The Albinism Association of Nigeria (AAN) has called on the federal government to implement the national policy on albinism established in 2019.
This appeal was made during a one-day meeting with the albinism community and other disability groups to mark International Albinism Awareness Day in Lagos.
The theme for this year’s event was ‘10 years of IAAD: A decade of collective progress.’
Bisi Bamishe, the executive director of AAN, expressed concern that people with albinism still face discrimination and social exclusion from education, healthcare, and employment.
“Persons with albinism are suffering, and it seems there is no hope, even though a national policy supporting our way of living was initiated,” Bamishe stated.
“There is a need to review and implement this policy due to the ongoing negative circumstances faced by PWAs.”
She emphasized the importance of preventing and treating skin cancer, noting that it is the “greatest enemy” of people with albinism.
“The government should provide for cancer treatment, regular skin checks, and sunscreen in all teaching hospitals across the six geopolitical zones of the country,” she added.
Adenike Oyetunde-Lawal, the general manager of the Lagos State Office for Disability Affairs (LASODA), represented by deputy director Kilani Toluwalope, said issues affecting PWAs are a top priority.
“LASODA remains committed to addressing their issues. While resolutions may not be immediate, we will continue to offer support,” Oyetunde-Lawal said.
“Regarding skin cancer, we are working with the dermatology unit in LASUTH. Albinos can testify that we take the issue of cancer very seriously because it is very dangerous.”
