Pat Bollard

Pat has 35 years in secondary school teaching and now works in counselling and hypnotherapy. 

Pat’s interest in the work of TASCA stems from the fact that thalassaemia is present in her extended family as well as her mother who is a carrier.

Pat’s husband suffers from a chronic condition so she understands first-hand the physical, emotional and mental difficulties that are associated with an ongoing medical condition, for both patients and their family.

Peter Verveniotis

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 working in a local government early intervention program, 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.

Joanne Mucciacciaro

Jo has a background in accounting and bookkeeping and has come to know about TASCA through a dear friend with thalassaemia.

This has led Jo to join the committee of TASCA. Jo is committed to making a positive difference to TASCA and people living with genetic blood disorders.

Karen Parr

Karen moved to Melbourne in August 2018 and has a strong background in science engagement roles. She also established Australia's Cell and Gene Catalyst, a joint venture that aims to accelerate Australia's Cell and Gene industry and ensure everyone in Australia has access to advanced therapeutics.

Karen has worked in both science and conservation communication and engagement roles. Having lived in London for two years, Karen continues to embrace her passion for adventure and travel.  Experiencing new cultures and people has broadened her mind and her outlook on life.

While Karen does not have a personal connection to thalassaemia or sickle cell conditions, Serving the community brings balance to her life, and TASCA caught Karen’s interest because of her background in life sciences.

Dean Karvelas

Dean is in senior level management for a large multinational in the automotive IT industry and working on several startups business on his spare time.

As a Beta Thalassaemia carrier, Dean is committed to improving the overall quality of life and ongoing care for Thalassaemia patients and believes this starts with good communication and education programs helping to spread knowledge and understanding to clinicians and the broader community. All this with the end goal in mind - to cure Thalassemia and other related genetic disorders.

Dean is looking forward to bringing positive support and contributions to Thalassaemia community and being a valued member of the TASCA team.

Dr. John Malios

MB, BS, (Monash), FRACGP, MACLM. 

Dr John Malios is a general practitioner having practised in Oakleigh (1972 -2018) with an interest in Occupational Health and is an experienced medico legal examiner.  He was the Convenor of Medical Panels Victoria (2012-2017) and Deputy Convenor (2007-2012), and continues  to be on the Governor in Council’s List for appointment to a Medical Panel.

He has a long-standing interest in thalassaemia and was the Thalassaemia Counsellor – Queen Victoria Medical Centre (1973-1985), the Royal Women’s Hospital (1975-1978) and Clinical Assistant, Haematology Clinic, Royal Children’s Hospital (1975-1977).

Dr Malios has previously been active in promoting information and education regarding haemoglobinopathies and the role of screening in medical practice.

He was  co-author of a paper:  “Thalassaemia – a preventive approach”  RN Matthews, J Malios – Medical Journal of Australia, 1976. 

This paper was also the subject of a presentation in 1976 at the New York Academy of Science. 

Relevant current memberships:

• Life member Australian Medical Association (Vic)
• Life member Royal Australian College General Practice
• Member Australian College Legal Medicine
• Founding Member – Thalassaemia Society (now Thalassaemia and Sickle Cell Australia)

Cameron Mehmet

As a lifelong Thalassaemia patient and advocate, Cameron is passionate about ensuring equity and access to treatment for everyone. In his professional work, Cameron serves as the Director of Architeck Group, leading a team specialising in domestic renovations. Cameron's expertise extends to significant contributions in engineering, notably on landmark hospital and tunnel projects across Victoria. Outside of work, Cameron finds joy in spending time with his loving family and embarking on travel adventures to explore new cultures and landscapes.

Nick Moutzouris

Nick is a dedicated registered Early Childhood Teacher with extensive experience in the early childhood sector. He brings over eight years of valuable board experience as a member of the Australian Childcare Alliance Victoria. Additionally, Nick holds a Bachelor of Property and Real Estate from Deakin University, providing him with a diverse skill set. Eager to apply his expertise, Nick is enthusiastic about contributing to TASCA and furthering its objectives.

Sally Barton

Sally is an enthusiastic Health Promotions Officer with a bright and friendly personality. She takes great pride in her work as she educates the community about inherited blood conditions, carrier testing and blood donations. She also loves connecting with people, supporting those affected by these conditions. Sally is passionate about making a difference in the life of others 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.

Kate Johnson

As the Administration Officer at TASCA, Kate supports the administrative functions of the organisation including office processes, coordinating appointments and communications. She is dedicated to supporting the company’s mission of improving the lives of individuals affected by Thalassaemia and Sickle Cell Anaemia, and enthusiastic to provide support to the TASCA team and members. Outside of work, you could find Kate watercolour painting, pottering about the garden or cooking up a storm at home.