SummaryPatients with ESRD have extensive and unique palliative care needs, often for years before death. The vast majority of patients, however, dies in acute care facilities without accessing palliative care services. High mortality rates along with a substantial burden of physical, psychosocial, and spiritual symptoms and an increasing prevalence of decisions to withhold and stop dialysis all highlight the importance of integrating palliative care into the comprehensive management of ESRD patients. The focus of renal care would then extend to controlling symptoms, communicating prognosis, establishing goals of care, and determining end-of-life care preferences. Regretfully, training in palliative care for nephrology trainees is inadequate. This article will provide a conceptual framework for renal palliative care and describe opportunities for enhancing palliative care for ESRD patients, including improved chronic pain management and advance care planning and a new model for delivering highquality palliative care that includes appropriate consultation with specialist palliative care. To cure sometimes, to relieve often, and to comfort always-this is our work. This is the first and great commandment. And the second is like it. Thou shalt treat thy patient as thou wouldst thyself be treated. AnonymousApproximately 90,000 dialysis patients die each year in the United States, with a high annual unadjusted mortality rate of approximately 20% (1). The exact numbers of patients with ESRD who die without starting dialysis are unknown but estimated to be several fold higher. As of December 31, 2009, there were 397,796 people in the United States on dialysis (1). The prevalent population ages 75 years and older is the largest growing group, having nearly doubled since 1997 (1). Patients with ESRD experience an extremely high burden of symptoms similar to those symptoms of cancer patients hospitalized in palliative care settings (2-8), and they have extensive and unique palliative care needs, often for years before death (9,10). Dialysis patients are more frequently dying after withdrawal of dialysis (10%-15% in 1990 and 20% in 2004) (1), representing the second leading cause of death after cardiovascular disease. Unfortunately, most patients lack decision-making capacity at the time that the decision to withdraw dialysis is made and are not involved in these decisions (11). Most dialysis patients do not have an advance directive and have not had discussions with their family or health providers about their end-of-life care preferences (10), despite patients wanting to engage in these conversations (10,12). Even patients with advance directives often do not address health states in which they would no longer wish to continue dialysis (13,14). Only a minority of patients chooses to forgo cardiopulmonary resuscitation (10,15), because they are unaware of the poor likelihood of survival after cardiopulmonary resuscitation (16). Without advance care planning (ACP), neither family nor physicians is accurate in their predict...