Breast Cancer Network Australia
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Symptoms of breast cancer can include a lump in one breast or a change to the nipple or breast skin. Sometimes there are no symptoms and breast cancer is found through screening.
There are many risk factors for breast cancer, including age, lifestyle factors and medical history. About 5–10% of breast cancers are due to an inherited breast cancer gene such as BRCA1 or BRCA2.
Breast cancer sometimes has no symptoms, so regular checks are important for women aged 40 and over. Breast changes may not mean cancer, but see a doctor if you notice:
Many factors can increase your risk of breast cancer, but they do not mean that you will develop it. You can also have none of the known risk factors and still get breast cancer. If you are worried, speak to your doctor. For more information, visit Cancer Australia or Peter MacCallum Cancer Centre.
Most people with breast cancer do not have a strong family history, but a small number may have inherited a gene fault (also called a mutation) that increases their breast cancer risk.
To find out if you have inherited a gene mutation, talk to your doctor or breast cancer nurse about visiting a family cancer clinic or genetic oncologist. Your specialist may also be able to order genetic tests. In particular, women diagnosed before 40 years, those with triple negative breast cancer diagnosed before 60 years, and men with breast cancer should ask for a referral. Genetic testing is covered by Medicare for some, but not all, people; ask your doctor about this.
Breast Cancer Network Australia
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McGrath Foundation
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