In the heart of Ghana’s Upper East Region, the Bongo District is fighting a quiet but devastating battle. Over the last six years, this rural district has recorded a deeply worrying rise in leprosy cases, with 57 new cases reported from 2019 to September 2025. For many, the word “leprosy” conjures up images from distant history books, but in Bongo, it is a daily reality, one made worse by stigma and isolation. This troubling revelation came from Mr. Kpankpari Wononuo Bismark, the District Neglected Tropical Diseases (NTDs) Focal Person, in the documentary “Pains of the Forgotten: Leprosy, Stigma, and Resilience” produced by Ngamegbulam Chidozie Stephen of ApexNewsGH. In a candid conversation, Mr. Bismark described the situation as “alarming,” drawing attention to the many layers of hardship leprosy patients endure beyond their diagnosis. “Stigmatization in Bongo is very high,” Mr. Bismark lamented. “Some patients are isolated, left in separate rooms, made to live alone. This worsens their mental health.” For many, the fear of being shunned by neighbors and loved ones is just as crippling as the disease itself. Some wait until their symptoms are too severe to hide, seeking help only when sores and deformities make life unbearable. “When we identify leprosy early, we can treat it within nine months,” Mr. Bismark explained. “But when patients report late with sores and deformities, the damage remains for life.” The consequences of this fear-driven delay are profound. Advanced leprosy often leaves patients with lifelong disabilities, making it impossible for them to farm or work. In a region where most people depend on their hands to earn a living, the economic toll can be just as devastating as the physical suffering. “Most of them cannot do meaningful work because of deformities,” Mr. Bismark said. “That is why interventions from NGOs that provide small capital for farming, weaving, or soap-making are so helpful. These initiatives help reduce idleness and restore dignity.” But the challenges don’t end with stigma and economics. Mr. Bismark also pointed to the struggles of accessing medicine, which must be requested from the regional health directorate and sometimes runs out. Still, he remains optimistic about the impact of treatment: “The good thing is that when we start the medicine, transmission to others is minimized, even though sometimes we run out of drugs briefly.” The changing climate also brings fresh hardships for leprosy patients. During the harsh dry season, cracked skin can lead to open sores that quickly become infected. Without easy access to clean water and proper hygiene, these sores can become septic, threatening not just health but life itself. “NTDs are neglected diseases, and sadly, the people suffering from them are also neglected,” Mr. Bismark noted. “Many patients live far from clean water sources, making hygiene very difficult.” Water, sanitation, and hygiene (WASH) remain critical challenges. In remote villages, fetching water involves long, painful journeys, a heavy burden for those already weakened by disease. This lack of WASH infrastructure leaves patients especially vulnerable to complications and further social exclusion. Despite these daunting obstacles, hope persists in the form of early detection and community support. “Leprosy is airborne, and elephantiasis is caused by mosquito bites. Everyone is at risk. That is why we keep telling the community: support patients, don’t stigmatize them, because you never know when you could also be affected,” Mr. Bismark urged. The fight against leprosy in Bongo is not waged by government alone. Non-governmental organizations like the Development Research and Advocacy Center (DRAC), led by Executive Director Jonathan Adabre, are helping to fill the gap. DRAC’s holistic approach tackles both the practical and social sides of the disease. “With support from Anesved Fundación, we raise awareness about early signs of diseases like leprosy, elephantiasis, and yaws,” Adabre explained. “Many believe leprosy is genetic, but it takes up to 20 years to manifest. That misconception must end.” DRAC’s projects are as varied as they are vital. The organization has drilled ten boreholes across affected communities, ensuring that more families have access to clean, safe water. They have also formed water health committees to educate locals on hygiene practices, crucial for managing NTDs. But perhaps their most transformative work lies in supporting economic empowerment. DRAC provides training and materials for basket weaving and soap-making, linking patients and caregivers to markets. “Buyers come to the community to purchase baskets, and we provide materials and training,” Adabre says. These initiatives offer more than income; they restore a sense of purpose and connection. The story of leprosy in Bongo is one of pain, but also of resilience and hope. It is a reminder that diseases like leprosy do not just attack the body, they disrupt families, livelihoods, and entire communities. Breaking the cycle requires more than medicine. It calls for compassion, early detection, and the kind of holistic support that brings patients out of the shadows and back into the embrace of their community. As Bongo continues its fight, the district’s journey stands as a testament to the power of partnership, awareness, and above all, human dignity. WATCH THE VIDEO DOCUMENTARY BELOW: Source: Apexnewsgh.com/Ngamegbulam Chidozie Stephen
Pains of the Forgotten: Leprosy, Stigma, and Resilience in Ghana–VIDEO ATTACHED
A documentary by Ngambebulam Chidozie-Stephen (ApexNewsGH) Editor in Chief Leprosy is one of humanity’s oldest diseases, yet in 2024, it remains a pressing global health crisis. According to the World Health Organization (WHO), 188 countries and territories reported a total of 172,717 new cases last year. The impact is not evenly distributed; women and girls comprised over 40% of new patients, and children accounted for more than 9,000 cases. Most troubling, over 9,100 new sufferers were diagnosed with the most severe form, grade 2 disability, a diagnosis that can mean permanent deformity and a lifetime of hardship. While leprosy’s global shadow is long, its most profound pain is felt in places like Ghana’s Upper East Region. Here, in the Bongo district, a community of just over 120,000 people, leprosy remains a silent threat. From 2019 to September 2025, 57 cases were officially reported, and the true number may be higher due to fear, stigma, and misunderstanding. Leprosy is just one of many Neglected Tropical Diseases (NTDs) that persist in Ghana. These diseases, fourteen of which are endemic in the country, disproportionately affect the poorest, deepening cycles of poverty and exclusion. Pain Behind Closed Doors: Matilda’s Story In the tight-knit community of Bongo Balungu, Matilda Nyaaba’s life is defined not only by the disease itself but by the isolation it breeds. For ten years, Matilda endured unexplained symptoms, fainting spells, nosebleeds, and growing weakness, a mystery to both her and the health professionals she visited. “Each episode left me weaker,” Matilda shares, remembering the confusion and fear that accompanied each new symptom. The only constant in her life became her monthly trips for medicine. Her family, she explains, has been a source of support, but the wider community’s reaction has been another story. She describes a self-imposed solitude, “I advised myself to stay indoors. They would use my condition against me.” Even basic errands, like fetching water from the borehole, are shadowed by the fear of being shunned. Whispers followed her: “Some described my illness as HIV, others as a curse. This has deeply affected my mental health; I don’t know what I’m thinking anymore.” Yet, Matilda’s resilience endures. She dreams of more than just survival: “If the government could help, maybe by providing vocational training, I could regain my dignity and hope for a brighter future.” From Provider to Dependent: Ania’s Struggle Before leprosy, Aniah Lamisi was at the center of her family’s livelihood in Bongo Soe. Farming was her pride and her purpose. But illness arrived quietly, a tingling in her fingers, followed by the slow, cruel twist of her hands. Aniah’s life shrank as the disease progressed. She could no longer wield a hoe or prepare meals over an open fire without pain. Even fetching water, a lifeline in the village, became a daily ordeal. She reflects on her new reality: “Some people have lost everything, even their mental faculties. I can still care for myself, dress well, and sometimes mingle with groups. That’s how I console myself. But if I can’t farm, how do I feed myself? I just sit and eat, if there’s food. Who will work for me?” Her appeal is simple but urgent. “If the government can provide us with a vocation or manual labor, we could earn a living. Now, I just wait and hope for food. Even cooking is painful, but who else will do it for me?” In Bongo Swing, Mr. Adombire Ayuumbeo once embodied industry and self-reliance. He farmed, cut firewood, and harvested thatch, supporting his family with pride. But when leprosy struck, it took his independence, disfigured his body, and left him idle. He describes the loss with raw honesty: “Everything I used to do to earn a living is gone. Now I am helpless. I sit alone. Nobody helps me. Sometimes I think it would be better to die than live like this. People stigmatize you. I don’t know why God gave me this disease that people don’t respect. When I remembered all these things happening to me, my tears began to fall.” He issues a plea not just for himself, but for others like him: “If the government can help sustain our lives, they should do it. I vote, I have a voting ID. If the government has anything to help, we would appreciate it.” The Sustainable Development Goals (SDGs), specifically Goal 3: Good Health and Well-being, address neglected tropical diseases (NTDs) like leprosy under Target 3.3. This target states: “By 2030, end the epidemics of AIDS, tuberculosis, malaria, and neglected tropical diseases, and combat hepatitis, waterborne diseases, and other communicable diseases.” This means that the global community, through the United Nations and its member states, has committed to eliminating NTDs, including leprosy, as public health problems by 2030. The aim is to reduce illness, disability, stigma, and death caused by these diseases through prevention, early detection, treatment, and improved access to health services, especially for vulnerable populations. In essence, the SDGs recognize that fighting NTDs is essential for achieving universal health coverage, reducing inequalities, and promoting the well-being of all people, particularly those living in poverty and marginalized communities. Ending NTDs like leprosy not only improves health outcomes but also supports broader development goals such as education, gender equality, and economic productivity. The rising trend of leprosy in Bongo is confirmed by Mr. Bismark Kpankpari Wononuo, the district’s Disease Control Officer, who doubles as the NTDs coordinator. He explained that the numbers increase every year. He credits increased detection to community volunteers but warns that the real challenge is stigma. According to him, “Many don’t come early for treatment due to discrimination. Early detection is key; if we treat early, within nine months, it can be cured. But when affected persons decide to report late, it causes deformities to remain for life.” He further sends a clear message to the community by letting them know that Leprosy is treatable and that early detection is crucial. “Everybody is at risk.” However, he acknowledged that there are









