News and Updates

January 9, 2017

TASCS Australia reaches out to the Turkish and Islamic Communities

On the 8th December, the office of TASCS Australia was honoured to receive two prominent members of Australia‚Äôs Turkish community. Our first guest, Mr Mustafa Yilmaz […]
January 9, 2017

TASCS Australia visits Maria Vamvakinou Member for Calwell

On Tuesday 6th December, as representative of TASCS Australia, I had the distinct pleasure of visiting Maria Vamvakinou who is the federal member for Calwell. Our […]
December 28, 2016


On the afternoon of the 5th December 2016, the passing of Sotirios Katakouzinos, left behind an immense but unfortunately unknown legacy. A legacy that poses to […]

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About our foundation

Our Mission

The Thalassaemia and Sickle Cell Society of Australia (TASCS Australia) is a not-for-profit community organisation dedicated to:

(A) Serving as a support network for Australians affected by genetic blood disorders (also known as "genetic haemoglobinopathies") like thalassaemia and sickle cell anaemia.
(B) Seeking to raise public awareness of genetic blood disorders within Australia, and the need to encourage the public to be tested for these conditions.
(C) Encouraging healthy members of the public to donate blood to the Australian Red Cross Blood Service, as fellow Australians who are affected by genetic haemoglobinopathies, require regular blood transfusions in order to live and manage their condition.

Interesting Fact:

According to medical scientists, it is believed that chronic blood conditions like thalassaemia and sickle cell anaemia, are genetic adaptions or disorders that sought to provide some protection to humans from malaria.

Useful information

How Can I Find Out If I Am A Carrier Of Thalassaemia Or Another Haemoglobin Condition?

Ask your GP for a blood test "for haemoglobin disorders". Family history is also very important so keep in mind immediate or extended family and if thalassaemia is known in your family history.

When Is The Best Time To Have A Test If I Am A Carrier?

You can have it at any time, but the best time is before you start a family. Ask the GP to give you a test if you are planning a family, or are at the start of pregnancy.

I Have Been Diagnosed With Thalassaemia Minor (Carrier). What Should I Worry About?

People with beta thalassaemia trait will usually experience no health problems other than a mild anemia. You may have beta/alpha thalassaemia trait and not know it.

Thalassaemia minor (carrier) is generally asymptomatic and usually does not present any significant symptoms. Please note that a disease is termed asymptomatic if a patient carries a disease or infection but experiences no symptoms.

Our concern is that they be aware that they may pass down their thalassaemia gene to their children. If their partner also has thalassaemia minor, they then have a 25% (1 in 4) chance with each pregnancy of having a child with thalassaemia major.

If people know that they have this 25% chance BEFORE they start a family, they can then discuss their family planning options with health professionals, such as Genetic Counsellors. The family planning options available to them may alter their chances of having a child affected by thalassaemia.