Trusted Resources: News & Events
Latest announcements and gatherings
Vaso-Occlusive Crisis: The Future of Treating Patients With Sickle Cell Disease in Emergency Departments
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Corinna Schultz, MD, Shares How Pediatricians Can Discuss Sickle Cell Trait With Patients, Families
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From Early Hypothesis to Clinical Data About Reducing Vaso-Occlusive Episodes with Arginine Therapy
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Corinna Schultz, MD: Does Sickle Cell Trait Get Discussed?
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Claudia Morris, MD, Uncovers Potential New Mechanism of Action for Hydroxyurea
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Arginine Therapy Shows Positive Impacts on Sickle Cell Disease in ASH 2022 Data
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MARAC Advisory Statement: Update on Penicillin Shortages
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23andMe, Morehouse School of Medicine and the Sickle Cell Foundation of Georgia Inc. launches the Sickle Cell Carrier Status Awareness Program
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Why genetic engineering experts are putting a spotlight on Victoria Gray’s case
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New York Senate Bill 1839 and Assembly Bill 6430—Sickle Cell Disease Detection and Education Program
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$100,000 Grant Allows National Expansion in Expert Care of Sickle Cell Patients
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SCDAA Partners With Phi Beta Sigma Fraternity
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Sickle Cell Disease Association of America, Inc. and Hemanext® Inc. Form New Strategic Partnership
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Sickle Cell Disease: After Years of Neglect Some Promise for Sufferers
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Novartis wins Medicaid approval for new sickle cell drug in key US states
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Novel Sickle Cell Drug Causes Radical Results in End of Life Patients
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Edward Ivy, MD, MPH: A Comprehensive Perspective on Sickle Cell Disease
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Sickle Cell Management During the Blood Crisis With Edward Ivy, MD, MPH
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Regina Hartfield Is Now the CEO and President of SCDAA
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Q&A With Regina Hartfield, New CEO of the SCDAA
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Sickle Cell Disease Association of America, Inc. Names New CEO & President
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65th American Society of Hematology (ASH) Annual Meeting & Exposition
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P.O.W.E.R ECHO Project Community Health Worker (CHW) Training
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Annual National Sickle Cell Disease Association of America (SCDAA) Convention
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P.O.W.E.R ECHO Project Community Health Worker (CHW) Training
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2023 NHLBI Annual Sickle Cell Disease Research Meeting
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This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.