About eight years ago, Tegegn watched as Habitat for Humanity Ethiopia started building a home in Kombolcha. He had heard that leprosy survivors were eligible for housing and wanted to know more.
"After speaking to the Kombolcha Community Committee and registering, I still didn't think I would actually ever get a house", he said. "I waited six months before I heard that construction would begin."
Ali Mohammed Ali, the chairman and founder of the Community Committee who works with Habitat for Humanity, used to live in a shack above a sewer. "My family was always sick," he said. "The smell came through the cracks in the floor and the unhealthy conditions made things worse." Now that Ali and his family have moved into a new house that has changed. "We are rarely sick."
Others, like Tegegn, have many more challenges.
"People like Tegegn have a family, no income and no proper housing. We held a series of meetings and information sessions in the community," Ali commented. "This created awareness about people with disabilities, such as Tegegn, before they became neighbors." The sessions provided critical information on the transmission of leprosy, a bacterial disease that slowly eats away the skin and nerves, causing deformities and disfigurement.
"It was widely believed that leprosy was easily transmittable or that it was a curse," commented Ali, "when in fact it comes from overexposure to another person who is suffering from it." The sessions had a noticeable impact on other families considered to be vulnerable— the disabled, orphans and those affected by HIV/AIDS.
Today, Tegegn and his family live in a home with a 4 by 4 meter living room, and a 2.5 by 4-meter bedroom. "It's like living in a palace," said Tegegn. "We now have a much more normal life." His wife Taitu, who never had leprosy herself, was also discriminated against because she was married to Tegegn.