Here's an announcement of a webinar on on children's health data you might want to attend:
DataSpeak: New Findings from the 2007 NSCH
The MCH Information Resource Center, funded by the Maternal and Child Health Bureau at the Health Resources and Services Administration (HRSA), is pleased to announce the next program in the DataSpeak Series: "New Findings from the 2007 National Survey of Children's Health (NSCH).
"This will be one of the very first presentations on the results of this important survey. The NSCH, funded and directed by MCHB, administered by the National Center for Health Statistics and disseminated on the Data Resource Center website, examines the physical and emotional health of children from birth through 17 years of age. Emphasis is placed on factors that may be related to the well-being of children, including medical homes, family interactions, parental health, school experiences, and neighborhood safety.
This Web conference will provide an overview of the survey methodology, discuss potential applications of the survey as well as selected findings, and provide information about accessing National- and State-level survey data online and highlight key State-level survey results.
Details and Registration
This program will take place on Tuesday, June 2, 2009, 2:00 - 3:00 p.m. ET (1pm Central, 12noon Mountain, 11am Pacific). For full program details, please visit the MCHIRC Web site at: http://www.mchb.hrsa.gov/mchirc/dataspeak/events/2009/0602/index.htm
To register for this event, please go to DataSpeak registration at:http://www.mchb.hrsa.gov/mchirc/dataspeak/register.htm
When you register, you will receive the details on how to participate in the Web conference. There is no cost to participate in this program.If you have any questions at all, please contact MCHIRC at email@example.com , or 202-842-2000.
About the Data Resource Center
The CAHMI Data Resource Center (DRC) website is a user-friendly and interactive resource that offers users immediate access to standardized results from the NSCH and the National Survey of Children with Special Health Care Needs datasets. The overarching goal of the DRC is to advance evidence-based program planning, evaluation, policy and advocacy. DRC users can view state-level summary profiles, generate rankings across all states, and interactively produce downloadable tables and graphs. The DRC website also provides tools and resources to help users learn about, interpret and present data findings. The website is designed to meet the needs of people with data skills of all levels - from beginning to advanced. Expert help from DRC staff is readily available by email: firstname.lastname@example.org or phone: (503) 494-1930.