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

03/02/2020

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

Join Us in Raising Awareness for These Causes in March

03/02/2020

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

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

02/28/2020

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

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

02/28/2020

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

Getting to Know: Aimee Lee Russell, Programs Associate

02/28/2020

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

2020 Health Leadership Conference

02/27/2020

2020 Health Leadership Conference Event Location: Tampa, FL The 2020 National Health Council (NHC) Health Leadership Conference (HLC) was a success, with 104 attendees from

Surprise Medical Billing Update

02/24/2020

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

Patient-Journey Mapping Toolbox

02/21/2020

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

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

02/20/2020

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