Unveiling of New AAN President In Abuja
On September 22nd, 2022 . Jake Epelle, the founder and CEO of The Albino Foundation (TAF) announced his resignation as...
Cost of living with Albinism in Nigeria
Albinism is a rare genetic disorder whereby one is not born with the usual amount of melanin pigment in the...
Skin cancer kills many persons with albinism in Nigeria —Association
The Albinism Association of Nigeria has raised the alarm that many of its members in the country are dying of...
Bisi Bamishe Becomes Albinism Association Of Nigeria President, As Jake Epelle Resigns
Mr. Jake Epelle, The Founder and CEO of The Albino Foundation (TAF) has announced his resignation as the National President...
New State Executive officers of AAN Lagos Chapter
Meet the the New State Executive officers of AAN Lagos Chapter
Persons With Disabilities In Lagos Want More Inclusion Ahead Of 2023 Polls
More than two million Persons With Disabilities, PWDs, under the aegis of the Joint National Association of Persons with Disabilities,...
Albinism Group Advocates Innovation to Bridge Disability Gap in Nigeria
The Albinism Association of Nigeria (AAN) has called for increased innovation to drive sustainable development, which will help close the...
AAN Calls For Better Life For Persons With Albinism, Introduces National Officers
The Albinism Association of Nigeria (AAN) has reiterated the call for better life for persons with albinism in the country....