People with disabilities (PWD), who constitute 25% of the adult U.S. population, consistently report a higher prevalence of psychological distress than do people without disabilities (Okoro et al., 2009). The COVID-19 pandemic represents a uniquely challenging period of time during which systematic and interpersonal forms of ableism have exacerbated pre-existing mental health disparities for PWD (Lund et al., 2020). The pandemic has also disrupted crucial care services, including mental health treatment, routinely used by PWD (Drum et al., 2020). Pre-pandemic studies focusing on individuals with intellectual and developmental disabilities highlighted disability-specific barriers, such as stigmatizing attitudes and lack of disability awareness among providers, as major factors hindering access to mental health services (Whittle et al., 2018). However, little research has examined how such barriers, along with other demographic and psychosocial factors known to influence treatment access, have shaped PWD’s mental health service use since the start of the COVID-19 pandemic.
In an article published in Rehabilitation Psychologyopens in new window, an interdisciplinary team led by Katie Wang at the Yale School of Public Health addressed this research question by conducting a two-wave survey among 183 U.S. adults with a wide range of visible (e.g., cerebral palsy) and invisible (e.g., autoimmune and chronic pain conditions) disabilities. In the fall of 2020 and 2021, participants completed measures assessing demographic and disability characteristics, pandemic-related stressors (e.g., worries about COVID-19), depression, anxiety, disability-specific barriers to accessing mental health services (e.g., anticipated disability stigma from providers, concerns about accessibility), perceived need for mental health services, and mental health service use. The authors found that anticipated disability stigma from providers significantly predicted a lower likelihood of mental health service use. They also found that specific subpopulations of the disability community (i.e., women, transgender and gender-diverse individuals, individuals with pre-pandemic mental health conditions, and younger individuals) have greater mental health needs and that low-income PWD were less likely to use mental health services.
The findings from this study provide initial vital descriptive data pertaining to the mental health service use patterns of PWD during the COVID-19 pandemic. Given that anticipated disability stigma from providers was identified as a significant barrier to mental health service use, the authors underscore the urgency of providing disability competency training and stigma reduction interventions to mental health professionals. Additionally, they emphasize that when researchers and practitioners develop and implement mental health interventions for PWD, it is especially important for them to do so with an eye toward addressing the needs of multiply marginalized members of the disability community.
This article is in the Clinical Psychology topic area.

