In many parts of the world, including Africa, individuals living with Non-Communicable Diseases (NCDs) face a significant challenge: the lack of systematic data collection. This gap not only leaves their needs unaddressed but also undermines the value of their lives. Dr. Tim Evans, Assistant Director-General of the World Health Organization, aptly pointed out that where people are not counted, their lives are not valued. This statement underscores the critical importance of comprehensive data collection in understanding and addressing the burden of NCDs, particularly diabetes. For people living with diabetes, this lack of data has profound implications. Diabetes is a chronic disease that requires lifelong management to prevent complications such as cardiovascular disease, kidney failure, and lower limb amputations. However, without accurate information on the prevalence, treatment, and outcomes of diabetes, it is challenging for healthcare providers to tailor care to individual needs.
Priviledge Laimoni and the End Diabetes Stigma Pledge logo In Zimbabwe, as in many parts of the world, individuals living with non-communicable diseases (NCDs) face not only the physical challenges of their conditions but also the harsh realities of stigma and discrimination. This is particularly evident in educational settings, where children with NCDs, such as type 1 diabetes, are often denied enrollment or face barriers to accessing education due to misconceptions and ignorance. This issue is not unique to Zimbabwe; it is a global phenomenon that affects millions of individuals living with NCDs worldwide. The International Society for Pediatric and Adolescent Diabetes ( ISPAD ) has recognized this challenge and has developed guidelines to support the inclusion and well-being of students with diabetes in schools. However, despite these efforts, stigma and discrimination persist, highlighting the need for greater awareness, advocacy, and action to ensure that every child, regardless