This paper explores the crucial role of legislation, sector skills standards, and organizational policies in promoting and maximizing the rights of users in health and social care. It examines factors that can hinder user empowerment, such as loss of independence and social exclusion, and analyzes how communication between care workers and individuals contributes to a positive and rights-respecting environment. The paper also delves into the tensions that arise when balancing individual rights with the care provider's duty to protect, using a case study to illustrate the potential risks of harm. Finally, it reviews current legislation, codes of practice, and policies related to medication handling and assesses the effectiveness of procedures for administering medication within a health and social care setting.