Hope for HIE is a wonderful organization full of other dedicated families in similar situations. Every day new parents join on Facebook or read this website full of questions, uncertainty, and searching for hope. Maybe you got here because you searched for “What is HIE? Hypoxic-Ischemic Encephalopathy.” I feel like I’ve gained some perspective on what our process was like regardless […]
A devastating loss suffered by two families brought them closer together than they could have ever imagined. Becky and Krista connected through Hope for HIE’s online forums over the loss of their children to HIE. They got even closer when discussing the fears of having another baby after the trauma they had both had in their previous birth experiences. They […]
For families of children with an HIE diagnosis, the journey can be lonely. Often, other families don’t look like ours. Their lives aren’t the same. Their routines are different. Hope for HIE has been organizing retreats focused on moms for the last four years, which for so many women have been life-changing, giving them a chance to connect with moms […]
We bet you can’t look at this photo without smiling. HIE kiddo Remi got to try her hand at skiing with an adaptive ski program. And she had a blast! Remi’s mom heard about the program when they went to a ski show at the beach. Her husband insisted they sign Remi up. Jamie was nervous at first, but then […]
After the loss of her son Carter, Kelli Durham wanted to do something to keep his memory alive. She decided one of the best ways to do that was to donate in his honor. “I wanted his life/memory to be as impactful to other people as it was to me,” Kelli said. And immediately Hope for HIE came to mind. […]
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