Breast Cancer Risk Charleston SC - Family History and BRCA Testing | Hope Integrative Medicine
October 30, 2026 · 1:11
How family history changes breast cancer screening, who should consider genetic counseling, who counts as high risk, and what dense breasts mean.
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Transcript
Breast cancer: family history, genetic testing and when to start screening early. Here are three things to know. About 1 in 8 U.S. women will be diagnosed with breast cancer in her lifetime. For women at average risk, the current guideline is simple: a mammogram every two years from age 40 through 74. But some women need to start earlier or add other tests. The U.S. Preventive Services Task Force recommends a brief risk assessment for women with a personal or family history of breast, ovarian, tubal or peritoneal cancer, or ancestry linked to BRCA gene changes. If it points to higher risk, genetic counseling comes next, and testing if appropriate. For women at high risk, the American Cancer Society recommends a breast MRI and a mammogram every year, typically starting at age 30. The MRI is added, not used in place of the mammogram. And if your report says dense breasts, ask your provider whether more imaging makes sense. Read the full article at hopeintegrativemed.com.
Frequently Asked Questions
Ask about breast, ovarian, tubal and peritoneal cancer on both sides of the family, including your father's side, which is easy to overlook, and the age each person was diagnosed.
Women with a lifetime risk of about 20 to 25 percent or more, a known BRCA1 or BRCA2 gene change or an untested parent, sibling or child with one, radiation to the chest before age 30, or certain inherited syndromes such as Li-Fraumeni or Cowden syndrome.
No. For women at high risk, the American Cancer Society recommends a yearly MRI added to a yearly mammogram, not used in its place.