A non-governmental organization, CrimsonBow Sickle Cell Initiative, is calling on the Federal Government to increase health funding and review policies on non-communicable diseases (NCDs), including sickle cell disorder.

At its monthly free clinic for 400 sickle cell patients, Founder Timi Edwin stressed the need for prevention rather than only treatment. 

“We must stop stigmatising people with sickle cell. They need regular medical care, free or affordable drugs, and an environment that supports their mental health,” Edwin said.

The clinic, supported by Lafarge Africa, provided routine tests, free medication, vaccination, and counselling. Patients also received guidance on managing the condition, especially during cold weather.

Lafarge Africa’s Corporate Communications Head, Mrs Ginikanwa Frank-Durugbor, said the partnership was part of their corporate social responsibility to improve lives.

Medical experts at the event urged parents to know their genotype before marriage and ensure constant care for their children. Beneficiaries expressed gratitude, noting that sickle cell care is often expensive and out of reach for many.

Edwin concluded:

“Every consultation and every smile shared today is a step toward a future where sickle cell no longer steals potential, dreams, or lives.”