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Essay Undergraduate 1,144 words

Health Disparities in Diabetes: Race, Income, and Policy

~6 min read 6 sections Health · Diabetes
Abstract

This paper examines the health disparities that arise in diabetes management and prevention, with a focus on how race, income, disability, and access to patient education shape outcomes. Drawing on peer-reviewed research, the paper explores how Black patients and those living in poverty face elevated risks of developing diabetes, how individuals with intellectual and developmental disabilities are disproportionately affected, and how gaps in patient autonomy and patient education further widen these disparities. The paper concludes that meaningful legislative reform and a clear policy framework are essential for delivering equitable, high-quality care to all patients regardless of location, income, or disability status.

Key Takeaways
  • Introduction: Diabetes and Health Disparities: Framing how information access drives diabetes disparities
  • Race and Income as Drivers of Diabetes Disparities: Race and poverty elevate diabetes risk and prevalence
  • Disability and Elevated Diabetes Risk: Intellectual disabilities linked to higher diabetes rates
  • Patient Autonomy and the Limits of Patient Education: Autonomy gaps undermine effective diabetes education
  • The Role of Legislation and Policy Reform: Policy frameworks needed to close care gaps
  • Conclusion: Legislation and education key to equitable diabetes care
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What makes this paper effective

  • Integrates multiple peer-reviewed sources to build a layered argument about the causes of diabetes-related health disparities across race, income, and disability.
  • Uses direct quotations strategically to anchor empirical claims, then follows each with interpretive analysis that advances the argument.
  • Maintains a clear, consistent thesis — that disparities stem from systemic gaps in education, autonomy, and policy — throughout each section.

Key academic technique demonstrated

The paper demonstrates effective use of the "quote-then-analyze" technique: each block quotation from the literature is immediately followed by a sentence or two explaining what the evidence means in the context of the paper's argument. This prevents evidence from standing alone and shows the reader how each source supports the central claim about legislative and educational reform.

Structure breakdown

The paper opens by framing the central question — whether lack of access to information produces diabetes health disparities — and moves through four contributing factors: race and poverty, intellectual and developmental disability, patient autonomy, and policy gaps. Each section builds on the last, and the conclusion synthesizes all four threads into a call for legislative action. The structure is linear and cumulative, making it easy to follow the progression of the argument.

Essay 1,144 words

Introduction: Diabetes and Health Disparities

Diabetes is a chronic and progressive disease that leads patients to seek the help of medical professionals across various stages and time frames. From surgery to patient education to physical therapy, diabetes treatment can be a daunting task that may require complex, multi-faceted effort. Such complexity can lead to severe disparities in treatment and in the prevalence of the disease.

If patient education is at the forefront of chronic disease management and prevention, it stands to reason that patient education — or the lack thereof — may be creating the kinds of health disparities seen in diabetes. Patients who receive information about diabetes and lifestyle choices to prevent it may reduce their chances of developing the disease compared to those who do not. The central question, then, is: what kinds of health disparities arise in diabetes as a result of lack of access to information?

Lack of access to information can occur for several reasons. As a physician or nurse, one must educate patients on the choices they have for treatment and help guide them through recovery from diabetes-related complications. Professionals must also educate patients on prevention. Failure to educate a patient in a way that builds genuine understanding can lead to ineffective patient care. Among the factors most often researched in this area are race and income.

Race and Income as Drivers of Diabetes Disparities

Race and income play a large role in diabetes outcomes. They shape access to care based on geographic location and potential cultural lifestyle factors. Researchers studying racial and income disparities in diabetes found a higher prevalence of the disease among Black individuals compared to White individuals:

"We found a race–poverty–place gradient for diabetes prevalence for Blacks and poor Whites. The odds of having diabetes were higher for Blacks than for Whites. Individual poverty increased the odds of having diabetes for both Whites and Blacks. Living in a poor neighborhood increased the odds of having diabetes for Blacks and poor Whites" (Gaskin et al., 2014, p. 2147).

Furthermore, those living in impoverished areas were more prone to developing diabetes. People from impoverished backgrounds may not have access to recreational activities or high-quality food that would support a healthier lifestyle. From a cultural standpoint, dietary patterns in some communities may also contribute to a higher prevalence of the disease. Such findings can help direct attention toward the areas in healthcare most in need of improvement, so that appropriate services can reach the populations most affected.

While race and income are significant contributors to health disparities, other aspects of a person's identity — such as disability status — can also play a critical role.

Disability and Elevated Diabetes Risk

One article describing health disparities among individuals with diabetes found that adults with developmental and intellectual disabilities developed diabetes at a higher rate than those without such disabilities. "Disparities in prevalence were most notable among women, younger adults, and those residing in rural or high-income neighbourhoods. Adults with intellectual and developmental disabilities are at high risk of developing and being hospitalized for diabetes" (Balogh, Lake, Lin, Wilton, & Lunsky, 2014, p. 235).

If people with intellectual and developmental disabilities develop diabetes at a disproportionately higher rate, this points to systemic gaps in how their health is managed. Understanding and addressing these gaps is essential to delivering equitable care to one of the most vulnerable patient populations.

2 Sections Hidden · 270 words
Patient Autonomy and the Limits of Patient Education140 words
In order to understand what can be done to reduce these disparities, one concept that must be considered is patient autonomy. "Patient autonomy is a gradual, time-changing process of (re-)constructing autonomy through…
The Role of Legislation and Policy Reform130 words
The most significant change must occur at the legislative level, specifically in policy. "As a result of a gap in provincial legislation, healthcare providers…

Conclusion

Diabetes is a chronic disease that requires effort across many areas of healthcare. Although medical professionals such as nurses can seek to educate patients on lifestyle choices and management strategies, the deeper problem lies in patient autonomy — and in what strategies can help strengthen it or, at the very least, offer meaningful alternatives. Patients require assistance in understanding what must be done both to prevent diabetes and to manage it effectively.

Legislation can lay the foundation from which medical professionals implement sound and effective practices. These practices can be constructed to accommodate new research identifying where health disparities lie and to address those disparities in a targeted manner. Everything required to deliver high-quality patient care must emerge from a carefully constructed framework — one that can only be achieved through sound, equitable legislation.

References

Abdool, R., Szego, M., Buchman, D., Justason, L., Bean, S., Heester, A., . . . Kaufman, H. (2016). Difficult healthcare transitions. Nursing Ethics, 23(7), 1.

Balogh, R. S., Lake, J. K., Lin, E., Wilton, A., & Lunsky, Y. (2014). Disparities in diabetes prevalence and preventable hospitalizations in people with intellectual and developmental disability: a population-based study. Diabetic Medicine, 32(2), 235–242.

Gaskin, D. J., Thorpe, R. J., McGinty, E. E., Bower, K., Rohde, C., Young, J. H., . . . Dubay, L. (2014). Disparities in diabetes: The nexus of race, poverty, and place. American Journal of Public Health, 104(11), 2147–2155. doi:10.2105/ajph.2013.301420

Lindberg, C., Fagerstrom, C., Sivberg, B., & Willman, A. (2014). Concept analysis: patient autonomy in a caring context. Journal of Advanced Nursing, 70(10), 2208–2221. doi:10.1111/jan.12412

Key Concepts in This Paper
Health Disparities Diabetes Prevention Race and Poverty Patient Autonomy Patient Education Intellectual Disability Chronic Disease Legislative Reform Healthcare Access Equitable Care
Cite This Paper
PaperDue. (2026). Health Disparities in Diabetes: Race, Income, and Policy. PaperDue. https://www.paperdue.com/study-guide/health-disparities-diabetes-race-income-policy-2164429

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