President of the Society Calls on Educational Institutions to Allocate Scholarships for Thalassemia and Hereditary Blood Disorder Patients
President of the Society Calls on Educational Institutions to Offer Scholarships for Patients with Thalassemia and Hereditary Blood Disorders
Dr. Ahmed Shamsan Al-Maqrami, President of the Yemeni Society for Thalassemia and Hereditary Blood Disorders, called on schools, universities, and all educational institutions to support patients suffering from thalassemia and hereditary blood disorders and to enable them to enjoy their right to education.
In his speech at the Third Charity Festival in Support of Thalassemia and Kidney Failure Patients — organized yesterday morning by the Student Activities Department at the University of Science and Technology — Dr. Al-Maqrami urged all educational institutions to provide free seats and scholarships for patients whose difficult living conditions have stood in the way of their access to education.
He praised the role of the University of Science and Technology in supporting humanitarian causes and encouraging those eager to pursue their education.
The celebration featured several artistic and musical performances promoting humanitarian and charitable work. The organizers also held a charity bazaar to support patients with thalassemia and kidney failure.
