13/03/2026
The Invisible Illness
Not every illness is visible.
Yet the battles within the body can be very real.
In celebration of International Women’s Day, I had the privilege of speaking about a condition often referred to as the “invisible illness.” For a long time, I hesitated to speak openly about it because it is widely misunderstood and can easily stigmatize those who live with it.
At the event hosted by the Association of Nigerian Female Students (AFNS), I spoke about the misconceptions surrounding lupus, the need to create safe spaces where women can speak about their health struggles without fear, and messages of hope for those living with chronic illnesses today.
Systemic Lupus Erythematosus (SLE) is a condition that mimics many other illnesses, which often makes it difficult to diagnose. Sadly, many sufferers have been misunderstood, misdiagnosed, or even accused of having spiritual problems. Yet with proper medical care, awareness, and healthy lifestyle management, many lupus warriors can live meaningful and purposeful lives.
To every Lupus warrior and everyone living with a chronic health condition who shows up each day despite the uncertainty of how their body may respond, I see you.
You are strong. You are resilient.
I am deeply grateful to the for the opportunity to represent them and for the honour of receiving an award on behalf of the selfless and sacrificial work of SafinatEmenego in championing the cause of lupus warriors.
My sincere thanks to the leadership of the Association of Nigerian Female Students for providing this platform and for continuing to champion the cause of resilient and purposeful women.
It was also an honour to share the stage with remarkable women including the Mandate Secretary for Women’s Affairs Secretariat in the FCT, Hon. Benjamins-Laniyi, Aisha Shuaibu, ,the TOS Group, and PrettyDarkDiva.
This month, I stand in solidarity with all Lupus Warriors.
