About Us
The Thalassemia Patients' Friends Association is a Palestinian non-profit organization founded in 1996 by patients, their families, and professionals and other interested men and women. Registered under license number 96/2014 by the Palestinian Ministry of the Interior, with the Palestinian Ministry of Health as the competent authority, the association strives to represent the voice of patients and promote their rights before the community and decision-makers. The association operates in the West Bank and Gaza Strip through main centers, subcommittees, and a wide network of volunteers. It is an active member of the Thalassemia International Federation (TIF), the Thalassemia Arab Federation (TATAF), and the Palestinian National Committee for Hemoglobinopathies.
Our Mission:
Enhancing community awareness and health education to reduce new births of thalassemia, improve the quality of life of patients and support their families, and empower patients as partners in community work.
Our Vision:
A society free of new births to thalassemia patients by 2030
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