1 in 5 children in the United States have a special health care need. This National Center for a System of Services for Children and Youth with Special Health Care Needs (CYSHCN) is here to support these children, their families/caregivers and the professionals who care for them.

Learn More About the National Center and the Blueprint for Change

 

What We Do

The goal of the National Center for a System of Services for Children and Youth with Special Health Care Needs (CYSHCN) is to advance and strengthen the system of services for CYSHCN, their families and caregivers at the community, state and national levels.

The work of the National Center is grounded in the Blueprint For Change: A National Framework for a System of Services for CYSHCN. The Blueprint for Change presents a vision for how to improve the system of services for CYSHCN through improved equity, access, quality of life and family well-being and financing.

To accomplish this goal, the National Center will:

  • Convene families/caregivers, youth, public health professionals, clinicians and others to guide all project activities.
  • Develop and disseminate a Roadmap to support implementation of the Blueprint for Change.
  • Convene state teams co-led by Title V and families/caregivers to test Blueprint implementation strategies.
  • Provide technical assistance, training, and support on Blueprint Implementation.
  • Evaluate all project activities.

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Professional Tools & Resources

Blueprint for Change Strategies: At-a-Glance Overview

View details on the 40 strategies outlined in the Blueprint for Change: A National Framework for a System of Services for CYSHCN. The strategies are categorized by the 4 critical areas of focus: health equity, family & child well-being and quality of life, access to services, and financing of services.

Aligning Your Work With the Blueprint for Change

The National Center developed this worksheet and accompanying crosswalk to support Title V programs in aligning their work and priorities with the Blueprint for Change: Guiding Principles for a System of Services for Children and Youth with Special Health Care Needs (CYSHCN) and their families. 

Virtual Town Hall: Charting a New Course for CYSHCN

Watch our virtual town hall Charting a New Course for CYSHCN: Introducing a new National Center for a System of Services. This Town Hall was open to the public and in particular to clinicians, families/caregivers, individuals with special health care needs/disabilities, public health professionals and any other partners serving CYSHCN.  

Population Health and Medical Home: Strategies to Support Title V Programs

Looking to learn more about the medical home national performance measure? This short 15 minute presentation and accompanying slide deck provides an overview of how Title V programs measure access to medical home and presents examples of medical home population health approaches.

Tools and Resources for Medical Home Implementation

This section provides practical tools and resources to assist families, practices and others with pediatric medical home implementation and related efforts to enhance collaboration between professionals and families.

National Performance/Outcome Measures and Blueprint Framework Crosswalk

Title V programs can use this crosswalk tool to help understand how current efforts align with the Blueprint framework and prioritize future efforts and optimize impact in serving CYSHCN.

Blueprint for Change Virtual Cafes

The National Center is hosting a series of virtual cafes, crafted for Title V CYSHCN Programs. These virtual cafes provide an interactive space to foster collaboration and facilitate meaningful conversations, share insights and connect with fellow Title V CYSHCN programs and professionals.

National Survey of Children’s Health Resources

National Survey of Children’s Health Data Briefs
The National Center for a System of Services for CYSHCN, in collaboration with the Altarum Institute, is developing annual data briefs based on the National Survey of Children’s Health data. These data briefs offer insight into national trends and progress in advancing the system of services for CYSHCN.
National Survey of Children’s Health Factsheets
In collaboration with the Altarum Institute, the National Center developed state factsheets based on the National Survey of Children’s Health data. These factsheets focus on critical areas from the Blueprint for Change and include demographic details to help states monitor progress towards addressing health care inequities among CYSHCN.


Title V Needs Assessment Tools and Resources

The tools and resources in this section are meant to support states and jurisdictions throughout their current and ongoing needs assessment activities. 

NSCH Indicators by Blueprint Critical Area

Explore how National Survey of Children's Health (NSCH) indicators align with critical areas of the Blueprint for Change. States and jurisdictions can use this tool to help monitor their progress on advancing the Blueprint during their current and ongoing needs assessment activities.

AMCHP Needs Assessment Workshop

It Takes a Village: How to Integrate the Blueprint for Change and Equitable Partnerships into your Title V Needs Assessment.

Title V Needs Assessment Focus Group Questions

Focus group questions to help understand how the systems of care serving CYSHCN can work better, particularly from the perspective of families, caregivers, and youth with lived expertise.

Connecting Your Needs Assessment With the Blueprint for Change

This resource was created for state or jurisdiction Title V CYSHCN programs to approach their needs assessment process in alignment with the Blueprint for Change. 

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Contact Us

Need technical assistance or support? Submit your inquiries to our team using our contact us form. 

Contact Us

 

 

The National Center for a System of Services for CYSHCN is supported by the Health Resources and Services Administration (HRSA) of the U.S. Department of Health and Human Services (HHS) as part of an award totaling $1,500,000 with no funding from nongovernmental sources. The information or content are those of the author(s) and do not necessarily represent the official views of, nor an endorsement, by HRSA, HHS or the U.S. Government.

Last Updated

05/23/2024

Source

American Academy of Pediatrics