Opportunity Information: Apply for CDC RFA DD11 1105
Apply for CDC RFA DD11 1105
- The Centers for Disease Control and Prevention in the health sector is offering a public funding opportunity titled "Craniofacial Malformations Information for Affected Families, Health Care Providers, and School Professionals" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.073 Birth Defects and Developmental Disabilities Prevention and Surveillance.
- This funding opportunity was created on May 19, 2011 and posted on May 19, 2011.
- Applicants must submit their applications by Jul 18, 2011. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- The funding agency has allocated a total of $900,000.00 to eligible and selected applicants.
- Each selected applicant is eligible to receive up to $300,000.00 in funding.
- The number of recipients for this funding is limited to 2 candidate(s).
- Eligible applicants include: Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled Additional Information on Eligibility.
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Opportunity Summary:
The Centers for Disease Control and Prevention (CDC) offered a discretionary cooperative agreement funding opportunity titled "Craniofacial Malformations Information for Affected Families, Health Care Providers, and School Professionals" (Funding Opportunity Number: CDC RFA DD11-1105). The main goal of this program was to improve how people affected by craniofacial malformations find, understand, and use information and services. In practical terms, the opportunity focused on producing and widely sharing reliable, current resources that help families navigate care, help health care providers deliver appropriate and informed services, and help school professionals better support children in educational settings.
A central purpose of the grant was to develop and disseminate information on strategies that increase access to health care services and reduce or eliminate disparities in access. This emphasis suggests the program was not only about creating educational pamphlets or fact sheets, but also about identifying and promoting real-world approaches that help families obtain needed care. That could include guidance on overcoming common barriers such as limited availability of specialized craniofacial teams, geographic distance from providers, insurance and cost obstacles, language and health literacy challenges, and gaps in care coordination between medical systems and schools. By prioritizing disparities, the program implicitly recognized that some populations may face systematically greater difficulties obtaining timely diagnosis, treatment, follow-up services, and supportive resources.
Another major aim was to develop and disseminate up-to-date educational materials about craniofacial malformations for three specific audiences: affected families, relevant health care providers, and school professionals. The framing indicates an intent to tailor materials to the needs of each group. For families, the materials would likely focus on understandable explanations of conditions, treatment pathways, and available supports, along with practical information for day-to-day decision-making and advocacy. For health care providers, the educational content would be expected to reflect current knowledge and best practices relevant to screening, referral, care coordination, and family-centered communication. For school professionals, the materials would likely address how craniofacial conditions can affect learning, speech, hearing, social experiences, and classroom participation, and how schools can provide appropriate accommodations and supports in collaboration with families and clinicians.
The opportunity aligned with Healthy People 2020 focus areas, specifically Maternal, Infant, and Child Health, Access to Health Services, and Oral Health. That alignment highlights why craniofacial malformations were treated as a public health concern rather than only a specialized clinical topic. Craniofacial conditions often intersect with early childhood development and long-term health outcomes, and many involve dental, orthodontic, and surgical needs as well as speech and hearing services. By explicitly referencing access and oral health, the funding announcement underscored the importance of connecting families to comprehensive services and ensuring that information supports timely and equitable care.
Administratively, this was a CDC cooperative agreement, meaning the agency likely anticipated substantial involvement during the project period, such as collaboration on planning, review of materials, coordination with broader CDC priorities, or shared evaluation expectations. The opportunity was posted on May 19, 2011, with an original and final application closing date of July 18, 2011, and it was later archived on August 17, 2011. The estimated total funding amount was $900,000, with an expected two awards. Individual awards were projected to range from $150,000 (floor) to $300,000 (ceiling). There was no cost sharing or matching requirement, reducing the financial burden on applicants and making participation more feasible for organizations that might not have large pools of unrestricted funds.
Eligibility was listed as unrestricted, meaning it was open to a wide range of entity types, subject to any clarifications in the full announcement. The program fell under CFDA 93.073, "Birth Defects and Developmental Disabilities Prevention and Surveillance," placing it within CDC efforts to address birth defects and developmental disability prevention, surveillance, and public health practice. For applicants or interested parties who had trouble accessing the full announcement, the CDC Procurement and Grants Office, Technical Information and Management Section (TIMS), provided a contact phone number (770-488-2700) for general submission inquiries. No direct additional information link was provided in the source data, and applicants were directed to use the "Full Announcement" area referenced in the posting.
Frequently Asked Questions (FAQs)
What is the title of this CDC funding opportunity?
The opportunity was titled "Craniofacial Malformations Information for Affected Families, Health Care Providers, and School Professionals."
What is the Funding Opportunity Number (FON)?
The Funding Opportunity Number was CDC RFA DD11-1105.
What type of funding mechanism was used?
This was a discretionary cooperative agreement, which generally indicates CDC expected substantial involvement during the project period (for example, collaboration on planning, review of materials, coordination with CDC priorities, and/or shared evaluation expectations).
What was the main goal of the program?
The main goal was to improve how people affected by craniofacial malformations find, understand, and use information and services.
What kinds of activities did the opportunity emphasize?
The opportunity emphasized producing and widely sharing reliable, current resources that help families navigate care, help health care providers deliver appropriate and informed services, and help school professionals better support children in educational settings.
Was this opportunity only about creating educational materials?
No. While educational materials were a major component, a central purpose was also to develop and disseminate information on strategies that increase access to health care services and reduce or eliminate disparities in access. This suggests attention to practical approaches that help families obtain needed care, not just general information products.
What does "reducing disparities in access" mean in the context of this program?
Based on the description, it refers to improving access to needed care for groups that face systematically greater barriers to timely diagnosis, treatment, follow-up services, and supportive resources. The opportunity highlighted barriers such as limited availability of specialized craniofacial teams, geographic distance, insurance and cost obstacles, language and health literacy challenges, and gaps in care coordination between medical systems and schools.
Who were the intended audiences for the educational materials?
The program identified three specific audiences: (1) affected families, (2) relevant health care providers, and (3) school professionals.
What types of information were materials for families expected to cover?
The description indicates family-focused materials would likely include understandable explanations of conditions, treatment pathways, and available supports, along with practical information to support day-to-day decision-making and advocacy.
What types of information were materials for health care providers expected to cover?
The description indicates provider-focused materials would be expected to reflect current knowledge and best practices relevant to screening, referral, care coordination, and family-centered communication.
What types of information were materials for school professionals expected to cover?
The description indicates school-focused materials would likely address how craniofacial conditions can affect learning, speech, hearing, social experiences, and classroom participation, and how schools can provide appropriate accommodations and supports in collaboration with families and clinicians.
How did this opportunity relate to Healthy People 2020?
It aligned with Healthy People 2020 focus areas including Maternal, Infant, and Child Health; Access to Health Services; and Oral Health.
Why was oral health specifically relevant to this opportunity?
The opportunity description noted that many craniofacial conditions involve dental, orthodontic, and surgical needs, as well as speech and hearing services, underscoring the importance of connecting families to comprehensive services and supporting timely, equitable care.
When was the opportunity posted?
It was posted on May 19, 2011.
What were the application due dates?
The original and final application closing date was July 18, 2011.
When was the opportunity archived?
It was archived on August 17, 2011.
What was the estimated total funding amount?
The estimated total funding amount was $900,000.
How many awards were expected?
The opportunity anticipated two awards.
What was the projected funding range per award?
Individual awards were projected to range from $150,000 (floor) to $300,000 (ceiling).
Was there a cost-sharing or matching requirement?
No. The opportunity specified there was no cost sharing or matching requirement.
Who was eligible to apply?
Eligibility was listed as unrestricted, meaning it was open to a wide range of entity types (subject to any clarifications that may have been included in the full announcement).
What CFDA number was associated with this funding?
The program fell under CFDA 93.073, "Birth Defects and Developmental Disabilities Prevention and Surveillance."
What broader CDC program area did this opportunity fit within?
Based on CFDA 93.073, it fit within CDC efforts related to birth defects and developmental disabilities prevention, surveillance, and public health practice.
Where were applicants directed for full details?
Applicants were directed to use the "Full Announcement" area referenced in the posting. No direct additional information link was provided in the source data.
Who could be contacted for submission-related questions if someone had trouble accessing the full announcement?
The CDC Procurement and Grants Office, Technical Information and Management Section (TIMS) was listed for general submission inquiries at 770-488-2700.
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