- Who We Are
- What is HIE?
- For Parents
- For Clinicians & Partners
- Get Involved
We’re continuously building out more resources to help educate HIE families, clinicians and researchers. We are happy to provide these free of charge in print to any NICU, PICU, clinic or other support entity that interfaces with HIE families.
We also offer newly diagnosed family support boxes for NICU and PICU distribution.
If you would like to request printed materials, free of charge for your clinic or hospital, click below:
If the form does not populate due to restrictions from your healthcare system internet provider, please email your request to us.
We have created an educational piece for families to be used during the NICU experience. This includes our HIE NICU timeline, developed in conjunction with our Medical Advisory Board.
Medical offices and hospitals typically have places for their physicians, nurses, nurse practitioners and other staff to display information on supporting services and organizations. Use this front and back card to communicate the importance of referring families to Hope for HIE.
Print this one page informational flyer and use to educate anyone who may be curious about HIE, the causes and how it is typically treated.
Feel free to share, download or print this graphic that explains more of how the brain functions.
We’re sharing the most common diagnoses that come from HIE, as well as the time that most families whose children experience these may get a diagnosis.
The basics on the connection, incidence and treatment of Infantile Spasms and HIE.
Educational materials written to be handed out to families whose children are at-risk for developing Infantile Spasms.
Educational materials written for providers (pediatricians, family practice physicians, pediatric neurologists) on ways to communicate with patients about Infantile Spasms.
As a part of the PCORI-funded Neonatal Seizure Registry project, we are happy to share additional materials created through this initiative.
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