The Catalyst Center created two interactive worksheets for Title V program staff, family leaders, and other stakeholders. These worksheets provide an overview of Title V, and Medicaid and the Children’s Health Insurance Program (CHIP). Each worksheet includes resources you can use to find and insert state-specific information to help demonstrate the importance of Title V, Medicaid and CHIP for children with special health care needs (CSHCN). The worksheets were created as companion materials to the Catalyst Center’s Public Insurance Programs and Children with Special Health Care Needs: A Tutorial on the Basics of Medicaid and the Children’s Health Insurance Program (CHIP).
I AM THE ARCHIVE.PHP FILE
Archives
State Statutes & Regulations on Dietary Treatment of Disorders Identified Through Newborn Screening
Every state has a Newborn Screening (NBS) Program which screens newborns for a variety of health conditions, including selected inborn errors of metabolism (IEMs) and other genetic disorders. Individuals with genetic conditions identified through NBS programs often require Modified Low Protein Foods (MLPFs), medical foods, dietary supplements, or other dietary treatments as well as enteral feeding supplies. Due to the wide-ranging funding mechanisms across states, coverage for these categories of products and supplies varies based on type of insurance coverage (e.g., public or private), type of health plan (e.g., individual, group, HMO), and any coverage and or related services that Title V or other state programs may fund.
This resource provides information about state-specific legislation that mandates the coverage of medically necessary foods by employer-sponsored health insurance and Medicaid, and coverage and related services funded by other state programs such as Title V or relief funds. It also details the covered services as well as any benefit limits or age and income restrictions. This report builds on a 2008 report of the same name by Alissa Johnson, and an update to that report from the Catalyst Center and the National Coordinating Center for the Regional Genetics Networks (NCC) published in 2016.
Webinar: Addressing Health Coverage Inequities among CSHCN in Your State
An hour-long webinar held on June 20, 2016 to “get acquainted” with the tutorial, Health Care Coverage and Financing for Children with Special Health Care Needs: A Tutorial to Address Inequities. MCH staff from Alaska and Michigan share strategies they use to work towards health equity for CSHCN in their states.
View detailed webinar description
Financing the Special Health Care Needs of Children in Foster Care: A Primer
This primer focuses on an often overlooked population of children and youth with special health care needs: children and youth in foster care.
Just the Facts: The 411 on Health Insurance for Young Adults Ages 18 – 30 in Florida
This guide is designed to provide basic information, action steps and deadlines to help young adults in Florida stay focused and on track with health insurance.
The Affordable Care Act and Children and Youth with Special Health Care Needs: Opportunities and Challenges
Maternal and Child Health Town Hall meeting, American Public Health Association annual meeting, Boston, MA.