If you have a history of breast cancer and a mutation in an inherited breast cancer gene (i.e., BRCA1/2, PALB2, ATM, or CHEK2), you may be eligible to contribute to tumor genomics studies that are being conducted through the Inherited Cancer Registry (ICARE). Through this effort, we are researching: - breast cancer characteristics - factors associated with outcomes, including treatments - studying genomics of the tumors to better understand pathways to tumor development, which can hopefully lead
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Do you have a history of breast cancer and a mutation in an inherited breast cancer gene (i.e., BRCA1, BRCA2, PALB2, ATM, and/or CHEK2)? Please consider joining our study at https://redcap.link/ICAREconsent if you have an inherited breast cancer gene mutation. In those with a breast cancer diagnosis, we are doing free genomic testing on tumor samples to better understand inherited breast cancers. Once you enroll in our study, we will assess your eligibility for this and other focused research ef
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#OnTheAirWithFACC: Tributes and Support for those Impacted by Cancer Marjorie Bellamy is a breast cancer survivor from Orlando, Florida, whose journey began at just 26 years old with a Stage 2B diagnosis. Eight years later, she faced a recurrence, triple-negative Stage 3C breast cancer and learned she carries the BRCA1 mutation. Though advised to undergo 19 cycles of chemotherapy and radiation, Marjorie chose a different path after deep research, reflection, and prayer. She pursued an alternativ
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