I have a strong family history of breast cancer that includes grandmothers and aunts on both my mothers and fathers sides who were diagnosed and died as a result of the disease. I believe all but one grandmother were diagnosed young (30s). My only first-degree female family membermy motheris 67 and (knock on wood) cancer free, which my healthcare providers have cited as a reason for me not be highly concerned about genetic susceptibility (i.e. BRCA1/2). Instead Ive been advised to be vigilant about my screening practices (monthly self exams and yearly doctors visits) and plan to get regular mammograms in a few years (Im now 32). I also pay attention to preventive dietary and lifestyle recommendations from clinical studies and try to incorporate this advice into my life. Beyond that, I think about starting mammograms early (maybe 35?) and also consider MRI screening.
Id like to hear from anyone else with similar family history and concerns: What do you think about early screening and genetic testing? Any precautions youre taking that I havent mentioned?




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