7 April 2025 · Global Partnership for Zero Leprosy

The Patient’s Charter for Leprosy Care: Patient Rights and Responsibilities

The Patient’s Charter for Leprosy Care is a vital document designed to empower individuals affected by leprosy by clearly outlining their rights and responsibilities within the healthcare system. It ensures that care is delivered with transparency, accountability, and respect, fostering an environment where patients receive the dignity and quality treatment they deserve.

This Charter provides a framework for equitable access to high-quality healthcare, enabling informed decision-making and active participation in treatment and recovery. It serves as a guide for patients to navigate the healthcare system while also emphasizing their role in maintaining their health and well-being.

At its core, this document establishes a foundation for collaboration between patients and healthcare providers, built on mutual respect, trust, and shared responsibility. By recognizing both patient rights and responsibilities, the Charter promotes fairness and ensures that healthcare remains person-centered.

The rights outlined in this Charter affirm every patient’s access to quality care, respectful treatment, and clear medical information. Patients should be well-informed about their condition, treatment options, and available support. At the same time, the Charter highlights patient responsibilities, such as open communication, adherence to medical advice, and respect for healthcare providers—contributions essential to the success of treatment.

Ultimately, the Patient’s Charter for Leprosy Care aims to create a healthcare experience that is respectful, safe, and effective. By fostering trust, accountability, and empathy, it encourages a strong partnership between patients and healthcare providers, ensuring the best possible health outcomes.

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