S3E3 | Living with Sickle Cell

In this thought-provoking episode of we sit down with Abi, the founder of 'Sickle First', a charity dedicated to supporting those affected by sickle cell disease. With both hosts carrying the sickle cell trait, this conversation is deeply personal as we explore the realities of living with sickle cell, both as a child and an adult. Abi opens up about her own journey with sickle cell and the crucial work she’s doing through 'Sickle First ' to raise awareness and provide vital advocacy support to the sickle cell community. We also discuss the importance of knowing your genotype, not just for health reasons, but also in the context of relationships and dating. The episode also addresses the significant issue of hospital mistreatment faced by sickle cell patients, highlighting the need for improved care, understanding, and education within the healthcare system. This episode is a must-listen for anyone wanting to gain a deeper understanding of sickle cell disease, its impact on everyday life, and the ways we can all do better to support those living with it. Tune in for an enlightening conversation that aims to raise awareness, encourage empathy, and inspire change. Don’t forget to like, subscribe, and share this episode to help spread awareness about sickle cell disease. Sickle Cell, Sickle Cell Disease, Sickle Cell Awareness, Sickle First, Sickle Cell Trait, Living With Sickle Cell, Health Awareness, Genotype Testing, Know Your Genotype, Dating With Sickle Cell, Sickle Cell Support, Sickle Cell Warrior, Hospital Mistreatment, Chronic Illness Awareness, Health Equality, Sickle Cell Community, Genetic Testing, Awareness Matters, Healthcare Reform, Patient Care, Sickle Cell Education, Invisible Illness, Health And Relationships, Sickle Cell Charity, Sickle Cell Advocacy, Sickle Cell Voices, Living With Chronic Illness, Health Talk.