Peter is of Greek descent and shows resilience and strength in facing the challenges of living with Beta Thalassaemia.  Peter is passionate about supporting and advocating for others who share his condition.

As an Early Childhood teacher, Peter uses his knowledge and personal experiences to assist families navigating the complexities of the health system and accessing vital services.  He is a dedicated advocate for patients and the community, providing guidance and support to those in need.

Peter enjoys participating in awareness days to educate the community around what it’s like living with thalassaemia and to increase awareness of genetic blood conditions.

Peter serves as a consumer advisor for the Monash Health Blood Committee, helping to shape policies and initiatives that benefit individuals with blood conditions.

Despite some health challenges he faces just like many others living with the condition, Peter remains positive and dedicated to making a difference in the lives of those around him.

Sally is an enthusiastic Health Promotions Officer at Thalassaemia and Sickle Cell Australia. 
She takes great pride in her work as she educates the community about genetic blood 
conditions, carrier testing and blood donations. She also loves connecting with people, 
supporting those affected by these conditions. Sally is dedicated to creating a positive 
impact in the lives of people across Australia.

When she's not working, Sally enjoys camping, hiking and being surrounded by nature. She 
also loves time with family and reading a good book at home

Peter Verveniotis, who has been living with thalassemia major for nearly 50 years, and Sally Barton, a health promotions officer at Thalassemia and Sickle Cell Australia. The discussion covers various aspects of thalassemia, including diagnosis, treatment, community attitudes, and future perspectives.

Key points include:

Peter's experience with regular blood transfusions and the physiological challenges of thalassemia major

The impact of diagnosis on family dynamics and community stigma

Sally's role in educating high school and university students about thalassemia

Advancements in treatment options, including chelation therapy and potential gene therapy

The importance of coordinated, multidisciplinary care for thalassemia patients

The role of community support in helping patients feel less isolated

Proposals for future initiatives, including an international conference and journal editorials

The episode provides valuable insights into living with thalassemia and the ongoing efforts to improve care and awareness for this rare genetic condition.



Peter Verveniotis and Sally Barton, Thalassaemia and Sickle Cell Australia ( TASCA)

The Health Design Podcast brought to you by the Journal of Health Design(www.journalofhealthdesign.com). Features interviews with the world's leading health design experts including clinicians, designers, patients, authors and researchers. Better health by design.

New tracks tagged #Genetic Condition