduce the severity, overcome or overcome the effects, consequences and negatives of Down syndrome through: • Solidarity, integration, and assistance to families who have newborns characterized by the syndrome. • Enumeration and inventory of old and new cases and at birth, providing the necessary services immediately for both newborns and parents, and linking the family to the association by providing rehabilitation, education, and psychological and scientific guidance, and for parents to know how to deal with these newborns/children and how to raise and raise them in a correct and sound manner that ensures that the family, society, and nation benefit from them. In addition to direct and indirect support according to the circumstances and grades of families. • Striving to develop health, psychological, educational, and employment services by mobilizing the various segments of society and raising the level of the general sense of responsibility on the part of those in charge of these fields towards paying attention to this group and providing all of their deserved needs and supplies, just like their healthy peers, and facilitating their involvement in society and removing any barriers that arise in this regard. The special. • Providing training, rehabilitative and educational courses for children with Down Syndrome from birth until adulthood, to help in normal growth by accelerating motor, linguistic, developmental and social development with the aim of integrating them into society and qualifying them to carry out their living, life and social duties without the need to depend on others.. • Taking the hands of parents of children with the syndrome in identifying the syndrome and understanding and accepting practical and rehabilitative training by involving them in the therapeutic and training programs offered to their children as they are the main party completing the rehabilitative and training doses. • Providing introductory and awareness programs about the syndrome, its causes, and how to deal with it, to different segments and groups of society, with the aim of reducing its incidence rates, by avoiding its causes. • Providing awareness programs about the negative aspects of the syndrome and its harmful accumulations on the individual who suffers from it and on society, to all workers in the medical field and in this field - to give it more attention in scientific research and to find/develop methods for early detection and advanced treatment of its physiological effects, through establishing Seminars, workshops, continuing education programs and encouraging research related to them. • Consolidating relations with local, foreign, professional, and civil associations, clubs, and schools for children with special needs, and clarifying and highlighting the true picture of the syndrome in the local and international circles to provide and provide the correct understanding of it, and in return, ensure the proper and correct treatment of them by everyone. • Establishing an information center to support and encourage studies, research, and specialized services related to the syndrome, its sufferers, and ways to develop and improve their lives. • Work to develop and invest the association’s inputs to cover activities and obligations.