WATCH THE VIDEO HERE As Nigeria marks National Albinism Day, the Albinism Association of Nigeria (AAN) has reaffirmed its commitment to advocating for the rights, health, and inclusion of persons with albinism (PWAs), urging the government and relevant stakeholders to adopt inclusive policies that address their unique challenges. Established in 2019, AAN has been at the forefront of championing the welfare of persons with albinism across the country. Through targeted advocacy, education, and partnerships, the association has significantly contributed to increased societal acceptance, reduced school drop-out rates among children with albinism, and greater attention to their health needs at national forums. According to the organisation, this year’s theme, Protect Your Skin, Be Sun Smart underscores the pressing need to address the health vulnerabilities of PWAs, especially those resulting from sun exposure. Due to the absence of melanin—the natural pigment that protects the skin from harmful ultraviolet (UV) rays—persons with albinism are prone to painful sunburns, premature skin aging, vision problems, and an increased risk of skin cancer. AAN emphasized preventive measures such as the regular use of broad-spectrum sunscreen (SPF 30 or higher), wearing protective clothing including wide-brimmed hats and sunglasses, avoiding peak sunlight hours, and seeking routine medical checkups for early detection of skin conditions. In a statement shared with Business Post, Mrs Bisi Bamishe, National President of AAN, made a strong appeal to the government: “We are calling on the Nigerian government to include sunscreen in the list of essential medicines under the National Health Insurance Scheme (NHIS). Sunscreen is not a luxury for persons with albinism—it is a necessity for survival.” She further stressed the need for more tangible support “Government should provide free or subsidized protective gear and health services to persons with albinism, especially in rural and underserved areas.” Highlighting the importance of awareness and capacity building, Mrs. Bamishe said, “We urge health workers and teachers to receive proper training on the specific needs of persons with albinism. This will go a long way in improving service delivery and reducing stigma in schools and health centres.” She also emphasized the importance of legal protections. “The Discrimination Against Persons with Disabilities (Prohibition) Act must be enforced. It is not enough to have laws on paper; we need full implementation to ensure justice and inclusion.” “We call for public education campaigns to reach deep into rural communities where harmful myths and stereotypes still persist. Awareness is key to acceptance.” AAN also stressed the need for capacity building initiatives to empower community advocates and peer support systems. As National Albinism Day is observed, AAN urges Nigerians to stand in solidarity with persons with albinism and work collectively to create a more inclusive, informed, and equitable society.
National Albinism Day: AAN Reiterates Call for Inclusive Policy
