Who We Are
Welcome to Thalassaemia Care Australia, a dedicated organisation committed to improving the lives of individuals and families affected by haemoglobin disorders. Founded in 1994, we have been at the forefront of advocacy, education, and support for those living with conditions like thalassaemia and sickle cell disease.
Our mission is to empower individuals living with genetic blood disorders to lead fulfilling lives. We aim to provide comprehensive support, from medical care to emotional well-being, ensuring that every patient has access to the resources they need.
What We Do
We actively engage with healthcare providers, policymakers, and the community to advocate for equitable access to high-quality care and research funding for haemoglobin disorders.
Through school visits, public events, and media campaigns, we aim to raise awareness and reduce the stigma associated with haemoglobin disorders. We also provide educational resources to help individuals understand their genetic status and the importance of carrier testing.
We offer a range of support services, including peer support groups, social events, and educational workshops, to provide holistic care for those affected by haemoglobin disorders.
Our dedicated team of healthcare professionals, volunteers, and advocates work tirelessly to make a positive impact. We are united by a common goal: to make the world a better place for those living with genetic blood disorders.
Your support can make a difference. Whether it’s through volunteering, donations, or partnerships, there are numerous ways you can contribute to our cause.
- Phone: (07) 4577 8142
- Address: 95 Learmouth Street, Tahara, Victoria 3301
- Email: [email protected]