Genetic risk for cancer in the family
Sometimes, cancer runs in families.
You may realise this when:
- Several family members have had the same or related types of cancer
- The diagnosis was made at an unusually young age
- A known mutation (such as BRCA1/2) is present
This doesn’t mean you will develop cancer, but it does mean that you may be able to detect it early or lower your personal risk.
What if the test is not covered by insurance?
Some patients choose to seek further clarification, even when testing is not publicly funded.
I offer:
- Guidance on which tests are useful
- Transparent discussion of what these tests can and cannot show
- Support in deciding when to wait and when to act
What can you expect at Moleküli?
- A personal assessment: What might indicate a hereditary cancer risk?
- Test guidance: Which test is appropriate for your situation?
- Coordination of the test (if you choose to proceed)
- An easy-to-understand explanation of your results
- Written summary for you, your family and your doctors
How does it work?
- A test kit is sent to your home
- You do a cheek swab (no blood required)
- We meet online for a convenient, stress-free experience