Providing social support and advocacy for patients and carers

LEARN MORE

The Thalassaemia and Sickle Cell Society of NSW is a registered charity that was formed in 1978 as a non-profit, self-help group organised by the families of children suffering from thalassaemia, sickle cell anaemia and other haemoglobinopathies.

MORE ABOUT US

Counselling

We provide confidential counselling sessions to help our members.

READ MORE

Resources

Access key information through videos and fact sheet resources.

READ MORE

Get Involved

With your support we can help make a difference in the lives of patients and carers.

READ MORE

Thalassaemia & Sickle Cell Anaemia are some of the most commonly inherited genetic disorders in Australia

We provide more advice for people around testing for these disorders along with more information about what to do once diagnosed. Your support helps people deal with symptoms and discuss family planning options before they start a family.

FIND OUT MORE

Latest News & Events

International Thalassaemia Day & Nurse of the Year Award 2025

Join us in celebrating International Thalassaemia Day 2025, a global day of awareness and unity.

READ MORE

INTERNATIONAL THALASSAEMIA DAY 2025

This 8th of May, mark International Thalassaemia Day 2025 with us as we embrace this year’s theme:

READ MORE