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Family's Genetic Curse: 80% Cancer Risk Unveiled
2 Dec
Summary
- Lynch syndrome dramatically increases cancer risk up to 80%.
- Genetic testing is the only way to detect Lynch syndrome.
- Colorectal cancer rates have surged in young Americans.

Tiffany Graham Charkosky's family history of colon cancer, which claimed her mother at 31 and uncle at 46, led to a startling discovery: Lynch syndrome. This hereditary genetic mutation significantly elevates the risk of developing various cancers, including colorectal, by up to 80%. Diagnosed around age 30, Tiffany faced a daunting reality, prompting her to undergo rigorous screenings and preventative surgeries.
Lynch syndrome affects approximately one in 300 Americans, yet most remain unaware due to the reliance on genetic testing. This lack of awareness is particularly concerning as colorectal cancer diagnoses are surging among young adults, with rates for teenagers already seeing a dramatic increase. The syndrome's genetic basis lies in mutations that impair DNA repair mechanisms, leading to uncontrolled cell growth.
Inspired by her journey, Tiffany authored 'Living Proof: How Love Defied Genetic Legacy' to empower others facing similar risks. Her experience underscores the critical importance of genetic awareness and proactive health management in confronting inherited cancer predispositions, offering hope and agency to those navigating this challenging diagnosis.




