Helping Children and Families with Sickle Cell Disease

The CDF Foundation supports children and families impacted by sickle cell disease through care, resources, and advocacy.

Helping Children and Families with Sickle Cell Disease

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Sickle Cell Disease (SCD) is a complex genetic disorder that impacts over 100,000 individuals in the United States, presenting life-altering challenges to those living with it. This chronic condition affects the shape and function of red blood cells, leading to severe pain, organ damage, and a reduced quality of life. Alongside sickle cell disease, many individuals face similar struggles due to other illnesses that also require ongoing care and attention. Despite the prevalence of these conditions, those affected often encounter a lack of understanding, limited resources, and insufficient support, intensifying the hardships they endure.

At the Caleb Duplan Foundation (CDF), we are deeply committed to addressing these challenges. We recognize the need for more awareness, comprehensive care, better educational resources, and a stronger community of support for people dealing with long-term health conditions.

Our approach focuses on empowering individuals affected by sickle cell disease and other chronic illnesses by ensuring they have access to the care, support, and advocacy they need. By fostering a strong sense of community and providing unwavering support, we aim to make a lasting impact on the lives of those living with these conditions, helping them lead healthier, more fulfilling lives. Our ultimate goal is to create a future where no one affected by sickle cell disease or any illness has to face these challenges alone.