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Research Grants is a grant from the Sickle Cell Disease Association of America, Inc. (SCDAA) that funds investigator-initiated research to improve understanding, treatment, and quality of life for individuals with sickle cell disease. Since 1972, SCDAA has served as the national voice for SCD, working through 55-plus member organizations across 30 states.
Funded projects may address pathophysiology, complications, health disparities, clinical interventions, and community-based approaches. Eligible applicants include researchers at academic and medical institutions; HBCUs and health-equity-focused institutions are encouraged to apply. Awards typically range from $25,000 to $50,000 for pilot or seed projects, with amounts varying by funding cycle.
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Sickle Cell Disease Association of America, Inc. Association of America, Inc. We serve as the national voice for sickle cell disease working to resolve issues surrounding this rare disease and sickle cell trait. Since 1972, our organization has been on the forefront of improving the quality of health, life and services for individuals, families and communities affected by this rare disease and related conditions.
Our 55+ member organizations span 30 states. Black History Month 2026: Dr. Charles Drew Our final #SCDHistoryHighlight of 2026 explores the life and career of Dr. Charles Drew, a pioneering physician whose work paved the way for our modern-day blood banking system. Thanks to his research, individuals with sickle.....
Black History Month 2026: Dr. Marilyn Hughes Gaston This week, meet Dr. Marilyn Hughes Gaston, whose dedication and passion for health care led her to pave the way for equity. Dr. Gaston’s special focus on sickle cell disease helped shape our understanding of the..... SCDAA Earns 2025 Candid Gold Seal of Transparency SCDAA is proud to announce that we have earned a 2025 Candid Gold Seal of Transparency!
This recognition demonstrates our commitment to trust and clarity. We encourage you to view our profile to learn more about..... Black History Month 2026: Dr. Roland Scott Our next #SCDHistoryHighlight shines a light on the life and legacy of the "father of sickle cell disease" - Dr. Roland B.
Scott. Dr. Scott's groundbreaking research and dedication to patients during a time of..... Babies born internationally each year with SCD African-Americans have Sickle Cell Trait (SCT) People in the United States have sickle cell disease (SCD) Black Americans have sickle cell disease (SCD) National Program Initiatives SCD C.
A. R. E.
S. Consortium The mission of this initiative is to raise awareness about the importance of clinical trials and why it’s beneficial for sickle cell warriors to participate in them. Sickle Cell Disease Association of America, Inc. (SCDAA) actively works with legislators and regulators at both the state and federal levels to advance SCD policies.
Community Health Worker Training If you have a passion for community health or you have been personally affected by SCD, SCDAA encourages you to apply for community health worker (CHW) training. Find A Member Organization Near You: Please select an option before clicking Find!
According to the current listing, eligibility includes: Researchers at academic or medical institutions working on SCD; HBCU and health‑equity‑focused institutions like Morehouse School of Medicine are encouraged. Confirm the full requirements in the official notice before applying.
The current listing shows often $25,000–$50,000 for pilot or seed projects (varies by year). Verify award ceilings, matching requirements, and allowable costs in the official notice.
Research Grants is funded by Sickle Cell Disease Association of America, Inc. (SCDAA). Verify program details on the funder's official page before applying.
Start from the official opportunity page linked in this listing — it carries the sponsor's submission instructions.
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