The Thalassaemia International Federation (TIF) is a non-profit, non-governmental organisation founded in 1986 by a small group of patients and parents representing mainly National Thalassaemia Associations in Cyprus, Greece, UK, USA and Italy.
Read more about The Thalassaemia International Federation (TIF) here:
Since 1996 TIF has issued a vast number of diverse publications on thalassaemia and sickle cell disease, many of which are used as reference texts for academics, healthcare professionals, patient-support organisations and individual patients.
New editions are regularly produced to keep up with scientific progress and novel concepts. You can download the resources directly from the TIF website or from the links given below: