Across all health care settings, the crucial role played by family caregivers (FCs) is often overlooked. FCs are defined as relatives, friends, or neighbors who provide unpaid patient care, assisting with physically, emotionally, and socially demanding tasks. 1 With medical advancements that have extended the lives of many patients with cancer and with most cancer care now being delivered in outpatient settings, the responsibilities placed on FCs have become increasingly complex and prolonged. In the United States, the monetary value of care provided by FCs is estimated to exceed $475 billion US dollars per year, a figure comparable with over a quarter of the nation's total health care costs. 2 FCs are not only our partners in care but also patients in their own right. In this regard, research on the impact of cancer on FCs paints a concerning picture: The physical and psychological well-being among FCs of patients with cancer is up to five-fold worse than that reported by the general population, and the psychological distress experienced by FCs often surpasses that of the patients they care for. [3][4][5][6] This hidden morbidity is most often in the form of anxiety, which is present in approximately 40% of caregivers of patients with cancer (compared with 28% in patients they care for) 7 ; depression is present in approximately 35% (compared with 23%). 7,8 An even higher prevalence of anxiety has been reported in caregivers of patients with malignant brain tumors, who witness profound changes in the patient's cognitive function and personality that may be perceived as particularly distressing. 9,10