The Disability Equity Collaborative’s goal is to empower and support healthcare organizations, practitioners, and policy makers in implementing evidence-based, accessible care for their patients with disabilities.
To help achieve this goal, DEC facilitates three special interest groups (SIGs) and hosts monthly webinars alternating between these three subject areas. DEC’s webinars engage a broad spectrum of stakeholders, including researchers, advocates, policymakers, payers, providers, and more.
Recent Webinars
The IDD Toolkit: Tools to Enhance Care for Adults with IDD↗
August 2026
Janet Shouse, BJ, Program Coordinator for the IDD Toolkit at Vanderbilt Kennedy Center for Excellence in Developmental Disabilities, presents an overview of the IDD Toolkit, a free online resource to help clinicians provide better care to adults with IDD. The Toolkit offers easy-to-use guidance and checklists for clinicians, as well as several resources for patients with IDD and their families or support persons.
Disability Perspectives on the Adverse Effects of Medical Ableism↗
March 2026
Dr. Jae Kennedy discusses preliminary findings from his grant-funded project, supported by the National Institute on Child Health and Human Development (R01HD116323). The study uses data from the 2025 National Survey of Health and Disability (sample: n=2,506 adults with disabilities) to investigate disability-related problems with healthcare access and utilization problems in four domains: physical access, information access, informed decision-making, and respect from providers. These problems were linked to clinically or economically important health and healthcare outcomes.
Health and Disability Related Social Needs↗
February 2025
Dr. Jen Oshita, Lauren Levinton, and Dr. Carol Haywood present their work to identify and understand the social factors contributing to the disability community’s health disparities and healthcare outcomes. Pilot research revealed that chronic disability and health-related social risks are exceptionally common among patients in large, urban academic medical centers, and healthcare workers have poor awareness of these patient characteristics.