Read more about family history
Family History & Cancer FAQs
1. Does having a family history of cancer increase my risk?
Yes. If a close relative had cancer—especially the same type or at a young age—your risk is increased.
2. Which cancers are commonly hereditary?
Breast, ovarian, colorectal, prostate, and pancreatic cancers are often linked to inherited gene mutations.
3. When should I consider genetic testing?
If multiple family members had the same cancer under age 50 or if you have a known family mutation.
4. How early should screenings begin?
Start screenings 5–10 years earlier than your relative’s diagnosis age. Consult your doctor for guidance.
5. Can lifestyle reduce inherited risk?
Yes. Healthy eating, regular activity, no smoking, and limiting alcohol can all reduce cancer risk.
6. What is a hereditary cancer syndrome?
Inherited gene mutations (like BRCA or Lynch) that significantly raise cancer risk across generations.
7. Can I pass this risk to my children?
Yes. Children of mutation carriers have a 50% chance of inheriting the same gene.
8. How does family history affect treatment?
It may influence surgery choices, follow-up screenings, and use of targeted therapies.
9. Are there family support networks?
Yes. Groups like FORCE and Bright Pink offer support, resources, and community events.
10. How often should I update my family history?
Update it regularly, especially after new diagnoses in relatives. Share with your doctor.
