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.
Justifications for Social Welfare Projects
The deteriorating living conditions of thousands of families affected by thalassemia and other hereditary blood disorders.
The inability of many families to meet basic needs due to their constant engagement in securing safe blood transfusions and providing essential healthcare.
Malnutrition among individuals with thalassemia and hereditary hemolytic anemia, in addition to suffering from these chronic genetic conditions.
Justifications for Psychological Support Projects
The lives of those affected by thalassemia and genetic blood disorders are marked by suffering, pain, and anxiety. These patients need to be filled with hope, optimism, and joy in order to better cope with their chronic illnesses.
The interaction of children with thalassemia with their peers, engaging in games and activities, helps to foster a sense of connection and love, while also equipping them with valuable life skills.
Families of patients need to learn various methods and techniques to alleviate pain and create moments of happiness for their children.
Social Welfare and Psychological Support Projects