Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2020 Aug 27.
Published in final edited form as: J Health Soc Behav. 2020 May 19;61(2):190–207. doi: 10.1177/0022146520921371

The Psychological Consequences of Disability over the Life Course: Assessing the Mediating Role of Perceived Interpersonal Discrimination

Eun Ha Namkung 1, Deborah Carr 2
PMCID: PMC7450392  NIHMSID: NIHMS1618371  PMID: 32425066

Abstract

We examine whether perceived interpersonal discrimination mediates the association between disability and psychological well-being (depression, negative and positive affect), and how these processes differ across the life course. Data are from two waves (2004-2006; 2013-2014) of the Midlife in the United States (MIDUS) (n = 2,503). Perceived discrimination accounts for 5 to 8 percent of the association between disability and the three mental health outcomes. Moderated mediation analyses reveal significant age differences; perceived discrimination is a stronger explanatory mechanism among midlife (ages 40-64) relative to older (age 65+) adults. Disability stigma takes a heightened psychological toll at midlife, a life stage when adults are expected to be able-bodied and interact with a diverse social network which may be a source of interpersonal mistreatment. Among older adults, for whom impairment is expected and common, the psychological impact of disability may operate through other pathways. We discuss implications for research and practice.


Disability encompasses any condition of the body or mind that makes it difficult to engage in activities and interact with one’s environment. More than 20 million U.S. adults report that they cannot do or have “a lot” of difficulty with seeing, hearing, mobility, communication, cognition, or self-care (National Center for Health Statistics 2017). Rates of impairment among young and midlife adults have risen dramatically in recent years, alongside population aging and a corresponding increase in physical limitation (Brown et al. 2017; Joffe-Walt 2013). Persons with disability are vulnerable to compromised emotional well-being due in part to their lower levels of social integration and activity, diminished sense of self-efficacy, poorer quality employment, reduced work hours, and financial strain (Brown and Barrett 2011; Caputo and Simon 2013; Freedman et al. 2017; Yang 2006).

We propose that experiences of interpersonal discrimination -- or the microaggressions and slights that occur in day-to-day interactions – also may contribute to the poorer emotional well-being of persons with disability. Research consistently shows that persons with mental illness (Russinova et al. 2011), “visible” conditions like hearing-aid use (Erler and Garstecki 2002), and physical conditions that limit daily activities like walking or lifting (Namkung and Carr 2019) are vulnerable to discriminatory and demeaning treatment. However, we know of no studies that formally evaluate the extent to which interpersonal discrimination contributes to mental health differentials between those with versus without impairment, nor the extent to which these patterns vary over the life course. Disability is more prevalent, expected, and accepted among older adults relative to their working-age counterparts, and may render them less vulnerable to distressing interpersonal mistreatment. About 15 percent of middle-aged adults in the United States have some difficulty performing basic daily activities and this proportion rises steadily with age, reaching 30 percent among persons ages 65 and older (Brown et al. 2017). Because health problems and accompanying impairments are increasingly common with advancing age, older adults may be less likely to experience and less emotionally vulnerable to interpersonal mistreatment, relative to their younger counterparts (Menec and Perry 1995).

We use data from two waves of the Midlife in the United States (MIDUS) survey, a random sample survey of more than 3,000 men and women ages 35 to 84 in 2004-05, to examine prospectively: (1) the extent to which the effects of disability on three dimensions of psychological well-being (depressive symptoms, negative affect, and positive affect) are mediated by perceived interpersonal discrimination; and (2) whether the relative explanatory power of perceived discrimination differs across four life course stages (young adulthood, early midlife, later midlife, and old age). Analyses are adjusted for demographic, health, and psychological characteristics that may confound associations among disability, perceived discrimination, and well-being. Identifying potentially modifiable factors that compromise the psychological well-being of U.S. adults with impairment is an important public health concern (Krahn et al. 2015). Interpersonal mistreatment of persons with disability could further undermine the well-being of this already vulnerable population.

BACKGROUND

Psychological Consequences of Disability

Disability refers to a condition that impairs one’s ability to perform activities of daily living (ADLs) such as walking up a flight of stairs, or instrumental activities of daily living (IADLs), which encompass complex behaviors like preparing meals (Verbrugge and Jette 1994). Adults with impairments that are not accommodated may struggle to carry out activities, maintain social relationships, and live independently. They also may quit work or abandon leisure activities that were once a source of pleasure, and may feel their independence and autonomy are undermined (Freedman et al. 2017). Consequently, impairment is associated with heightened depressive symptoms, and compromised daily mood, life satisfaction, and self-esteem (Caputo and Simon 2013; Freedman et al. 2017; Mancini and Bonanno 2006), with prospective studies documenting that effects operate from disability to distress, rather than vice-versa (Gayman, Turner and Cui 2008; Yang 2006).

The association between disability and compromised mental health is consistent with key themes of the stress paradigm (Pearlin et al. 2005). Stressors encompass acute events, such as losing one’s job, and chronic strains, such as a long-term impairment, that undermine well-being. Chronic strains are particularly detrimental to emotional well-being, due to their extended duration and capacity to spill over into multiple life domains, including work and family. Persistent stress exposure also threatens one’s immune, digestive, cardiovascular, sleep, and reproductive systems, which render one vulnerable to psychological distress (Carr, 2014; Pearlin et al. 2005). Disability also may diminish one’s internal coping resources, including mastery and self-esteem, as well as external coping resources including social support. Coping resources are critical to sustaining emotional well-being in the face of chronic stress (Carr, Cornman and Freedman 2019; Turner and Noh 1988; Yang 2006).

Stress perspectives identify a further process through which a stressor undermines mental health; the primary stressor (e.g., disability) may trigger secondary stressors such as financial insecurity, work strains, involuntary unemployment, or marital conflict, which may further erode one’s well-being (Shandra 2018; Turner and Turner 2004). We propose that discriminatory or demeaning interpersonal encounters are a potentially important yet under-explored secondary stressor through which disability undermines mental health. Interpersonal mistreatment of persons with impairment could threaten their well-being directly, consistent with research on the negative psychological consequences of discrimination including racism (Williams and Williams-Morris 2000), sexism (Pavalko, Mossakowski and Hamilton 2003), sizeism (Carr and Friedman 2005), ageism (Vogt Yuan, 2007), and homophobia (Bostwick et al. 2014). Perceived discrimination also can amplify the harmful psychological consequences of vulnerability factors like obesity (Tsenkova et al. 2011).

Stigmatization and Perceived Discrimination toward Persons with Disability

Classic stigma theories assert that persons with impairment may be devalued and mistreated by others. Goffman (1963:3) defined stigma as any personal attribute that is “deeply discrediting” to its possessors; these attributes include “blemishes of individual character,” “abominations of the body,” and “tribal stigmata.” Persons with functional limitations arguably fall into the former two categories. Goffman’s writings suggested that persons with disabilities are “disqualified from full social acceptance” (p. 3) both because their condition is unappealing to others and may be viewed as a signal that the person is not fully capable of carrying out their expected social roles. Especially in capitalist societies where being able-bodied is viewed as a marker of competence and capacity to work, persons with activity-limiting impairments also may be treated as if they possess a “blemish of individual character” -- a malingerer who is exaggerating or faking their symptoms to evade work and other responsibilities (Lingsom 2008). Contemporary conceptualizations of stigmatization underscore that this devaluation is carried out by social institutions and individuals who denigrate and exclude. This mistreatment may encompass institutional discrimination which blocks access to education, employment, and healthcare, and interpersonal slights and microaggressions that may undermine one’s well-being (Link and Phelan 2001).

Discrimination against persons with functional limitations is prohibited by law in the United States. The Americans with Disability Act (ADA), passed by Congress in 1990 and amended in 2008, prohibits discrimination on the basis of disability in many settings including employment, public services (e.g., transportation), public accommodations, and telecommunications. The ADA also requires employers to provide reasonable accommodations to qualified individuals with a disability. The ADA is based on a broad definition of “disability” which covers both mental and physical conditions; a condition need not be severe or permanent to qualify an individual for accommodations (Jasper 2008). Despite these formal protections, legal cases and media reports of persons being mistreated on the basis of health problems, even relatively minor ones such as back problems, controlled diabetes, or a speech impediment, are common (McMahon and Shaw 2005). For example, workers with activity limitations earn less, receive less training and benefits, are less likely to participate in decision-making, and are more likely to exit employment, relative to their counterparts without such conditions (Schur et al. 2009). Institutional discrimination also is documented in health care settings; patients with poorer self-rated health are more likely to report receiving inferior services, compared to their counterparts in better health (LaVeist, Rolley and Diala 2003).

Yet institutional discrimination represents a modest share of all stigmatizing encounters. Other subtle yet pernicious forms of stigmatization including interpersonal slights may affect psychological well-being, especially for those whose health and functioning are already compromised (Link and Phelan 2001). Studies based on large national surveys of U.S. adults (Namkung and Carr 2019) and smaller regional samples (Brown 2017; Kilpatrick and Taylor 2018), as well as studies focused on persons with psychiatric conditions (Kassam, Williams and Patten 2012) and visible conditions such as hearing-aid use (Erler and Garstecki 2002) show that persons with disability experience microaggressions in everyday life, including bullying and disrespectful treatment. Likewise, focus group interviews of persons with sensory or physical limitations revealed they often felt they were treated like “second-class citizens,” and that their intelligence and skills were underestimated (Keller and Galgay 2010: 249-50).

We use data from a nationally representative sample of U.S. adults to explore whether persons with difficulty performing daily activities report compromised mental health, and the extent to which these associations are accounted for by perceived interpersonal discrimination. Drawing on stigma theories, we separately evaluate three subtypes of interpersonal mistreatment (treated disrespectfully, treated as if one has a character flaw, and harassment/insults), as well as a composite measure (encompassing all three subscales), to identify the specific ways stigmatization may undermine well-being.

Life Course Differences in Disability-Related Discrimination and its Psychological Consequences

We also evaluate whether perceived interpersonal discrimination is an equally powerful mediator of the disability-mental health link at four distinctive life course stages: young adulthood, early midlife, later midlife, and old age. We expect that interpersonal mistreatment will be a particularly strong mediator for working age persons relative to their older counterparts, because disability among older persons may be more culturally normative and expected, thus treated less harshly. Disablement diminishes individuals’ “abilities to act in necessary, usual, [and] expected…ways in their society” (Verbrugge and Jette 1994: 3). Thus, impairment may be seen as more discrediting to working-age persons, as it violates expectations regarding physically and economically active, independent, and “able-bodied” adults (McPherson 1994). Because functional impairment is less common in young (age 30-39) and middle (age 40-64) adulthood relative to old age (age 65+), it may be a more salient personal characteristic that elicits stigmatizing treatment from others (Barreto and Ellemers 2015).

Structural factors also may contribute to greater stigmatization of persons with disability in midlife versus later life. The size and diversity of one’s social networks and life spaces diminish with age, such that working-age persons interact in a wider array of social settings and with a more extensive network of persons who may be the source of stigmatization (Baker, Bodner and Allman 2003). By contrast, older adults’ social networks diminish, especially upon retirement, such that they tend to interact with a smaller and more close-knit group of friends, relatives, and confidantes (Charles and Carstensen 2010); this more selective social circle may be less inclined to mistreat an older adult with impairment (Luong, Charles and Fingerman 2011). Older adults with impairment may be treated with support and empathy, whereas their younger counterparts may be treated with disdain or disrespect in their workplace or other peripheral social connections (Menec and Perry 1995).

Age-related changes in emotion regulation also may affect how persons with impairment respond emotionally to unkind or stigmatizing personal encounters. Older adults have less extreme emotional responses to stress, and a greater capacity to see the “good” even in unpleasant situations, relative to their younger counterparts (Charles and Carstensen 2010). This capacity to see the positive (and ignore or diminish the negative) is especially the case with interpersonal encounters. Older adults report fewer interpersonal tensions, experience less stress following such tensions, and are more likely to respond passively and avoid arguments, relative to younger adults, even when objective levels of interpersonal tensions are held constant (Birditt and Fingerman 2005; Birditt, Fingerman and Almeida, 2005; Charles and Carstensen 2008).

Finally, the experience of disablement changes over the life course, such that disability tends to be more severe and multifaceted among older adults (National Center for Health Statistics 2017). Consequently, other secondary stressors such as difficulty navigating one’s home, reduced social participation, social isolation, and a diminished sense of autonomy may be more salient for older adults’ mental health, relative to the secondary stressor of interpersonal mistreatment (Brown 2015; Brown and Barrett 2011). Thus, we carry out moderated mediation analyses to examine whether the strength of perceived discrimination as a mediator of the disability-mental health relationship differs in young adulthood (age 30-39), early (age 40-49) and late (age 50-64) midlife, and later life (age 65+).

We consider three conceptually and statistically distinct dimensions of psychological well-being (depressive symptoms, negative affect, and positive affect), given well-established age differences in how individuals experience and report their mental health symptoms. Positive affect refers to pleasant emotions such as feeling happy, whereas negative affect reflects unpleasant moods such as sadness or nervousness during the past 30 days (Watson, Clark and Tellegen 1988). Older adults tend to report more frequent positive affect, less frequent negative affect, and more frequent co-occurrence of the two, relative to younger persons (Charles and Carstensen 2010). Depressive symptoms, as measured in the MIDUS, refer to a period of two weeks or more over the past year in which one experienced symptoms such as sadness and lethargy (Kessler, Mickelson and Williams 1999). Given this relatively long period of retrospection, older adults’ depressive symptom reports may be understated, reflecting recall and positivity biases (Knauper and Wittchen 1994; Reed and Carstensen 2012).

We adjust all analyses for demographic, health, and psychosocial factors that may confound statistical associations among disability, discrimination, and mental health. Persons from socially and economically disadvantaged groups, including women, ethnic minorities, and persons of lower socioeconomic status are especially vulnerable to physical disability (Brown et al. 2017; Krahn et al. 2015), discriminatory treatment (Carr, Jaffe and Friedman 2008; Kessler et al. 1999), and compromised mental health (Kessler et al. 1999). We adjust for body mass index (BMI) and chronic health conditions as they are associated with elevated disability risk (Kassam et al. 2012; Krahn et al. 2015), perceived discrimination (Carr and Friedman 2005; Kessler et al. 1999), and psychological well-being (Carr and Friedman 2005). We adjust for trait neuroticism which may render one particularly cognizant of and emotionally reactive to unpleasant encounters such as interpersonal mistreatment (Carr et al. 2008). Finally, we control for baseline mental health measures to address concerns regarding possible endogeneity among reports of perceived discrimination and mental health.

DATA AND METHODS

Data

Analyses are based on data from the National Survey of Midlife Development in the United States (MIDUS), a longitudinal survey of a national probability sample of non-institutionalized, English-speaking adults ages 25 to 74 in 1995-1996 who were selected via random digit dialing from working telephone banks in the continental United States (MIDUS 1, n = 7,108). Study participants were re-interviewed at ages 35-84 in 2004-2006 (MIDUS 2, n = 4,963), and ages 43-94 in 2013-2014 (MIDUS 3, n = 3,294). Retention rates are 75% between MIDUS 1 and MIDUS 2, and 77% between MIDUS 2 and MIDUS 3, after adjusting for mortality (Radler and Ryff 2010). (For further detail, see https://www.icpsr.umich.edu/icpsrweb/ICPSR/series/203).

We use MIDUS 2 and MIDUS 3 to prospectively examine associations between disability and perceived discrimination reported at MIDUS 2, and psychological outcomes assessed in MIDUS 3. We use data from MIDUS 2 only to ascertain associations between disability status and contemporaneous perceived interpersonal discrimination; a prospective exploration of disability status at one wave and perceived discrimination ten years later would raise concerns regarding the instability of impairment over lengthy time periods (Lin and Kelley-Moore 2017).

Our analytic sample includes respondents who completed both a telephone interview and self-administered questionnaire in MIDUS 2 and MIDUS 3 (n = 2,555). We excluded 52 respondents whose disability status is missing, resulting in a final analytic sample of 2,503 persons. Item-specific missing data are less than 1% across all variables, except body weight, which is 3.9%. We indicate these cases with a dichotomous “weight missing” variable because refusal to report one’s weight is correlated with poorer mental health and more frequent reports of discrimination, relative to normal weight persons (Carr et al. 2008; Chau et al. 2013).

Measures

Psychological well-being.

Depressive symptoms are assessed with the World Health Organization (WHO) Composite International Diagnostic Interview (CIDI) Short Form (Kessler et al. 1999). Participants indicated whether they “felt sad, blue, or depressed” or “lost interest in most things” for two weeks or more within the past 12 months. Those who endorsed either item were asked seven follow-up questions (yes or no) assessing the specific symptoms experienced: (1) lose interest in most things; (2) feel more tired out or low on energy than is usual; (3) lose your appetite; (4) have more trouble falling asleep than usual; (5) have a lot more trouble concentrating than usual; (6) feel down on yourself, no good, or worthless; and (7) think a lot about death. Consistent with previous MIDUS studies (Namkung, Greenberg and Mailick 2016; Robinson, Sutin and Daly 2017), we constructed a depressive symptoms score based on these two measures, with scores ranging from 0 to 7 (0 = no two-week period of depressed affect or anhedonia in the last 12 months; 7 = more depressive symptoms).1

Positive and negative affect are assessed with subsets of the Affect Balance Scale (Bradburn 1969). Positive affect (α = 0.89) captures how often during the past 30 days the respondent felt: cheerful; in good spirits; extremely happy; calm and peaceful; satisfied; and full of life. Negative affect (α = 0.80) refers to how often during the past 30 days they felt: so sad nothing could cheer you up; nervous; restless or fidgety; hopeless; everything was an effort; and worthless. Response categories range from 1 (none) to 5 (all the time) and are averaged such that higher scores reflect more frequent positive or negative affect (Mroczek and Kolarz 1998). The zero-order correlation between the negative affect and depression outcomes was 0.40, affirming their statistical and conceptual distinctiveness.

Disability.

Disability is assessed in the self-administered questionnaire with items adapted from the SF-36, capturing difficulty with nine activities of daily living (Ware and Sherbourne 1992). Participants are asked, “how much does your health limit you in doing each of the following: lifting or carrying groceries; bathing or dressing yourself; climbing several flights of stairs; bending, kneeling, or stooping; walking more than a mile; walking several blocks; walking one block; vigorous activity (e.g. running, lifting heavy objects); moderate activity (e.g. bowling, vacuuming)?” Response categories are not at all, a little, some, and a lot. We classify participants as having a limitation if they reported at least “some” difficulty on any of the nine items, consistent with previous MIDUS analyses (Friedman 2016; Namkung and Carr 2019). The most common limitation reported among persons with impairment is vigorous activity (90 percent), followed by kneeling, bending or stooping (46 percent) and walking a mile (41 percent). We conducted sensitivity analyses in which we use a more stringent measure, classifying persons as having a disability if they indicated “a lot” on any of the nine items. Multivariate results were remarkably consistent regardless of the measure used, yet model fit was superior with the broader measure (at least “some” impairment). The former measure also provides a sufficient subsample size for mediated moderation analyses testing effects of age group by impairment status (Sensitivity analyses are presented in Appendix Tables 1a and 1b).

We carried out additional sensitivity analyses using a measure of new onset cases of impairment (i.e., persons who reported “some” difficulty at MIDUS 2 but not MIDUS 1). Model fit was superior and effect sizes larger for our original measure; we suspect this reflects both statistical power and the fact that the new onset cases are of shorter duration. As such, they may be less consequential for mental health than impairments of longer duration which increase one’s exposure to potential discrimination (Supplementary analyses presented in Appendix Table 2).

Perceived interpersonal discrimination.

Perceived interpersonal discrimination (α = 0.91) refers to how often on a day-to-day basis a respondent experiences each of the following (Kessler et al. 1999): (1) treated with less courtesy; (2) treated with less respect than other people; (3) receive poorer service at restaurants or stores; (4) people act as if you are not smart; (5) people act afraid of you; (6) treated as if dishonest; (7) treated as if not as good as others; (8) called names or insulted; and (9) threatened or harassed. Response categories are never, rarely, sometimes, and often. Responses are averaged, and scores range from 1 to 4, where a 4 reflects greater frequency of perceived daily mistreatment.

We conducted sensitivity analysis in which we used three subscales of perceived mistreatment, consistent with MIDUS analyses showing three conceptually and statistically distinct subtypes of perceived discrimination (Carr et al. 2008; Namkung and Carr 2019). Lack of respect (α = 0.91) indicates the frequency with which one was treated with less courtesy or respect than other people; received poorer service than other people; treated as if not smart or not as good as other people. Blemish of character (α = 0.72) refers to the frequency with which one is treated as if they are dishonest or are frightening to others. Insulted/harassed (α = 0.82) refers to the frequency with which one is insulted and threatened/harassed. We focus largely on the overall scale, as results were highly consistent across the three subscales.

Age group.

We created four categories of: young adulthood (ages 30-39), early midlife (ages 40-49), late midlife (ages 50-64), and later life (age 65 or older), consistent with earlier studies of impairment over the life course (Namkung and Carr 2019).

Control variables.

All analyses are adjusted for demographic and socioeconomic characteristics at baseline (MIDUS 2) that are established correlates of psychological well-being and perceived discrimination: gender (1 = female; 0 = male), race/ethnicity (1= racial or ethnic minority; 0 = non-Hispanic white), marital status (1 = currently married; 0 = unmarried), education (less than high school, high school graduate (reference), some college, college graduate or higher), and employment status (1 = currently working; 0 = not working). We adjust for two physical health indicators, body mass index (BMI) and the presence of at least one of 27 medical conditions in the past 12 months (e.g., asthma, hypertension). BMI is calculated from participants’ self-reported height and weight, and classified into four categories (underweight/normal (reference), overweight, obese, refusal/don’t know), consistent with those used by the National Heart, Lung and Blood Institute (NHLBI 1998). Underweight status (i.e., BMI less than 18.5) was not associated with discrimination or psychological well-being, so we combined this very small category with normal weight. Finally, we adjust for the personality trait neuroticism (α = 0.74) using an established four-item scale (Rossi 2001). Respondents indicate how much each of four adjectives describes them: moody, worrying, nervous, and calm (reverse coded). Responses are averaged and range from 1 to 4, with higher scores indicating higher levels of neuroticism.

Analytic Plan

We first conduct bivariate analyses comparing all measures by disability subgroup; we conduct t-tests for continuous measures and chi-square tests for categorical variables. Second, we estimate ordinary least squares (OLS) regression models to identify the effects of baseline functional limitation and perceived discrimination (MIDUS 2) on the three well-being outcomes at the ten-year follow-up (MIDUS 3). Third, we estimate structural equation models to evaluate the extent to which the longitudinal associations between functional limitations and well-being are mediated by perceived interpersonal discrimination. Fourth, we test the moderating role of life course stage in the mediation patterns (i.e., conditional indirect effects) and in the direct associations between functional impairment and psychological outcomes. Our final conceptual model with moderated mediation by age group is presented in Figure 1.

Figure 1. A Conceptual Model of Moderated Mediation.

Figure 1.

Note. M2 = MIDUS 2, M3 = MIDUS 3. Path C’ indicates direct effect of disability on psychological outcomes, and path C indicates total effect, a combination of the direct effect and indirect effect (path A x path B) of disability.

All analyses are performed in Stata version 15. For the (moderated) mediation analyses, we use the sem and nlcom commands to estimate the structural equation models using the maximum likelihood method. To test the presence of significant mediation or indirect effects, path A (functional impairment → perceived discrimination) and path B (perceived discrimination → psychological outcomes) coefficients are multiplied (Preacher and Hayes 2008).2 All mediation analyses are adjusted for baseline psychological outcome measures (only for path B), and sociodemographic, health, and personality covariates (both for paths A and B). We also test differential mediation effects for disability via perceived discrimination across the four age groups. We evaluate moderation effects by age group by including two-way interactions on all three paths (i.e., functional impairment x age group on paths A and C, perceived discrimination x age group on path B). Moderated mediation is documented when mediation effects of perceived discrimination (i.e., the purported pathway linking disability status with mental health) differ significantly by age group

RESULTS

Bivariate Analysis

Table 1 shows that about half of the analytic sample (47%) reports at least some functional impairment at baseline (MIDUS 2). Persons with disability are overrepresented among older adults (ages 65+), women, and unmarried persons. A socioeconomic gradient also is evident, such that adults with impairment are less likely to be employed and have fewer years of education relative to those without impairment. Disability is linked to higher rates of obesity and chronic medical conditions: adults with (versus without) disabilities are more likely to be classified as obese (36 vs. 18 percent) and to report a chronic condition (88 vs. 64 percent). They also report significantly higher levels of neuroticism (M = 2.12 vs. 1.98) and more frequent interpersonal discrimination (M = 1.46 vs. 1.37) than adults without impairment. Persons with impairment also report significantly higher scores on all three discrimination subscales, including disrespectful treatment (M = 1.59 vs. 1.47), insults or harassment (M = 1.33 vs. 1.29), and being treated as if they have a character flaw (M = 1.26 vs. 1.21). They also report poorer mental health, with significantly more depressive symptoms and negative affect and lower levels of positive affect at both study waves.

Table 1.

Univariate and Bivariate (by Disability Status) Statistics

Total No
disability
(2004-06)
Any
disability
(2004-06)
Group
difference 2
Variables 1 %, M (SD) %, M (SD) %, M (SD)
Baseline characteristics
Age group
 Young adulthood (age 30-39) 6% 9% 3% p < .001
 Early midlife (age 40-49) 23% 30% 15%
 Late midlife (age 50-64) 45% 45% 45%
 Later life (age 65 or older) 26% 16% 37%
Gender (1 = female) 56% 50% 63% p < .001
Race/ethnicity (1 = minority) 8% 8% 7% p = .626
Marital status
 Currently married 72% 76% 68% p < .001
 Previously married (widowed, divorced, separated) 20% 15% 26%
 Never married 8% 9% 7%
Education
 Less than a high school diploma 5% 3% 7% p < .001
 High school graduate 24% 20% 29%
 Some college 28% 27% 28%
 College degree or higher 43% 50% 35%
Working status (1 = currently working) 67% 77% 56% p < .001
Body weight
 Under- or normal weight 32% 38% 24% p < .001
 Overweight 38% 41% 36%
 Obese 26% 18% 36%
 Refused to report weight 4% 3% 5%
Any medical condition (1 = yes) 75% 64% 88% p < .001
Neuroticism (range = 1-4) 2.05 (0.62) 1.98 (0.62) 2.12 (0.62) p < .001
Perceived discrimination (range = 1-4) 1.41 (0.49) 1.37 (0.46) 1.46 (0.51) p < .001
 Lack of respect subscale (range = 1-4) 1.53 (0.62) 1.47 (0.56) 1.59 (0.62) p < .001
 Blemish of character subscale (range = 1-4) 1.31 (0.51) 1.29 (0.49) 1.33 (0.54) p < .05
 Harassment subscale (range = 1-4) 1.24 (0.46) 1.21 (0.43) 1.26 (0.49) p < .01
Mental health outcomes
Depressive symptoms (range = 1-7)
 Baseline (M2) 0.58 (1.68) 0.43 (1.44) 0.76 (1.91) p < .001
 Follow-up (M3) 0.56 (1.65) 0.38 (1.34) 0.77 (1.92) p < .001
Positive affect (range = 1-5)
 Baseline (M2) 3.46 (0.68) 3.58 (0.64) 3.32 (0.71) p < .001
 Follow-up (M3) 3.44 (0.72) 3.57 (0.67) 3.30 (0.74) p < .001
Negative affect (range = 1-5)
 Baseline (M2) 1.47 (0.53) 1.39 (0.45) 1.57 (0.45) p < .001
 Follow-up (M3) 1.46 (0.57) 1.36 (0.48) 1.58 (0.64) p < .001
N 2,503 1,339 1,164
Percent (%) 53% 47%

M = mean; SD = standard deviation

Source. Midlife Development in the United States (MIDUS), second wave (2004-2006; M2) and third wave (2013-2014; M3). Baseline refers to 2004-06 and follow-up refers to 2013-14.

Notes.

1

Missingness was less than 1% across all control and outcome variables.

2

Chi-square tests (for categorical variables) and t-tests (for continuous variables) were used to assess significant differences between the two groups.

To provide a fuller descriptive portrait of how disability is experienced over the life course, we carried out supplemental descriptive analyses showing age differences in the specific types of discrimination and health conditions reported by persons with impairment (see Appendix Tables 3a and 3b). Young and midlife persons with impairment report significantly more frequent experiences on each of the nine discrimination items, relative to both older adults with impairment and their age peers without impairment. Interestingly, among older adults, persons with versus without disability do not differ significantly in their responses to any of the nine discrimination items, suggesting that disability-related discrimination is highest in midlife, yet is not detected among older adults. The specific health conditions experienced by persons with disability in each age group also differ significantly. Among younger and midlife persons with impairment, the most common conditions are visible (e.g., tooth problems) or directly affect mobility (most notably joint problems) whereas older persons also report frequent chronic conditions like high blood pressure (see Appendix Table 3b). Overall, these results suggest that daily experiences of persons with versus without impairment are distinct for midlife persons, yet do not differ starkly among retirement-age adults.

Longitudinal Associations among Disability, Discrimination, and Well-being

OLS Regression.

We first examine prospective associations between disability and the three psychological outcomes. Table 2 shows OLS regression coefficients for our focal predictors only (full results presented in Appendix Tables 4a-c): Model 1 estimates the effects of disability, adjusting for sociodemographic characteristics, health, and neuroticism; Model 2 incorporates baseline mental health, and Model 3 further adds perceived discrimination. Persons with disability report significantly more depressive symptoms (B = 0.19, p < .001) and negative affect (B = 0.15, p < .001) and less positive affect (B = −0.14, p < .001) at the ten-year follow-up, adjusting for all covariates (see Model 1). These effects diminish by 15 percent (depressive symptoms), 33 percent (negative affect), and 50 percent (positive affect) yet remain sizeable and statistically significant after baseline psychological symptoms are controlled (see Model 2). The effects of disability status further diminish by 6 percent for depressive symptoms and 3 percent for positive and negative affect when perceived discrimination is added to Model 3.

Table 2.

Effects of Disability Status and Perceived Discrimination at Baseline (MIDUS 2) on Psychological Well-Being Outcomes at Follow-up (MIDUS 3)

Depressive symptoms
Model 1 Model 2 Model 3
b (SE) b (SE) b (SE)
Disability status a .19 (.04)*** .16 (.04)*** .15 (.04)***
Young adulthood (age 30-39) b .35 (.09)*** .22 (.09)* .21 (.09)*
Early midlife (age 40-49) b .34 (.06)*** .23 (.06)*** .23 (.06)***
Late midlife (age 50-64) b .22 (.05)*** .16 (.05)** .16 (.05)**
Baseline depressive symptoms .15 (.01)*** .15 (.01)***
Perceived discrimination .16 (.04)***
Constant −1.03 (.09)*** −.78 (.09)*** −.94 (.10)***
Adjusted R2 0.07 0.13 0.14
Negative affect
Model 1 Model 2 Model 3
b (SE) b (SE) b (SE)
Disability status a .15 (.02)*** .09 (.02)*** .09 (.02)***
Young adulthood (age 30-39) b .15 (.05)** .04 (.04) .02 (.04)
Early midlife (age 40-49) b .10 (.03)** .01 (.03) −.00 (.03)
Late midlife (age 50-64) b .02 (.03) −.05 (.02)* −.06 (.02)*
Baseline negative affect .47 (.02)*** .46 (.02)***
Perceived discrimination .08 (.02)***
Constant −.46 (.05)*** −.60 (.04)*** −.68 (.05)***
Adjusted R2 0.22 0.36 0.36
Positive affect
Model 1 Model 2 Model 3
b (SE) b (SE) b (SE)
Disability status a −.14 (.02)*** −.07 (.01)*** −.07 (.01)***
Young adulthood (age 30-39) b −.17 (.04)*** −.10 (.03)** −.09 (.03)**
Early midlife (age 40-49) b −.09 (.02)*** −.01 (.02) −.01 (.02)
Late midlife (age 50-64) b −.03 (.02) .02 (.02) .03 (.02)
Baseline positive affect −.30 (.01)*** .30 (.01)***
Perceived discrimination −.04 (.01)**
Constant 1.01 (.04)*** −.43 (.06)*** −.39 (.06)***
Adjusted R2 0.18 0.36 0.37

Source. Midlife Development in the United States, second wave (MIDUS 2) and third wave (MIDUS 3).

Note. Models used z-scores for all three outcomes. All models adjusted for gender, race/ethnicity, marital status, education, current employment status, BMI category, has one or more chronic conditions, and trait neuroticism.

a

Reference categories are no disability, and

b

age 65+.

*

p < .05

**

p <.01

***

p <.001.

Structural Equation (Mediation) Analyses.

Path analyses reveal the direct and indirect pathways linking disability and perceived discrimination with the three psychological outcomes. Figures 2 through 4 display results of the mediation analyses; coefficients are plotted for ease of interpretation (Summary of the results also are presented in Appendix Table 1a). Figure 2 shows that persons with impairment report more frequent daily discrimination (B = 0.166, p < .001), and discrimination in turn predicts increased depressive symptoms from baseline to follow-up (B = 0.079, p < .001), net of all covariates. Similarly, perceived daily discrimination is associated with decreased positive affect (B = −0.020, p < .01, see Figure 3) and increased negative affect (B = 0.041, p < .001, see Figure 4).

Figure 2. Perceived Interpersonal Discrimination Mediating Longitudinal Association between Disability and Depressive Symptoms.

Figure 2.

Note. Values are based on z-scores. Models are adjusted for age group, gender, race, marital status, education, employment status, BMI category, having one or more chronic conditions, and neuroticism. Regression coefficients and [95% confidence intervals] are presented. The values shown on underside of model path “physical disability → depressive symptom” indicate the total effect and the ones on upside of the path indicates the direct effect. M2 = MIDUS 2, M3 = MIDUS 3.

*** p <.001

Figure 4. Perceived Interpersonal Discrimination Mediating Longitudinal Association between Disability and Negative Affect.

Figure 4.

Note. Values are based on z-scores. Models are adjusted for age group, gender, race, marital status, education, employment status, BMI category, having one or more chronic conditions, and neuroticism. Regression coefficients and [95% percentile confidence intervals] are presented. The values shown on underside of model path “physical disability → negative affect” indicate the total effect and the ones on upside of the path indicates the direct effect. M2 = MIDUS 2, M3 = MIDUS 3.

*** p <.001

Figure 3. Perceived Interpersonal Discrimination Mediating Longitudinal Association between Disability and Positive Affect.

Figure 3.

Note. Values are based on z-scores. Models are adjusted for age group, gender, race, marital status, education, employment status, BMI category, having one or more chronic conditions, and neuroticism. Regression coefficients and [95% percentile confidence intervals] are presented. The values shown on underside of model path “physical disability → positive affect” indicate the total effect and the ones on upside of the path indicates the direct effect. M2 = MIDUS 2, M3 = MIDUS 3.

** p <.01; *** p <.001

Perceived discrimination accounts for a modest proportion of the link between physical impairment and well-being. Indirect effects of impairment are 0.13 for depressive symptoms (p = .01), 0.07 for negative affect (p < .01), and −0.003 for positive affect (p < .05). In total, 8.2% of the total effect of impairment on depressive symptoms is mediated through perceived discrimination. The proportions of total effects mediated (effect ratios) are 5.2% for positive affect and 7.3% for negative affect. Supplementary analyses (see Appendix Table 5, for summary) for the three discrimination subscales reveal that disrespectful treatment shows the greatest mediation effects (effect ratios are 8.5% for depressive symptoms, 4.1 for positive affect, and 8.6 for negative affect). The association between disability and positive affect was mediated by disrespectful treatment only. Being treated as if one had a character flaw and being insulted/harassed mediated the effects of disability on both depressive symptoms and negative affect, although these effects ratios were considerably lower than for disrespectful treatment.

Moderated Mediation Analyses

Finally, we evaluate the extent to which the mediation processes documented in Figures 2 through 4 vary by life course stage. We find that associations between functional impairment and perceived discrimination are significantly moderated by age group such that associations are stronger for working-age adults than those aged 65 or older (chi2(3) ranges from 10.85 to 11.26, p <. 05 for the models on three psychological outcomes). Similarly, we find evidence of significant moderation for the disrespectful treatment subscale (chi2(3) ranges from 11.15 to 11.67, p <. 05). However, we do not detect significant moderation for the subscales of blemished character and insult/harassment.

As Figure 5 shows, the moderated mediation effects are statistically significant for the outcomes of depressive symptoms and negative affect, but not positive affect. Perceived interpersonal discrimination significantly mediates the association between impairment and negative affect (left panel) for early (B = 0.026, p < .05) and late (B = 0.013, p < 0.05) midlife adults aged 40 to 49 and 50 to 64, respectively. By contrast, discrimination is not a significant mediator for adults aged 65+. Similarly, the right-hand panel shows a significant mediation effect in the association between impairment and depressive symptoms among late midlife adults ages 50 to 64 only (B = 0.016, p < .05). Comparable results emerged when we used the subscale of disrespectful treatment, but not for the subscales of blemished character and harassment.

Figure 5. Differential Mediation Effects of Perceived Discrimination in the Association between Functional Impairment and Psychological Well-Being by Life Stage.

Figure 5.

Note. Bar graphs quantify mediation or indirect effects and error bars on each bar indicate 95% confidence intervals based on bootstrapped resampling.

We found no statistically significant interactions between age and perceived discrimination (path B) nor between age and impairment in models predicting psychological well-being (path C), regardless of whether the composite or subscale measures of interpersonal mistreatment were used. Overall, the direct impacts of functional impairment and perceived discrimination on the three psychological well-being measures do not differ significantly by age, although the extent to which discrimination mediates the impairment-mental health linkage is significantly larger among working age versus older adults.

DISCUSSION

Our study is the first we know of to explore prospectively whether the link between disability and three aspects of psychological well-being is accounted for by perceived interpersonal discrimination. Recognizing that physical impairment is considered normative in later life, and is more highly stigmatized for younger persons (Namkung and Carr 2019), we also examined whether the psychological consequences of impairment differ by life course stage, and the extent to which perceived discrimination accounts for these effects.

Three main findings emerged. First, disability is a significant predictor of all three psychological outcomes, even after controlling for baseline measures of mental health and covariates. However, these effects were not moderated by age, demonstrating that the negative consequences of disability for mood and depressive symptoms are similar in magnitude among young, midlife, and older adults. Our findings are consistent with prior studies documenting strong linkages between disability and depression (Turner and Noh 1988; Yang 2006) or mood (Caputo and Simon 2013), and further reveal that positive aspects of mental health are undermined by disability for persons of all ages. This is an important finding, as our measure of disability was broad and encompasses persons with relatively modest level of impairments (i.e., “some” difficulty on any of nine daily activities, such as climbing a few flights of stairs), whereas previous studies focus on the severity of impairment and well-being (Caputo and Simon 2013; Freidman et al. 2017; Yang 2016). We found that these effects remained sizeable and statistically significant after BMI and chronic medical conditions were controlled. Thus, our results suggest that even a slightly diminished capacity to carry out expected roles – a condition affecting nearly half of MIDUS respondents -- can be a source of distress for adults over the life course, underscoring the importance of identifying why and how, so that effective interventions may be developed.

Second, our mediation analyses revealed that the link between disability and well-being is partly accounted for by perceived interpersonal discrimination, with this mediator accounting for 5 to 8 percent of the association. Although this is a modest proportion mediated, even a small proportion of total effect mediated may have important practical implications when the total effect is large (Preacher and Kelley 2011). Disability status has large and significant effects on negative and positive affect (see R-square in the regression Model 1), with larger effects than other sociodemographic characteristics, medical conditions, and BMI category. Thus, even a modest mediation effect of disability via interpersonal mistreatment suggests a potential site for practical intervention.

Our moderated mediation analyses further revealed that these patterns held only for midlife adults, and not for young or retirement-age adults. The youngest MIDUS participants came of age and entered the labor force following the 1990 passage of the ADA. As such, they may have received more responsive accommodations, the benefit of school-to-work or work-based initiatives, and more thoughtful treatment in their work and social encounters in adulthood (Shandra and Hogan 2008). However, given the relatively small number of younger adults in our sample, the non-significant results also may reflect statistical power. The distinctive ways that disability affects the lives of younger adults warrants further exploration.

For midlife persons with impairment, who have more expansive social networks and life spaces than their older counterparts, interpersonal mistreatment and microaggressions perpetuated by service providers, colleagues, and significant others are significantly more frequent (as shown in Appendix Table 3a). These discriminatory encounters may constitute a chronic strain that is consequential for one’s everyday life, making them a critical pathway linking impairment status with psychological well-being (Baker et al. 2003; Charles and Carstensen 2010; Luong et al. 2011).

For older adults, a very different scenario emerged. While disability was a significant predictor of mental health outcomes among those ages 65+, experiences of discrimination were not a significant mediator. Supplemental descriptive analyses showed that older persons with impairment reported significantly less frequent mistreatment along all nine specific indicators, relative to their younger counterparts. Moreover, among older adults, those with impairment did not report significantly more frequent discriminatory treatment on any of the nine items, relative to their age peers without impairment. This may reflect the fact that disability is normative and expected, and thus less likely to be stigmatized in later life (Menec and Perry 1995). Moreover, older adults’ more narrowly drawn social networks and life spaces may limit their encounters to a close-knit group of significant others who may be less inclined to mistreat them (Baker et al. 2003; Charles and Carstensen 2010; Luong et al. 2011).

Our results suggest that secondary stressors other than perceived discrimination -- such as social isolation, a diminished sense of self-efficacy, and reduced activity -- may be more powerful mechanisms linking disability to psychological well-being among older adults (Brown and Barrett 2011; Caputo and Simon 2013; Freedman et al. 2017; Yang 2006). We carried out supplementary mediation analysis, and evaluated the extent to which environmental mastery, autonomy, perceived control, family relationship strains, and marital strain mediated the association between disability and psychological well-being among older adults. Not one was a statistically significant mediator; we suspect that potential pathways not included in the MIDUS, such as time use and changes in daily activities, may be plausible yet unexplored mechanisms. We encourage future research identifying the specific pathways through which disability undermines the psychological well-being of older adults.

Third, we found that one subtype of discrimination, being treated disrespectfully, is particularly consequential for the well-being of persons with disability. Our supplemental analyses (shown in Appendix Table 5) revealed the greatest mediation effect for this subscale, and also found that it was the only subscale that mediated the association between disability and positive affect. We speculate that disrespectful treatment is particularly distressing for persons with impairment because of its breadth, pervasiveness, and the feelings of demoralization it may engender. Disrespect conveys claims about one’s competence and undermines one’s dignity, making it particularly painful (Janoff-Bulman and Werther 2008). By contrast, insults and harassment are relatively infrequent (see Appendix Table 3a), so persons with impairment may attribute this mistreatment to traits of the person doing the stigmatizing rather than internalizing the experience (Major, Quinton and McCoy 2002). Future studies should delve more fully into the particular subtypes of interpersonal discrimination that are especially harmful, paying close attention to disrespectful treatment given the centrality of respect to human dignity (Janoff-Bulman and Werther 2008).

Our results also convey a broader message for the study of stress and mental health; the explanatory mechanisms linking a stigmatized identify, such as disablement, and psychological well-being may differ markedly by social location. Our moderated mediation analyses clearly show that perceived interpersonal discrimination was a significant pathway linking disability with psychological well-being for working-age but not older adults. The use of moderated mediation analyses may be a useful tool for understanding the consequences of secondary stressors more generally. One reason why studies may fail to detect significant pathways linking stigma to well-being is that a particular pathway may be significant for one subgroup only, a pattern that may be concealed or ‘cancelled out’ using a coarser approach. Documenting for whom a secondary stressor is harmful also will inform appropriate practices and interventions.

Limitations

Our study has several limitations that bear on the generalizability of the results and motivate future research. First, the stronger mediation effects detected among midlife versus older persons may reflect cohort rather than age effects, such that members of the Baby Boom and Generation X cohorts are more sensitive to experiences of discrimination, relative to older cohorts. However, while there is evidence that cohort membership may affect one’s awareness of and willingness to report discrimination (Namkung and Carr 2019), it is less clear that cohort membership would affect emotional responses to this discrimination among persons with impairment. Given compelling literature on age differences in emotional responses to difficult interpersonal encounters (Charles and Carstensen 2010), we find age moderation arguments more persuasive, although these contrasts could be further fleshed out in future analyses.

Second, we used a broad self-reported measure of impairment, rather than a specific measure of the impairment-related condition. However, self-reported function is widely considered an important patient-centered measure (Brown et al. 2017) that is a robust predictor of subsequent adverse health outcomes including mortality risk (Carey et al. 2004). Third, the MIDUS relies on perceptions rather than formally documented or confirmed reports of mistreatment. Further, our analysis did not consider whether one attributes the mistreatment to their own impairment or to a character flaw of the person doing the discrimination. However, perceiving that one is mistreated (regardless of the cause) is stressful in its own right, and may have important consequences for the perceiver’s well-being.

Fourth, MIDUS does not obtain detailed information on underlying diagnoses or conditions that specifically undermine functioning, limiting our capacity to explore how experiences of discrimination may vary based on the specific health condition. To partially address this limitation, we examined whether persons with versus without impairment differed with respect to the medical conditions experienced over the prior 12 months. Persons with disability reported higher rates of 25 of the 27 conditions considered. Further, our multivariate and moderated mediation analyses barely changed in magnitude or significance when medical conditions were adjusted. Thus, our results suggest that it is the manifestation of one’s conditions, such as difficulty walking, that elicits mistreatment from others rather than the underlying conditions. Future studies could further distinguish “visible” versus “invisible” health conditions, as the former may render one particularly vulnerable to discriminatory treatment and the mental health consequences thereof.

Finally, we considered only life course stage as a moderator; it is plausible that the mediation effects of discrimination we documented also may be more pronounced for persons with other social or economic disadvantages, including persons with lower levels of education, ethnic minorities, or women. We conducted supplemental analyses and found no significant differences on the basis of gender (results available from authors). Future studies with larger subsamples of ethnic minorities and economically disadvantaged persons should further explore factors that intensify or diminish the mediating role of perceived discrimination for understanding the mental health of persons with impairment.

Despite these limitations, our study reveals that perceived interpersonal discrimination is a pathway through which disability undermines three distinctive aspects of mental health, especially for midlife adults. These findings have potentially important implications for public health. The proportion of working-age persons either reporting a physical impairment or receiving disability payments has increased steadily over the past two decades (Joffe-Walt 2013). Theoretical writings suggest that specific stigmas eliciting negative reactions from others may change over time as knowledge, values, and public acceptance of “devalued” conditions and behaviors change (Goffman 1963). As more individuals experience relatively young onset of physical limitations, biases may be reduced because awareness of disability-based inequities may increase. However, if disability continues to prematurely befall (and becoming associated with) members of historically stigmatized groups including persons of lower socioeconomic status, ethnic minorities, and persons with mental health conditions or obesity, the stigma may intensify.

We focused specifically on interpersonal discrimination that occurs in daily encounters with coworkers, service providers, and even friends and family. Educating personal caregivers for persons with impairment as well as service providers across a range of industries is critical. Persons with impairment – especially those of working-age -- may avoid or delay seeking services like home repairs and bank loans, or may not reach out to kin or neighbors for personal care as a way to protect themselves from mistreatment. The latter is particularly troubling, as persons with impairment have disproportionately high rates of 25 of the 27 health conditions considered in our study. Efforts to minimize stigmatization and mistreatment of persons with functional limitation may be critical in mitigating this accumulation of disadvantage and the implications thereof for their overall well-being (Link & Phelan, 2001).

Supplementary Material

Tables 1-5

Footnotes

1.

In preliminary analyses, we considered an alternative measure based on four depressive symptoms, dropping the three somatic symptoms (low energy, trouble sleeping, lost appetite). Our multivariate results were virtually identical. For example, using the four-item outcome, the coefficient of disability on depressive symptoms in Model 3 of Table 2 was 0.15 (SE=.04) versus 0.16 (SE=.04) when the seven-item outcome was used. Thus, we present results based on the full scale, to retain comparability with prior MIDUS studies (all models available from authors).

2.

The nlcom command in Stata calculates standard errors using the delta method, which assumes a normal distribution of the products of path A and path B coefficients as well as interaction terms. Bootstrapping, a nonparametric resampling procedure, is an alternative method for testing mediation that does not impose the assumption of normality on the sampling distribution. Bootstrapping involves repeatedly sampling from the data set and estimating the indirect or mediation effect in each resampled data set. We conduct bootstrapping based on 1,000 random resamples of the data to obtain standard errors and confidence intervals of indirect effects (Preacher and Hayes 2008; Preacher, Rucker and Hayes 2007).

Contributor Information

Eun Ha Namkung, Lurie Institute for Disability Policy, The Heller School for Social Policy and Management, Brandeis University.

Deborah Carr, Department of Sociology, Boston University.

REFERENCES

  1. Baker Patricia S., Bodner Eric V., and Allman Richard M.. 2003. “Measuring Life‐Space Mobility in Community‐Dwelling Older Adults.” Journal of the American Geriatrics Society 51(11): 1610–1614. [DOI] [PubMed] [Google Scholar]
  2. Barreto Manuela, and Ellemers Naomi. 2015. “Detecting and Experiencing Prejudice: New Answers to Old Questions.” Advances in Experimental Social Psychology 52: 139–219. [Google Scholar]
  3. Birditt Kira S., and Fingerman Karen L.. 2005. “Do We Get Better at Picking Our Battles? Age Group Differences in Descriptions of Behavioral Reactions to Interpersonal Tensions.” The Journals of Gerontology Series B: Psychological Sciences and Social Sciences 60: P121–P128. [DOI] [PubMed] [Google Scholar]
  4. Birditt Kira S., Fingerman Karen L., and Almeida David M.. 2005. “Age Differences in Exposure and Reactions to Interpersonal Tensions: A Daily Diary Study.” Psychology and Aging 20: 330–340. [DOI] [PubMed] [Google Scholar]
  5. Bostwick Wendy B., Boyd Carol J., Hughes Tonda L., West Brady T., and McCabe Sean Esteban. 2014. “Discrimination and Mental Health among Lesbian, Gay, and Bisexual Adults in the United States.” American Journal of Orthopsychiatry 84: 35–44. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bradburn Norman M. 1969. The Structure of Psychological Well-Being. Chicago: Aldine. [Google Scholar]
  7. Brown Robyn L. 2015. “Perceived Stigma among People with Chronic Health Conditions: The Influence of Age, Stressor Exposure, and Psychosocial Resources.” Research on Aging 37(4): 335–360. [DOI] [PubMed] [Google Scholar]
  8. Brown Robyn Lewis. 2017. “Understanding the Influence of Stigma and Discrimination for the Functional Limitation Severity—Psychological Distress Relationship: A Stress and Coping Perspective.” Social Science Research 62:150–160. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Brown Robyn Lewis and Barrett Anne E.. 2011. “Visual Impairment and Quality of Life among Older Adults: An Examination of Explanations for the Relationship.” The Journals of Gerontology: Series B. 66B: 364–373. [DOI] [PubMed] [Google Scholar]
  10. Brown Rebecca. T., Diaz-Ramirez L. Grisell, Boscardin W. John, Lee Sei J., and Steinman Michael A.. 2017. “Functional Impairment and Decline in Middle Age: A Cohort Study.” Annals of Internal Medicine 167(11): 761–768. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Caputo Jennifer, and Simon Robin W.. 2013. “Physical Limitation and Emotional Well-Being: Gender and Marital Status Variations.” Journal of Health and Social Behavior 54: 241–257. [DOI] [PubMed] [Google Scholar]
  12. Carey Elise C., Walter Louise C., Lindquist Karla, and Covinsky Kenneth E.. 2004. “Development and Validation of a Functional Morbidity Index to Predict Mortality in Community‐Dwelling Elders.” Journal of General Internal Medicine 19(10): 1027–1033. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Carr Deborah. 2014. Worried Sick: How Stress Hurts Us and How to Bounce Back. New Brunswick, NJ: Rutgers University Press. [Google Scholar]
  14. Carr Deborah, Cornman Jennifer C., and Freedman Vicki A.. 2019. “Do Family Relationships Buffer the Impact of Disability on Older Adults’ Daily Mood? An Exploration of Gender and Marital Status Differences.” Journal of Marriage and Family 81(3): 729–746. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Carr Deborah and Friedman Michael. 2005. “Is Obesity Stigmatizing? Body Weight, Perceived Discrimination and Psychological Well-Being in the United States.” Journal of Health and Social Behavior 46: 244–259. [DOI] [PubMed] [Google Scholar]
  16. Carr Deborah, Jaffe Karen and Friedman Michael. 2008. “Perceived Mistreatment among Obese Americans: Do Race, Class, and Gender Matter?” Obesity 16 (Supplement): S60–68. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Charles Susan T. and Carstensen Laura L.. 2008. “Unpleasant Situations Elicit Different Emotional Responses in Younger and Older Adults.” Psychology and Aging, 23(3): 495–504. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Charles Susan T., and Carstensen Laura L.. 2010. “Social and Emotional Aging.” Annual Review of Psychology 61: 383–409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Chau Nearkasen, Chau Kénora, Mayet Aurélie, Baumann Michèle, Legleye Stéphane, and Falissard Bruno. 2013. “Self-Reporting and Measurement of Body Mass Index in Adolescents: Refusals and Validity, and the Possible Role of Socioeconomic and Health-Related Factors.” BMC Public Health 13(1): 815–831. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Erler Susan F. and Garstecki Dean C.. 2002. “Hearing Loss-and Hearing Aid-Related Stigma: Perceptions of Women with Age-Normal Hearing.” American Journal of Audiology 11(2): 83–91. [DOI] [PubMed] [Google Scholar]
  21. Freedman Vicki A., Carr Deborah, Cornman Jennifer C., and Lucas Richard. 2017. “Impairment Severity and Evaluative and Experienced Wellbeing among Older Adults: Assessing the Role of Daily Activities.” Innovation in Aging. 10.1093/geroni/igx010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Friedman Elliott M. 2016. “Self‐reported Sleep Problems Prospectively Increase Risk of Disability: Findings from the Survey of Midlife Development in the United States.” Journal of the American Geriatrics Society 64(11): 2235–2241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Gayman Matthew D., Turner R. Jay, and Cui M. 2008. “Physical Limitations and Depressive Symptoms: Exploring the Nature of the Association.” Journal of Gerontology: Social Sciences 63(4): S219–S228. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Goffman Erving. 1963. Stigma: Notes on the Management of Spoiled Identity. Englewood Cliffs, NJ: Prentice-Hall. [Google Scholar]
  25. Janoff-Bulman Ronnie, and Werther Amelie. 2008. “The Social Psychology of Respect: Implications for Delegitimization and Reconciliation” Pp. 145–170 in The Social Psychology of Intergroup Reconciliation, ed. by Nadler A, Malloy T, and Fisher J. New York: Oxford. [Google Scholar]
  26. Jasper Margaret C. 2008. Americans with Disabilities Act. Oxford University Press, USA. [Google Scholar]
  27. Joffe-Walt Chana. 2013. “Unfit for Work: The Startling Rise of Disability in America.” National Public Radio (March 22, 2013). http://apps.npr.org/unfit-for-work/, accessed September 1, 2019. [Google Scholar]
  28. Kassam Allya, Williams Jeanne, and Patten Scott. 2012. “Perceived Discrimination among People with Self-Reported Emotional, Psychological, or Psychiatric Conditions in a Population-Based Sample of Canadians Reporting a Disability.” The Canadian Journal of Psychiatry 57(2): 102–110. [DOI] [PubMed] [Google Scholar]
  29. Keller Richard M. and Galgay Corinne E.. 2010. “Microaggressive Experiences of People with Disabilities” Pp. 241–267 In Microaggressions and Marginality: Manifestation, Dynamics, and Impact, edited by Sue DW. Hoboken, NJ: John Wiley & Sons Inc. [Google Scholar]
  30. Kessler Ronald C., Mickelson Kristin D., and Williams David R.. 1999. “The Prevalence, Distribution, and Mental Health Correlates of Perceived Discrimination in the United States.” Journal of Health and Social Behavior 40: 208–230. [PubMed] [Google Scholar]
  31. Kilpatrick Quentin K. and Taylor John. 2018. “Racial/Ethnic Contrasts in the Relationships between Physical Disability, Perceived Discrimination, and Depressive Symptoms.” Journal of Racial and Ethnic Health Disparities 5(6): 1–9. [DOI] [PubMed] [Google Scholar]
  32. Knäuper Bärbel, and Wittchen Hans-Ulrich. 1994. “Diagnosing Major Depression in the Elderly: Evidence for Response Bias in Standardized Diagnostic Interviews?” Journal of Psychiatric Research 28(2): 147–164. [DOI] [PubMed] [Google Scholar]
  33. Krahn Gloria L., Walker Deborah K., and Correa-De-Araujo Rosaly. 2015. “Persons with Disabilities as an Unrecognized Health Disparity Population.” American Journal of Public Health 105(Suppl 2): S198–S206. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. LaVeist Thomas A., Rolley Nicole C., and Diala Chamberlain. 2003. “Prevalence and Patterns of Discrimination among U.S. Health Care Consumers.” International Journal of Health Services 33: 331–344. [DOI] [PubMed] [Google Scholar]
  35. Lin Jielu, and Kelley-Moore Jessica. 2017. “Intraindividual Variability in Late-Life Functional Limitations among White, Black, and Hispanic Older Adults: Implications for the Weathering Hypothesis.” Research on Aging 39(4): 549–572. [DOI] [PubMed] [Google Scholar]
  36. Link Bruce G., and Phelan Jo C.. 2001. “Conceptualizing Stigma.” Annual Review of Sociology 27: 363–385. [Google Scholar]
  37. Lingsom Susan. 2008. “Invisible Impairments: Dilemmas of Concealment and Disclosure.” Scandinavian Journal of Disability Research 10(1): 2–16. [Google Scholar]
  38. Luong Gloria, Charles Susan T., and Fingerman Karen L.. 2011. “Better with Age: Social Relationships across Adulthood.” Journal of Social and Personal Relationships 28(1): 9–23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Major Brenda, Quinton Wendy J., and McCoy Shannon K.. 2002. “Antecedents and Consequences of Attributions to Discrimination: Theoretical and Empirical Advances.” Advances in Experimental Social Psychology 34: 251–330. [Google Scholar]
  40. Mancini Anthony D. and Bonanno George A.. 2006. “Marital Closeness, Functional Disability, and Adjustment in Late Life.” Psychology and Aging 21(3): 600–610. [DOI] [PubMed] [Google Scholar]
  41. McMahon Brian T. and Shaw Linda R.. 2005. “Workplace Discrimination and Disability.” Journal of Vocational Rehabilitation 23(3): 137–143. [Google Scholar]
  42. McPherson Barry D. 1994. “Sociocultural Perspectives on Aging and Physical Activity.” Journal of Aging and Physical Activity 2(4): 329–353. [Google Scholar]
  43. Menec Verena H. and Perry Raymond P.. 1995. “Reactions to Stigmas: The Effect of Targets’ Age and Controllability of Stigmas.” Journal of Aging and Health 7(3): 365–383. [DOI] [PubMed] [Google Scholar]
  44. Mroczek Daniel K., and Kolarz Christian M.. 1998. “The Effect of Age on Positive and Negative Affect: A Developmental Perspective on Happiness.” Journal of Personality and Social Psychology 75(5): 1333–1349. [DOI] [PubMed] [Google Scholar]
  45. Namkung Eun Ha and Carr Deborah. 2019. “Perceived Interpersonal and Institutional Discrimination among Persons with Disability: Do Patterns Differ by Age.” Social Science and Medicine. 10.1016/j.socscimed.2019.112521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Namkung Eun Ha, Greenberg Jan S., and Mailick Marsha R.. 2016. “Well-being of Sibling Caregivers: Effects of Kinship Relationship and Race.” The Gerontologist 57(4): 626–636. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. National Center for Health Statistics. 2017. Health, United States, 2016: With Chartbook on Long-term Trends in Health; Hyattsville, MD. [PubMed] [Google Scholar]
  48. National Heart, Lung and Blood Institute (NHLBI). 1998. Clinical Guidelines on the Identification, Evaluation, and Treatment of Overweight and Obesity in Adults: The Evidence Report (NIH Publication No. 98–4083). U.S. Department of Health and Human Services. [Google Scholar]
  49. Pavalko Eliza K., Mossakowski Krysia N., and Hamilton Vanessa J.. 2003. “Does Perceived Discrimination Affect Health? Longitudinal Relationships between Work Discrimination and Women’s Physical and Emotional Health.” Journal of Health and Social Behavior 44(1): 18–33. [PubMed] [Google Scholar]
  50. Pearlin Leonard I., Schieman Scott, Fazio Elena M., and Meersman Stephen C.. 2005. “Stress, Health, and the Life Course: Some Conceptual Perspectives.” Journal of Health and Social Behavior 46(2): 205–219. [DOI] [PubMed] [Google Scholar]
  51. Preacher Kristopher J. and Hayes Andrew F.. 2008. “Asymptotic and Resampling Strategies for Assessing and Comparing Indirect Effects in Multiple Mediator Models.” Behavior Research Methods 40: 879–891. [DOI] [PubMed] [Google Scholar]
  52. Preacher Kristopher J., Rucker Derek D., and Hayes Andrew F.. 2007. “Addressing Moderated Mediation Hypotheses: Theory, Methods, and Prescriptions.” Multivariate Behavioral Research 42(1): 185–227. [DOI] [PubMed] [Google Scholar]
  53. Preacher Kristopher J., and Kelley Ken. 2011. “Effect Size Measures for Mediation Models: Quantitative Strategies for Communicating Indirect Effects.” Psychological Methods 16: 93–115. [DOI] [PubMed] [Google Scholar]
  54. Radler Barry T., and Ryff Carol D.. 2010. “Who Participates? Accounting for Longitudinal Retention in the MIDUS National Study of Health and Well-Being.” Journal of Aging and Health 22(3): 307–331. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Reed Andrew E., and Carstensen Laura L.. 2012. “The Theory behind the Age-Related Positivity Effect.” Frontiers in Psychology 3(339): 1–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Robinson Eric, Sutin Angelina, and Daly Michael. 2017. “Perceived Weight Discrimination Mediates the Prospective Relation Between Obesity and Depressive Symptoms in US and UK Adults.” Health Psychology 36(2): 112–121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. Rossi Alice S. 2001. “Developmental Roots of Adult Social Responsibility” Pp. 227–320 in Caring and Doing for Others: Social Responsibility in the Domains of Family, Work, and Community, edited by Rossi AS. Chicago, IL: University of Chicago Press. [Google Scholar]
  58. Russinova Ziatka, Griffin Shanta, Bloch Phillippe, Wewiorski Nancy J., and Rosoklija Ilina. 2011. “Workplace Prejudice and Discrimination toward Individuals with Mental Illnesses.” Journal of Vocational Rehabilitation 35(3): 227–241. [Google Scholar]
  59. Schur Lisa, Kruse Douglas, Blasi Joseph, and Blanck Peter. 2009. “Is Disability Disabling in All Workplaces? Workplace Disparities and Corporate Culture.” Industrial Relations: A Journal of Economy and Society 48: 381–410. [Google Scholar]
  60. Shandra Carrie L. 2018. “Disability as Inequality: Social Disparities, Health Disparities, and Participation in Daily Activities.” Social Forces 97(1): 157–192. [Google Scholar]
  61. Shandra Carrie L., and Hogan Dennis P.. 2008. “School-to-Work Program Participation and the Post-High School Employment of Young Adults with Disabilities. Journal of Vocational Rehabilitation 29(2): 117–130. [PMC free article] [PubMed] [Google Scholar]
  62. Tsenkova Vera K., Carr Deborah, Schoeller Dale A., and Ryff Carol D.. 2011. “Perceived Weight Discrimination Amplifies the Link between Central Adiposity and Nondiabetic Glycemic Control (HbA1c).” Annals of Behavioral Medicine 41(2): 243–251. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Turner R. Jay, and Noh Samuel. 1988. “Physical Disability and Depression: A Longitudinal Analysis.” Journal of Health and Social Behavior 23–37. [PubMed] [Google Scholar]
  64. Turner J. Blake, and Turner R. Jay. 2004. “Physical Disability, Unemployment, and Mental Health.” Rehabilitation Psychology 49(3): 241–249. [Google Scholar]
  65. Verbrugge Lois M. and Jette Alan M.. 1994. “The Disablement Process.” Social Science & Medicine 38(1): 1–14. [DOI] [PubMed] [Google Scholar]
  66. Vogt Yuan Anastasia S. 2007. “Perceived Age Discrimination and Mental Health.” Social Forces 86(1): 291–311. [Google Scholar]
  67. Ware John E. Jr, and Sherbourne Cathy D.. 1992. “The MOS 36-Item Short-Form Health Survey (SF-36): I. Conceptual Framework and Item Selection.” Medical Care 30: 473–483. [PubMed] [Google Scholar]
  68. Watson David, Clark Lee Anna, and Tellegen Auke. 1988. “Development and Validation of Brief Measures of Positive and Negative Affect: The PANAS Scales.” Journal of Personality and Social Psychology 54(6): 1063–1070. [DOI] [PubMed] [Google Scholar]
  69. Williams David R. and Williams-Morris Ruth. 2000. “Racism and Mental Health: The African American Experience.” Ethnicity and Health 5(3–4): 243–268. [DOI] [PubMed] [Google Scholar]
  70. Yang Yang. 2006. “How Does Functional Disability Affect Depressive Symptoms in Late Life? The Role of Perceived Social Support and Psychological Resources.” Journal of Health and Social Behavior 47:355–372. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Tables 1-5

RESOURCES