This book examines the idea of a fundamental entitlement to health and healthcare from a human rights perspective.
The volume is based on a particular conceptual reasoning that balances critical thinking and pragmatism in the context of a universal right to health. Thus, the primary focus of the book is the relationship or contrast between rights-based discourse/jurisprudential arguments and real-life healthcare contexts. The work sets out the constraints that are imposed on a universal right to health by practical realities such as economic hardship in countries, lack of appropriate governance and lack of support for the implementation of this right through the provision of appropriate resource allocation. It queries the degree to which the existence of this legally enshrined right and its application in instruments such as ICESCR and the UDHR can be more than an ephemeral aspiration but can, actually, sustain, promote and instil good practice. It further asks if social reality and the inequalities that present themselves therein impede the implementation of laudable human rights, particularly within marginalised communities and cadres of people. It deliberates on what States and global bodies do, or could do, in practical terms to ensure that such rights are moved beyond the aspirational and become attainable and implementable. Divided into three parts, the first analyses the notion of a universal inalienable right to health(care) from jurisprudential, anthropological, legal, and ethical perspectives. The second considers the translation of international human rights norms into specific jurisdictional healthcare contexts. With a global perspective it includes countries with very different legal, economic and social contexts. Finally, the third part summarises the lessons learnt and provides a pathway for future action.
The book will be an invaluable resource for students, academics and policy-makers working in the areas of health law and policy, and international human rights law.
