Familial Cancer
Understanding cancer risk starts with your family history.
Rosalind Genetics helps individuals and families understand inherited cancer risks and take action early with expert counselling, testing, and support.
Protecting your family
While most cancers occur by chance, some are passed down through inherited gene changes (mutations), often affecting people at younger ages or appearing across multiple generations.
If you or a relative have had certain types of cancer – such as breast, ovarian, bowel, or prostate – or were diagnosed unusually young, genetic testing may help explain why. It can also empower you and your family to take proactive steps around screening, treatment, or prevention.
Who is this service for?
You may benefit from familial cancer genetic testing if:
You or a close relative have had cancer at a young age
There are multiple relatives with the same or related cancers
There is a history of rare or unusual cancer types
There’s a known mutation in the family (such as BRCA1/2 or Lynch syndrome)
You’re a clinician seeking support for patient risk assessment
You don’t need to meet all these criteria. Our team can help determine whether testing is appropriate based on your personal and family history.
“Knowing I carried the BRCA1 gene was scary at first, but it gave me a clear path forward. Rosalind helped me understand my risk and take control of my health, for myself and for my daughters.”
– Claire, age 42
What to expect
1
Referral
Get a referral from your GP to Rosalind Genetics.
2
Consult
Speak to our genetic counselling team about your options in a telehealth consult online.
3
Family History
Discuss your family history and whether testing is appropriate.
4
Undergo testing
Undertake testing (if needed). We’ll explain what it covers and what results mean.
5
Results
Receive your results with clear guidance and emotional support.
6
Next steps
Follow-up care, referrals, and screening advice if needed.
1. Get a referral
From your GP, obstetrician, or fertility specialist.
2. Consultation
Meet with one of our genetic counsellors (in person or via telehealth).
3. Family history
Discuss your family history and whether testing is appropriate.
4. Undertake testing
Undertake testing (if needed). We’ll explain what it covers and what results mean.
5. Results
Receive your results with clear guidance and emotional support.
6. Next steps
Plan your next steps with confidence, whatever the outcome.
What can we test for?
Depending on your family history, we may recommend:
- BRCA1/2 testing for hereditary breast and ovarian cancer
- Lynch syndrome screening for bowel and endometrial cancers
- Panel testing for other cancer-related genes (e.g. prostate, pancreatic, melanoma)
- Predictive testing if a known familial mutation has been identified
- Targeted testing of tumour tissue or family members when relevant
We’ll always explain your options clearly in a genetics consultation. Every test is discussed carefully during your consultation, and no decision is made without your informed consent.
Medicare and costs
Many familial cancer services are eligible for Medicare rebates, especially if clinical or family history criteria are met. We’ll let you know upfront if any out-of-pocket costs apply, and you’re never obligated to proceed with testing after consultation.
Why Choose Rosalind?
Rosalind’s clinical team has deep expertise in familial cancer genetics and works closely with oncologists and other specialists across Australia.
We specialise in:
- Thorough, evidence-based risk assessment
- Clear, compassionate counselling to help you navigate complex information
- Coordination with your care team for prevention and screening strategies
Frequently Asked Questions
Do I need a referral?
Yes. You’ll need a referral from a GP or specialist to access this genetic testing service.
If I test positive, does that mean I’ll get cancer?
Not necessarily. It means you may be at increased risk, and can benefit from earlier or more frequent screening.
What if there’s already a known mutation in my family?
We may recommend predictive testing to see if you’ve inherited the same gene change.
Can my family members be tested too?
Yes. If a mutation is identified, other relatives can be offered counselling and testing.
How long do results take?
Most results are available in 3 to 6 weeks. Your counsellor will explain the expected timeline during your appointment.
Have more questions?
Reach out to us at gene@rosalindgenetics.com or call us on 1300 042 132.