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Creates a culturally and linguistically tailored national mental health awareness and outreach campaign aimed at Hispanic and Latino parents, caregivers, youth, and school personnel, and requires two related federal studies: one on mental health status and crisis services for Hispanic and Latino youth and one on strategies to boost the Hispanic/Latino mental health workforce. The bill directs HHS to complete a review of prior outreach, develop and implement the campaign within a year, coordinate across federal agencies and community groups, and submit public reports to Congress; it authorizes limited funding for the campaign and the two studies.
The bill directs modest federal funding and targeted data collection to improve culturally and linguistically tailored outreach, training, and policy guidance for Hispanic/Latino youth mental health — at the cost of added federal spending, administrative burdens, privacy risks, and the potential for unmet demand if local service capacity and program design are insufficient.
Hispanic and Latino youth will have greater awareness of mental-health symptoms and culturally/linguistically tailored resources, increasing early identification and likelihood of receiving support.
Parents, teachers, and school staff will receive youth mental health first-aid training and schools/community sites will gain access to screenings and on-site consultations, improving early response and connections to care for children.
Federal and local policymakers will receive timely, disaggregated data and a report to inform targeted, culturally tailored policy recommendations (including ways to increase 9-8-8/hotline use) to reduce mental-health and substance-use disorders among Latino youth.
Taxpayers and the federal budget will face increased spending (the bill authorizes $5M/year for outreach plus ~$2M in study authorizations), which could require trade-offs or divert funds from other priorities.
Students and families may have needs identified through screenings and outreach that local systems cannot meet, producing unmet demand, longer waitlists, and frustration.
Collecting and publicly reporting disaggregated data risks privacy harms for small subgroups, providers, and patients if de-identification is inadequate.
Introduced November 20, 2025 by Andrea Salinas · Last progress November 20, 2025