First Black Child Diagnosed with Progeria, AKA Aging Disease

Ontlametse-Phalatse-Progeria

The elfin child with the big personality and bright smile calls herself “the first lady” and dreams of the future. Unfortunately, doctors say 12-year-old Ontlametse Phalatse has only, perhaps, another couple of years to live, says the Associated Press.

“I call myself a first lady because I’m the first black child with this disease … Which other black child do you know with this disease?” she challenged.

Ontlametse is the first black child diagnosed with Progeria, a rare and fatal genetic condition that accelerates the aging process, the Progeria Research Foundation said.

Nobody knows how many kids in the world have it. In a two-year campaign to identify them, the Progeria Research Foundation says the number of children diagnosed around the world has soared from 48 to 80 on five continents. The foundation’s executive director, Audrey Gordon, says only two Africans have been diagnosed and both live in South Africa — Ontlametse and a 5-year-old white girl. That is probably because South Africa, an economic powerhouse, offers some of the best medical care on the continent.

Gordon says there are several black holes on the map in her office studded with colored tacks where they have found children living with progeria. “We know that there are children (with progeria) in Africa, in China and Russia, but we just can’t seem to get to them,” she said in a telephone interview from the foundation’s office in Peabody, Massachusetts.

Ontlametse’s mother, Bellon Phalatse, says her baby was born looking normal but that she realized early on that something was wrong…

[Full Story]

  • John Stamos

    Awe, man. Poor kid, at least she's being positive.