The Advocacy Program at TLMIB (The Leprosy Mission International Bangladesh) plays a pivotal role in promoting the rights and well-being of individuals affected by leprosy. This initiative aims to raise awareness, reduce stigma, and empower marginalized communities through a concerted effort to advocate for policy changes, access to healthcare, and social inclusion. In the past year, we have made significant strides toward achieving our advocacy goals, creating a more supportive environment for those impacted by leprosy.


Key Highlights of the Advocacy Program

  • Awareness Campaigns:

    One of the core components of our advocacy efforts has been the implementation of awareness campaigns aimed at educating the general public about leprosy. These campaigns have targeted various platforms, including social media, local communities, and educational institutions, to dispel myths and misconceptions surrounding the disease. By utilizing informative workshops, distribution of educational materials like BCC, flipchart, pictural message, visual presentation, different media communications, billboards, etc. and engaging storytelling. These initiatives have not only informed people about leprosy but also encouraged community discussions that foster understanding and acceptance.

  • Policy Engagement

    To create systemic change, TLMIB has actively engaged with local and national policymakers to advocate for the inclusion of leprosy services within the broader health system. We have successfully organized a series of roundtable discussions and consultations with key stakeholders, including government officials and health authorities. Through these dialogues, we highlighted the need for comprehensive leprosy services, which led to the inclusion of leprosy in the national health agenda. Our advocacy has contributed to increased funding and resources for leprosy treatment and care, ensuring that affected individuals receive the necessary support.

  • Empowerment of Affected Individuals

    Central to our advocacy work is the empowerment of individuals affected by leprosy. TLMIB has facilitated capacity-building trainings, orientations, workshops for local Leprosy People’s Organizations (LPOs) to enhance their advocacy skills and enable them to effectively represent their communities. These interventions have equipped LPO members with tools for effective communication, negotiation, and leadership, allowing them to engage with stakeholders and advocate for their rights confidently. The impact of these training sessions is evident, as LPOs have successfully influenced local policies and garnered support for community-led initiatives.

  • Collaboration with Civil Society

    We recognize that collaboration is essential for effective advocacy. TLMIB has formed strategic partnerships with various civil society organizations, NGOs, and grassroots movements to amplify our advocacy efforts. Through these collaborations, we have coordinated joint campaigns, shared resources, and exchanged best practices, resulting in a unified voice for individuals affected by leprosy. Our collective efforts have raised public awareness and garnered support from diverse sectors, including education, healthcare, and human rights.

  • Monitoring and Evaluation

    To assess the effectiveness of our advocacy initiatives, TLMIB has implemented a robust monitoring and evaluation framework. This framework allows us to track progress, gather feedback from stakeholders, and adjust our strategies accordingly. Our evaluations indicate that our advocacy efforts have led to increased community awareness, improved access to leprosy services, and a notable reduction in stigma towards affected individuals. These outcomes reaffirm our commitment to creating lasting change in the lives of those impacted by leprosy.

Looking ahead, TLMIB is committed to further strengthening our advocacy program. We plan to expand our awareness campaigns to reach underserved populations, particularly in rural areas where access to information is limited. Additionally, we will continue to engage with policymakers to ensure that leprosy remains a priority in health discussions and that the voices of affected individuals are heard and respected.

Moreover, we aim to enhance our partnerships with other organizations working in the field of leprosy, disability rights and health equity. By fostering collaborative relationships, we can utilize resources and expertise to address the broader issues faced by individuals affected by leprosy.

The Advocacy Program at TLMIB is making significant strides in promoting the rights and well-being of individuals affected by leprosy. Through awareness campaigns, policy engagement, empowerment initiatives, and collaboration with civil society, we are working towards a future where leprosy is recognized, treated, and integrated into mainstream health services. We remain committed to our mission of achieving zero transmission, zero disability, and zero discrimination for those impacted by leprosy in Bangladesh. Thank you for your continued support as we strive to create a more inclusive and equitable society for all.