PRESS RELEASE
National Albinism Day 2025: AAN Calls for Greater Protection,
Health Equity, and Inclusion for Persons with Albinism
As Nigeria commemorates National Albinism Day today, the Albinism Association of Nigeria (AAN) is calling for greater awareness, protection, and inclusion of persons with albinism (PWAs). The association urges the government to take concrete steps to address the unique health and social challenges faced by this often-overlooked population.
In a statement issued to mark the occasion, Dr. (Mrs.) Bisi Bamishe, National President of AAN, emphasized this year’s theme: “Protect Your Skin, Be Sun Smart.” The theme highlights the urgent need for preventive care and public education to safeguard the health and dignity of people with albinism across the country.
Dr. Bamishe noted that persons with albinism, who lack melanin the pigment that protects the skin from harmful ultraviolet (UV) radiation are particularly vulnerable to a range of health complications. These include painful sunburns, premature skin aging, severe visual impairments due to light sensitivity, and an alarmingly high risk of skin cancer, especially among those living in rural areas with limited access to protective resources.
To reduce these risks, the AAN encourages:
- Consistent use of broad-spectrum sunscreen with an SPF of 30 or higher;
- Wearing of sun-protective clothing, including wide-brimmed hats and long sleeves;
- Avoiding outdoor activities during peak sunlight hours;
- Regular medical check-ups for early detection and treatment of skin-related issues.
The AAN is also urging the Nigerian government at all levels to:
- Recognize sunscreen as an essential medicine under the National Health Insurance Scheme (NHIS);
- Provide free or subsidized healthcare and protective gear to persons with albinism;
- Train healthcare workers and educators on the specific needs of PWAs;
- Fully implement and enforce the Discrimination Against Persons with Disabilities (Prohibition) Act;
- Launch nationwide public education campaigns, especially in rural and underserved communities.
To ensure long-term impact, the association is advocating for stronger policy implementation, data collection on persons with albinism, increased collaboration with NGOs and international development partners, and strengthened community-based advocacy through peer support networks.
Dr. Bamishe expressed profound appreciation to all those who have supported the association since its founding in 2019. She acknowledged the vital contributions of members, volunteers, donors, media partners, and stakeholders such as the National Commission for Persons with Disabilities (NCPWD), the Disability Rights Fund (DRF), state governments, and the Joint National Association of Persons with Disabilities (JONAPWD).
“Together, let us commit to a Nigeria where persons with albinism are safe, empowered, and included,”
Dr. Bisi Bamishe, National President, AAN
