In this podcast, Sam talks to thalassaemia patient and aspiring author Kristina. 

We talk about self-empowerment through knowledge, the importance of mental health support as well as work and career choice.

Join us as we explore topics that are relevant right now to patients and families living with genetic blood disorders in Australia.

Views and opinions expressed on this podcast are those of the host and guests and do not necessarily express TASCA's official policy and position.

This week, Sam talks to Ella from Brisbane about challenges her young family faced when both her sons were diagnosed with a form of transfusion-dependent thalassaemia. We explore topics around support, awareness in the community and building resilience in these challenging times.

In TASCA's first podcast, Sam talks with TASCA's Vice-Chair, Robbin, about life as a thalassaemia and sickle cell affected family during the current COVID-19 quarantine.

Join us as we explore topics that are relevant right now to patients and families living with genetic blood disorders in Australia.

Views and opinions expressed on this podcast are those of the host and guests and do not necessarily express TASCA's official policy and position.