Sickle Cell News and Information

Scholarships will be awarded to applicants with sickle cell who present the best combination of a creative and persuasive essay, excellent recommendations, and superior academic standing. The application is open to all eligible students (inclusions/exclusions noted above). Applicants need not be on a Pfizer product to apply. Treatment regimen will have no bearing on application eligibility nor will it impact the scholarship selection process, as awardees will be chosen by

Rare Disease Day is a globally coordinated movement dedicated to rare diseases, striving for equity in social opportunities, healthcare, and access to diagnosis and therapies for people living with a rare disease. Since its creation in 2008, Rare Disease Day has played a crucial role in building an international rare disease community—multi-disease, global, and diverse, yet united in purpose. Rare Disease Day is observed every year on 28 February (or 29 February in leap years

The Sick Cells Inaugural Therapeutics Conference is a space to explore the future of sickle cell therapeutics through education, storytelling, and policy insights. Want to learn more about clinical trials and new therapies for sickle cell? Join warriors, patients, caregivers, healthcare professionals, and advocates as we: Break down barriers to clinical trial participation Share powerful patient stories Explore the policy landscape shaping access to treatment November 13, 2

Don’t just survive your next ER visit — learn how to take control, speak up, and get the care you deserve . This powerful session will give you the tools to: Communicate with confidence using medical language Understand triage levels & why your care can’t wait Build your personal care plan so you’re always ready Activate your support team & advocates This isn’t another lecture — it’s an interactive, life-changing experience designed to help sickle cell warriors and families

Dear Friends and Community Partners, The Sickle Cell Foundation of Georgia, Inc. stands proudly as the boots on the ground for the sickle cell community. Every day, we work alongside dedicated leaders across the nation who give their time, heart, and expertise to serve individuals and families impacted by sickle cell disease. As we look ahead to the SCDAA 2026 National Conference , we want to ensure that every Executive Director —especially those leading small and under-reso

This study is endorsed by The Sickle Cell Foundation of Georgia's CEO, Tabatha McGee. Read her letter of support here .