So I am working on a presentation about challenges in increasing uptake of genetic counseling and testing in BW and one of the most interesting things I’m finding in the literature is that BW underestimate their risk for breast cancer
Which tells me that breast cancer organizations and medical professionals are not doing a good job of educating BW
At least two professional organizations recommend that BW undergo a comprehensive risk assessment for breast cancer at age 30 due to the fact that BW are a high risk group to develop breast cancer
If you’re a breast cancer organization and reaching BW is not a top priority what are you doing?