The Africa Albinism Network (AAN) has issued a powerful call to the African Committee of Experts on the Rights and Welfare of the Child (ACERWC), highlighting that the lack of sun protection for children with albinism is no longer just a health issue, but a critical matter of climate justice and child rights.
In a statement delivered during the 47th Session in Lesotho, AAN pointed out that more than half of persons with albinism in Africa live in rural communities.
These areas are often the hardest hit by intensifying climate change and simultaneously have the least access to sunscreen, shade, and specialised healthcare.
To address these systemic barriers, AAN proposed a six-point plan for Member States:
1. Sunscreen as Essential Medicine: Governments should include sunscreen on the Essential Medicines List, invest in local production, and ensure it is freely or affordably available in rural clinics and schools.
2. National Action Plans: States are urged to adopt national plans aligned with the AU Plan of Action on Albinism (2021–2031).
AAN specifically commended Zambia for its leadership in launching its National Action Plan on 17 April 2026.
3. Inclusive Education: Advocacy was made for stronger protections against bullying and the provision of “reasonable accommodations,” such as large-print materials and additional time during examinations.
4. Public Awareness: Sustained campaigns are needed to challenge myths and misconceptions to foster respect and dignity.
5. Specialised Healthcare: Expansion of dermatological, low vision, and psychosocial services, particularly in underserved rural regions.
6. AU Special Envoy: AAN called on the African Union to expedite the appointment of a Special Envoy on Albinism to ensure sustained continental coordination.
The network reaffirmed its commitment to working with the Committee and young people with albinism to ensure that every child can live in safety and good health.
SOURCE: AAN/DisabilityNewsGH.com
