The Sickle Cell Struggle: Advocacy, Unity, and the Power of Community Collaboration
Sickle cell patients can be anywhere, but are there effective community-based strategies to help with psychosocial challenges? Dr. Titilope Fasipe and Jemela Williams share their perspectives.
How Can Sickle Cell Providers Advocate for Equitable Diagnostics?
Maya Bloomberg shares how providers can assist with raising sickle cell education and awareness, screening recommendations, and increasing patient self-advocacy.