Indicators of Healthy Aging: A Guide to Explore Healthy Aging Data through Community Health Improvement

Collecting, analyzing, and translating relevant and robust data on older adults.

For over a century, public health interventions – from vaccines to food safety and vector control – have contributed to Americans’ longevity, and state and local health departments play a key role in supporting their communities by promoting healthy living. Healthy aging programs uniquely dovetail with local health department Community Health Improvement Plans (CHIPs).  Both allow health departments and partnering organizations to understand and address healthy aging priorities through data.

An analysis conducted by the National Association of County and City Health Officials (NACCHO), found that most CHIPs include priorities that, while not specifically addressing older adults (e.g., 65 years of age and older), could be adapted for healthy aging programs. These priorities include chronic diseases, including heart disease, diabetes, stroke, and cancer, as well as substance use, depression, and other mental health conditions.

To develop and strengthen age-friendly public health systems, a more comprehensive set of healthy aging indicators is needed to help health departments and community partners at the local, state, tribal, and territorial levels measure and identify population-level health disparities and inequities. Additionally, Community Health Improvement (CHI) partners need a robust, unified source of secondary data that aligns with healthy aging indicators to inform strategic and action planning.

This guide, developed by Trust for America’s Health (TFAH) and the National Association of County and City Health Officials (NACCHO) and with funding from The John A. Hartford Foundation, is designed to augment NACCHO’s Mobilizing for Action through Planning and Partnerships (MAPP) framework. MAPP is the most widely used CHI framework among governmental public health departments and, increasingly, community-based organizations, nonprofit hospital systems, and community health centers that lead or engage in CHI processes. This also serves as a resource for health departments seeking to attain Age-Friendly Public Health Systems (AFPHS) recognition.

Download your free copy of the Guide.

TFAH President & CEO Dr. J. Nadine Gracia speaks to JHU’s Public Health on Call podcast about the steps necessary to improve state and national emergency response readiness.

J. Nadine Gracia, M.D., MSCE, President and CEO of the Trust for America’s Health (TFAH), joined the Johns Hopkins Bloomberg School of Public Health podcast, Public Health on Call to discuss the nation’s and states’ readiness to respond to public health emergencies and the findings of TFAH’s Ready or Not 2023: Protecting the Public’s Health from Diseases, Disasters, and Bioterrorism report.

“As we transition out of the emergency phase of the pandemic, now is not the time to turn our focus away from public health,” Dr. Gracia told podcast host Dr. Joshua Sharfstein.  In addition, Dr. Gracia highlights the importance of sustained public health funding, as well as a  focus on health equity. Listen to the full interview.

TFAH hosted the  Congressional Briefing and National Webinar, Ready or Not 2023 on May 3, where a panel of experts discussed national emergency preparedness and areas for additional focus.

TFAH Applauds OMB for Recognizing the Need for Improved Race and Ethnicity Data

The 2020 Census revealed a country increasingly characterized by its diverse population. The proportion of non-Hispanic white people, though still the largest racial or ethnic group, has decreased as the nation’s overall diversity index climbs. This dynamic landscape demands a reevaluation of federal regulations about population data collection which have remained unchanged for over two decades.

The United States finds itself grappling with the complexities of its ever-evolving racial and ethnic composition and the interplay between race and health. It is well-documented that race, while a sociopolitical construct, is inextricably linked to health outcomes. Having complete and accurate data about all population groups, while also protecting individual privacy, is key to effectively addressing the myriad public health challenges facing the nation and contending with structural discrimination. Trust for America’s Health (TFAH) supports a reevaluation of the way the nation collects and analyzes race and ethnicity data. As the country’s demographics continue to shift, so too must our approach to understanding and addressing health disparities.

In June 2022,  Dr. Karin Orvis, Chief Statistician of the United States, announced her office’s intention to begin a formal review process to revise the Office of Management and Budget’s (OMB) Statistical Policy Directive No. 15 (Directive No. 15): Standards for Maintaining, Collecting, and Presenting Federal Data on Race and Ethnicity. Six months later, an interagency technical working group spanning 20 federal agencies published an initial set of recommendations and invited public comment. TFAH submitted comments, applauding OMB for undertaking the process as well as the working group’s governing principles and proposals, and offering technical input.

The pervasive influence of structural racism and discrimination in the U.S. has led to stark disparities in health and well-being. For instance, Black Americans, burdened by the legacy of redlining and underinvestment in communities, experience higher rates of chronic diseases such as diabetes, hypertension, obesity, asthma, and heart disease than their white counterparts. Furthermore, their life expectancy at birth is nearly six years lower than that of white Americans.

The urgent need for accurate and comprehensive race and ethnicity data is highlighted by a series of health crises, from the maternal health crisis among Black women, owed to factors such as variation in healthcare quality, underlying chronic conditions, structural racism, and implicit bias, to the disproportionate impact of COVID-19 on people of color. As we strive to address these issues, precise data can illuminate the unique needs of different populations, helping to guide resource allocation and the development of targeted interventions.

For example, as the COVID-19 pandemic unfolded, it became evident that communities of color were disproportionately affected. Race and ethnicity data, while uneven across jurisdictions, proved invaluable in pinpointing these disparities, catalyzing in many places a more equitable distribution of tests, vaccines, and healthcare resources. Furthermore, such data has been critical in deciphering the disparate impacts of events like Hurricane Katrina on distinct New Orleans zip codes and unmasking the systemic racism at the heart of the Flint water crisis.

While these health crises have been acknowledged, we continue to require accurate data to comprehend the disaggregated effects of these events, and others, on particular population subgroups, the recovery and resilience of specific subgroups, and the outcomes experienced by these subgroups. This understanding will ensure the strategic development and application of policies and programs, ultimately bolstering our collective pursuit of health equity.

America’s ever-changing demographics, shaped by immigration and migration patterns, necessitate a reevaluation of the current racial and ethnic categories used in the Census and other data sets. Updated and accurate data can expose the distinct health challenges faced by different subgroups, enabling policymakers and public health officials to respond effectively. For example, accurate data could reveal disparities in access to nutrient-dense foods or mental health services, providing valuable insight for targeted public health initiatives.

A more granular approach to race and ethnicity data could also help identify and address additional public health challenges, such as subgroup-specific obesity trends, mental health conditions, and substance use disorder rates. By understanding the needs of different populations, public health officials can develop targeted interventions that address specific needs, such as culturally-sensitive dietary education and exercise programs—bolstered by communities that foster and enable healthful lifestyles, rather than obstructing them—or mental health services that are thoughtfully tailored to the experiences of specific communities.

TFAH underscores the significance of reevaluating Directive No. 15 in order to more accurately account for the variegated tapestry of contemporary America. By refining our methodology for gathering and studying race and ethnicity data—in part by enhancing data collection techniques and working to ensure that the assembled information genuinely represents the experiences of diverse populations—we can more adeptly comprehend public health needs within the United States and devise equitable resolutions for our most urgent health challenges.

As the primary entities responsible for implementing public health policies and interventions, state and local governments are uniquely positioned to address the specific needs of their diverse populations. Therefore, it is important for state and local governments to update and improve their data collection methods in a manner similar to what the OMB is proposing. Collaboration between federal, state, and local governments, as well as community organizations, is key to improved data collection and sharing. Through these efforts, state and local governments can align their data collection practices with any updated OMB standards.

In this era of rapid demographic change, the quest for health equity demands a renewed commitment to complete, accurate, actionable data. As we strive for a more equitable and inclusive society, it is imperative that our approach to public health reflects and respects the unique experiences of all Americans. Only by understanding the intricate connections between race, ethnicity, and health can we begin to dismantle the structural barriers that perpetuate disparities and chart a course towards a healthier, more equitable future for all.

 

Improving Minority Health Requires Addressing Social and Economic Disparities

The data tell the story. Members of certain racial and ethnic groups in the U.S. have, on average, worse health outcomes, including higher rates of chronic and infectious disease, than do their white counterparts. According to the National Institutes of Health, American Indian and Alaska Native people have a greater chance of having diabetes than any other racial group and are twice as likely as whites to have diabetes. Black adults in the U.S. are nearly twice as likely to develop diabetes compared to white adults. Asian Americans are 40 percent more likely to have diabetes than are whites, and Hispanic and Latino adults are also more likely to have diabetes than are whites.

Cancer is another disease for which people of color experience higher disease and death rates than do white people, according to the National Cancer Institute, typically due to social, environmental, and economic disadvantages. People of color also often have less access to healthcare screening and services, experience a lower quality of care, and face discrimination and bias when they do seek care. Black men have the highest prostate cancer mortality rate among all U.S. population groups, Black women have a lower incidence of breast cancer than white women but a higher mortality rate, and American Indian and Alaska Native people have higher death rates from kidney cancer than other racial and ethnic groups.

Health disparities are preventable differences in the burden of disease or in opportunities to achieve optimal health as experienced by racial and ethnic groups. Health disparities are among the many ways in which both the legacy of and present-day structural racism impact the disease burden and life expectancy of people of color. At the root of these disproportional health burdens are historic patterns of systematic inequities which have led to communities disadvantaged by poverty, exposure to pollution and environmental risks, unstable housing, limited employment opportunities and lack of access to healthy food, quality education, transportation, and healthcare. These differential disease burdens are rooted in differences that go beyond personal choices. They occur at the systems level, are rooted in centuries of structural racism, and were exacerbated by the COVID-19 pandemic.

Solutions can be found in policy action to create conditions in every community that allow all residents to achieve optimal health. Conditions such as access to safe and affordable housing; access to healthy foods, transportation, education, employment, and healthcare; jobs that pay a living wage and a built environment that supports physical activity. Building such communities will require a multi-sector and intentional focus on health equity and should start by targeting resources to communities most in need.

Trust for America’s Health’s (TFAH) recommendations for policy action that will advance health equity include:

  • The Federal government should be a leader in advancing health equity by making it a priority and by ensuring accountability to health equity goals in all federal agencies, policies, and programs.
    • Update: The Biden-Harris Administration’s American Rescue Plan and other COVID-19 response measures were designed to mitigate the impacts of the pandemic, with households of color being at particular risk for negative health and economic impacts during the emergency. Numerous programs including cash relief to low-and-middle income people, expansion of food and nutrition security programs, rent payment programs, and lower health insurance marketplace premiums helped Americans weather the pandemic. Of concern, is that many of these programs and program flexibilities will expire with the end of the public health emergency in May 2023.
    • Update: On his first day in office, President Biden signed Executive Order 13985 Further Advancing Racial Equity and Support for Underserved Communities Through the Federal Government which instructed Federal agencies “to redress inequities in their policies and programs that serve as barriers to equal opportunity”.
  • Congress should further develop and expand funding for programs that serve communities that are under-resourced and marginalized, including enacting and funding the Health Equity and Accountability Act and expanding investment for the Centers for Disease Control and Prevention’s (CDC) Racial and Ethnic Approaches to Community Health (REACH) program and its Healthy Tribes program so that all approved applicants are funded.
  • Government at all levels and the healthcare sector should work together to ensure that health data is complete, shareable, and disaggregated (while still protecting individual privacy) so that the impact of health conditions, disease threats, health policies and interventions on specific population groups are known. All health data should be collected and disaggregated by race and ethnicity and other demographic factors. Investments in modernizing the nation’s public health data infrastructure are needed to meet these goals.
  • The Biden Administration should create, and Congress should fund, a strategy and programs to address the root causes of health inequities including providing at least $100 million in FY 2024 for the expansion of the social determinants of health program at CDC.
  • The federal government should prioritize the elimination of poverty by raising the national minimum wage, expanding programs to make higher education more accessible to lower-income people, growing federal supports for affordable housing and childcare and by expanding nutrition support programs such as the Supplemental Nutrition Assistance Program (SNAP) and the Special Supplemental Nutrition Program for Women, Infants and Children (WIC).
  • Federal and state governments should ensure that all Americans have access to health insurance and have job-protected paid leave for illness or to care for a family member who is ill.
  • Federal and state governments should expand programs that support families including child tax credits, earned income tax credits, and programs that support childcare, early childhood education programs, school meal programs, and school-based Medicaid health services programs.

For more information about the data and policy solutions summarized in this news feature see TFAH’s Blueprint report for the 2021 Administration and Congress, The Promise of Good Health for All: Transforming Public Health in America.

 

TFAH President & CEO Dr. J. Nadine Gracia discusses the 2023 Ready or Not report

Dr. J. Nadine Gracia, President and CEO of the Trust for America’s Health (TFAH), discussed the results of TFAH’s  Ready or Not 2023: Protecting the Public’s Health from Diseases, Disasters, and Bioterrorism report with the Public Health Review Morning Edition.

Dr. Gracia highlights the report’s findings that “the public health system has been chronically underfunded” and notes that “Congress and lawmakers should provide increased and sustained funding in support of the public health infrastructure.” Listen to the full interview.

On May 3 at 2PM ET, TFAH will host the  Congressional Briefing and National Webinar, Ready or Not 2023. Register today to learn more about the nation’s emergency preparedness.

Unseen Guardians: Measles Outbreak Highlights Public Health’s Crucial Role and Evolving Challenges

Local health officials and CDC work together to stamp out Ohio measles outbreak

In 1912, the United States formally recognized measles—a highly contagious viral infection causing fever, cough, runny nose, red eyes, and a characteristic rash in milder cases, while leading to pneumonia, encephalitis, and death in more severe instances—as a nationally notifiable disease. For centuries, this ubiquitous childhood ailment afflicted millions. In the first decade of reporting, an annual average of 6,000 measles-related fatalities were recorded in the U.S.

The introduction of the first measles vaccine in 1963, with its near-perfect efficacy, marked a turning point. The vaccine was later combined with those for mumps and rubella (MMR) in 1971, and varicella (MMRV) in 2005, providing children protection against several diseases in a single shot. Bolstered by this potent new preventive tool, the Centers for Disease Control and Prevention (CDC) set a goal in 1978 to eliminate measles from the country. This objective was realized in 2000, thanks to robust vaccination campaigns, the introduction of a second dose in 1989 to increase efficacy, and rigorous disease surveillance systems.

In the new millennium, measles appeared a relic of the past, but the specter of outbreaks returned—first in the 2014-15 Disneyland episode, and then in the largest outbreak in decades in 2019. Declining vaccination rates, fueled by skepticism and misinformation, left vulnerable communities exposed. The 2019 outbreak primarily affected unvaccinated children in communities with low vaccination rates across 31 states, such as ultra-Orthodox Jewish communities in New York and vaccine hesitant regions in Washington. Travelers imported the virus, sparking infections among the unvaccinated.

One such measles outbreak erupted in Ohio in 2022. Between November 2022 and February 2023, when the outbreak was declared over, 85 cases were reported, primarily affecting children under five, with 36 hospitalizations. Among the 85 cases, 80 were unvaccinated, including 25 infants too young to receive their first dose.

To quell the outbreak, a team of epidemiologists from the CDC worked in concert with Columbus Public Health to track cases, identify and notify exposed residents, and understand the spread of the virus. Dr. Mysheika Roberts, Columbus’s health commissioner, led the outbreak response, raising awareness of the disease through public information and education, and promoting and easing access to vaccination.

In addition to the on-the-ground work of state and local health departments, the CDC plays a vital, often behind-the-scenes role in supporting those departments and safeguarding public health. It provides robust disease surveillance systems, expert guidance, technical assistance, and financial support, enabling locally targeted interventions and infrastructure improvements.

Though the latest outbreak was successfully contained, the Ohio measles episode may portend further challenges. Vaccine hesitancy, a complex and deeply ingrained phenomenon, threatens to erode hard-won public health gains and could precipitate resurgent outbreaks. The issue has multifaceted roots including mistrust in science and institutions, and misinformation amplified on digital platforms. In communities of color, vaccine hesitancy is compounded by longstanding health disparities and medical mistreatment.

The COVID-19 pandemic exacerbated the problem, with routine vaccination rates falling due to school closures and disrupted well-child doctor visits. A recent Kaiser Family Foundation poll revealed that, amid the politicization of COVID-19 vaccines and school mandates, over a third of parents with children under 18 believe they should have the choice to not vaccinate their children against measles, mumps, and rubella, even at the risk of others’ health. This represents a 52% increase compared to 2019. During the 2021-22 school year, kindergarten vaccination coverage fell to roughly 93%, leaving about 250,000 kindergartners potentially unprotected against measles.

Tackling vaccine hesitancy and strengthening our public health systems requires a multifaceted national approach. Federal, state, and local governments should invest in accessible, science-based education campaigns that dispel myths and foster trust. Working with local partners, public health agencies are developing tailored, culturally sensitive vaccine education and access programs that bridge gaps in understanding and acceptance.

The Ohio measles outbreak serves as a stark reminder that the fight against vaccine-preventable diseases remains ongoing, the indispensable role of the public health workforce, and the critical need for a robust public health system. Increased, sustained, and flexible public health funding is key to having such a system. As is growing a diverse workforce to ensure that those shaping policy and delivering services reflect the communities they serve. By taking these steps, among others, we can reduce vaccine hesitancy, create a more robust public health system, and foster an environment of trust in science. Doing so can protect the hard-won progress made against measles and other diseases, safeguard the health and well-being of generations to come, and pave the way for a more equitable future.

Improving Americans’ Nutrition Security Requires Legislative Action

Q&A with Dr. Hilary Seligman:

Hilary Seligman, M.D., MAS, is a professor at the University of California, San Francisco, with appointments in the Departments of Medicine, Epidemiology, and Biostatistics. Her research and advocacy work focuses on food insecurity, its health implications, and the needed policy responses.

 

TFAH: Food insecurity is obviously a serious problem in the United States. Can you also talk about the issue of nutrition insecurity and the relationship between the two?

Dr. Seligman:
First, it’s important to recognize that the food-security construct always considered access to nutrition, not just calories. But, the sector’s new focus on nutrition security has helped emphasize the importance of providing not just food but food that meets people’s health and nutrition needs. The construct of nutrition security is also strongly related to issues of equity and the massive burden of early mortality in our country that is related to poor diets.


TFAH: Can food banks and charitable food networks address hunger and improve nutrition?

Dr. Seligman: Yes, of course they can, and they must. The charitable food system as a whole has made massive investment and progress in this area over the last decade. What I do want to call attention to though is that the same forces that make it difficult for individuals to afford and prepare healthy food make it difficult for the charitable food system to distribute healthy food. Healthy alternatives almost always cost more, they are often perishable, and they often require more preparation time which can be costly to provide. So, although there has been strong investment and tremendous progress at the system level, there is still a lot to be done. It will always be cheaper to distribute a box of mac and cheese than it will be to distribute a peach.


TFAH: You’ve been a leader in grassroots anti-hunger programs in the San Francisco area, programs like EatSF, a healthy food voucher program. Are these programs making a difference in food insecurity for San Francisco families and children?

Dr. Seligman: EatSF is one of a rapidly growing ecosystem of state and local food voucher programs and produce prescription programs in the U.S. These programs have functioned as a way for local leaders and health systems to say: We see we have this critical problem of nutrition insecurity in our community, this is not acceptable in the richest county in the U.S., and we are going to do something about it. I think that is amazing, and I am privileged to be a part of that movement. But, let’s be honest, the nutrition security problem in the U.S. is not going to be solved by small local programs. We need a systems-based approach. We need better policies to address nutrition security, and we need to rectify the way in which our current policies work better for white people than they do for people who are not white.


TFAH: Can you say more about that? How does current policy work better for white people than for people of color?

Dr. Seligman: SNAP program policies are a good example. In order for able bodied adults to receive SNAP benefits they have to be working. For a myriad of reasons, Black people are less likely to be able to secure employment. They are therefore less likely to be able to meet the work requirements that would allow them to enroll in SNAP, even if they are food insecure.


TFAH: You direct the National Clinician Scholars Program at the UCSF School of Medicine. The goal of the program is to train clinicians to be change-agents in order to improve their patients’ health. Are clinicians and the healthcare system doing enough to address the social determinants of health? Are they well-prepared to treat their patients who have obesity?

Dr. Seligman: Traditionally, healthcare in the U.S. has focused on treating, not preventing, disease in individuals. The evidence is very clear that this is the worst way to approach obesity: first to do it at the treatment stage (when obesity has already developed, rather than to prevent the onset of obesity) and second to do it by attempting to change people’s behaviors, rather than changing the environments that resulted in the onset of obesity to begin with. So, although I hate that we need to be having this discussion at all, we do. We do because the U.S. has completely failed at prevention efforts and at policy and environmental approaches to obesity prevention for decades. So now, what needs to be done? Obesity and poor diets are the biggest drivers of healthcare costs in the country— so the healthcare system has to get involved (whether it is traditionally in their wheelhouse or not), and the best way to do this is by addressing social determinants of health and food environments. It is not a comfortable fit for the healthcare system, but there really is no other choice. And because it is not a comfortable fit and requires a new way of thinking about healthcare and new kinds of engagement and policy change, we have to nurture the next generation of healthcare leaders to be able to tackle these really complicated problems.


TFAH: What are the links between public policy and obesity? What policy actions or changes would you like to see enacted?

Dr. Seligman: Oh, there are so many of them—dozens if not more are being discussed as potential approaches for the next Farm Bill. At the federal level alone, there are policy levers that Congress, USDA, and the FDA have authority over that could help reverse obesity trends. Let’s start with an enormous one: SNAP. Early in my career I worked on health literacy, and I was always challenged by the lack of existing infrastructure to reach people with effective health literacy interventions. Food insecurity is not like that. SNAP works. It reaches almost 50 million people in the U.S. annually. It is available in every county nationwide. It helps families to afford more nutritious food. So, we have the tools, we have the evidence, and we have the infrastructure to solve food insecurity in the U.S. What we lack is the political will. We need to expand SNAP eligibility to all the people who aren’t receiving the food they need but who are not currently eligible for benefits, and we need to raise benefit rates to allow for the purchase of healthy food. If these changes are made, it is very clear to me that they will have a substantial impact on obesity rates and on public health.


TFAH: There  were a number of waivers in federal food programs like SNAP, WIC, and school meals, during the COVID-19 pandemic to better reach individuals and families during the public health emergency. Are there any lessons we can learn from these policy changes?

Dr. Seligman: Yes! The predominant lesson is: these programs work. Food insecurity rates did not increase nearly as much as anticipated during the pandemic, although there were certainly vast disparities in how the pandemic impacted different communities. Why didn’t rates of food insecurity rise as much as anticipated? Because we had the will to do the things we knew—based on a tremendous amount of evidence— would make a difference. When we make it easier for people to enroll in SNAP, more people have access to benefits and food insecurity falls. When we provide money on debit cards to replace the meals not being served in schools, food insecurity falls. When stimulus checks were sent to people across the U.S. in response to the pandemic, low-income households reported that food was the first or second most covered item from the stimulus money.

The really optimistic lesson is that we know how to address hunger, nutrition security, and obesity prevention through good public policy. Now we just have to keep these programs in place as interest in the pandemic wanes.

Additional Resources:

Brief: Legislative Priorities for the 118th Congress

Report:  State of Obesity 2022

Priority Issue: Obesity /Chronic Disease

This interview was originally published as a part of TFAH’s 2022 State Of Obesity: Better Policies for a Healthier America report.

Public Health’s Role in Supporting Family Caregivers

According to a September 2022 report by the National Alliance for Caregiving (NAC) and  the National Association of Chronic Disease Directors, Chronic Disease Family Caregiving Through a Public Health Lens, there are 53 million family caregivers in America-that’s nearly one i five families. Furthermore, the number of caregivers will continue to rise as people aged 65 or older are expected to almost double by the year 2060. At that time, the nation will have reached a milestone of one in four people responsible for providing care for a family member with a chronic disease, serious illness, or a disability.

The report, which was supported by a grant from the John A. Hartford Foundation, found that caregivers are taking on caregiving responsibilities for adults with increasingly complex needs due to raising rates of chronic disease, Alzheimer’s Disease and other types of memory and dementia issues.

Caregivers in Need

Providing care for an ill family member is a demanding task often made more complicated by geographically dispersed families and the need for two wage-earners.

Source: Caregiving for Family and Friends – A Public Health Issue

According to a NAC and National Association of Chronic Disease Directors Roundtable, in 2020,23 percent of caregivers reported worsening health due to caregiving. Of those caregivers, 60 percent reported difficulty when addressing their own health needs. TFAH has recommended establishing a comprehensive paid family and medical leave policy that ensures paid time off to address family health or caregiving needs for all employees.

Equity in Caregiving

Of the nation’s 53 million family caregivers, an estimated 61 percent are Non-Hispanic white, 17 percent are Hispanic, 14 percent are African American, and 5 percent are Asian American and/or Pacific Islander. As the need for care grows, the need for caregiver systems that are integrated into the community, and culturally and language appropriate is critical. Innovations in technology, such as telemedicine and translation tools, can assist in allowing both long-distance and non-English speaking caregivers have the support they need from public health programs and their communities. Culturally designed approaches and relationship building within communities will enable greater understanding of, support for, and interaction with the nation’s caregivers.

How Can the Public Health System Support Caregivers?

Support for the nation’s caregivers is a public health issue especially in light of demographic changes that will make the need for family caregiving even greater in the future. The public health system has  a critical role to play in supporting family caregivers and their ability to provide care through care coordination and assistance integrating home care with more formal healthcare services. Public health systems should work to create family caregiving support infrastructure and should team with other entities that can have a role in supporting caregivers including healthcare systems and providers, insurers, community-based organizations, faith-based organizations, and employers.

Conclusion

Caregivers are a vital part of the nation’s healthcare system and need the support of the public health sector. Policies should support the nation’s existing and growing number of caregivers to allow them to provide care while protecting their own health, well-being, and financial security.

Additional TFAH Age-Friendly Public Health Systems initiative Resources on Family Caregiving

Michigan Conference Seeks to Advance an Interconnected, Age-friendly Public Health System

Michigan is a leader in the movement to create a more age-friendly public health system by creating partnerships throughout the health and public health sectors within the state. In October 2022, over 120 aging and health leaders and innovators gathered at Michigan State University for the state’s first-ever Strategically Partnering for Age-Friendly Health in Michigan Conference to collaborate on a shared vision to advance age-friendly policies and practices across the state.

The conference, jointly hosted by The Michigan Health Endowment Fund, Michigan Public Health Institute, and Trust for America’s Health, emphasized the need for age-friendly policies to benefit everyone, not just older adults, due to their focus on the social conditions that support optimal health.

One of the key themes of the conference was the importance of integrating age-friendly principles into the ecosystem of society and information sharing across care delivery, between hospitals and home care providers, for example. Dr. Aaron Guest, a national leader in aging and public health, spoke on the connections between social determinants of health and healthy aging, and the importance of creating an age-friendly environment that addresses the social and economic factors that promote good health and well-being.

Structural racism and health disparities were also discussed as significant obstacles to ensuring equitable access to care and culturally responsive, age-friendly care. Black older adults in Michigan experience lower rates of health insurance coverage and greater rates of chronic health conditions compared to their white counterparts. Furthermore, the Detroit Area Agency on Aging found that the death rate of Detroit adults in their 50s is 122 percent higher than the rest of the state.

Overall, the conference sought to chart the course for an age-friendly future within the state, acknowledging the challenges ahead but also the progress made, especially in light of the COVID-19 pandemic. The pandemic’s disproportionate impact on communities of color and older adults illustrates the importance of addressing the upstream social determinants of health and integrating age-friendly policies into public health systems.

TFAH is proudly committed to a continued partnership with the Michigan Public Health Institute and will continue to help support Michigan’s Age Friendly Public Health System initiative in the future.

This article is based on the Age-Friendly Conference Envisions as Interconnected Michigan blog, published by the Michigan Health Endowment Fund.

Read more on TFAH’s Age Friendly Public Health Systems and Age Friendly Public Health Systems Initiative Page.

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