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This emerging population of adolescent and young adult (AYA) patients with KS seeking care makes it increasingly important to understand the unique experiences and perspectives of these individuals. This qualitative study explored (1) the psychosocial well\u2010being of AYA with KS and (2) resources and support systems AYA with KS utilize to cope with challenges related to their diagnosis. This study included 13 participants ages 14\u201323 (<jats:italic>M<\/jats:italic> age 16\u2009years) who completed semi\u2010structured individual interviews. Reflexive thematic analysis was used. Three themes were generated concerning psychosocial well\u2010being, resources, and support systems of AYA with KS: (1) \u201cI'm a little different\u201d\u2014Rejecting stigmatization and integrating a diagnosis of KS into one's identity, (2) \u201cLet it out\u201d\u2014Lessons learned when disclosing one's diagnosis of KS to others, and (3) \u201cThey accept me for who I am\u201d\u2014The building blocks of a support system. Participants largely viewed KS as part of themselves but not their whole identity and expressed not wanting to be labeled by others as \u201cdisabled.\u201d Participants voiced that disclosing KS to trusted others often provides a sense of relief, and that it is important to have a varied support system that includes individuals like parents, friends, and romantic partners. This study improves the understanding of what support resources AYA with KS are using, or not using, and provides insights into their psychosocial well\u2010being, which in turn may help providers implement effective clinical interventions and promote better psychosocial outcomes for this growing patient population.<\/jats:p>","DOI":"10.1002\/jgc4.70074","type":"journal-article","created":{"date-parts":[[2025,6,24]],"date-time":"2025-06-24T07:09:37Z","timestamp":1750748977000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Finding acceptance: How adolescents and young adults with Klinefelter Syndrome navigate identity, disclosure, and support"],"prefix":"10.1002","volume":"34","author":[{"ORCID":"https:\/\/orcid.org\/0009-0006-4973-9035","authenticated-orcid":false,"given":"Abigail","family":"Tubman","sequence":"first","affiliation":[{"name":"Graduate Program in Genetic Counseling Northwestern University  Chicago Illinois USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8556-2509","authenticated-orcid":false,"given":"Jaclyn L.","family":"Papadakis","sequence":"additional","affiliation":[{"name":"Department of Psychiatry &amp; Behavioral Health Ann &amp; Robert H. 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