Given the exceptional economic circumstances our country is facing—conditions that affect citizens in general and patients with thalassemia and hereditary blood disorders and their families in particular—these individuals endure the compounded burden of illness and poverty, along with challenges such as displacement, unemployment, and the constant pressure of securing medical care for their loved ones.
In response to these difficult conditions and the urgent needs of thousands of affected families, the Association develops and proposes humanitarian projects to governmental bodies and cooperating organizations. These projects aim to provide partial support for essential material and nutritional needs, with priority given to the most vulnerable families in the capital city and surrounding areas.