Synopsis

Thalassaemia is a group of inherited blood disorders that affect red blood cell production. First recognised in the 1920s, its most severe form ‘thalassaemia major’ once caused life-threatening anaemia, organ failure, and early death if untreated. The introduction of regular blood transfusions in the 1960s improved survival, but led to iron overload, which can damage vital organs. Iron chelation therapies, including oral medicines like deferiprone and deferasirox, are now central to long-term care. 
In Australia, thalassaemia is more common among people with Mediterranean, Middle Eastern, South Asian, and Southeast Asian heritage. Genetic screening before or during pregnancy and at birth helps detect and prevent severe disease early. Curative treatments have advanced, from stem cell transplants to promising gene therapies.
Ongoing research in Australia and globally aims to refine these therapies, improve iron regulation, and reduce complications, offering hope for a future where thalassaemia is manageable or even curable.

Bio

Dr Jim Vadolas leads the Immunohaematology Group at the Hudson Institute of Medical Research and is a recognised leader in the field of red blood cell disorders. His research spans both inherited and acquired forms of anaemia, with a focus on developing innovative therapeutic approaches aimed at prevention, treatment, and cure. His group is at the forefront of applying cutting-edge technologies—including lentiviral gene therapy, RNA interference (RNAi), and CRISPR-based genome editing, to advance translational solutions for chronic haematological disorders.

How to Participate

This is an in-person only event, so please join us at the Greek Centre, on Level M.

See our speaker live, ask questions during the Q&A and hobnob with fellow participants before and after the event.

We look forward to seeing you there.

Sponsors

We thank Ithacan Philanthropic Society and AHEPA for the kind donations that made this seminar possible.

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