Opportunity Information: Apply for HRSA 19 060
The Transforming Health Care for Children and Youth with Epilepsy (CYE) Program is a discretionary federal grant opportunity from the U.S. Department of Health and Human Services, Health Resources and Services Administration (HRSA). Listed under Funding Opportunity Number HRSA-19-060 and CFDA 93.110, the program is designed to improve how children and youth with epilepsy receive care, especially when they live in rural communities or other medically underserved areas where specialty services and coordinated systems of care are often harder to access. The central goal is to expand access to coordinated, high-quality services delivered through a patient- and family-centered medical home approach, meaning care is intended to be organized, continuous, and built around the needs of the child and family rather than fragmented across separate providers.
A key feature of the opportunity is its focus on building and supporting quality improvement (QI) networks. Instead of funding isolated projects, HRSA is aiming to strengthen multi-partner networks that can test, measure, and spread better practices across clinical sites and communities. These networks are expected to use quality improvement methods to make practical changes in workflows, referral pathways, communication routines, and care coordination so that the overall system works better for children and youth with epilepsy. The intent is not only to deliver services, but also to create repeatable improvements that can be maintained and shared.
Applicants are expected to address four main content areas. First, the program prioritizes increasing access to epilepsy specialists by using telehealth and telemedicine strategies. This emphasis reflects the reality that many families in rural or underserved regions may be hours away from pediatric neurology or comprehensive epilepsy centers. Telehealth approaches can reduce travel burden, shorten wait times, and help local clinicians consult with specialists more quickly, which can be critical for diagnosis, medication management, seizure control planning, and ongoing follow-up.
Second, the program highlights increasing family engagement at multiple levels across the health care system. This goes beyond patient education and includes meaningful involvement of families in planning, decision-making, and feedback processes. In practice, this could mean integrating family perspectives into clinic quality improvement efforts, incorporating family advisory roles, and ensuring families are treated as core members of the care team. The broader aim is to make services more responsive, culturally appropriate, and aligned with what families actually need to manage epilepsy day to day.
Third, the program seeks to improve transitions from pediatric to adult health care. Transition is often a high-risk period for youth with chronic neurologic conditions, where gaps in care can lead to missed appointments, medication issues, reduced adherence, and worsening health outcomes. The grant opportunity encourages efforts that create clearer pathways and supports for adolescents and young adults as they move from pediatric specialists and pediatric primary care into adult systems, including planning, readiness assessment, and coordination between providers.
Fourth, the program focuses on strengthening communication, collaboration, and co-management between primary care providers and epilepsy specialty providers. Many children and youth with epilepsy rely on primary care for ongoing needs, while specialists handle seizure-related management. HRSA is encouraging models where roles are clear, information flows reliably, and care is co-managed rather than siloed. This can include shared care plans, consistent feedback loops after specialist visits, and improved referral and follow-up processes so families are not left navigating a disconnected system.
From a funding standpoint, the opportunity is structured as a grant with an award ceiling of $416,000, with HRSA expecting to make approximately seven awards. The opportunity was originally posted on January 11, 2019, with an original closing date of April 11, 2019. Eligibility is listed broadly as "Others" with additional clarification referenced in the full announcement, suggesting that organizations beyond typical categories may be eligible depending on HRSA's detailed criteria.
Overall, this grant opportunity is aimed at changing the practical experience of care for children and youth with epilepsy in underserved settings by building quality improvement networks that expand specialty access through telehealth, elevate family engagement, make pediatric-to-adult transitions safer and more organized, and improve day-to-day coordination between primary care and specialty epilepsy services.Apply for HRSA 19 060
- The Department of Health and Human Services, Health Resources and Services Administration in the health sector is offering a public funding opportunity titled "Transforming Health Care for Children and Youth with Epilepsy" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.110.
- This funding opportunity was created on Jan 11, 2019.
- Applicants must submit their applications by Apr 11, 2019. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- Each selected applicant is eligible to receive up to $416,000.00 in funding.
- The number of recipients for this funding is limited to 7 candidate(s).
- Eligible applicants include: Others (see text field entitled Additional Information on Eligibility for clarification).
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Frequently Asked Questions (FAQs)
What is the Transforming Health Care for Children and Youth with Epilepsy (CYE) Program?
The Transforming Health Care for Children and Youth with Epilepsy (CYE) Program is a discretionary federal grant opportunity offered by the U.S. Department of Health and Human Services (HHS), Health Resources and Services Administration (HRSA). It focuses on improving how children and youth with epilepsy receive care, especially in rural communities and other medically underserved areas.
Which agency is offering this funding opportunity?
This opportunity is offered by HRSA, which is part of HHS.
What is the Funding Opportunity Number (FON) for this grant?
The Funding Opportunity Number is HRSA-19-060.
What is the CFDA number for this program?
The CFDA number listed for this program is 93.110.
What is the main goal of the CYE Program?
The central goal is to expand access to coordinated, high-quality services for children and youth with epilepsy through a patient- and family-centered medical home approach, with particular emphasis on rural and medically underserved settings where specialty care and coordinated systems are often harder to access.
What does a patient- and family-centered medical home approach mean in this program?
In this program, a patient- and family-centered medical home approach means care is intended to be organized, continuous, and built around the needs of the child and family, rather than being fragmented across separate providers. The approach emphasizes coordination and continuity over time.
Why does the program emphasize rural and medically underserved areas?
The program emphasizes these areas because specialty services and coordinated systems of care can be difficult to access in rural or underserved regions. Families may face long travel distances, limited availability of epilepsy specialists, and gaps in care coordination.
What is a key feature of this grant opportunity?
A key feature is the focus on building and supporting quality improvement (QI) networks. HRSA is aiming to strengthen multi-partner networks that can test, measure, and spread better practices across clinical sites and communities, rather than funding isolated projects.
What is meant by a quality improvement (QI) network in this opportunity?
A QI network refers to a multi-partner group of organizations and stakeholders working together to use quality improvement methods to make practical, measurable, and repeatable changes that improve systems of care. The goal is to create improvements that can be maintained and shared across sites and communities.
What kinds of improvements are QI networks expected to work on?
Networks are expected to use QI methods to improve workflows, referral pathways, communication routines, and care coordination, so the overall care system works better for children and youth with epilepsy.
Is the program focused only on providing services?
No. The intent is not only to deliver services, but also to create repeatable improvements that can be maintained and shared, strengthening the broader system of care through quality improvement networks.
What are the four main content areas applicants are expected to address?
Applicants are expected to address four main content areas: (1) increasing access to epilepsy specialists using telehealth and telemedicine, (2) increasing family engagement across the health care system, (3) improving transitions from pediatric to adult health care, and (4) strengthening communication, collaboration, and co-management between primary care providers and epilepsy specialty providers.
How does the program propose increasing access to epilepsy specialists?
The program prioritizes strategies that use telehealth and telemedicine to connect children and youth with epilepsy to specialty expertise. This is intended to reduce travel burden, shorten wait times, and enable faster consultation between local clinicians and specialists.
Why is telehealth a major emphasis in this funding opportunity?
Telehealth is emphasized because many families in rural or underserved regions may live hours away from pediatric neurology or comprehensive epilepsy centers. Telehealth can help improve access to diagnosis support, medication management, seizure control planning, and ongoing follow-up.
What does the program mean by increasing family engagement?
Family engagement in this program goes beyond patient education. It includes meaningful involvement of families in planning, decision-making, and feedback processes, and may include integrating family perspectives into clinic QI efforts and including families in advisory or care-team roles.
How is family engagement expected to improve care?
The broader aim is to make services more responsive, culturally appropriate, and better aligned with what families need to manage epilepsy day to day, by treating families as core members of the care team and incorporating their feedback into system improvements.
What does the program focus on regarding transitions to adult care?
The program seeks to improve transitions from pediatric to adult health care by supporting clearer pathways and supports for adolescents and young adults, including planning, readiness assessment, and coordination between pediatric and adult providers.
Why are pediatric-to-adult transitions highlighted as important?
Transition is described as a high-risk period for youth with chronic neurologic conditions. Gaps in care during this time can contribute to missed appointments, medication issues, reduced adherence, and worsening health outcomes.
What does strengthening co-management between primary care and specialists mean?
It means improving communication, collaboration, and shared responsibility between primary care providers and epilepsy specialty providers so care is not siloed. Examples mentioned include shared care plans, consistent feedback loops after specialist visits, and improved referral and follow-up processes.
Who is the intended population this program aims to benefit?
The program is aimed at improving care for children and youth with epilepsy, with special attention to those living in rural communities or other medically underserved areas.
How much funding is available per award?
The award ceiling is $416,000.
How many awards does HRSA expect to make?
HRSA expects to make approximately seven awards.
When was the opportunity originally posted and when did it close?
The opportunity was originally posted on January 11, 2019, and had an original closing date of April 11, 2019.
What type of grant is this?
It is described as a discretionary federal grant opportunity.
Who is eligible to apply based on the information provided?
Eligibility is listed broadly as "Others," with additional clarification referenced in the full announcement. This suggests organizations beyond typical categories may be eligible depending on HRSA's detailed criteria in the complete funding announcement.
Does the information provided include detailed eligibility requirements?
No. The information provided indicates eligibility is "Others" and notes that additional clarification is in the full announcement, but it does not include the detailed eligibility criteria itself.
What is the overall purpose of this grant opportunity in practical terms?
Overall, the opportunity is aimed at improving the real-world experience of care for children and youth with epilepsy in underserved settings by building QI networks that expand specialty access through telehealth, elevate family engagement, make transitions to adult care safer and more organized, and improve coordination between primary care and specialty services.
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