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National Minority Health Month--Using Data for Advocacy
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The DRC is a project of the CAHMI supported by the Health Resources and Services Administration, Maternal and Child Health Bureau.

Access New Online Data from the 2009-10 National Survey of Children with Special Health Care Needs

April is National Minority Health Month. In honor of this year's theme--"Health Equity Can't Wait. Act Now in Your Community"--the Data Resource Center for Child and Adolescent Health (DRC) announces new data available on our website. In order to better understand and advocate for minority children with special health care needs (CSHCN), the DRC website lets you compare important key indicators and outcomes for CSHCN by race/ethnicity, highest educational level in the household, and two new measures of complexity. Here are a few examples of findings you can access on the DRC website:

  • Among the 46% of CSHCN who experience 4 or more functional difficulties, only half have access to community based services
  • The 14% of CSHCN who meet 4 or more qualifying CSHCN Screener criteria are half as likely to experience quality care within a medical home as those whose conditions are less complex
  • Hispanic CSHCN are most likely to lack insurance coverage

 

 

existUsing Data to Reduce and Eliminate Health Disparities

 

Disparities continue to exist in the health status of minority CSHCN in the United States. Data showing the differences in health status and access to care among minority children in the United States are an important tool in eliminating disparities and improving the health and well-being of all children.

 

Recently released data from the 2009-10 National Survey of Children with Special Health Care Needs reveal that: 

For additional information on disparities among all children, please visit the race/ethnicity 2007 NSCH Disparities Profile.

 

 

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