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Hope for HIE - Support for Hypoxic Ischemic Encephalopathy


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Hope for HIE is a worldwide nonprofit organization serving families whose children have been diagnosed with or experienced HIE at birth or sometime during early childhood. We have a comprehensive support network providing much-needed psychosocial support. We are also committed to working with neonatal and postnatal providers to help connect families, participate in any research studies and provide educational materials. 

If you are interested in receiving our materials (we ship them worldwide!), please submit a request to our Vice President of Professional Outreach at http://www.hopeforhie.org/requestmaterials

Please let me know if you have any thoughts of ways you wish to collaborate, or questions that I can answer from this parental perspective.


Betsy Pilon, President, Hope for HIE



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