This is a CDC research program for organizations that already run or partner with specialized spina bifida clinics: component A funds longitudinal data collection in the National Spina Bifida Patient Registry, and component B implements and evaluates the UMPIRE protocol for young children with myelomeningocele. If you are a small business or other organization with no connection to spina bifida patient care or research data, do not bother applying; the money goes to clinics and research groups,
- Best for
- Specialized spina bifida clinics already contributing to the National Spina Bifida Patient Registry, Research organizations and universities that can run longitudinal data collection and analysis, Clinics able to implement and evaluate the UMPIRE protocol for young children with myelomeningocele, Tribal, state, county, and city health or education agencies with access to spina bifida patient populations
- Not for
- Businesses with no connection to spina bifida care, research, or patient data, Organizations without access to a specialized spina bifida clinic or relevant patient population, Applicants seeking general operating funding or unrelated health programs
These are our matcher’s estimates for a typical business in each industry. A real match depends on your size, your state and what you need the money for — check your own fit.