Who we are

A charitable trust registered in Kenya, restoring the dignity of people with albinism.

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The foundation

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Meet Dr. Prabha Choksey →

What we do

Eye care, education support, awareness, and community empowerment.

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Programs

 

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Help a child with albinism. Share your love and kindness with those in need.

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Our focus

There is a strong link between a child’s sight and their learning, their performance in school, and their education.

That is why our work begins with the eyes and continues into the classroom. With our partners NCBA Bank, 3Z Foundation, M-Pesa Foundation Academy and others, we give the Gift of Sight, the Gift of Education, and Wings to Fly to children with albinism who are orphans or come from extremely poor backgrounds in Kenya.

The urgency is not ours alone to claim. The United Nations reports that in some countries a majority of persons with albinism die of skin cancer between the ages of 30 and 40 — from a cause that sunscreen, protective clothing and a routine skin check can prevent. The same lack of melanin leaves most with permanent visual impairment. Sight, sunscreen and school fees are not charity; they are the difference between a short life and a full one.

Albinism in focus

Understanding albinism

Albinism occurs in every country and every ethnic group on earth. What differs is how common it is — and how dangerous it is to live with.

1 in 1,400Estimated prevalence of albinism in parts of Tanzania
1 in 5,000Upper estimate across parts of sub-Saharan Africa
1 in 17,000Prevalence across Europe and North America
June 13International Albinism Awareness Day

Prevalence figures: United Nations and the Office of the High Commissioner for Human Rights. Estimates vary by country and study.

Dr. Choksey with sponsored students at the NCBA cheque-handover

Scholarships

A child without education is like a bird without wings

Our scholarship program keeps children with albinism in school. In 2026 it is paying the fees of 124 learners — 25 of them in pre-primary, 84 across the primary grades, and 15 in senior and secondary school. The youngest were born in 2023; the eldest are sitting Form 4.

In 2017, beneficiary Goldalyn Kakuya Tanga made history as the best-performing student in the Kenya Certificate of Primary Education, scoring 455 out of 500 and outperforming 993,718 candidates nationwide.

She proved to the world that disability is never inability.

Apply for our scholarship

Advocacy & awareness

Our approach

Our Albinism Advocacy and Awareness Program provides information and services to people with albinism, their families and the public.

Our teams are made up of educators, medical professionals, trained parents and experts in their fields. Across Africa, myths still put children with albinism in danger. Facts, spoken often and by the right people, are how that ends.

“Multiple and intersecting discrimination on the grounds of both disability and colour.”

The United Nations, on what people with albinism face

Areas of focus

  1. 01

    Discrimination advocacy

    Standing with people with albinism who face stigma, abuse or exclusion, and with families forced to flee for their children’s safety.

    Five siblings who fled DR Congo
  2. 02

    Educational advocacy

    Guiding parents, students and educators on the support learners with low vision need to thrive in regular schools, and speaking up when a child is turned away.

    Challenging our children to lead
  3. 03

    Awareness day

    Leading Kenya’s International Albinism Awareness Day activities each June 13, alongside communities worldwide, and backing the artists who carry the message further.

    “Creek” on the Nairobi stage
  4. 04

    Policy research

    Researching the policies that shape the lives of people with albinism, and working with government bodies to reach children in more counties of Kenya.

    Working with NCPWD
Report abuse

Is a child with albinism in danger?

If a child is at immediate risk in Kenya, call the police on 999 or 112, or Childline Kenya on 116, free from any phone. Then tell us. We will support the child and family, confidentially.

Report to the foundation

For parents & guardians

Adapting to a diagnosis of albinism takes education, support, love, and time. A few suggestions for the journey ahead.

Need more help? Contact us

Feelings of sadness, fear, helplessness, and anger are normal. Take time to process how you feel so you can be a support for your family.
Acknowledge progress and celebrate successes. Stay in the present: you only need to handle the phase in front of you and stay one step ahead.
Educate yourself so you can answer questions about your child’s appearance or vision, and raise awareness among colleagues, neighbors, friends, and family.
Small adjustments to the physical environment can make your child much more comfortable.
Whenever possible, let your child find their own creative solutions to visual challenges.
Parenting a child with albinism doesn’t require special skills. The most important thing is that your child is a unique human being, treasured for who they are.
Children adapt naturally, holding objects closer or standing nearer the TV. They often see more than you expect and can ride bikes, play sports, read, and make friends.
Ask for help. Tap into the foundation’s community, meet adults with albinism, listen to their stories, and join our events or webinars.

Our partners

We are grateful to everyone who helps give the Gift of Sight, the Gift of Education, and Wings to Fly.

Global Albinism AllianceProud memberGlobal Albinism Alliance
NCBA BankEducation since 2015NCBA Bank
Women Ophthalmologists WorldwideEye careWomen Ophthalmologists Worldwide
M-Pesa Foundation AcademyEducationM-Pesa Foundation Academy
Albinism Foundation in AfricaSun protectionAlbinism Foundation in Africa

With thanks also to the National Council for Persons with Disabilities and 3Z Foundation.