Wide Range of resources on complex issues

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.

Notice of Benefit and Payment Parameters for 2021

The National Health Council (NHC) appreciates the opportunity to comment on the Centers for Medicare & Medicaid Services’ (CMS’) Proposed Rule entitled, “HHS Notice of

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Join Us in Raising Awareness for These Causes in March

Join Us in Raising Awareness for These Causes in March By Theo Smith, Communications Intern Patient advocacy organizations work tirelessly to educate, promote, advocate, and

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Office of Minority Health and Health Equity (OMHHE) Strategic Priorities Public Docket

The National Health Council (NHC) appreciates the opportunity to provide comments as the Food and Drug Administration’s (FDA’s) establishes its Office of Minority Health and

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Request for Proposals: Building an Interactive Tool Patient Journey Mapping Toolbox

Founded in 1920, the National Health Council (NHC) brings diverse organizations together to forge consensus and drive patient-centered health policy. The NHC provides a united

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Getting to Know: Aimee Lee Russell, Programs Associate

Getting to Know: Aimee Lee Russell, Programs Associate Following is a Q&A to get to know Aimee Lee Russell, Programs Associate, who began working at

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2020 Health Leadership Conference

2020 Health Leadership Conference Event Date: Feb. 14, 2020 Event Location: Ft. Lauderdale, FL Agenda (download) Sponsorship: Premier: BIO, Eli Lilly, Johnson & Johnson, Mallinckrodt,

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Surprise Medical Billing Update

By Maddie Mason, Senior Associate, Policy Surprise medical bills, which are unexpected medical bills that come after someone with insurance inadvertently receives care from an

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Patient-Journey Mapping Toolbox

Patient-Journey Mapping Toolbox Understanding the patient’s journey with disease is critical as it enables understanding the context of the patient experience, the natural history of

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PFMPD Webinar Series: Rare-Disease Listening Sessions with NORD and the FDA

PFMPD Webinar Series: Rare-Disease Listening Sessions with NORD and the FDA By Aimee Lee Russell, Associate, Programs This blog highlights the first webinar in our

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