On National Albinism Day 2025, the Albinism Association of Nigeria (AAN) has called on the Nigerian government to prioritize the health and rights of persons with albinism (PWAs) by subsidizing protective gear and strengthening anti-discrimination laws.
The group also appealed for increased awareness about sun protection and inclusion for persons with albinism across the country.
Under the theme “Protect Your Skin, Be Sun Smart,” the National President of AAN, Dr. Bisi Bamishe, emphasized the critical need for preventive care, public education, and decisive government action to safeguard the health and dignity of people with albinism in Nigeria.
In her statement, Dr. Bamishe highlighted that persons with albinism lack melanin, the pigment that protects the skin from harmful ultraviolet radiation, making them extremely vulnerable to painful sunburns, premature skin aging, and significantly higher risks of developing skin cancer.
To mitigate these risks, AAN recommended regular use of broad-spectrum sunscreen (SPF 30+), wide-brimmed hats, long-sleeved clothing, sunglasses.
“Prolonged exposure to the sun poses serious health risks for persons with albinism, especially those living in rural areas with limited access to protective resources and healthcare services,” Dr. Bamishe added.
The association also urged PWAs to attend routine medical checkups for early detection of skin changes.
AAN called on the Nigerian government at all levels to implement concrete support measures, specifically appealing for the inclusion of sunscreen as an essential medicine under the National Health Insurance Scheme and provision of free or subsidized protective gear for persons with albinism.
“Provide free or subsidized protective gear and health services to PWAs. Train healthcare providers and teachers on the specific needs of persons with albinism.
“Enforce anti-discrimination laws and ensure full implementation of the Discrimination Against Persons with Disabilities (Prohibition) Act; and support public education campaigns targeting rural communities,” the AAN president added.
Dr. Bamishe emphasized that achieving long-term positive change would require strengthened policy implementation, improved data collection, strategic partnerships with NGOs and private sector actors, and enhanced capacity building for community-based advocacy.
The association expressed appreciation to its members, volunteers, donors, media partners, and collaborating state governments, as well as the National Commission for Persons with Disabilities, Disability Rights Fund, and Joint National Association for Persons with Disabilities.
“Together, let us commit to a Nigeria where persons with albinism are safe, empowered, and included,” Dr. Bamishe said.
Established in 2019, AAN has worked to address unique challenges faced by persons with albinism, including health risks, stigma, and discrimination. The organization reports achieving increased community awareness and acceptance, reduced school dropout rates among children with albinism through targeted support programs, and greater recognition of albinism-related health challenges at national health forums.
By His Divine Grace, we shall all sail through by the involvement of the necessary organization and The AAN as a whole