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

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A Surreal Beginning

A Surreal Beginning

April 8th, 2021  | Family Stories  |  By Naomi Lichtenstein Shicker

Up until 2.5 years ago, I, like most people, had never heard of HIE. Since April is HIE Awareness month, I decided to write a little about our experience. It was Sunday, October 7, 2018. Once again, I hadn’t felt the baby moving. I drove to the hospital to get monitored, thinking it would be like the last few times […]

Just Say HIE Podcast Launches

Just Say HIE Podcast Launches

April 5th, 2021

We are excited to share that the first episode of our new Just Say HIE podcast has been published! Episode 1 is with our own Annie Goeller, long time Board of Directors member, communication and marketing guru, and crafter, grower and nurturer of HIE Awareness Month! The podcast has been picked up and is available on Spotify, Amazon and will […]

Finding Hope: HIE Awareness Month Reflection

Finding Hope: HIE Awareness Month Reflection

April 5th, 2021  | Family Stories

Hope for HIE *The first year * As days passed by, we were still waiting for big things to happen. Eliana still hadn’t cried, opened her eyes or even showed signs of a suck/swallow reflex. This was hard. She still wasn’t holding her own temperature and they were trying to get her sodium levels balanced. She had so much happening. […]

HIE Awareness Month – Team Swag

HIE Awareness Month – Team Swag

March 9th, 2021

April is HIE Awareness Month! Get in on the theme of TEAM HOPE and grab some swag to help promote awareness, education and support! Adult & Kid Sizes  Infant & Toddler Sizes Car & Home Items

Welcoming Crystal Kostick to the Board of Directors

Welcoming Crystal Kostick to the Board of Directors

March 8th, 2021  | Advocacy

We are excited to announce that Crystal Kostick has joined the Hope for HIE Board of Directors. As a long time “super volunteer” at Hope, Crystal has been a member of the retreat planning committee, has served as a moderator of our Colorado subgroup, attended the 2019 Child Neurology Foundation Peer-to-Peer Support Training representing the organization, and has worked to […]

SHARE YOUR HIE STORY

One of the ways many HIE families work through the trauma of their journey is sharing their story to help other families who will find us in their own HIE journey. We hope you’ll take a few minutes and share yours with us. We’ll publish it to our Family Stories blog!

Share Your Story

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