Hope for HIE – Hypoxic Ischemic Encephalopathy Hope for HIE – Hypoxic Ischemic Encephalopathy



Every day, we face questions and search for answers that will help us on our HIE journey. Whether you’re new to HIE, or a seasoned veteran, our resource area is a great place to find helpful information.

Our resources will help you think about the questions to ask, and the choices and options to consider on your HIE journey.

Here, you’ll find tools, links to local resources and maybe even a few tips/tricks to make life easier. All of our content is gathered, written and developed by other HIE parents and family members.

Please remember that not all information will be specific to you or your family. These resources shouldn’t replace any medical advice or direction you may receive from your professional caregiving team. This is simply a place where we can share our resources and develop a listing of everything from therapies to educational reading and self care.


Posts are updated regularly and are sent in by HIE parents all over the world. Do you like to write? Have a topic you have some knowledge/experience with?

Resource Blog

Want to tell us your story? E-mail our Website Manager.


Handouts, flyers and contact cards you can pass along to your local hospital, social worker/case manager, education advocate or medical professional. In the meantime, be sure to ask your providers to add Hope for HIE’s website to their resource directory so more families can find us!

Printable Resources


We’ve worked to bring together a comprehensive hub to learn more about participating in clinical trials and research studies, active trials, and the latest research.

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