Redefining Advocacy and Care for Sickle Cell Disease | Dr. La'Shardae Scott | TEDxFaurotPark скачать в хорошем качестве

Redefining Advocacy and Care for Sickle Cell Disease | Dr. La'Shardae Scott | TEDxFaurotPark

Sickle cell doesn’t discriminate—but our healthcare systems do. In this powerful TEDx talk, Dr. La’Shardae Scott shares her personal journey as a mother, advocate, and changemaker, challenging the racial biases that shape sickle cell care. Watch as she redefines advocacy and inspires a new standard of equity, compassion, and accountability in healthcare. Dr. La’Shardae Scott, DSW, MSW, CHES, is President and CEO of the Scott Center for Observation, Treatment, and Transition, leading efforts in infant mortality, mental health, and the pediatric-to-adult transition for sickle cell patients. She has secured vital funding and co-developed the CDC’s manual Oral Health Management in Sickle Cell Patients. Her partnerships with Ohio hospitals have improved care transitions and outcomes for vulnerable populations. A passionate advocate and mother of two children living with sickle cell disease, Dr. Scott serves on several health equity boards and the NASW-Ohio Region 1 Board. She holds degrees from Eastern Michigan University and a Doctorate of Social Work in Administration and Leadership from the University of Kentucky. This talk was given at a TEDx event using the TED conference format but independently organized by a local community. Learn more at https://www.ted.com/tedx