HIE Support & Educational Resources

Hope for HIE is the premiere global organization dedicated to improving the quality of life for children and families impacted by HIE - hypoxic ischemic encephalopathy. The organization hosts a comprehensive support network for families, 6000+ strong and growing every day, and continuously publishes new educational materials for explaining HIE that clinicians can use with families, and hosted Q&A's with Hope for HIE's Medical Advisory Board. 

• Resources for clinicians and researchers
• HIE overview for newly diagnosed families
• HIE NICU overview translated into six languages
• Newly diagnosed support boxes and printable materials request form (all free to clinicians)

April is global HIE Awareness Month. A comprehensive toolkit, links to events, and other resources can be found at HIEawarenessmonth.com.

Questions? Feel free to email Betsy Pilon, Executive Director at betsy@hopeforhie.org.