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Parents require sufficient information and support to understand what \u201cdoing something and doing nothing\u201d really means when learning about nonsurgical options. This may take the form of health literacy support, asking how parents are given access to meaningful and understandable information, as well as psychosocial support and psychological care. Timely psychological assessment and interventions that support informed decision-making actions are an essential aspect of holistic care for children and youth with DSD and their parents. Without actionable tools or approaches, parents cannot make informed decisions about their child\u2019s health and, as such, health literacy is a key attribute to aid decision making for both parents and children. As individuals with DSD become increasingly adept at building resourcefulness and gathering and applying knowledge about their bodies, limiting irreversible surgeries in childhood can afford wider life choices. To this end, an educated and informed comprehensive and helpful multidisciplinary group understands and embodies, as a whole team, the need for compassionate, emotionally supportive, and validating care in all interactions with parents of children and individuals with DSD. The paper draws on the primary author\u2019s experiences working with the charity, dsdfamilies, concluding with actionable approaches that include supporting personal knowledge through health literacy, examining team-based psychological care, and psychosocial approaches across the lifespan. <\/jats:p>","DOI":"10.1159\/000525452","type":"journal-article","created":{"date-parts":[[2022,6,10]],"date-time":"2022-06-10T21:00:54Z","timestamp":1654894854000},"page":"228-237","source":"Crossref","is-referenced-by-count":9,"title":["Listening to Individuals with Differences in Sex Development or Intersex and Their Families: \u201cNot Doing Surgery Does Not Mean Doing 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