Educational Programme
Developing and delivering a multimodal educational programme for patients, families and healthcare professionals.
TIF Education is the central hub for the Thalassaemia International Federation’s educational conferences, meetings, workshops and webinars on thalassaemia and other haemoglobin disorders.
It brings together our global educational activities in one secure and easy‑to‑use online environment, making it simpler to discover upcoming events, participate and stay connected over time.
TIF is based in Nicosia, Cyprus, and its work extends worldwide through country visits, workshops and meetings with competent bodies. It forms networks with health authorities, patient organisations, medical and scientific communities, academic institutions, public‑health‑related agencies and the pharmaceutical industry, and has been in official relations with the World Health Organization (WHO) since 1996.
The Thalassaemia International Federation (TIF) is a patient‑oriented, non‑profit, non‑governmental umbrella organisation, established in 1986 by a small group of patients and parents who were active in national thalassaemia associations in Cyprus, Greece, the UK, the USA and Italy.
Today, TIF brings together a broad network of member associations and partners from many countries across the world, representing the global thalassaemia community and working to safeguard the rights of patients to quality health and other care.
To address the needs of the global thalassaemia community and to achieve its mission, TIF’s work is organised around several key pillars:
Developing and delivering a multimodal educational programme for patients, families and healthcare professionals.
Building collaborations and networks with competent health authorities and international partners.
Designing and implementing targeted projects to support prevention and care at country and regional level.
Contributing to and promoting research efforts in the field of thalassaemia and related haemoglobin disorders.
TIF Education is developed and supported by a diverse global community of patients, parents, healthcare professionals and experts who share a common commitment to improving the lives of people with thalassaemia and other haemoglobin disorders.
The overall direction and priorities of TIF’s educational work are guided by the Federation’s governance and leadership bodies, which ensure that all activities remain aligned with our mission, vision and strategic plans.
TIF’s educational activities bring together international medical experts, nurses and other healthcare professionals, patient leaders and advocates, policy‑makers and partner organisations who contribute as speakers, authors, reviewers and mentors across our events and digital platforms.
“Through this broad and inclusive community, TIF Education ensures that every activity reflects real‑world needs and promotes practical, patient‑centred solutions.”
TIF organises a wide range of educational events designed to share knowledge, strengthen skills and support collaboration among patients, families, healthcare professionals and other stakeholders in the field of thalassaemia and haemoglobin disorders.
Through TIF Education, you can explore and participate in different types of educational activities, including:
High‑level global meetings bringing together experts, patient representatives and policy‑makers to discuss advances, challenges and priorities in thalassaemia care and prevention.
Region‑focused meetings addressing specific needs, health‑system contexts and policies in different parts of the world.
Practical activities focused on capacity building, clinical management, laboratory practice and patient empowerment.
Regular online events providing updates, case discussions and focused learning opportunities, often later made available through TIF’s digital platforms.
This platform has been developed to bring all TIF educational events together in one place, offering a clear overview of upcoming activities and secure online tools to support registration, participation and follow‑up.
With a single TIF Education account, participants can manage registrations across multiple events, view their upcoming and past activities, access their certificates and, where relevant, review accommodation bookings and payment history.
In addition to in‑person and hybrid events, TIF offers dedicated digital platforms that extend access to education, training and resources for patients, families and healthcare professionals worldwide.
The TIF e‑Academy hosts structured online courses for patients, families and healthcare professionals on key aspects of thalassaemia and sickle cell disease, combining expert content with flexible, self‑paced learning.
“It is designed to complement TIF’s conferences and meetings, allowing participants to deepen and update their knowledge between events.”
The TIF e‑Academy hosts structured online courses for patients, families and healthcare professionals on key aspects of thalassaemia and sickle cell disease, combining expert content with flexible, self‑paced learning.
“It is designed to complement TIF’s conferences and meetings, allowing participants to deepen and update their knowledge between events.”
Since 2010
International conferences, regional meetings, workshops, and webinars
Educational activities delivered across multiple regions and health systems.
Patients, families, healthcare professionals, and other stakeholders reached
Learners reached through TIF’s e‑Academy and the TIFLIX video library.
By taking part in TIF’s educational activities, you help strengthen knowledge, improve care and support better outcomes for people living with thalassaemia and other haemoglobin disorders around the world.