Research Approaches to Improve the Care and Outcomes of People Living with Spina Bifida

The purpose of this funding opportunity is to identify health care and clinic practices that are associated with the best outcomes for people living with spina bifida (SB) and to communicate and encourage adoption of best practices by SB clinics including providing needed educational/informational resources


for the SB patient and provider communities, health care professionals, families, and educators.
Related Programs

Rare Disorders: Research, Surveillance, Health Promotion, and Education

Department of Health and Human Services

Agency: Department of Health and Human Services

Office: Centers for Disease Control and Prevention - ERA

Estimated Funding: $1,736,500

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Other Eligible Applicants include the following: Alaska Native and Native Hawaiian Serving Institutions; Eligible Agencies of the Federal Government; Faith-based or Community-based Organizations; Hispanic-serving Institutions; Historically Black Colleges and Universities (HBCUs); Indian/Native American Tribal Governments (Other than Federally Recognized); Regional Organizations; Tribally Controlled Colleges and Universities (TCCUs) ; U. S. Territory or Possession.

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