Founder of the Albino Foundation, Jake Epelle, says the concession of the Joint Admission and Matriculation Board, JAMB, for ...

The government has reiterated its directive to all local government authorities to allocate funds for the purchase of special skin-protection oil for people with albinism, with Sh1.9 billion ...

Every parent looks forward to their child’s firsts. As adoptive parents, my husband and I crammed years’ worth of firsts into ...

Stares, taunts fill life of black twin, 10, with albinism; brother unaffected. Oct. 1, 2009— -- Kenyen and Khari Flowers are 10-year-old, African-American fraternal twin brothers. Born 25 minutes ...

Albinism is a rare condition. It is a genetic disorder which is characterized by the inadequate production of the pigment melanin. The disorder may be inherited from the parents. The condition is not ...

When Megan McMorris, 41 an interior designer from Denver, found out that her daughter Louise, now 9, was born with albinism, she was "devastated." "Myself and my husband had so many thoughts running ...

Abia State Government provides support, including cash and rice, to people with albinism, HIV/AIDS patients, and sickle cell ...

Stacy Omirin got the surprise of her life when she gave birth to twin boys in February 2019. Omirin knew she was carrying two babies — but she never imagined they would have different skin colors.

Learn about organizations working to protect albinos from guesome attacks. Aug. 26, 2010 — -- In Tanzania, life with albinism is a near death sentence. Fifty-seven people with albinism have been ...

When you purchase through links on our site, we may earn an affiliate commission. Here’s how it works. The series "Imaginary Earths" speculates what the world might be like if one key aspect of life ...

President Peter Mutharika has moved to protect people with albinism by ordering security and law enforcement agencies to ...