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Equal access to quality healthcare for every patient with Thalassemia across the world

Thalassemia International Federation (TIF) is a non-profit, non-governmental patient-driven organization founded in 1987. TIF is an umbrella organization involving 108 national Thalassemia associations and other members from over 55 countries across the world.

TIF has been engaged in a number of activities that focused on addressing the needs for quality information of patients and other relevant stakeholders/partners, including health care professionals, parents/carers and the community at large.

TIF is committed to strengthen its involvement and contribution to the national and global initiatives and efforts for a more patients’ orientated approach to health care as part of its mission for establishing equal access of every patient to quality health care that includes their own perspective.