As part of the programme to mark the World Cancer Day 2025, the Albinism Association of Nigeria (AAN) has called for the inclusion of skin cancer in the National Health Insurance Scheme (NHIS).
In a statement to mark the 2025 World Cancer Day, which is commemorated on February 4 globally, the President of AAN, Dr. Mrs. Bisi Bamishe said sunscreen, wide-brimmed hats, and protective clothing should be made accessible and affordable, especially to low-income persons with albinism (PWAs), through government intervention programmes and corporate social responsibility initiatives.
The AAN used the 2025 World Cancer Day, observed under the theme ‘United by Unique,’ to amplify the voices of persons with albinism in Nigeria. The theme speaks to the power of unity in addressing the global cancer burden.
In addition, the AAN called on the federal, state, and local governments, the legislative arms at all levels, well-meaning individuals, local and international donors, and relevant stakeholders to stand with persons with albinism in the fight against skin cancer.
“We call on lawmakers at all levels to pass and implement policies that recognise and address the specific health challenges of persons with albinism, including budgetary allocations for skin cancer prevention and treatment.
She urged the Federal Ministry of Health and Social Welfare (FMoH&SW) to integrate free and subsidised skin cancer treatment, early screening, and regular dermatological check-ups for persons with albinism in public hospitals.
According to Bamishe, the absence of structured government interventions, including access to free or subsidised skin cancer treatments, preventive measures such as sunscreen distribution, and specialised dermatological care, has left our community in a state of despair. “Without immediate action, we will continue to witness the preventable deaths of our members,” lamented Bamishe.
Similarly, she stated that special appreciation goes to the Lagos State Government that has spent over N20 million on skin cancer patients in the last two years as well as the provision of sunscreen, hats and umbrellas. “We hope other states can follow suit as much as possible,” Bamishe added.
She said, “We seek collaboration with global health organisations, donor agencies, and research institutions to develop long-term solutions that will improve the healthcare and quality of life for PWAs in Nigeria.
“There is a need for nationwide educational campaigns to enlighten both PWAs and the general public on the importance of early detection, preventive measures, and available treatment options.”
According to the president of the AAN, “The lives of our community members are precious, and we cannot afford to remain passive in the face of this growing crisis. We stand united by unique challenges, but we also believe in the collective power of government intervention, public support, and global solidarity to change the narrative for persons with albinism in Nigeria.”
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