Rare Disease Day and Myths and Misconceptions about Sickle Cell Anemia

Welcome back to another episode! Join Lucy as we discuss myths and misconceptions surrounding Sickle Cell Anemia, Rare Disease Day, and how you can support Sickle Cell Programs within your region, or even the American Sickle Cell Anemia Association. Creative and have sickle cell anemia? Send in your artwork, photographs, stories, and more to [e-mail]. Your art could be featured in an episode! Sickle Talk is owned and operated by the American Sickle Cell Anemia Association and funded by viewers and listeners like you. Thank you!