Thalassemia and hereditary blood disorder patients face difficult circumstances that hinder many of them from achieving their goals and ambitions. One of the main challenges is their inability to continue secondary and higher education. They are more vulnerable to dropping out of school, which makes their future more challenging, especially if they do not receive a good education or a job that aligns with their capabilities and health conditions. This affects their ability to secure a better life for themselves and their families. From this perspective, the association aims to support these young men and women, encouraging them to pursue further education and academic development. The association calls on various organizations to stand by them by providing opportunities for free education and scholarships. Many have proven academic excellence and have excelled among their peers, demonstrating that illness is not an obstacle to achieving dreams and ambitions.
Justifications for Educational Projects
Most youth with thalassemia and hereditary blood disorders are unable to pursue higher education due to their families’ difficult living conditions.
Youth with thalassemia and hereditary blood disorders have many ambitions and future aspirations like others, and it is everyone’s duty to support and empower them to obtain proper qualifications and integrate into the job market.
Girls with thalassemia and sickle cell anemia are more vulnerable to isolation and neglect, which negatively impacts their mental health. Supporting them in continuing their education offers a glimmer of hope for a better life.