ONG DIKO

ONG DIKO is a Nigerien African non-governmental development and humanitarian organisation with a universal vocation and based on ethical values ​​that guide its work. It was created on October 22, 2006 by young progressive students and rights activists under the name “Association pour le Secours aux Populations Vulnérables (ASPV)”. In 2009, this association evolved into an NGO by  ministerial decree with the name DIKO, which means “SUPPORT” in the Djerma language.

Its mission is to support vulnerable populations, particularly women, children, and people with special needs, by promoting social justice, combating inequality, and respecting human rights. They operate using an approach based primarily on human rights.

ONG DIKO works to prevent water-related diseases, hygiene, and sanitation, including hepatitis A and E caused by the consumption of water or food contaminated by faecal matter. Their interventions focus on access to safe drinking water and adequate sanitation through targeted awareness-raising, advocacy, capacity building, the provision of hygiene kits and infrastructure, etc., for the benefit of vulnerable populations. Their commitment to the fight against hepatitis goes far beyond their daily advocacy efforts, raising awareness among authorities, training healthcare personnel, and increasing access to health centres. With 10 years of experience in the field, they have developed in-depth expertise and a nuanced understanding of the multiple facets of this public health issue. Their holistic approach translates into significant involvement in [mention other specific areas of expertise here, for example:

• Prevention and early detection: They have implemented targeted community awareness campaigns, using innovative approaches to inform at-risk populations about the modes of transmission, the importance of screening, and the benefits of early treatment.
• Psychosocial support for patients and their families: Aware of the emotional and social impact of hepatitis, they offer psychosocial support, support groups, and resources to help patients cope with the disease and improve their quality of life.
• Promoting favourable public policies: Their expertise allows us to actively contribute to the development and implementation of public policies aimed at strengthening prevention, screening, treatment, and access to care for people living with hepatitis.
• Research and data collection: They actively participate in the collection of epidemiological data and studies aimed at better understanding the prevalence of hepatitis in our specific context, as well as evaluating the effectiveness of implemented interventions.
• Advocacy for access to affordable treatment: They actively engage in advocacy to ensure equitable and affordable access to antiviral treatments and other necessary care for people with hepatitis.
• Capacity building for local stakeholders: Beyond training healthcare personnel, they work to build the capacity of community organisations and local stakeholders so they can play an active role in the fight against hepatitis within their communities.