Vision & Mission
Guided by patients’ needs and experiences, the Thalassaemia International Federation (TIF) works to advance the prevention and treatment of thalassaemia and other haemoglobin disorders, make knowledge more accessible and ensure that patients’ voices inform the decisions that affect their lives.
What this means for patients
Our vision and mission reflect a commitment to meaningful change in people’s lives. We work towards a future in which everyone living with thalassaemia or another haemoglobin disorder can benefit from: 
- Quality care throughout life
Timely diagnosis, appropriate treatment and coordinated support that responds to changing needs. - Knowledge and confidence
Clear, reliable information to understand their condition and make informed decisions about their care. - A meaningful voice
Opportunities to shape the healthcare policies, services and research that affect them. - Dignity and inclusion
Respect for their rights and the opportunity to participate fully in education, employment and community life.
Explore our Pillars of Work to discover how we put this commitment into practice.
Also:
Click below to download and read the TIF Constitution.
Get in touch:
If you would like to help us by getting involved, please CONTACT US.