Hi, redditors!
We’re genetic counseling experts with the National Society of Genetic Counselors. Genetic counselors help people understand and adapt to the medical and, psychological aspects of diseases that run in families. Those of us participating today specialize in helping people understand their cancer risk, screening and treatment options.
In honor of Breast Cancer Awareness Month, we’re here to discuss:
- how family history contributes to breast cancer risk;
- options for patients with a family history of breast cancer, including genetic testing, cancer screening, and mechanisms to reduce cancer risk.;
- the role of genetic counselors in developing a personalized cancer screening plan;
- the “Angelina Jolie effect” and what’s important to know about her decision to undergo a double mastectomy
- and how to talk with family members about cancer and genetic testing.
NSGC serves as an integral resource for patients, prospective students and healthcare providers interested in learning more about genetic counseling. Here’s a bit about those of us answering your questions today:
Mary E. Freivogel, MS, CGC: I am President-elect of NSGC and an NSGC Cancer Expert. In addition to my role with NSGC, I am the Senior Manager of Clinical Service Lines at Invision Sally Jobe Breast Centers. I can discuss the hereditary aspects of cancer and how patients can understand genetic test results, develop a specific plan to address their cancer risks, and share relevant information with family members.
Jessica M. Salamone, ScM, CGC: I am the Director of Genetic Counseling and Cancer Risk Assessment at Elizabeth Wende Breast Care in Rochester, NY. I love helping families think about the differences between genetic and sporadic cancers and how genetic testing may benefit them. Topics such as insurance coverage criteria and how testing may impact your future management are imperative in making such a huge decision. I’m here to help individuals move through the process and take the best action for their personal situation.
Jennifer Scalia Wilbur, MS: I am the Clinical Program Manager of the Cancer Genetics and Prevention Program for Care New England hospitals in Rhode Island. I started this program 15 years ago and have seen more than 7,000 high-risk patients over the course of my career. Helping patients more accurately estimate their cancer risk has been incredibly rewarding, as I have witnessed the detection of cancers at earlier stages (where treatments were avoided), as well as the prevention of cancers in both my patients and their family members. Talking about your personal and/or family cancer history and the option of cancer genetic testing can be extremely overwhelming, however we have recognized that most patients feel empowered with this knowledge, especially when they have played an active part in the decision making process.
We’ll be back at 12:30 p.m. EST to answer your questions, ask us anything!
Want to know more about how genetics affects your risk for diseases, or how to capture your family health history? Sign up for our free webinar on Nov. 2
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