Opportunity Information: Apply for CDC RFA DP16 1602
The Centers for Disease Control and Prevention (CDC), through its National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), released this FY16 cooperative agreement funding opportunity to strengthen epilepsy-related programs, services, and outcomes by working through national partnerships. The opportunity recognizes epilepsy as a chronic neurological condition involving recurrent seizures, affecting an estimated 2.9 million people in the United States with active epilepsy (meaning physician-diagnosed epilepsy that is currently being treated or includes at least one seizure in the past year). The CDC frames epilepsy not only as a medical issue, but also as a major public health and equity issue, since people with epilepsy often have multiple other chronic conditions, are more likely to live in lower-income households, report disability at higher rates, and experience reduced health-related quality of life. The burden is also economic, with epilepsy associated with an estimated $15.5 billion each year in medical costs plus lost or reduced earnings and productivity.
A major problem highlighted in the announcement is the gap between need and appropriate clinical care. Using 2010 National Health Interview Survey findings, CDC notes that only 57.7% of adults with epilepsy and uncontrolled seizures received appropriate care in the sense of seeing a neurologist or epilepsy specialist. The CDC links delayed recognition of seizures and inadequate treatment to serious consequences such as continued seizures, injuries, disability, possible brain damage, and increased risk of early death. In other words, the FOA is motivated by the idea that better-connected systems, better-trained providers, and stronger community supports can change real outcomes for people living with a complex condition.
The announcement also stresses that epilepsy remains widely recognized but poorly understood, even among people who personally know someone with epilepsy. While overt negative stereotypes have declined over time, CDC points out that many people still do not know basic seizure first aid and often report fear and safety concerns about being around someone who has seizures. That lack of understanding fuels stigma, which can isolate people with epilepsy and limit participation in everyday life such as school, work, and community activities. Because of this, the FOA treats public education and stigma reduction as central outcome areas rather than optional add-ons.
The opportunity is closely tied to the Institute of Medicine (IOM) 2012 report, "Epilepsy Across the Spectrum: Promoting Health and Understanding," which documented national gaps and proposed 13 recommendations for action. CDC indicates it has a key role in 12 of those recommendations, including improving education for health professionals, improving the delivery and coordination of community services, engaging media to increase accurate awareness and reduce stigma, and expanding education for people with epilepsy and their families. The FOA reflects that roadmap and was also shaped by feedback gathered from more than a dozen stakeholder groups during the agency's engagement process, signaling that CDC expects a broad, partnership-driven approach rather than isolated projects.
Programmatically, the FOA supports three core public health functions applied to epilepsy: building workforce competency (so professionals and systems are better prepared to respond to epilepsy-related needs), mobilizing community partnerships and actions (so services and supports are coordinated and accessible), and educating and empowering people about epilepsy (so individuals, families, and the public have practical knowledge, confidence, and tools). These functions are intended to work together, with national partners acting as catalysts that can influence practice, service delivery, and public understanding at scale.
The long-term goals described are concrete and outcome-oriented: increasing the number of people with epilepsy who receive appropriate and timely medical care; improving social participation such as employment and school attendance; decreasing public stigma; and ultimately improving health and quality of life for people with epilepsy. The funding mechanism is a discretionary cooperative agreement, meaning CDC expects to have substantial involvement with awardees in shaping, monitoring, and supporting the work rather than simply issuing funds with minimal interaction.
Key administrative details include the funding opportunity title "Improving Epilepsy Programs, Services, and Outcomes through National Partnerships," funding opportunity number CDC-RFA-DP16-1602, and CFDA number 93.850. Eligibility is listed as unrestricted, which generally means a wide range of organizations may apply if they can meet the program and administrative requirements. The original application closing date was April 7, 2016. CDC anticipated making 2 awards, with an award ceiling of $4,000,000, indicating large, nationally oriented projects designed to influence systems, partnerships, and public impact rather than small local demonstrations.Apply for CDC RFA DP16 1602
- The Centers for Disease Control - NCCDPHP in the health sector is offering a public funding opportunity titled "Improving Epilepsy Programs, Services, and Outcomes through National Partnerships" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.850.
- This funding opportunity was created on 2015-12-03.
- Applicants must submit their applications by 2016-04-07. (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 $4,000,000.00 in funding.
- The number of recipients for this funding is limited to 2 candidate(s).
- Eligible applicants include: Unrestricted.
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