
Tamara Hussong Milagre
President – Evita Cancro
Lisbon, Portugal
Hereditary cancers account for over 10% of all cases, yet many individuals with genetic mutations go undiagnosed because of limited testing criteria and misconceptions about risk factors. Driven by a strong family history of breast and ovarian cancer, she sought genetic counseling and discovered a BRCA1 mutation—highlighting that even healthcare professionals can miss crucial hereditary risks, especially when paternal family history is overlooked. After this discovery, Ms. Tamara opted for proactive surgeries to reduce cancer risk and openly shared their journey to raise awareness of genetic testing. Their experience revealed how limited communication within families and the healthcare system can delay or prevent life-saving interventions. A relative, unaware of the shared mutation, was later diagnosed with advanced breast cancer that could have been detected earlier through genetic testing. Through advocacy and education, the writer emphasizes the urgent need for accessible genetic testing, improved awareness, and open discussions to prevent missed opportunities for early detection and intervention in hereditary cancer. Ms. Tamara’s team is championing the YCBH campus and the 2024 Initiative – First Circle Awareness programs of the BCYW Foundation in Portugal.
