Birth Defect Research for Children (www.birthdefects.org) has started a new network for heart defect support groups and families who have children with Congenital Heart Defects (CHDs). to provide information about the latest research on the connections between CHDs and environmental exposures. Briefs for new studies will be posted on this site each month. Families and support groups for CHDs are also invited to post their comments.
posted by Birth Defect Research for Children @ 12:35 PM
sponsors this site to provide abstracts of research and news on Agent Orange and Birth Defects. If you would like to share your name and e-mail with other veteran families, please contact betty@birthdefects.org.
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