Mitchell Bays Turner was born a healthy vivacious boy on February 27, 2012. “It wasn’t until the morning of his baptism, when Mitchell was three-months-old, that his mother, Meg McElwain, noticed bruising on his legs. The next day, she took him to the pediatrician who recommended a blood test. The results of which showed Mitchell was anemic and had an extremely high white blood cell count. Mitchell and his mother were sent directly to Novant Health Hemby Children’s Hospital.”


That day, Mitchell Bays Turner was diagnosed with a rare form of Infant Acute Lymphocytic Leukemia (ALL); he was given a 40% chance of survival. The family immediately started treatment.


Over the course of Mitchell’s two year battle with childhood cancer, he enduring long hospital stays, harsh chemotherapy drugs and isolation from family, including his older brother, Frank. Mitchell did achieve remission, but later relapsed.


Mitchell died due to complications from the intense chemotherapy and antibiotic medications. He died just weeks after his second birthday; he lived only 774 days.


His parents, Meg McElwain and Frank Turner, III, are committed to serving families who are experiencing life-threatening pediatric illness and the unexpected financial hardships that come along with it. For them, Mitchell’s Fund is way of coming alongside these families in support and honoring their son’s memory.

Mitchell Bays Turner Pediatric Fund

1307 W. Morehead Street
Suite 207
Charlotte, NC 28208

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