Abstract / Summary
Since July 1, 2026, pancreatic disability has been recognized as a disability category eligible for registration in South Korea. This policy change acknowledges that diabetes management requires not only individual effort but also coordinated healthcare, welfare services, and social support. The registration system is intended for individuals with severe pancreatic endocrine dysfunction who require continuous insulin therapy and intensive glycemic management and are at high risk of severe hypoglycemia or diabetic ketoacidosis. Although the new system provides access to essential healthcare, welfare, educational, and employment support, disability registration may also raise concerns about psychological adjustment, disclosure of health information, stigma, and discrimination. Its implementation should therefore be accompanied by comprehensive counseling and information services that enable patients and families to make informed decisions about available resources. In this process, diabetes educators play a key role in reducing stigma, supporting self-management, and promoting social participation and quality of life.