Our Impact Initiatives
Making a Difference
We offer educational resources, advocacy, and community programs that improve the quality of life for individuals with Sickle Cell Disease and their families.
Podcast
The Sickle Cycle Podcast explores intersectionality of the medical, social, and personal impacts of sickle cell disease. Each episode features patients, caregivers, clinicians, and researchers sharing lived experiences, treatment breakthroughs, and tools for advocacy and care.
Scholarship
Financial support for students with sickle cell disease provides them with resources needed to succeed academically. The scholarship reduces barriers to learning, encourage consistent enrollment, and empower recipients with long‑term success. The application is currently open and deadline is July 3, 2026. More information can be found here.
Community Events
Our engagements include blood drives and genotype screening to help fight sickle cell disease (SCD). Increasing awareness of genotype status helps people learn whether they have SCD or carry the trait. Many individuals with SCD depend on transfusions to prevent life‑threatening complications and improve quality of life. By getting tested and donating blood, it strengthens support for people affected by SCD.
Speaker
We speak at events, meetings, briefings, and conferences to inform audiences and raise awareness about the medical, social, and systemic barriers individuals living with sickle cell disease face. By engaging healthcare professionals, educators, advocates, and community leaders, we help audiences better understand the impact of sickle cell disease and how they can support improved care, equity, and awareness.