people living with albinism living with albinism standing strong people living people with albinism

Albinism Awareness Day: STILL STANDING STRONG!

by Onyinye Okeke August 30, 2020

written by Onyinye Okeke August 30, 2020

By Onyinnye Okeke

Albinism is an inherited genetic condition that reduces the amount of melanin pigment formed in the skin, hair, and/or eyes. Albinism affects all racial backgrounds, ethnic group, and sex.

According to statistics, Nigeria is ranked among the highest in the world with an estimated figure of two million people living with albinism in the country. Over 600,000 Nigerians living with albinism suffer discrimination from their families, schoolmates, and peers.

In most cases, we find families practicing infanticide on babies born with albinism. Other times, people living with albinism are neglected, denied care and education because family considers them worthless. As a result, they lack the confidence to compete with their peers.

There is a need to create a conducive environment for persons living with albinism.
The Albino Foundation (TAF) is the organization in Nigeria that empowers people living with albinism.

5 Truths about Albinism;

People with Albinism do not have red eyes or special powers.
Albinism is caused by genetic changes in both parents passed down from previous generations, not by a curse or infidelity.
Albinism does not affect mental capacity.
Albinism is present in many cultures and many animal species.
People with albinism often have very poor eyesight.

International Albinism Awareness Day is celebrated on 13th June every year. This year’s theme is “Still Standing Strong”.

This is a call to recognize, celebrate, and stand in solidarity with persons with albinism around the world, and to support their cause.
Despite all these challenges, persons with albinism remain positive and are STILL STANDING STRONG!

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Albinism Awareness Day: STILL STANDING STRONG!

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