Children with albinism share their stories on CRTV Bamenda
On the eve of International Albinism Awareness Day 2026, two children supported by AWA spoke on CRTV Bamenda.
- +237 674 715 263
- contact@awaforcharity.org
- Mon–Fri 9:00 am – 5:00 pm
Without protection, skin burns quickly and skin cancer can follow.
Most people with albinism have low vision, which affects learning and daily life.
False beliefs lead to stigma, exclusion and, in the worst cases, violence.
Many children and adults miss out on school, work and community life.
Albinism is a curse or a punishment.
Albinism is a genetic condition passed on by both parents. It is no one's fault.
You can catch albinism by touching someone.
Albinism is not contagious. You cannot catch it.
People with albinism have magical powers.
This belief puts lives at risk. People with albinism are ordinary people with the same rights as everyone.
A genetic condition in which the body produces little or no melanin, the pigment that colours skin, hair and eyes. It affects people of all backgrounds.
Yes. Most have low vision, which glasses, magnifiers, large print and a seat near the board can help with.
Sunscreen (SPF 50+), wide-brimmed hats, long sleeves, and staying in the shade between 10 am and 4 pm.
Yes. Albinism does not affect intelligence. With simple classroom support, learners with albinism do well.
Give, sponsor a child's education, volunteer, partner with us, or share accurate information about albinism.
35,000 FCFA
covers one year of public secondary school tuition and PTA fees for a learner with albinism.
Sponsor a Child
I am a woman with albinism. I know what it feels like to burn under the sun with no sunscreen to protect your skin. I know what it is like to sit in class and struggle to read the board. And I know the stares, the whispers and the myths that make people treat you as less than human.
These were not stories I read about. They were my own experiences, and as I grew up and trained as a nurse, I saw many other persons with albinism going through the same pain, often with even less support. Children were dropping out of school. Families did not know how to protect their loved ones. Too many were suffering in silence.
That is why I founded AWA in Bamenda in 2016. I wanted no person with albinism in Cameroon to face these challenges alone.
Today, our work is practical and focused. We protect skin and eyes, keep children in school, keep people safe, help families earn a living, and change minds in our communities.
I did not do this alone. I am deeply grateful to everyone who believed in this vision from the very beginning: my family, friends, mentors and early supporters who encouraged me and told me, “You can do it.” Your faith gave me the courage to start. Thank you as well to our members, volunteers, Board, partners and donors, who continue to carry this vision forward with us.
“Together, we can make every person with albinism safe, included and able to thrive.”
Ngom Maceline Anwi
Founder and Executive Director, registered nurse
“AWA did not simply bring sunscreen and vision aids; they restored our confidence.”
Community focal person
Read more stories
We are based in Bamenda. Our programmes are active in the North-West and South-West regions, and we are expanding to other regions of Cameroon.
On the eve of International Albinism Awareness Day 2026, two children supported by AWA spoke on CRTV Bamenda.
How partners, members and donors keep sunscreen reaching people with albinism in Cameroon.
Making learning data work for every learner, including learners with albinism.
Your support protects health, education, safety and dignity.