HERN strives to create and continually maintain an anti-racist research paradigm.

We are committed to: building a platform for sharing experiences with health and health care that is meaningful for all people; prioritizing topics that are specifically relevant for racial justice; learning about how health experiences and inequality intersect; and continually challenging white privilege within our network.

"You're getting the feel of someone, instead of just seeing their words on paper. There's a richness you can get."

Erika Cottrell, PhD, Oregon Health & Science University

"If the interview is helpful to others, it’s helpful to me. I hope it helps at least one person realize they are not alone."

Health Experiences Participant

"It's a move from anecdote to science. We need to do it with the assurance that we're not just collecting the outlier story, but rigorously collecting the full diversity of patient experiences and representing them responsibly."

Rachel Grob, PhD, University of Wisconsin-Madison

"I want my experiences to help other people, even if it’s just one person."

Health Experiences Participant

Read more about our work

"Listening to other people's stories was always helpful for me… I just thought it would be really cool to be a part of that."

Health Experiences Participant

"Delivering patient-centered care requires putting the patient rather than the clinician at the center of the care process."

David Atkins, MD, MPH, Department of Veterans Affairs

"I have battled with depression for most of my life, and like the idea of being able to help others with my own story."

ELEVATING PATIENT VOICES

The Health Experience Research Network (HERN) brings patients’ voices to American health care. HERN is a non-commercial, non-profit group, part of an international movement (DIPEx International) to share patient stories.

 

HERN strives to create and continually maintain an anti-racist research paradigm. We are committed to: building a platform for sharing experiences with health and health care that is meaningful for all people; prioritizing topics that are specifically relevant for racial justice; learning about how health experiences and inequality intersect; and continually challenging white privilege within our network.

 

UNDERSTANDING PEOPLE’S EXPERIENCES WITH HEALTH AND ILLNESS

We use qualitative research methods to provide you with real information from patients about their experiences with a particular topic or condition. 

Take a look at our first modules on Young Adults with Depression, Cancer Risk That Runs in Families and Veterans with Traumatic Brain Injury. Other modules on a variety of topics are currently underway.

View topics

REPRESENTING A WIDE RANGE OF PERSPECTIVES

We seek to describe the widest range of experiences from patients' points of view.

Learn more about our methods

DESCRIBING COMPLEX STORIES

We identify key themes in patient stories, arranging their contributions so that people can find the themes that matter to them most, when they matter the most.

Learn more about what we do

WE’RE LISTENING

We want to know which topics or conditions you'd like us to explore in the future.

Contact us
©2019 Health Experiences Research Network