Questions to Ask Your Doctor

Do I have any red flags in my personal or family history that could indicate hereditary cancer risks?
Are there specific cancers that are more common within my family?
Based on my family history, what is my likelihood of carrying a genetic mutation?
If someone in my family has a hereditary cancer mutation, should I be tested even if I don't have a personal history of cancer?
How do factors such as my age, gender, and lifestyle impact my cancer risk?
Can you explain what early-onset cancers are and why they may indicate hereditary cancer?
Could any existing symptoms (e.g., unusual lumps, fatigue) be warning signs of cancers with genetic links?
If I have no family members with cancer, does that mean my risk is low?

Should I consider genetic testing based on my personal or family history?
What does genetic testing involve, and what kind of mutations does it look for?
Will my health insurance cover the cost of genetic testing?
How accurate are genetic tests, and what are their limitations?
How long will it take to get the results of genetic testing, and how are they delivered?
If the test identifies a mutation, what does that mean for my health and cancer risk?
Can genetic testing determine the best preventative actions or treatments if I test positive?
If a mutation is identified, what steps do I take to inform my relatives?

What preventative measures can I take if my genetic test indicates higher cancer risk?
How often should I schedule screenings if I have hereditary risk factors?
Are there lifestyle adjustments I can make to lower my risk?
What early detection or monitoring methods are best for me (e.g., mammograms, colonoscopies)?
Are there medications or supplements I should consider to reduce my risk?
Could a prophylactic surgery (e.g., mastectomy, hysterectomy) be an option for me?
What role does genetic counseling play in creating a prevention plan?
Are there clinical trials or research studies I might qualify for?
How do I prepare my body for possible treatments if cancer is diagnosed?
If cancer is detected, how does knowing it is hereditary affect treatment options?

How should I communicate my genetic test results to family members?
Are my children at risk of inheriting a genetic mutation I may carry?
Should my siblings, parents, or other relatives consider testing as well?
How do I explain hereditary cancer risks to younger children or teenagers?
Should family members with existing cancers also consider genetic testing?
My family members live in another state; how can they access genetic services?
Will my family need to follow different screening protocols based on my test results?
If I don’t test positive for a mutation but have family members who do, what does that mean for me?