Treatment and Services for Health and Wellness
Operates 13 tribally and federally operated residential treatment facilities located across the U.S. to address substance use disorder (SUD) and/or co-occurring mental health disorders (COD) among American Indian and Alaska Native (AI/AN) youth and their families at no cost. Provides a range of education and culture-based prevention initiatives, evidence-based and practice-based models of treatment, family strengthening and recreational activities designed to help AI/AN youth overcome challenges related to mental health and substance use. Promotes holistic, culturally responsive care that integrates clinical services with traditional healing, spiritual values, and cultural identification in a substance-free residential environment to support AI/AN youth in achieving their treatment goals and leading healthy, resilient lives.
Offers evidence-based, voluntary programs that provide families with regular, planned home visits from qualified health, social service, and child development professionals. Supports at-risk pregnant people and parents with children up to kindergarten entry with resources to raise physically, socially, and emotionally healthy children. Provides guidance on parenting and health topics, such as breastfeeding, safe sleep practices, injury prevention, nutrition, and childcare solutions. Seeks to improve maternal and child health, prevent child abuse and neglect, encourage positive parenting, and promote child development and school readiness.
Provides a directory of national, state, and local programs and services to support recovery, rehabilitation and community reintegration for military service members, veterans, their families, and caregivers. Helps connect individuals to a range of services and resources, including substance use disorder (SUD) treatment and recovery support.
Offers appropriate follow-up support services for individuals identified with sickle cell disease and sickle cell trait. Aims to improve care for sickle cell disease and reduce the number of individuals who do not receive follow-up care. Services are provided through local community-based organizations located in 21 states across the U.S.
Supports 5 coordinating centers that serve states in their respective regions to expand access to quality care for patients with sickle cell disease. Works with sickle cell centers, primary care sites, community-based organizations, parents, and patients to provide coordinated, comprehensive, culturally competent, and family-centered care.