Albinism is a genetic condition that affects people of all races and backgrounds. It occurs when the body produces very little or no melanin, which is the pigment that gives colour to the skin, hair, ...

THE albino community has shared harrowing experiences of discrimination, harmful myths and threats of ritual exploitation that continue to endanger their lives. Many describe being ostracised by ...

Honey badgers are not actually named for their love of honey, in fact, they raid bee hives to loot the delicious, protein-rich larva inside, which seems like an overly complicated way to get protein.

A UN expert on Wednesday urged increased efforts to promote the implementation of laws to protect people with albinism in Portugal, ensuring their equitable access to education, health, and employment ...

Fresh trauma arrives with every election season in Tanzania for 42-year-old Mariam Staford. For most, the fiesta-like rallies and songs, along with the campaign messages, signal a chance for people to ...

Human rights activists are urgently calling for legal safeguards against ritual-related violence and protection for people living with albinism in Zambia. But can such movements bring real change to ...

Misty Glam Company has crowned Anita Chidiebube Dike as the Albinism Advocacy Queen 2025, at the grand finale of Nigeria’s first-ever Albinism Advocacy Pageant. Themed “Beauty in Inclusivity”, the ...

The Department of Women, Youth and Persons with Disabilities is using September to highlight that people with albinism, who have a rare genetic condition affecting melanin production, face not only ...

Albinism is a rare genetic condition marked by little to none of the pigment melanin, which is responsible for the color in hair, skin, and the irises of the eyes. This results in a range of very pale ...

Hajia Humu Suala na mama of six children – three of dem get albinism, even tho she and her husband Abdul Rahim Sambo dia skin colour dey black. Humu Sambo say her second child get golden hair when she ...

The mother of a two-year-old girl with albinism has welcomed funding for research into improving eyesight for children with the condition. Her daughter Amelia is severely visually impaired as a result ...