TIF's Mission, Vision, and Pillars

TIF’s Mission:

“The promotion and implementation of national control programmes for the prevention and treatment of thalassaemia and other haemoglobin disorders in every affected country.”

TIF’s Vision:

“Equal access to quality health care for every patient with thalassaemia and other haemoglobin disorders across the world.”

TOOLS TO ACHIEVING TIF’s Mission:

  • Creating new and strengthening existing associations
  • Country Delegation Visits
  • Educational Programme
  • Building up networks, partnerships and collaborations with relevant stakeholders

Educational Programme

Thalassaemia International Federation (TIF) has developed an internationally-recognised educational programme, with the objective to continuously educate health professionals, patients and their families, the community at large and policy-makers, based on four pillars:

  • The organisation of educational events including conferences, workshops and seminars at the national, regional and international level;
  • The preparation, translation and distribution of publications;
  • The preparation, organisation and contribution in courses, e.g., electronic educational platform and ENERCA, and;
  • The preparation and organisation of educational courses for patients and parents, e.g., the Expert Patients' Programme and Capacity Building

In this section you can read more about each pillar of TIF’s Educational Programme.