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The National Health Council (NHC) announces the theme of the 2022 Science of Patient Engagement Symposium, From Research to Action: Health Equity for All. Over the past couple of years, the COVID-19 pandemic has upended the world, and health inequities among historically underrepresented racial/ethnic groups have magnified. The science of understanding the patient has never been more important. Specifically, health equity research, where diverse patients are at the core of scientific inquiry, is imperative to tackling these issues.
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The NHC team will present an overview of the 2021 NHC Revenue Report findings to NHC patient group members.
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The National Health Council (NHC) and its partners have undertaken a process to create a Blueprint for developing patient-centered core impact sets, or PC-CIS, to address inconsistencies between what is important to patients to the information typically collected in research and care. A PC-CIS is a patient-derived and -prioritized list of impacts a disease and/or its treatments have on a patient and his/her life as well as that of their family and caregivers.
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