Mariamu Stanford, a soft-spoken, 28-year-old single mother from rural Tanzania, has earned a grim distinction: She's one of only two people with albinism -- a group that has faced discrimination in East Africa -- to survive a brutal attack by those wanting to sell the limbs of albinos on the black market.
In her first interview with American journalists, Stanford greeted ABC News visitors with a shy smile, wearing a short-sleeve blouse that revealed the scars of her ordeal.
Last October, men armed with machetes entered her hut and began cutting at her arms in a gruesome attempt to amputate them, Stanford told ABC News.
"In the middle of the night, a group of men stormed in and said, 'We are going to cut your arm off, and if you scream we'll cut the other arm off,'" she said. "And then they started to chop my right arm off. And because I was screaming, they also started to do the same with the other."
After her attackers fled, it took six full hours for Stanford to get medical treatment. Five months pregnant at the time, she lost both arms and her unborn child.
A devout Christian and member of her church choir, Stanford was caught up in a grisly trade inspired by a renegade set of witch doctors; they claim potions made of the blood, skin or bones of an albino can make people wealthy and bring good luck.
We spoke just outside the two-room mud-floor building, where she lives with her parents, four young siblings and her son, a toddler. Her artificial limbs, donated by a well-wisher, lay discarded because they were painful and cumbersome.
Despite Tanzania's reputation as a tourist mecca known for safaris and visits to Mount Kilimanjaro, people with albinism are being hunted down like animals. Since 2007, 54 Tanzanian albinos, including children, have been murdered by gangs of men who hack off arms, legs or genitals. Observers said even more cases of attacks have gone unreported.
Tanzania is arguably the worst place in the world to be born with albinism -- a hereditary genetic condition caused by two recessive genes resulting in little or no pigment production in the hair, skin or eyes. The country has one of the largest populations of albinos in the world -- an estimated 170,000 -- and they are being targeted for their white skin.
Officials say ignorance, prejudice, traditional beliefs and poverty are behind the epidemic of albino killings. In a country where per capita income is $442 a year, the limb of a person with albinism can fetch almost anywhere from $500 to $2,000.
It doesn't help matters that many in Tanzania still live according to superstition. For decades, people with albinism have been thought of as ghosts and bad omens. It is also believed that albinos don't die; they just disappear.
"I was always hearing these tales, people here believe that albinos do not die, they disappear so I was always wondering how I am going to disappear," Stanford said.
The idea that the body parts of albinos can bring wealth is a recent phenomenon. Some have been known to use human hair from albinos woven into fishing nets for good luck.
At the Mwanza homestead of witch doctor Jackson Kanyerere, who offers his patients medical and spiritual care, he told ABC News that the person who started this superstition wasn't even a witch doctor.