Injustice arises when equity is not a central consideration in health care interventions-a reality made more apparent during the COVID-19 pandemic. Pediatric palliative care is a proven intervention that enhances care and is associated with decreased suffering for children with serious illness and their families. 1 However, nearly two-thirds of countries lack access to pediatric palliative care despite a clear need. 2 Children in low-and middle-income countries experience disproportionately high illnessrelated morbidity and mortality, an inequity highlighted in pediatric cancer. More than 80% of US children with cancer will survive 5 years, compared with less than 30% of children with cancer living in low-and middle-income countries; this injustice is more striking when considering that more than 80% of global pediatric cancer cases occur in these countries. 3 For children with cancer living in lowand middle-income countries, improving integration of pediatric palliative care is just as crucial as improving access to life-extending therapies to decrease family suffering and improve quality of life.There are several barriers to early integration of pediatric palliative care worldwide, including the health system infrastructure, access (to primary and specialized palliative care, medications, and interdisciplinary clinicians), funding, education, health care professionals' perceptions, patient and family perceptions, and cultural adaptation. McNeil and colleagues 4 reported their efforts to understand physician-associated barriers to pediatric palliative care integration in a cross-sectional survey study of physicians in 17 Latin American countries that assessed palliative care perceptions and comfort in providing primary palliative care. 4 Of note, the authors systematically approached adaptation and translation of their previously used Assessing Doctors' Attitudes on Palliative Treatment (ADAPT) survey for physicians in Latin America. Their efforts to translate, iteratively review, back-translate, and pilot the survey before broad dissemination helped enhance the face validity and cultural sensitivity of their instrument. The authors partnered with local collaborators to distribute the survey and achieved a 39.9% response rate with a total of 874 participants. Of participating physicians, 34.1% were in general pediatrics, 26.7% in pediatric hematology/oncology, 4.0% in pediatric palliative care, and 35.2% in other pediatric and medical subspecialties. Among participants, 44.4% reported some training in palliative care and 65.3% had access to palliative care consultation.McNeil and colleagues 4 described 2 major findings. First, physicians' perceptions of pediatric palliative care aligned well with World Health Organization guidance in general (mean alignment, 83.0%). This finding suggests that physicians in Latin America have an accurate understanding of pediatric palliative care and its components despite limited access to pediatric palliative care services. However, Latin American physicians held misconception...