This collection of breast health resources represents the most critical dimensions of the mammography debate: general critiques of screening, ethical concerns about informed consent, the profound issue of overdiagnosis and overtreatment (particularly with DCIS), and the importance of rethinking cancer terminology. It also covers systematic reviews, registry data, the measurable risks of radiation and treatment harms, and the growing evidence for alternatives such as active surveillance. Together, these categories provide a comprehensive framework for understanding not only the scientific and clinical issues, but also the ethical and human consequences of breast cancer screening. For informed care, this structured evidence base ensures patients and clinicians can make decisions grounded in transparency, balance, and respect for patient autonomy.