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Educational resources
Practical information for teachers, parents, health workers and communities who want to support people with albinism.
Adopted and adapted for the Cameroonian context. It explains how albinism affects learning, and gives clear guidance on low-vision support, classroom accessibility, sun protection at school and creating an inclusive, bullying-free classroom.
21 February 2026: pilot workshop and teachers’ survey.
The draft is being finalised and tested in classrooms by ten teachers.
Review by pedagogic inspectors and education practitioners, then the final booklet is produced.
Schools and teachers can register their interest in receiving the final booklet by writing to contact@awaforcharity.org.
How is albinism passed from parents to children? This short illustrated presentation explains it simply, through five family scenarios. It was developed after our pilot workshop on the Teacher’s Information Booklet, with Lancaster University, to help teachers, families and communities understand that albinism is genetic, is not contagious and is no one’s fault.
Five things you can do for your child.
Protect your child’s skin from birth: shade, a wide-brimmed hat, long sleeves and SPF 50+ sunscreen every day.
Have your child’s eyes tested early, and ask about low-vision aids.
Tell the school about your child’s needs and share the Teacher’s Information Booklet.
Check the skin regularly and see a health worker about any sore that does not heal.
Speak positively about albinism at home. Your child is capable and deserves every opportunity.
What people say, and what is true.
Albinism is a curse.
It is a genetic condition inherited from both parents.
Albinism is contagious.
You cannot catch albinism.
People with albinism cannot learn or work.
With sun protection and low-vision support, they succeed in school and every profession.
More guides and leaflets will be added here. In the meantime, see our sun-safety tips and tips for teachers.
