Frequently Asked Questions
Who should consider cancer genetic counseling?
You may wish to see a genetic counselor if you have a personal or family history of cancer. We welcome all individuals and families who have a concern about a cancer diagnosis or a family history of cancer.
What should I expect?
We provide risk assessment, genetic counseling and genetic testing to individuals affected with cancer and their at-risk relatives. We help patients navigate surveillance, prevention and treatment options, as well as other cancer prevention strategies.
How will my genetic test results impact my health care?
Our cancer genetics team partners with you to integrate your genetic testing results into your overall health care plan. That plan can include:
Cancer screenings: A high-risk surveillance strategy to reduce future risk by finding cancer in its very early stages.
Medications: Some medications can help reduce the risk of developing certain cancers.
Risk-reducing surgery: A procedure to remove high-risk tissues that could develop into cancer, such as breast or ovarian tissues.
Is there a difference between in-person or virtual appointment?
The only difference is that a same-day blood draw would be available for an in-person appointment if you decide to proceed with testing. If you are seen for a video visit, you can be sent an at-home cheek swab or saliva genetic testing kit or come in for a blood draw. Blood, saliva, and cheek swab samples have the same accuracy for genetic testing. Your genetic counselor will discuss sample collection options in detail during the consult.
What cancer syndromes do we see?
Please see Hereditary Cancer Syndromes webpage.
What if I don’t know my family cancer history?
Try to ask the most informed family members and communicate limitations to your doctor.