Most of us have heard of Sickle Cell disease, but what do we really know about it? In this episode, Paige shares her personal experience as a patient and advocate. Her conversation with Brenda and Elaine provides so much insight into what it is like to live with this disorder and the advances that are finally being made to provide relief for those who suffer its effects.

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The Centers for Disease Control has great information about sickle cell disease including: how the trait is passed on and how to get the best care .

The Red Cross provides a history of Sickle Cell Disease.

Sick Cells is a non-profit organization whose mission is “to elevate the voices of the sickle cell community and their stories of resilience—to ultimately influence decision-makers and propel positive change”

Bloodline: A Sickle Cell Warrior with Paige Hardy