As part of efforts to provide critical healthcare services and strengthen advocacy for social inclusion, the Albinism Association of Nigeria ...
The Albinism Association of Nigeria has called for urgent action to address the disproportionate burden of skin cancer among persons ...
When Mrs. Febishola Babatunde first held her newborn with albinism, she was stunned. “I was marvelled. What is this? Where ...
Despite their significant contributions to society, Persons with Albinism (PWAs) continue to suffer from endemic poverty, financial exclusion, and limited ...
Damilola Ibigbami, a 34-year-old woman with albinism from Osun State, urgently needs two million naira (NGN2,000,000) for life-saving surgery after ...
WARNING: Some of the images in the report are sensitive and might be disturbing to some viewers. The Gabriels are ...
The National President of the Albinism Association of Nigeria (AAN), Dr. Mrs. Bisi Bamishe, has appealed to the Nigerian government ...
The Lagos Albinism Awareness Foundation (LAAF) has commemorated the 2023 International Albinism Awareness Day (IAAD) 2023 with the theme: Inclusion ...
The Albinism Association of Nigeria (AAN) has called for continued engagement, recognition, and fair treatment for all workers. The group ...
Albinism is a rare genetic disorder where you are not born with the usual amount of melanin pigment in your ...
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