Community Engaged Education Materials for SCD Gene Therapy
Cayenne Wellness Center, Sickle Cell Consortium Axis Advocacy and SCAASF FREE AND OPEN TO THE ENTIRE SICKLE CELL COMMUNITY
New Data from CA SCDC: Sickle Cell Disease Activities October 2020 – January 2021
Advancing World-Class Science and Patient Engagement: CIRM’s Sickle Cell Disease Portfolio CIRM’s research programs.
End-of-Life Healthcare Utilization in Sickle Cell Disease and thePalliative Care Model
SCDC Program Findings and Activities + Future Directions
Diversifying the Blood Donor Pool: The need for African American donors to support Sickle Cell Patients
Adult Health Care for Sickle Cell Disease: How to Make it Better
This webinar is on collaboration and community in sickle cell. Dr. Nik Abdul Rashid and Ms. Linetta Barnes from Nevada will present on how a clinical group and community-based organization work together to improve care and quality of life for people living with sickle cell disease.
What's new at the Sickle Cell Disease Association of America (SCDAA) ? Presented by Ms. Beverley Francis-Gibson, SCDAA President and CEO, and Dr. Biree Andemariam, SCDAA Chief Medical Officer