We offer a wide range of resources on complex issues that impact all people with chronic conditions. Resources include member-specific services, frequent meetings and events, publications, and comments on rules and legislation.
Advances in Celiac Disease Research Funding: Honoring Our Dedicated Patient Community By Marilyn G. Geller, Chief Executive Officer, Celiac Disease Foundation During May, Celiac Disease
Recognizing Health Disparities Among Asian American, Native Hawaiians, and Other Pacific Islander Populations By: Lillian Witting, MPH, Coordinator, Research, Education and Programs Although the historical
Guest Post: Did you know that May is VHL Awareness month? By: Janet Thompson, Executive Director, VHL Alliance Von Hippel-Lindau disease, or VHL, is one
Guest Post: May is ALS Awareness Month! By: The ALS Association May is ALS Awareness Month, a time dedicated to raising awareness about ALS and
NHC Fair-Market Value (FMV) Calculator Session Event Time: 1:00 – 1:45 p.m. ET Event Location: Virtual The NHC wants to ensure that all stakeholders confidently
NHC Patient Experience Mapping Toolbox (PEMT) Session Event Time: 9:00 – 9:45 a.m. ET Event Location: Virtual Understanding the patient’s experiences living with disease is
Registration Is Now Open for the NHC’s Inaugural International Patient Forum By: Jennifer Schleman, SVP Communications & Governance Registration is open for the National Health
Implications of Mifepristone Ruling By: Allen Pinn, Coordinator, Policy In recent weeks, the drug mifepristone has gained national attention. Mifepristone, a drug prescribed for medication
The science of patient engagement must not take a back seat to rapid technological advancements in health care according to more than 160 nationally recognized policymakers, researchers, patients and patient advocates, and health care providers participating in the National Health Council’s (NHC) 2023 Science of Patient Engagement Symposium: Patient Empowerment in the Digital Era, held today at the National Press Club.