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Tiara Green: Empowering Patients with Rare Diseases and Bridging Healthcare Gaps

Prime Highlights:

Tiara Green’s career journey began with a passion for pediatric medicine but evolved into advocacy for patients with rare and chronic conditions.

She highlights her significant work in vulnerable communities, focusing on maternal, child health, and chronic disease management, particularly within African American populations.

Key Background:

Tiara Green, President of Accessia Health, a Richmond, Virginia-based nonprofit, is committed to addressing the disparities in healthcare for individuals with rare and chronic conditions. Green’s early dream of becoming a pediatrician evolved into a mission to advocate for patients who often face significant challenges in accessing treatment. From her initial work in community health and maternal-child care to managing public health programs for chronic diseases in Virginia, Green gained firsthand insight into the healthcare inequities faced by underserved communities, particularly African Americans.

Her work with the Virginia Department of Health left a lasting impact, especially as she witnessed the immense difficulties patients with chronic conditions such as diabetes and sickle cell disease endured in accessing care. These experiences inspired Green to pursue a path where she could make a more significant difference by helping patients navigate the complex healthcare system.

At Accessia Health, Green has found a platform to make her vision a reality. The organization’s focus on supporting individuals with rare and chronic diseases resonates deeply with her belief that healthcare should be accessible, affordable, and comprehensive. Green’s work goes beyond financial assistance, ensuring that patients receive a holistic approach to care. She stresses the importance of addressing social determinants of health, such as transportation, lodging, and medical equipment, which are often overlooked.

For over a decade, Green has worked tirelessly to bridge healthcare gaps, offering essential resources and a safety net for patients struggling with rare diseases. In her view, healthcare is a right, and the healthcare system must evolve to ensure all patients have the support they need to thrive.