Resource Details
New England Children with Genetic Disorders and Health Care Reform: Information and Recommendations for State Policymakers
Report includes data gathered from an online survey of families and parents of children with genetic disorders throughout New England identifying the greatest shortcomings of insurance coverage in the areas of habilitative services. The report also includes recommendations for state policymakers regarding gaps in insurance benefits, identifies opportunities for improving coverage and availability created under the ACA, and lists resources for both policymakers and consumers, including family leadership organizations, state insurance regulators, and centers for health care reform.
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Awareness Campaign (5)Breastfeeding (1)Care Coordination (9)Careers (2)Carrier Screening (6)Condition Specific (68)Consumer Advocacy (2)COVID-19 (60)Cystic Fibrosis (1)Diagnostic Test (2)Dismantling Racism/Implicit Bias (8)Diversity (1)Diversity, Equity, Inclusion and Justice (50)Education (393)ELSI (1)Emergency Preparedness (14)Evaluation (8)Family Health History (9)Family History (1)Family Support (114)Genetic Service System (76)Genetic Test (24)Genetics Privacy (3)Health Equity (5)Health Literacy (4)Healthcare Access (17)Healthcare Access and Financing (81)Healthcare Interpreting (69)LGBTQ+ (3)Medicaid (1)Medical Food (18)Medical Home (8)Microagressions (3)Multilingual (8)Newborn Hearing Screening (1)Newborn Screening (172)Newborn Screening Emergency Preparedness (1)Newborn Screening Family Support (2)Noninvasive Prenatal Screening (NIPS) (8)Pharmacogenetics (1)Policy (7)Pregnancy (1)Prenatal (2)Public Health (7)Public health genetics (13)Research (9)Secondary Findings (10)State Specific (3)Teleeducation (9)Telegenetics (76)Telehealth (1)Transition (22)Workforce (1)
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Administrators (23)Education (1)Educators (60)Evaluators (2)Family Support (27)Family-Led Organizations (21)Genetics Providers (372)Healthcare Interpreters (71)Healthcare Interpreting (15)Insurers (24)Midwives (6)Non-Genetics Providers (485)Patients and/or Families (365)Policymakers (34)Public Health (126)Regional Genetics Networks (97)Researchers (42)Students (50)Title V (9)