At Emory Healthcare, we understand many factors can impact your well-being and your ability to live a healthy life.
Where you live and how you live affects how easily and often you can access care services. These and other social determinants of health include the economy, education, the environment, food, housing, public safety and transportation.
When your doctors and nurses understand more about your life outside the exam room, our high-quality care can address all aspects of your life.
For this reason, we ask you to share more personal information with us. We don’t want to pry—we just want to help improve health care access for our community.
“We want to understand better who you are and what you need,” says Nicole Franks, MD, chief quality officer at Emory University Hospital Midtown. “Your information helps us understand how to care for you.”
Emory Healthcare is on a mission to understand health care inequalities and build trusting relationships with new and ongoing patients. We want patients and their families to feel comfortable enough to “tell us how to identify them and share what represents their culture,” Dr. Franks says. “We want to be intentional and not make any assumptions.”
Your Personal Information Impacts Your Health
When you update your personal information, you make it easier for us to give you the best care. “For example, if you don’t have a car and bus fare is an extra expense, tell us,” says Ildemaro Gonzalez, chief diversity, equity & inclusion officer at Emory Healthcare.
“We can provide transportation vouchers or connect you with a ride-share group,” Gonzalez says.
You can share information like this on our online portal (MyChart), at home, or by talking to your doctor or nurse during an office appointment, hospital visit or in the emergency room.
Data like your income, living situation, race, and sexual orientation and gender identity can greatly impact your health. When health systems started to collect race and ethnicity information, Gonzalez says, they uncovered different conditions and health events affect people of various backgrounds differently.
For example, we now know:
- Three times more African American women die during pregnancy than white women
- African American men and women experience glaucoma earlier. So, they should start screenings at age 40, while people of other backgrounds can wait until age 60
- Latinx children are more than twice as likely to face hunger as white children and adults
- LGBTQ+ youth are at greater risk for poor mental health, violence, homelessness and HIV than their non-LGBTQ+ peers
- Loneliness and social isolation in older adults can put them at risk for dementia and other serious medical conditions
- Patients with limited English proficiency can spend a longer time in a hospital – as many as 4 days longer for certain conditions
More recent studies show structural racism increases complications, including death rates, for minority patients with diabetes.
“The data allows us to see how we can tailor our services better to improve health outcomes,” Gonzalez says.
Of course, the choice to share personal information is voluntary. The more information we have, the more effectively we can provide the care you need.