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This qualitative study sought to explore the advocacy efforts and experiences among caregivers of children with Down syndrome across a range of intersecting identities and social contexts. Guided by the tenets outlined in the DisCrit framework (Annamma, Connor & Ferri, 2018), this study privileged the voices of 9 parent and caregiver advocates of children with Down syndrome, including Black and Hispanic families, families experiencing socioeconomic hardships and families with an additional dis/ability label underrepresented in research studies. Through a systematic inductive and comparative analysis of the data , themes emerged which outlined the processes by which caregivers mobilized to push past deficit-oriented perspectives held by professionals and the community-at-large, centering the value and potential of their children.