Eke
Foundation
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Port Harcourt, Nigeria

"My daughter will not grow up afraid."

When Ngozi's daughter was diagnosed with SS genotype, she was terrified. "I didn't know what to expect, and I was scared for her future," she recalls.

But instead of letting fear take over, Ngozi educated herself about SCD, connected with support groups, and became an advocate for her daughter.

"We talk openly about sickle cell in our home. My daughter knows her condition doesn't limit her dreams. She will not grow up afraid of what sickle cell might do to her."

Today, her daughter is a thriving young girl who knows she is a warrior. Ngozi has started a support network for mothers of children with SCD in her community.

"There's power in community. When you find other families who understand your journey, it changes everything. You realize you're not alone."

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