Jenna Scott’s pregnancy took a turn for the worse after eight months of being ideal, with symptoms like bleeding, dizziness, and abdominal pain surfacing. Despite her concerns, her OB-GYN dismissed them as normal pregnancy issues. It wasn’t until a year after giving birth that Scott was diagnosed with stage 4 colon cancer at the age of 31.
Scott’s case sheds light on the disparities in colon cancer screening and treatment, especially among people of color. Dr. Renee Williams, a gastroenterologist, highlights the impact of bias, social determinants of health, and lack of access on these disparities. Routine screening is crucial as early detection can lead to higher survival rates.
Efforts like community-based programs and state initiatives have shown promising results in reducing racial disparities in colon cancer outcomes. Patients are encouraged to advocate for themselves by initiating conversations about screening with their providers.
Scott’s personal journey underscores the importance of being proactive about one’s health and seeking second opinions when necessary. Awareness, early detection, and access to screening services are key in the fight against colon cancer.
Resources like the Colorectal Cancer Alliance aim to provide support and education on the matter. It is crucial to address provider bias and systemic inequities in colon cancer screening and treatment to improve outcomes for all individuals.
