Similar to other areas of society, debates around access to and ownership of an individual's digital information have taken center stage in health care. A decade ago, the idea of offering patients ready access to their clinical notes was a fringe idea. Today, information transparency in health care has become a pressing legislative and regulatory issue in the United States and elsewhere. 1 The 21st Century Cures Act of 2016 requires that clinicians and health care organizations give patients electronic access to the information in their electronic medical records. Rules to enact this legislative priority promulgated by the Office of the National Coordinator for Health Information Technology and the Centers for Medicare and Medicaid have substantially expanded the types of information that must be easily accessible to patients and readily exchanged among clinicians in electronic form. 2 These regulations around information blocking, which take effect on November 2, 2020, require health care organizations and clinicians to share the following eight note types: consultation, discharge summary, history & physical, imaging, laboratory, and pathology report narratives, procedure notes, and progress notes. 3 By 2022, patients will be able to access this information in their records through any third party app of their choosing. The hope is that this increased transparency will improve care and the delivery system for patients, families, and clinicians; that it will positively impact patient safety; and that it will contribute to health care value for all stakeholders. Patients receiving dialysis are at particular risk for fragmented care, given the complexity of their needs and the number of clinical sites and providers involved in their treatment. 4 While the Centers for Medicare and Medicaid Services has incentivized coordination across dialysis stakeholders, it did does specifically target greater health information exchange between providers. 5 The current lack of interoperability between disparate EHRs prompted calls for increased investment in improved data exchange specifically for dialysis patients, similar to the work supported by CMS through the Promoting Interoperability programs in place for hospitals