Genetic Counselling for Cancer
Some cancers run in families. Genetic counselling helps you understand whether an inherited risk may be present — and what you and your family can do about it.
About 5–10% of cancers are linked to an inherited change in a gene, such as BRCA1 and BRCA2 in breast and ovarian cancer, or Lynch syndrome in colorectal and uterine cancer.
Knowing about an inherited risk can change how a cancer is treated, and it allows family members to choose earlier screening or preventive steps. Counselling explains the benefits and limits of testing before any decision is made.
Consider genetic counselling if
- Several relatives on the same side of the family have had cancer
- Cancer was diagnosed at a young age (for example, breast cancer before 45)
- A relative has had breast and ovarian cancer, or cancer in both breasts
- A family member has a known cancer gene change (e.g. BRCA)
- You have been diagnosed with ovarian, pancreatic or male breast cancer
How it works
- 01
Family history
We map your family's cancer history over at least three generations.
- 02
Risk assessment
The pattern is assessed to judge whether testing would be useful.
- 03
Testing, if appropriate
A simple blood or saliva test, with consent after a full explanation.
- 04
A plan
Results are explained, with screening, preventive or treatment options for you and your family.
Questions about genetic counselling for cancer?
Share your reports or questions and our team will respond quickly. An enquiry is not an appointment — just the first, easy step.