Finding new ways to reach all Tanzanians with efforts to eliminate neglected tropical diseases
By Veronica Kabona, RTI International
In the heat of the day, fisherfolk draw their nets from the water. Their vessels dot the coastline in Kilwa, a coastal district in southern Tanzania that encompasses five islands. Fishing pays the bills and feeds the families of many in Kilwa.
But these fisherfolk—and their neighbors—are threatened by a disease spread by mosquitoes that is proving difficult to eliminate in certain areas, including Kilwa. Tanzanians, like Dr. Faraja Lyamuya from Tanzania’s Ministry of Health, are leading the charge to address these neglected tropical diseases (NTDs) and tailor treatment to reach all Tanzanians at risk, including fisherfolk.
“I love doing this work because I see how people are suffering and we know that if we can help them, they can avoid the effects of this disease,” Dr. Lyamuya said. “Our wish is that the next generation of Tanzanians won’t have any cases of it—that it will be out of the picture.”
Across Tanzania, health leaders like Dr. Lyamuya are working to reduce levels of this NTD called lymphatic filariasis (LF), a mosquito-borne parasitic disease, which can lead to disability, stigma, and pain. Today, more than 28 million Tanzanians are free from the risk of contracting it and developing elephantiasis and hydrocele—two conditions that can result from the disease.
“People become victims of disability because of elephantiasis,” Dr. Lyamuya explained. “It causes not only physical but also psychological damage. It makes them feel like outcasts…and leads to individual poverty, which also leads to poverty in the family and society at large.”
“People were suffering and in a lot of pain,” added Abdalah Mohamedi Milenge, a community drug distributor who works to reach his community with treatment and information about the disease. “After taking medicine, the problems have greatly reduced.”
“People become victims of disability because of elephantiasis,” Dr. Lyamuya explained. “It causes not only physical but also psychological damage. It makes them feel like outcasts…and leads to individual poverty, which also leads to poverty in the family and society at large.”
“People were suffering and in a lot of pain,” added Abdalah Mohamedi Milenge, a community drug distributor who works to reach his community with treatment and information about the disease. “After taking medicine, the problems have greatly reduced.”
Overcoming skepticism to eliminate lymphatic filariasis
Convincing people to take medicine was an initial challenge—one that education and outreach has helped to alleviate.
“People were less receptive [to the medicine] in the beginning because they thought it would affect men’s virility and have side effects,” Abdallah said. “Providing education to local villages and neighborhoods [on the safety and efficacy of the medicines] is important for motivating people.”