Dr. Alexia Mays
The only daughter and youngest child of Jesse and Leona Mays, Dr. Alexia Mays, shares her parent's belief in the importance of humanity and giving back.
Alexia has spend much of her life fighting for the rights of others; creating opportunities to help sickle cell warriors and their families, the homeless community, and children experiencing grief and loss.
Sickle Cell Advocacy is a personal mission for
Dr. Mays. She has lived with Sickle Cell (HBSS)her entire life. (her Mother died from Rare Blood disorder when she was 4, her Father died of Sickle Cell(HBSS) when she was 6).
Alexia formed the "Amaysing Kids' to assist children suffering loss and trauma. Having suffered the loss of her entire family by age 10, she understands the need for grief and loss counseling, peer support and resources to assist children as they grieve and heal.
Founded in 2020 to honor her deceased parents and brothers, the May5Foundation works to ensure quality of life for underserved communities.
The foundation works to provide resources, awareness, education, funding and advocacy.
Dr. Alexia Mays leads the efforts for change and the advancement of policies and practices that promote quality of life for those the foundation serve.