“The US Department of Health and Human Services’ Office of the National Coordinator for Health Information Technology (ONC) today released the ONC Guide to Getting and Using your Health Records, a new online resource for individuals, patients, and caregivers.  This new resource supports both the 21st Century Cures Act goal of empowering patients and improving patients’ access to their electronic health information and the recently announced MyHealthEData initiative. The new initiative, led by the White House Office of American Innovation and supported by ONC, empowers patients by giving them control of their healthcare information.  Other participants in the effort include the Centers for Medicare & Medicaid Services, National Institutes of Health, and the Department of Veterans Affairs. “It’s important that patients and their caregivers have access to their own health information so they can make decisions about their care and treatments,” said Don Rucker, M.D., national coordinator for health information technology. “This guide will help answer some of the questions that patients may have when asking for their health information.” Individuals’ ability to access and use their health information electronically is a measure of interoperability and a cornerstone of ONC’s efforts to increase patient engagement, improve health outcomes, and advance person-centered health. In fact, a new ONC data brief – PDF shows that in 2017, half of Americans reported they were offered access to an online medical record by a provider or insurer…” [h/t Pete Weiss]