Hi there,
I was just 12 years old when I was diagnosed with Systemic Lupus Erythematosus (SLE)—commonly known as lupus. Living with lupus since my teenage years has been a journey filled with highs and lows. While it hasn’t always been easy, I’ve worked hard not to let it define me.

The Labalaba Foundation (TLF) is doing incredible work to raise awareness about lupus in Nigeria. Through advocacy, education, and community support, TLF is improving the lives of those affected by this often misunderstood disease—including people like me.

If you can, please consider supporting this mission by clicking the “Donate Today” button. Every contribution helps us reach more people, provide more resources, and drive change.

Thank you so much for your support!