The Bahrain National Hereditary Anaemia Society has committed itself since its inception in 1991, the task of spreading awareness for genetic blood diseases prevalent in almost all Arab countries .oohm objectives of the association and the second goal is to improve patient care and services provided to them in cooperation with the Ministry of Health. To achieve those goals Assembly has sought the help of a group of people of this beloved country to hold seminars and issuing educational brochures and posters of these diseases. And access to large segments of the Bahraini public, which has become a praise to Allah a high degree of understanding of scientific concepts of genetic blood diseases. The Bahraini public is fully aware today of the need for early screening tests, especially before marriage which was supported by Assembly since its inception. That the Assembly many projects singled out the leading national project, a project that continues to examine the students for seven consecutive years at the expense of Assembly. It also projects the rehabilitation of patients for the labor market, and training and assistance in their access to the realization to fend for themselves rather than be a burden on others. As well as the delivery of patients to and from the hospital, along with entertainment programs that relieve them and their families. We also hope that everyone involved with us in the march towards a purposeful application of a national strategy to eliminate genetic blood diseases in Bahrain. In conclusion, we send a multitude of thanks and gratitude to everyone who participated and cooperate with us in this benevolent activities.