Opportunity Information: Apply for CDC RFA CK20 2001
The grant opportunity titled "Creutzfeldt-Jakob Disease (CJD) Increasing Educational Support for CJD Families and the Nation" is a discretionary funding announcement from the Centers for Disease Control and Prevention (CDC), specifically under the National Center for Emerging and Zoonotic Infectious Diseases (NCEZID). It is issued as a cooperative agreement, which typically means the CDC expects to have substantial involvement in the funded project beyond simply providing money. The focus of the opportunity is to strengthen educational support related to Creutzfeldt-Jakob Disease for affected families and for the broader public or professional audiences nationwide.
This opportunity is identified by Funding Opportunity Number CDC RFA CK20-2001 and is associated with CFDA Number 93.283. The eligible applicant pool is broad and effectively unrestricted in practice, allowing applications from states, political subdivisions of states, and other public and nonprofit private entities. In other words, state or local health departments, public agencies, universities, nonprofit organizations, and similar entities could potentially apply, as long as they fit within the public or nonprofit categories described.
The funding structure indicates a single expected award, with an award ceiling of $100,000. That combination suggests the CDC intended to support one primary recipient organization to carry out the core educational support activities, likely aiming for a centralized or nationally coordinated approach rather than multiple smaller regional awards. The original closing date for submissions was March 28, 2020, and the opportunity record was created on January 27, 2020.
In practical terms, the aim of a program like this is generally to improve access to accurate, consistent, and usable information about CJD. CJD is a rare, rapidly progressive, and fatal prion disease that creates intense needs for families, caregivers, and clinicians, including guidance on what to expect clinically, how to navigate diagnostic pathways and specialist referrals, what support services are available, and how to address infection control concerns in healthcare settings. Because CJD is uncommon, many healthcare providers and community support systems have limited experience with it, so educational materials and outreach can have outsized impact by reducing confusion, helping families make informed decisions, and supporting appropriate public health responses.
Overall, this CDC cooperative agreement opportunity was designed to fund one organization to enhance educational support capacity related to CJD, with national-level benefit in mind, using up to $100,000 and with eligibility open to governmental entities and nonprofit organizations.Apply for CDC RFA CK20 2001
- The Centers for Disease Control - NCEZID in the health sector is offering a public funding opportunity titled "Creutzfeldt-Jakob Disease (CJD) Increasing Educational Support for CJD Families and the Nation" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.283.
- This funding opportunity was created on 2020-01-27.
- Applicants must submit their applications by 2020-03-28. (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 $100,000.00 in funding.
- The number of recipients for this funding is limited to 1 candidate(s).
- Eligible applicants include: Unrestricted.
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Frequently Asked Questions (FAQs)
What is the name of this grant opportunity?
The opportunity is titled "Creutzfeldt-Jakob Disease (CJD) Increasing Educational Support for CJD Families and the Nation."
Which federal agency is offering this funding?
The funder is the Centers for Disease Control and Prevention (CDC), under the National Center for Emerging and Zoonotic Infectious Diseases (NCEZID).
What type of funding mechanism is this?
This is a cooperative agreement. That generally means CDC expects substantial involvement in the funded project, not just awarding funds and stepping back.
What is the main purpose of the award?
The purpose is to strengthen educational support related to Creutzfeldt-Jakob Disease (CJD) for affected families and for broader nationwide audiences (public and/or professional).
What is the funding opportunity number (FON)?
The Funding Opportunity Number is CDC RFA CK20-2001.
What is the CFDA number associated with this opportunity?
The opportunity is associated with CFDA Number 93.283.
Who is eligible to apply?
Eligibility is broad and effectively unrestricted in practice, allowing applications from states, political subdivisions of states, and other public and nonprofit private entities. Examples that could fit these categories include state or local health departments, public agencies, universities, and nonprofit organizations.
Is this limited to state governments only?
No. The eligible pool includes states and political subdivisions of states, but it also includes other public entities and nonprofit private entities.
Are for-profit organizations eligible to apply?
Based on the eligibility description provided, eligibility is described for public entities and nonprofit private entities. For-profit organizations are not named in the provided eligibility language.
How many awards does CDC expect to make?
CDC expected to make a single award.
What is the maximum award amount (award ceiling)?
The award ceiling is $100,000.
Does the grant appear designed for a national or regional approach?
Based on the single expected award and the educational support goal for families and audiences nationwide, it appears intended to support a centralized or nationally coordinated approach rather than multiple smaller regional awards.
What kinds of activities does this opportunity emphasize?
The emphasis is on improving access to accurate, consistent, and usable information about CJD and strengthening educational support capacity. The description highlights educational support for families, caregivers, clinicians, and other audiences who may have limited experience with CJD due to its rarity.
What needs is this education intended to address?
The opportunity description points to needs such as guidance on what to expect clinically, navigating diagnostic pathways and specialist referrals, understanding available support services, and addressing infection control concerns in healthcare settings.
Why does CDC focus on education for CJD?
CJD is described as rare, rapidly progressive, and fatal. Because it is uncommon, many healthcare providers and community support systems have limited experience with it, so educational materials and outreach can reduce confusion and support informed decision-making and appropriate public health responses.
What was the original application deadline?
The original closing date for submissions was March 28, 2020.
When was the opportunity record created?
The opportunity record was created on January 27, 2020.
Does the announcement describe how CDC will be involved after an award is made?
It does not list specific involvement activities, but it states the mechanism is a cooperative agreement, which typically indicates substantial CDC involvement beyond simply providing money.
Is the opportunity focused on helping families only, or broader audiences too?
It is focused on both. The description specifically references educational support for affected families and for broader public or professional audiences nationwide.
Is this opportunity strictly about research?
The information provided emphasizes educational support and outreach rather than research. The stated focus is strengthening educational support related to CJD.
What does the award size and number of awards suggest about the intended program design?
With one expected award and an award ceiling of $100,000, the structure suggests CDC intended to fund one primary recipient organization to carry out core educational support activities at a national level.
What is CJD in the context of this opportunity?
CJD is described here as a rare, rapidly progressive, and fatal prion disease that creates urgent informational and support needs for families, caregivers, and clinicians.
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