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‘We Deserve to Live!’ – Albino Association Demands FG Action on Skin Cancer Treatment
The President of the Albinism Association of Nigeria (AAN), Dr. Bisi Bamishe, has called on the government and relevant stakeholders to fast-track the inclusion of skin screening and treatment for persons with albinism under the National Health Insurance Scheme (NHIS).....KINDLY READ THE FULL STORY HERE▶
Dr. Bamishe made this appeal during her welcome address at the International Albinism Awareness Day (IAAD) celebration held in Abuja. This year’s event, themed “IAAD 2025: Demanding Our Rights: Protect Our Skin, Preserve Our Lives,” was organized by AAN to spotlight the health and social challenges faced by persons with albinism.
Describing the theme as a compelling call to action, she emphasized the urgent need to integrate skin-related healthcare into NHIS as a life-saving measure.
“The theme underscores the critical need to raise awareness about the health crises—particularly skin cancer—that disproportionately affect people with albinism. It is a reminder to government, civil society, media, and the public that we must not be left behind in matters of healthcare, protection, empowerment, and inclusion.”
Dr. Bamishe lamented that many individuals with albinism are unable to afford treatment for skin conditions, resulting in preventable deaths. She passionately urged the integration of skin screening and care services into the NHIS, stating that such a move would significantly improve survival and well-being.
“Harsh environmental conditions have led to an alarming rise in skin cancer cases among our members. Without access to treatment, we are losing lives every day. We urgently appeal for support to make skin care a part of NHIS—it would save lives and restore hope.”
She also addressed the educational disadvantages faced by students with albinism, particularly those stemming from visual impairments. Dr. Bamishe called on authorities to ensure full implementation of the National Albinism Policy on Education, including timely provision of learning aids to promote inclusive and equitable education.
“May this year’s celebration rekindle our collective commitment to protecting the rights and dignity of persons with albinism. Let it drive stronger advocacy, inclusive policies, and sustainable investment in our health, education, and overall well-being.”
Dr. Bamishe also highlighted the association’s recent achievements, including the expansion of state chapters to 26 (with more underway), official registration with JONAPWD, OPDs, NCPWD, and other key agencies, as well as increased national visibility and the acquisition of a fully equipped project office.
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